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Erschienen in: Clinical & Experimental Metastasis 2/2020

23.01.2020 | Review

Toll-like receptors: exploring their potential connection with post-operative infectious complications and cancer recurrence

verfasst von: S. D. Gowing, J. J. Cool-Lartigue, J. D. Spicer, A. J. E. Seely, L. E. Ferri

Erschienen in: Clinical & Experimental Metastasis | Ausgabe 2/2020

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Abstract

Cancer is the leading cause of death in North America. Despite modern advances in cancer therapy, many patients will ultimately develop cancer metastasis resulting in mortality. Surgery to resect early stage solid malignancies remains the cornerstone of cancer treatment. However, surgery places patients at risk of developing post-operative infectious complications that are linked to earlier cancer metastatic recurrence and cancer mortality. Toll-like receptors (TLRs) are evolutionarily-conserved sentinel receptors of the innate immune system that are activated by microbial products present during infection, leading to activation of innate immunity. Numerous types of solid cancer cells also express TLRs, with their activation augmenting their ability to metastasize. Similarly, healthy host-tissue TLRs activated during infection induce a prometastatic environment in the host. Cancer cells additionally secrete TLR activating ligands that activate both cancer TLRs and host TLRs to promote metastasis. Consequently, TLRs are an attractive therapeutic candidate to target infection-induced cancer metastasis and progression.
Literatur
1.
Zurück zum Zitat Miller KD, Siegel RL, Lin CC et al (2016) Cancer treatment and survivorship statistics, 2016. CA Cancer J Clin 66:271–289PubMedCrossRef Miller KD, Siegel RL, Lin CC et al (2016) Cancer treatment and survivorship statistics, 2016. CA Cancer J Clin 66:271–289PubMedCrossRef
2.
Zurück zum Zitat Statistics CCSsACoC (2017) Canadian cancer statistics 2017. Canadian Cancer Society, Ontario Statistics CCSsACoC (2017) Canadian cancer statistics 2017. Canadian Cancer Society, Ontario
3.
4.
Zurück zum Zitat Nguyen DX, Bos PD, Massague J (2009) Metastasis: from dissemination to organ-specific colonization. Nat Rev Cancer 9:274–284PubMedCrossRef Nguyen DX, Bos PD, Massague J (2009) Metastasis: from dissemination to organ-specific colonization. Nat Rev Cancer 9:274–284PubMedCrossRef
5.
Zurück zum Zitat Takeuchi H, Saikawa Y, Oyama T et al (2010) Factors influencing the long-term survival in patients with esophageal cancer who underwent esophagectomy after chemoradiotherapy. World J Surg 34:277–284PubMedCrossRef Takeuchi H, Saikawa Y, Oyama T et al (2010) Factors influencing the long-term survival in patients with esophageal cancer who underwent esophagectomy after chemoradiotherapy. World J Surg 34:277–284PubMedCrossRef
6.
Zurück zum Zitat Andreou A, Aloia TA, Brouquet A et al (2013) Margin status remains an important determinant of survival after surgical resection of colorectal liver metastases in the era of modern chemotherapy. Ann Surg 257:1079PubMedCrossRef Andreou A, Aloia TA, Brouquet A et al (2013) Margin status remains an important determinant of survival after surgical resection of colorectal liver metastases in the era of modern chemotherapy. Ann Surg 257:1079PubMedCrossRef
7.
Zurück zum Zitat Matull WR, Dhar DK, Ayaru L et al (2011) R0 but not R1/R2 resection is associated with better survival than palliative photodynamic therapy in biliary tract cancer. Liver Int 31:99–107PubMedCrossRef Matull WR, Dhar DK, Ayaru L et al (2011) R0 but not R1/R2 resection is associated with better survival than palliative photodynamic therapy in biliary tract cancer. Liver Int 31:99–107PubMedCrossRef
8.
Zurück zum Zitat Khan O, Goh S, Byrne B et al (2011) Long-term outcomes of extended proximal gastrectomy for oesophagogastric junctional tumours. World J Surg 35:2245–2251PubMedCrossRef Khan O, Goh S, Byrne B et al (2011) Long-term outcomes of extended proximal gastrectomy for oesophagogastric junctional tumours. World J Surg 35:2245–2251PubMedCrossRef
9.
10.
Zurück zum Zitat Uramoto H, Tanaka F (2012) Prediction of recurrence after complete resection in patients with NSCLC. Anticancer Res 32:3953–3960PubMed Uramoto H, Tanaka F (2012) Prediction of recurrence after complete resection in patients with NSCLC. Anticancer Res 32:3953–3960PubMed
11.
Zurück zum Zitat Sawabata N, Okumura M, Utsumi T et al (2007) Circulating tumor cells in peripheral blood caused by surgical manipulation of non-small-cell lung cancer: pilot study using an immunocytology method. Gen Thorac Cardiovasc Surg 55:189–192PubMedCrossRef Sawabata N, Okumura M, Utsumi T et al (2007) Circulating tumor cells in peripheral blood caused by surgical manipulation of non-small-cell lung cancer: pilot study using an immunocytology method. Gen Thorac Cardiovasc Surg 55:189–192PubMedCrossRef
12.
Zurück zum Zitat Pesta M, Fichtl J, Kulda V et al (2013) Monitoring of circulating tumor cells in patients undergoing surgery for hepatic metastases from colorectal cancer. Anticancer Res 33:2239–2243PubMed Pesta M, Fichtl J, Kulda V et al (2013) Monitoring of circulating tumor cells in patients undergoing surgery for hepatic metastases from colorectal cancer. Anticancer Res 33:2239–2243PubMed
13.
Zurück zum Zitat Papavasiliou P, Fisher T, Kuhn J et al (2010) Circulating tumor cells in patients undergoing surgery for hepatic metastases from colorectal cancer. Proc (Bayl Univ Med Cent) 23:11–14CrossRef Papavasiliou P, Fisher T, Kuhn J et al (2010) Circulating tumor cells in patients undergoing surgery for hepatic metastases from colorectal cancer. Proc (Bayl Univ Med Cent) 23:11–14CrossRef
14.
Zurück zum Zitat Fidler IJ (1970) Metastasis: quantitative analysis of distribution and fate of tumor emboli labeled with 125 I-5-iodo-2′-deoxyuridine. J Natl Cancer Inst 45:773–782PubMed Fidler IJ (1970) Metastasis: quantitative analysis of distribution and fate of tumor emboli labeled with 125 I-5-iodo-2′-deoxyuridine. J Natl Cancer Inst 45:773–782PubMed
15.
Zurück zum Zitat Tsubura E, Yamashita T, Sone S (1983) Inhibition of the arrest of hematogenously disseminated tumor cells. Cancer Metastasis Rev 2:223–237PubMedCrossRef Tsubura E, Yamashita T, Sone S (1983) Inhibition of the arrest of hematogenously disseminated tumor cells. Cancer Metastasis Rev 2:223–237PubMedCrossRef
16.
17.
Zurück zum Zitat Groot Koerkamp B, Rahbari NN, Buchler MW et al (2013) Circulating tumor cells and prognosis of patients with resectable colorectal liver metastases or widespread metastatic colorectal cancer: a meta-analysis. Ann Surg Oncol 20:2156–2165PubMedCrossRef Groot Koerkamp B, Rahbari NN, Buchler MW et al (2013) Circulating tumor cells and prognosis of patients with resectable colorectal liver metastases or widespread metastatic colorectal cancer: a meta-analysis. Ann Surg Oncol 20:2156–2165PubMedCrossRef
18.
Zurück zum Zitat Neki K, Kawahara H, Watanabe K et al (2013) Usefulness of circulating tumor cells after preliminary chemotherapy for prediction of response to further anticancer therapy in patients with initially unresectable metastatic colorectal cancer. Anticancer Res 33:1769–1772PubMed Neki K, Kawahara H, Watanabe K et al (2013) Usefulness of circulating tumor cells after preliminary chemotherapy for prediction of response to further anticancer therapy in patients with initially unresectable metastatic colorectal cancer. Anticancer Res 33:1769–1772PubMed
19.
Zurück zum Zitat Rahbari NN, Reissfelder C, Muhlbayer M et al (2011) Correlation of circulating angiogenic factors with circulating tumor cells and disease recurrence in patients undergoing curative resection for colorectal liver metastases. Ann Surg Oncol 18:2182–2191PubMedCrossRef Rahbari NN, Reissfelder C, Muhlbayer M et al (2011) Correlation of circulating angiogenic factors with circulating tumor cells and disease recurrence in patients undergoing curative resection for colorectal liver metastases. Ann Surg Oncol 18:2182–2191PubMedCrossRef
20.
Zurück zum Zitat Nespoli A, Gianotti L, Bovo G et al (2006) Impact of postoperative infections on survival in colon cancer patients. Surg Infect (Larchmt) 7(Suppl 2):S41–43CrossRef Nespoli A, Gianotti L, Bovo G et al (2006) Impact of postoperative infections on survival in colon cancer patients. Surg Infect (Larchmt) 7(Suppl 2):S41–43CrossRef
21.
Zurück zum Zitat Radu DM, Jaureguy F, Seguin A et al (2007) Postoperative pneumonia after major pulmonary resections: an unsolved problem in thoracic surgery. Ann Thorac Surg 84:1669–1673PubMedCrossRef Radu DM, Jaureguy F, Seguin A et al (2007) Postoperative pneumonia after major pulmonary resections: an unsolved problem in thoracic surgery. Ann Thorac Surg 84:1669–1673PubMedCrossRef
22.
Zurück zum Zitat Schussler O, Alifano M, Dermine H et al (2006) Postoperative pneumonia after major lung resection. Am J Respir Crit Care Med 173:1161–1169PubMedCrossRef Schussler O, Alifano M, Dermine H et al (2006) Postoperative pneumonia after major lung resection. Am J Respir Crit Care Med 173:1161–1169PubMedCrossRef
23.
Zurück zum Zitat Pisters PW, Hudec WA, Hess KR et al (2001) Effect of preoperative biliary decompression on pancreaticoduodenectomy-associated morbidity in 300 consecutive patients. Ann Surg 234:47–55PubMedPubMedCentralCrossRef Pisters PW, Hudec WA, Hess KR et al (2001) Effect of preoperative biliary decompression on pancreaticoduodenectomy-associated morbidity in 300 consecutive patients. Ann Surg 234:47–55PubMedPubMedCentralCrossRef
24.
Zurück zum Zitat Matsuo K, Prather CP, Ahn EH et al (2012) Significance of perioperative infection in survival of patients with ovarian cancer. Int J Gynecol Cancer 22:245–253PubMedCrossRef Matsuo K, Prather CP, Ahn EH et al (2012) Significance of perioperative infection in survival of patients with ovarian cancer. Int J Gynecol Cancer 22:245–253PubMedCrossRef
25.
Zurück zum Zitat Andalib A, Ramana-Kumar AV, Bartlett G et al (2013) Influence of postoperative infectious complications on long-term survival of lung cancer patients: a population-based cohort study. J Thorac Oncol 8:554–561PubMedCrossRef Andalib A, Ramana-Kumar AV, Bartlett G et al (2013) Influence of postoperative infectious complications on long-term survival of lung cancer patients: a population-based cohort study. J Thorac Oncol 8:554–561PubMedCrossRef
26.
Zurück zum Zitat Kinugasa S, Tachibana M, Yoshimura H et al (2004) Postoperative pulmonary complications are associated with worse short- and long-term outcomes after extended esophagectomy. J Surg Oncol 88:71–77PubMedCrossRef Kinugasa S, Tachibana M, Yoshimura H et al (2004) Postoperative pulmonary complications are associated with worse short- and long-term outcomes after extended esophagectomy. J Surg Oncol 88:71–77PubMedCrossRef
27.
Zurück zum Zitat Tsujimoto H, Ichikura T, Ono S et al (2009) Impact of postoperative infection on long-term survival after potentially curative resection for gastric cancer. Ann Surg Oncol 16:311–318PubMedCrossRef Tsujimoto H, Ichikura T, Ono S et al (2009) Impact of postoperative infection on long-term survival after potentially curative resection for gastric cancer. Ann Surg Oncol 16:311–318PubMedCrossRef
28.
Zurück zum Zitat Tokunaga M, Tanizawa Y, Bando E et al (2013) Poor survival rate in patients with postoperative intra-abdominal infectious complications following curative gastrectomy for gastric cancer. Ann Surg Oncol 20:1575–1583PubMedCrossRef Tokunaga M, Tanizawa Y, Bando E et al (2013) Poor survival rate in patients with postoperative intra-abdominal infectious complications following curative gastrectomy for gastric cancer. Ann Surg Oncol 20:1575–1583PubMedCrossRef
29.
Zurück zum Zitat Tan HJ, Hafez KS, Ye Z et al (2012) Postoperative complications and long-term survival among patients treated surgically for renal cell carcinoma. J Urol 187:60–66PubMedCrossRef Tan HJ, Hafez KS, Ye Z et al (2012) Postoperative complications and long-term survival among patients treated surgically for renal cell carcinoma. J Urol 187:60–66PubMedCrossRef
30.
Zurück zum Zitat Walker KG, Bell SW, Rickard MJ et al (2004) Anastomotic leakage is predictive of diminished survival after potentially curative resection for colorectal cancer. Ann Surg 240:255–259PubMedPubMedCentralCrossRef Walker KG, Bell SW, Rickard MJ et al (2004) Anastomotic leakage is predictive of diminished survival after potentially curative resection for colorectal cancer. Ann Surg 240:255–259PubMedPubMedCentralCrossRef
31.
Zurück zum Zitat Nespoli A, Gianotti L, Totis M et al (2004) Correlation between postoperative infections and long-term survival after colorectal resection for cancer. Tumori 90:485–490PubMedCrossRef Nespoli A, Gianotti L, Totis M et al (2004) Correlation between postoperative infections and long-term survival after colorectal resection for cancer. Tumori 90:485–490PubMedCrossRef
32.
Zurück zum Zitat den Dulk M, Marijnen CA, Collette L et al (2009) Multicentre analysis of oncological and survival outcomes following anastomotic leakage after rectal cancer surgery. Br J Surg 96:1066–1075CrossRef den Dulk M, Marijnen CA, Collette L et al (2009) Multicentre analysis of oncological and survival outcomes following anastomotic leakage after rectal cancer surgery. Br J Surg 96:1066–1075CrossRef
33.
Zurück zum Zitat Lin JK, Yueh TC, Chang SC et al (2011) The influence of fecal diversion and anastomotic leakage on survival after resection of rectal cancer. J Gastrointest Surg 15:2251–2261PubMedCrossRef Lin JK, Yueh TC, Chang SC et al (2011) The influence of fecal diversion and anastomotic leakage on survival after resection of rectal cancer. J Gastrointest Surg 15:2251–2261PubMedCrossRef
34.
Zurück zum Zitat Indelicato D, Grobmyer SR, Newlin H et al (2007) Association between operative closure type and acute infection, local recurrence, and disease surveillance in patients undergoing breast conserving therapy for early-stage breast cancer. Surgery 141:645–653PubMedCrossRef Indelicato D, Grobmyer SR, Newlin H et al (2007) Association between operative closure type and acute infection, local recurrence, and disease surveillance in patients undergoing breast conserving therapy for early-stage breast cancer. Surgery 141:645–653PubMedCrossRef
35.
Zurück zum Zitat Murthy BL, Thomson CS, Dodwell D et al (2007) Postoperative wound complications and systemic recurrence in breast cancer. Br J Cancer 97:1211–1217PubMedPubMedCentralCrossRef Murthy BL, Thomson CS, Dodwell D et al (2007) Postoperative wound complications and systemic recurrence in breast cancer. Br J Cancer 97:1211–1217PubMedPubMedCentralCrossRef
36.
Zurück zum Zitat Rueth NM, Parsons HM, Habermann EB et al (2011) The long-term impact of surgical complications after resection of stage I nonsmall cell lung cancer: a population-based survival analysis. Ann Surg 254:368–374PubMedCrossRef Rueth NM, Parsons HM, Habermann EB et al (2011) The long-term impact of surgical complications after resection of stage I nonsmall cell lung cancer: a population-based survival analysis. Ann Surg 254:368–374PubMedCrossRef
37.
Zurück zum Zitat Lerut T, Moons J, Coosemans W et al (2009) Postoperative complications after transthoracic esophagectomy for cancer of the esophagus and gastroesophageal junction are correlated with early cancer recurrence: role of systematic grading of complications using the modified Clavien classification. Ann Surg 250:798–807PubMedCrossRef Lerut T, Moons J, Coosemans W et al (2009) Postoperative complications after transthoracic esophagectomy for cancer of the esophagus and gastroesophageal junction are correlated with early cancer recurrence: role of systematic grading of complications using the modified Clavien classification. Ann Surg 250:798–807PubMedCrossRef
38.
Zurück zum Zitat Hayashi T, Yoshikawa T, Aoyama T et al (2015) Impact of infectious complications on gastric cancer recurrence. Gastric Cancer 18:368–374PubMedCrossRef Hayashi T, Yoshikawa T, Aoyama T et al (2015) Impact of infectious complications on gastric cancer recurrence. Gastric Cancer 18:368–374PubMedCrossRef
39.
Zurück zum Zitat Ohtsuka T, Kitajima Y, Takahashi T et al (2009) Infectious complications after gastric cancer surgery accelerate a rapid hepatic recurrence. Hepatogastroenterology 56:1277–1280PubMed Ohtsuka T, Kitajima Y, Takahashi T et al (2009) Infectious complications after gastric cancer surgery accelerate a rapid hepatic recurrence. Hepatogastroenterology 56:1277–1280PubMed
40.
Zurück zum Zitat Tsujimoto H, Ueno H, Hashiguchi Y et al (2010) Postoperative infections are associated with adverse outcome after resection with curative intent for colorectal cancer. Oncol Lett 1:119–125PubMedPubMedCentralCrossRef Tsujimoto H, Ueno H, Hashiguchi Y et al (2010) Postoperative infections are associated with adverse outcome after resection with curative intent for colorectal cancer. Oncol Lett 1:119–125PubMedPubMedCentralCrossRef
41.
Zurück zum Zitat Jackson RM, Rice DH (1990) Wound infections and recurrence in head and neck cancer. Otolaryngol Head Neck Surg 102:331–333PubMedCrossRef Jackson RM, Rice DH (1990) Wound infections and recurrence in head and neck cancer. Otolaryngol Head Neck Surg 102:331–333PubMedCrossRef
42.
Zurück zum Zitat Farid SG, Aldouri A, Morris-Stiff G et al (2010) Correlation between postoperative infective complications and long-term outcomes after hepatic resection for colorectal liver metastasis. Ann Surg 251:91–100PubMedCrossRef Farid SG, Aldouri A, Morris-Stiff G et al (2010) Correlation between postoperative infective complications and long-term outcomes after hepatic resection for colorectal liver metastasis. Ann Surg 251:91–100PubMedCrossRef
43.
Zurück zum Zitat Haruki K, Shiba H, Fujiwara Y et al (2013) Negative impact of surgical site infection on long-term outcomes after hepatic resection for colorectal liver metastases. Anticancer Res 33:1697–1703PubMed Haruki K, Shiba H, Fujiwara Y et al (2013) Negative impact of surgical site infection on long-term outcomes after hepatic resection for colorectal liver metastases. Anticancer Res 33:1697–1703PubMed
44.
Zurück zum Zitat Neal CP, Mann CD, Garcea G et al (2011) Preoperative systemic inflammation and infectious complications after resection of colorectal liver metastases. Arch Surg 146:471–478PubMedCrossRef Neal CP, Mann CD, Garcea G et al (2011) Preoperative systemic inflammation and infectious complications after resection of colorectal liver metastases. Arch Surg 146:471–478PubMedCrossRef
45.
Zurück zum Zitat Mirnezami A, Mirnezami R, Chandrakumaran K et al (2011) Increased local recurrence and reduced survival from colorectal cancer following anastomotic leak: systematic review and meta-analysis. Ann Surg 253:890–899PubMedCrossRef Mirnezami A, Mirnezami R, Chandrakumaran K et al (2011) Increased local recurrence and reduced survival from colorectal cancer following anastomotic leak: systematic review and meta-analysis. Ann Surg 253:890–899PubMedCrossRef
46.
Zurück zum Zitat Pucher PH, Aggarwal R, Qurashi M, Darzi A (2014) Meta-analysis of the effect of postoperative in-hospital morbidity on long-term patient survival. Br J Surg 101:1499–1508PubMedCrossRef Pucher PH, Aggarwal R, Qurashi M, Darzi A (2014) Meta-analysis of the effect of postoperative in-hospital morbidity on long-term patient survival. Br J Surg 101:1499–1508PubMedCrossRef
47.
Zurück zum Zitat Kawai T, Akira S (2011) Toll-like receptors and their crosstalk with other innate receptors in infection and immunity. Immunity 34:637–650PubMedCrossRef Kawai T, Akira S (2011) Toll-like receptors and their crosstalk with other innate receptors in infection and immunity. Immunity 34:637–650PubMedCrossRef
48.
49.
Zurück zum Zitat Kawai T, Akira S (2010) The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors. Nat Immunol 11:373–384PubMedCrossRef Kawai T, Akira S (2010) The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors. Nat Immunol 11:373–384PubMedCrossRef
50.
Zurück zum Zitat Jiang D, Liang J, Fan J et al (2005) Regulation of lung injury and repair by Toll-like receptors and hyaluronan. Nat Med 11:1173–1179PubMedCrossRef Jiang D, Liang J, Fan J et al (2005) Regulation of lung injury and repair by Toll-like receptors and hyaluronan. Nat Med 11:1173–1179PubMedCrossRef
51.
Zurück zum Zitat Lucas M, Stuart LM, Savill J, Lacy-Hulbert A (2003) Apoptotic cells and innate immune stimuli combine to regulate macrophage cytokine secretion. J Immunol 171:2610–2615PubMedCrossRef Lucas M, Stuart LM, Savill J, Lacy-Hulbert A (2003) Apoptotic cells and innate immune stimuli combine to regulate macrophage cytokine secretion. J Immunol 171:2610–2615PubMedCrossRef
52.
Zurück zum Zitat Sabroe I, Prince LR, Jones EC et al (2003) Selective roles for Toll-like receptor (TLR)2 and TLR4 in the regulation of neutrophil activation and life span. J Immunol 170:5268–5275PubMedCrossRef Sabroe I, Prince LR, Jones EC et al (2003) Selective roles for Toll-like receptor (TLR)2 and TLR4 in the regulation of neutrophil activation and life span. J Immunol 170:5268–5275PubMedCrossRef
53.
Zurück zum Zitat Fan J, Malik AB (2003) Toll-like receptor-4 (TLR4) signaling augments chemokine-induced neutrophil migration by modulating cell surface expression of chemokine receptors. Nat Med 9:315–321PubMedCrossRef Fan J, Malik AB (2003) Toll-like receptor-4 (TLR4) signaling augments chemokine-induced neutrophil migration by modulating cell surface expression of chemokine receptors. Nat Med 9:315–321PubMedCrossRef
54.
Zurück zum Zitat McDonald B, Spicer J, Giannais B et al (2009) Systemic inflammation increases cancer cell adhesion to hepatic sinusoids by neutrophil mediated mechanisms. Int J Cancer 125:1298–1305PubMedCrossRef McDonald B, Spicer J, Giannais B et al (2009) Systemic inflammation increases cancer cell adhesion to hepatic sinusoids by neutrophil mediated mechanisms. Int J Cancer 125:1298–1305PubMedCrossRef
55.
Zurück zum Zitat Clark SR, Ma AC, Tavener SA et al (2007) Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic blood. Nat Med 13:463–469PubMedCrossRef Clark SR, Ma AC, Tavener SA et al (2007) Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic blood. Nat Med 13:463–469PubMedCrossRef
56.
Zurück zum Zitat Schnare M, Barton GM, Holt AC et al (2001) Toll-like receptors control activation of adaptive immune responses. Nat Immunol 2:947–950PubMedCrossRef Schnare M, Barton GM, Holt AC et al (2001) Toll-like receptors control activation of adaptive immune responses. Nat Immunol 2:947–950PubMedCrossRef
57.
58.
Zurück zum Zitat Kim S, Takahashi H, Lin WW et al (2009) Carcinoma-produced factors activate myeloid cells through TLR2 to stimulate metastasis. Nature 457:102–106PubMedPubMedCentralCrossRef Kim S, Takahashi H, Lin WW et al (2009) Carcinoma-produced factors activate myeloid cells through TLR2 to stimulate metastasis. Nature 457:102–106PubMedPubMedCentralCrossRef
59.
Zurück zum Zitat Okamura Y, Watari M, Jerud ES et al (2001) The extra domain A of fibronectin activates Toll-like receptor 4. J Biol Chem 276:10229–10233CrossRefPubMed Okamura Y, Watari M, Jerud ES et al (2001) The extra domain A of fibronectin activates Toll-like receptor 4. J Biol Chem 276:10229–10233CrossRefPubMed
60.
Zurück zum Zitat Schaefer L, Babelova A, Kiss E et al (2005) The matrix component biglycan is proinflammatory and signals through Toll-like receptors 4 and 2 in macrophages. J Clin Invest 115:2223–2233PubMedPubMedCentralCrossRef Schaefer L, Babelova A, Kiss E et al (2005) The matrix component biglycan is proinflammatory and signals through Toll-like receptors 4 and 2 in macrophages. J Clin Invest 115:2223–2233PubMedPubMedCentralCrossRef
61.
Zurück zum Zitat Guillot L, Balloy V, McCormack FX et al (2002) Cutting edge: the immunostimulatory activity of the lung surfactant protein-A involves Toll-like receptor 4. J Immunol 168:5989–5992PubMedCrossRef Guillot L, Balloy V, McCormack FX et al (2002) Cutting edge: the immunostimulatory activity of the lung surfactant protein-A involves Toll-like receptor 4. J Immunol 168:5989–5992PubMedCrossRef
62.
63.
Zurück zum Zitat Yanai H, Ban T, Wang Z et al (2009) HMGB proteins function as universal sentinels for nucleic-acid-mediated innate immune responses. Nature 462:99–103PubMedCrossRef Yanai H, Ban T, Wang Z et al (2009) HMGB proteins function as universal sentinels for nucleic-acid-mediated innate immune responses. Nature 462:99–103PubMedCrossRef
64.
Zurück zum Zitat Hiratsuka S, Watanabe A, Sakurai Y et al (2008) The S100A8-serum amyloid A3-TLR4 paracrine cascade establishes a pre-metastatic phase. Nat Cell Biol 10:1349–1355PubMedCrossRef Hiratsuka S, Watanabe A, Sakurai Y et al (2008) The S100A8-serum amyloid A3-TLR4 paracrine cascade establishes a pre-metastatic phase. Nat Cell Biol 10:1349–1355PubMedCrossRef
65.
Zurück zum Zitat Imai Y, Kuba K, Neely GG et al (2008) Identification of oxidative stress and Toll-like receptor 4 signaling as a key pathway of acute lung injury. Cell 133:235–249PubMedPubMedCentralCrossRef Imai Y, Kuba K, Neely GG et al (2008) Identification of oxidative stress and Toll-like receptor 4 signaling as a key pathway of acute lung injury. Cell 133:235–249PubMedPubMedCentralCrossRef
66.
Zurück zum Zitat Biragyn A, Ruffini PA, Leifer CA et al (2002) Toll-like receptor 4-dependent activation of dendritic cells by beta-defensin 2. Science 298:1025–1029PubMedCrossRef Biragyn A, Ruffini PA, Leifer CA et al (2002) Toll-like receptor 4-dependent activation of dendritic cells by beta-defensin 2. Science 298:1025–1029PubMedCrossRef
67.
Zurück zum Zitat D'Arpa P, Leung KP (2017) Toll-like receptor signaling in burn wound healing and scarring. Adv Wound Care (New Rochelle) 6:330–343CrossRef D'Arpa P, Leung KP (2017) Toll-like receptor signaling in burn wound healing and scarring. Adv Wound Care (New Rochelle) 6:330–343CrossRef
68.
Zurück zum Zitat Braza F, Brouard S, Chadban S, Goldstein DR (2016) Role of TLRs and DAMPs in allograft inflammation and transplant outcomes. Nat Rev Nephrol 12:281–290PubMedCrossRefPubMedCentral Braza F, Brouard S, Chadban S, Goldstein DR (2016) Role of TLRs and DAMPs in allograft inflammation and transplant outcomes. Nat Rev Nephrol 12:281–290PubMedCrossRefPubMedCentral
69.
Zurück zum Zitat Macedo L, Pinhal-Enfield G, Alshits V et al (2007) Wound healing is impaired in MyD88-deficient mice: a role for MyD88 in the regulation of wound healing by adenosine A2A receptors. Am J Pathol 171:1774–1788PubMedPubMedCentralCrossRef Macedo L, Pinhal-Enfield G, Alshits V et al (2007) Wound healing is impaired in MyD88-deficient mice: a role for MyD88 in the regulation of wound healing by adenosine A2A receptors. Am J Pathol 171:1774–1788PubMedPubMedCentralCrossRef
71.
Zurück zum Zitat Prince LR, Whyte MK, Sabroe I, Parker LC (2011) The role of TLRs in neutrophil activation. Curr Opin Pharmacol 11:397–403PubMedCrossRef Prince LR, Whyte MK, Sabroe I, Parker LC (2011) The role of TLRs in neutrophil activation. Curr Opin Pharmacol 11:397–403PubMedCrossRef
72.
Zurück zum Zitat Greene CM, McElvaney NG (2005) Toll-like receptor expression and function in airway epithelial cells. Archivum Immunologiae et Therapiae Experimentalis 53:418–427PubMed Greene CM, McElvaney NG (2005) Toll-like receptor expression and function in airway epithelial cells. Archivum Immunologiae et Therapiae Experimentalis 53:418–427PubMed
73.
Zurück zum Zitat Hauber HP, Tulic MK, Tsicopoulos A et al (2005) Toll-like receptors 4 and 2 expression in the bronchial mucosa of patients with cystic fibrosis. Can Respir J 12:13–18PubMedCrossRef Hauber HP, Tulic MK, Tsicopoulos A et al (2005) Toll-like receptors 4 and 2 expression in the bronchial mucosa of patients with cystic fibrosis. Can Respir J 12:13–18PubMedCrossRef
74.
Zurück zum Zitat Zhang Z, Louboutin JP, Weiner DJ et al (2005) Human airway epithelial cells sense Pseudomonas aeruginosa infection via recognition of flagellin by Toll-like receptor 5. Infect Immun 73:7151–7160PubMedPubMedCentralCrossRef Zhang Z, Louboutin JP, Weiner DJ et al (2005) Human airway epithelial cells sense Pseudomonas aeruginosa infection via recognition of flagellin by Toll-like receptor 5. Infect Immun 73:7151–7160PubMedPubMedCentralCrossRef
75.
Zurück zum Zitat Kawai T, Akira S (2008) Toll-like receptor and RIG-I-like receptor signaling. Ann N Y Acad Sci 1143:1–20PubMedCrossRef Kawai T, Akira S (2008) Toll-like receptor and RIG-I-like receptor signaling. Ann N Y Acad Sci 1143:1–20PubMedCrossRef
76.
Zurück zum Zitat Ishida I, Kubo H, Suzuki S et al (2002) Hypoxia diminishes toll-like receptor 4 expression through reactive oxygen species generated by mitochondria in endothelial cells. J Immunol 169:2069–2075PubMedCrossRef Ishida I, Kubo H, Suzuki S et al (2002) Hypoxia diminishes toll-like receptor 4 expression through reactive oxygen species generated by mitochondria in endothelial cells. J Immunol 169:2069–2075PubMedCrossRef
77.
Zurück zum Zitat Fan J, Kapus A, Marsden PA et al (2002) Regulation of toll-like receptor 4 expression in the lung following hemorrhagic shock and lipopolysaccharide. J Immunol 168:5252–5259PubMedCrossRef Fan J, Kapus A, Marsden PA et al (2002) Regulation of toll-like receptor 4 expression in the lung following hemorrhagic shock and lipopolysaccharide. J Immunol 168:5252–5259PubMedCrossRef
78.
Zurück zum Zitat Hopkins PA, Fraser JD, Pridmore AC et al (2005) Superantigen recognition by HLA class II on monocytes up-regulates toll-like receptor 4 and enhances proinflammatory responses to endotoxin. Blood 105:3655–3662PubMedCrossRef Hopkins PA, Fraser JD, Pridmore AC et al (2005) Superantigen recognition by HLA class II on monocytes up-regulates toll-like receptor 4 and enhances proinflammatory responses to endotoxin. Blood 105:3655–3662PubMedCrossRef
79.
Zurück zum Zitat Nilsen N, Nonstad U, Khan N et al (2004) Lipopolysaccharide and double-stranded RNA up-regulate Toll-like receptor 2 independently of myeloid differentiation factor 88. J Biol Chem 279:39727–39735PubMedCrossRef Nilsen N, Nonstad U, Khan N et al (2004) Lipopolysaccharide and double-stranded RNA up-regulate Toll-like receptor 2 independently of myeloid differentiation factor 88. J Biol Chem 279:39727–39735PubMedCrossRef
80.
Zurück zum Zitat Medzhitov R, Preston-Hurlburt P, Janeway CA Jr (1997) A human homologue of the Drosophila Toll protein signals activation of adaptive immunity. Nature 388:394–397PubMedCrossRef Medzhitov R, Preston-Hurlburt P, Janeway CA Jr (1997) A human homologue of the Drosophila Toll protein signals activation of adaptive immunity. Nature 388:394–397PubMedCrossRef
81.
Zurück zum Zitat Kagan JC, Medzhitov R (2006) Phosphoinositide-mediated adaptor recruitment controls Toll-like receptor signaling. Cell 125:943–955PubMedCrossRef Kagan JC, Medzhitov R (2006) Phosphoinositide-mediated adaptor recruitment controls Toll-like receptor signaling. Cell 125:943–955PubMedCrossRef
82.
Zurück zum Zitat Kagan JC, Su T, Horng T et al (2008) TRAM couples endocytosis of Toll-like receptor 4 to the induction of interferon-beta. Nat Immunol 9:361–368PubMedPubMedCentralCrossRef Kagan JC, Su T, Horng T et al (2008) TRAM couples endocytosis of Toll-like receptor 4 to the induction of interferon-beta. Nat Immunol 9:361–368PubMedPubMedCentralCrossRef
83.
Zurück zum Zitat Basith S, Manavalan B, Yoo TH et al (2012) Roles of toll-like receptors in cancer: a double-edged sword for defense and offense. Arch Pharm Res 35:1297–1316PubMedCrossRef Basith S, Manavalan B, Yoo TH et al (2012) Roles of toll-like receptors in cancer: a double-edged sword for defense and offense. Arch Pharm Res 35:1297–1316PubMedCrossRef
84.
Zurück zum Zitat Malley R, Henneke P, Morse SC et al (2003) Recognition of pneumolysin by Toll-like receptor 4 confers resistance to pneumococcal infection. Proc Natl Acad Sci USA 100:1966–1971PubMedCrossRefPubMedCentral Malley R, Henneke P, Morse SC et al (2003) Recognition of pneumolysin by Toll-like receptor 4 confers resistance to pneumococcal infection. Proc Natl Acad Sci USA 100:1966–1971PubMedCrossRefPubMedCentral
85.
Zurück zum Zitat Park BS, Song DH, Kim HM et al (2009) The structural basis of lipopolysaccharide recognition by the TLR4-MD-2 complex. Nature 458:1191–1195PubMedCrossRef Park BS, Song DH, Kim HM et al (2009) The structural basis of lipopolysaccharide recognition by the TLR4-MD-2 complex. Nature 458:1191–1195PubMedCrossRef
86.
Zurück zum Zitat Hayashi F, Smith KD, Ozinsky A et al (2001) The innate immune response to bacterial flagellin is mediated by Toll-like receptor 5. Nature 410:1099–1103PubMedCrossRef Hayashi F, Smith KD, Ozinsky A et al (2001) The innate immune response to bacterial flagellin is mediated by Toll-like receptor 5. Nature 410:1099–1103PubMedCrossRef
87.
Zurück zum Zitat Miao EA, Andersen-Nissen E, Warren SE, Aderem A (2007) TLR5 and Ipaf: dual sensors of bacterial flagellin in the innate immune system. Semin Immunopathol 29:275–288PubMedCrossRef Miao EA, Andersen-Nissen E, Warren SE, Aderem A (2007) TLR5 and Ipaf: dual sensors of bacterial flagellin in the innate immune system. Semin Immunopathol 29:275–288PubMedCrossRef
88.
Zurück zum Zitat Uematsu S, Jang MH, Chevrier N et al (2006) Detection of pathogenic intestinal bacteria by Toll-like receptor 5 on intestinal CD11c+ lamina propria cells. Nat Immunol 7:868–874PubMedCrossRef Uematsu S, Jang MH, Chevrier N et al (2006) Detection of pathogenic intestinal bacteria by Toll-like receptor 5 on intestinal CD11c+ lamina propria cells. Nat Immunol 7:868–874PubMedCrossRef
89.
Zurück zum Zitat Uematsu S, Akira S (2009) Immune responses of TLR5(+) lamina propria dendritic cells in enterobacterial infection. J Gastroenterol 44:803–811PubMedCrossRef Uematsu S, Akira S (2009) Immune responses of TLR5(+) lamina propria dendritic cells in enterobacterial infection. J Gastroenterol 44:803–811PubMedCrossRef
90.
Zurück zum Zitat Uematsu S, Fujimoto K, Jang MH et al (2008) Regulation of humoral and cellular gut immunity by lamina propria dendritic cells expressing Toll-like receptor 5. Nat Immunol 9:769–776PubMedCrossRef Uematsu S, Fujimoto K, Jang MH et al (2008) Regulation of humoral and cellular gut immunity by lamina propria dendritic cells expressing Toll-like receptor 5. Nat Immunol 9:769–776PubMedCrossRef
92.
Zurück zum Zitat Bell JK, Botos I, Hall PR et al (2005) The molecular structure of the Toll-like receptor 3 ligand-binding domain. Proc Natl Acad Sci USA 102:10976–10980PubMedCrossRefPubMedCentral Bell JK, Botos I, Hall PR et al (2005) The molecular structure of the Toll-like receptor 3 ligand-binding domain. Proc Natl Acad Sci USA 102:10976–10980PubMedCrossRefPubMedCentral
93.
Zurück zum Zitat Cho WG, Albuquerque RJ, Kleinman ME et al (2009) Small interfering RNA-induced TLR3 activation inhibits blood and lymphatic vessel growth. Proc Natl Acad Sci USA 106:7137–7142PubMedCrossRefPubMedCentral Cho WG, Albuquerque RJ, Kleinman ME et al (2009) Small interfering RNA-induced TLR3 activation inhibits blood and lymphatic vessel growth. Proc Natl Acad Sci USA 106:7137–7142PubMedCrossRefPubMedCentral
94.
Zurück zum Zitat Harrison LI, Astry C, Kumar S, Yunis C (2007) Pharmacokinetics of 852A, an imidazoquinoline Toll-like receptor 7-specific agonist, following intravenous, subcutaneous, and oral administrations in humans. J Clin Pharmacol 47:962–969PubMedCrossRef Harrison LI, Astry C, Kumar S, Yunis C (2007) Pharmacokinetics of 852A, an imidazoquinoline Toll-like receptor 7-specific agonist, following intravenous, subcutaneous, and oral administrations in humans. J Clin Pharmacol 47:962–969PubMedCrossRef
96.
97.
Zurück zum Zitat Gantier MP, Irving AT, Kaparakis-Liaskos M et al (2010) Genetic modulation of TLR8 response following bacterial phagocytosis. Hum Mutat 31:1069–1079PubMedCrossRef Gantier MP, Irving AT, Kaparakis-Liaskos M et al (2010) Genetic modulation of TLR8 response following bacterial phagocytosis. Hum Mutat 31:1069–1079PubMedCrossRef
98.
Zurück zum Zitat Mancuso G, Gambuzza M, Midiri A et al (2009) Bacterial recognition by TLR7 in the lysosomes of conventional dendritic cells. Nat Immunol 10:587–594PubMedCrossRef Mancuso G, Gambuzza M, Midiri A et al (2009) Bacterial recognition by TLR7 in the lysosomes of conventional dendritic cells. Nat Immunol 10:587–594PubMedCrossRef
99.
Zurück zum Zitat Coban C, Igari Y, Yagi M et al (2010) Immunogenicity of whole-parasite vaccines against Plasmodium falciparum involves malarial hemozoin and host TLR9. Cell Host Microbe 7:50–61PubMedCrossRef Coban C, Igari Y, Yagi M et al (2010) Immunogenicity of whole-parasite vaccines against Plasmodium falciparum involves malarial hemozoin and host TLR9. Cell Host Microbe 7:50–61PubMedCrossRef
100.
Zurück zum Zitat Lee SM, Yip TF, Yan S et al (2018) Recognition of double-stranded RNA and regulation of interferon pathway by Toll-like receptor 10. Front Immunol 9:516PubMedPubMedCentralCrossRef Lee SM, Yip TF, Yan S et al (2018) Recognition of double-stranded RNA and regulation of interferon pathway by Toll-like receptor 10. Front Immunol 9:516PubMedPubMedCentralCrossRef
101.
Zurück zum Zitat Hasan U, Chaffois C, Gaillard C et al (2005) Human TLR10 is a functional receptor, expressed by B cells and plasmacytoid dendritic cells, which activates gene transcription through MyD88. J Immunol 174:2942–2950PubMedCrossRef Hasan U, Chaffois C, Gaillard C et al (2005) Human TLR10 is a functional receptor, expressed by B cells and plasmacytoid dendritic cells, which activates gene transcription through MyD88. J Immunol 174:2942–2950PubMedCrossRef
102.
Zurück zum Zitat Paget S (1989) The distribution of secondary growths in cancer of the breast. Cancer Metastasis Rev 8:98–101PubMed Paget S (1989) The distribution of secondary growths in cancer of the breast. Cancer Metastasis Rev 8:98–101PubMed
103.
Zurück zum Zitat Sleeman JP, Thiele W (2009) Tumor metastasis and the lymphatic vasculature. Int J Cancer 125:2747–2756PubMedCrossRef Sleeman JP, Thiele W (2009) Tumor metastasis and the lymphatic vasculature. Int J Cancer 125:2747–2756PubMedCrossRef
104.
Zurück zum Zitat Ran S, Volk L, Hall K, Flister MJ (2010) Lymphangiogenesis and lymphatic metastasis in breast cancer. Pathophysiology 17:229–251PubMedCrossRef Ran S, Volk L, Hall K, Flister MJ (2010) Lymphangiogenesis and lymphatic metastasis in breast cancer. Pathophysiology 17:229–251PubMedCrossRef
105.
Zurück zum Zitat Luddy KA, Robertson-Tessi M, Tafreshi NK et al (2014) The role of toll-like receptors in colorectal cancer progression: evidence for epithelial to leucocytic transition. Front Immunol 5:429PubMedPubMedCentralCrossRef Luddy KA, Robertson-Tessi M, Tafreshi NK et al (2014) The role of toll-like receptors in colorectal cancer progression: evidence for epithelial to leucocytic transition. Front Immunol 5:429PubMedPubMedCentralCrossRef
106.
Zurück zum Zitat Spicer JD, Brodt P, Ferri LE (2011) The role of inflammation in the early stages of liver metastasis. In: Brodt P (ed) Liver metastasis: biology and clinical management. Springer Science and Business Media, Berlin, pp 155–185CrossRef Spicer JD, Brodt P, Ferri LE (2011) The role of inflammation in the early stages of liver metastasis. In: Brodt P (ed) Liver metastasis: biology and clinical management. Springer Science and Business Media, Berlin, pp 155–185CrossRef
107.
Zurück zum Zitat Pearson HB, Pouliot N (2013) Modeling metastasis in vivo. In Jandial R (ed) Metastatic cancer: clinical and biological perspectives. Landes Bioscience, Melbourne Pearson HB, Pouliot N (2013) Modeling metastasis in vivo. In Jandial R (ed) Metastatic cancer: clinical and biological perspectives. Landes Bioscience, Melbourne
108.
Zurück zum Zitat Sutherland RM (1988) Cell and environment interactions in tumor microregions: the multicell spheroid model. Science 240:177–184PubMedCrossRef Sutherland RM (1988) Cell and environment interactions in tumor microregions: the multicell spheroid model. Science 240:177–184PubMedCrossRef
112.
113.
Zurück zum Zitat Maroldi R, Farina D, Borghesi A et al (2008) Perineural tumor spread. Neuroimaging Clin N Am 18:413–429PubMedCrossRef Maroldi R, Farina D, Borghesi A et al (2008) Perineural tumor spread. Neuroimaging Clin N Am 18:413–429PubMedCrossRef
114.
Zurück zum Zitat Dajon M, Iribarren K, Cremer I (2017) Toll-like receptor stimulation in cancer: a pro- and anti-tumor double-edged sword. Immunobiology 222:89–100PubMedCrossRef Dajon M, Iribarren K, Cremer I (2017) Toll-like receptor stimulation in cancer: a pro- and anti-tumor double-edged sword. Immunobiology 222:89–100PubMedCrossRef
115.
Zurück zum Zitat Huang B, Zhao J, Shen S et al (2007) Listeria monocytogenes promotes tumor growth via tumor cell toll-like receptor 2 signaling. Cancer Res 67:4346–4352PubMedCrossRef Huang B, Zhao J, Shen S et al (2007) Listeria monocytogenes promotes tumor growth via tumor cell toll-like receptor 2 signaling. Cancer Res 67:4346–4352PubMedCrossRef
116.
Zurück zum Zitat Kundu SD, Lee C, Billips BK et al (2008) The toll-like receptor pathway: a novel mechanism of infection-induced carcinogenesis of prostate epithelial cells. Prostate 68:223–229PubMedCrossRef Kundu SD, Lee C, Billips BK et al (2008) The toll-like receptor pathway: a novel mechanism of infection-induced carcinogenesis of prostate epithelial cells. Prostate 68:223–229PubMedCrossRef
117.
Zurück zum Zitat Grimmig T, Matthes N, Hoeland K et al (2015) TLR7 and TLR8 expression increases tumor cell proliferation and promotes chemoresistance in human pancreatic cancer. Int J Oncol 47:857–866PubMedPubMedCentralCrossRef Grimmig T, Matthes N, Hoeland K et al (2015) TLR7 and TLR8 expression increases tumor cell proliferation and promotes chemoresistance in human pancreatic cancer. Int J Oncol 47:857–866PubMedPubMedCentralCrossRef
118.
Zurück zum Zitat Cherfils-Vicini J, Platonova S, Gillard M et al (2010) Triggering of TLR7 and TLR8 expressed by human lung cancer cells induces cell survival and chemoresistance. J Clin Invest 120:1285–1297PubMedPubMedCentralCrossRef Cherfils-Vicini J, Platonova S, Gillard M et al (2010) Triggering of TLR7 and TLR8 expressed by human lung cancer cells induces cell survival and chemoresistance. J Clin Invest 120:1285–1297PubMedPubMedCentralCrossRef
119.
Zurück zum Zitat Luo JL, Maeda S, Hsu LC et al (2004) Inhibition of NF-kappaB in cancer cells converts inflammation-induced tumor growth mediated by TNFalpha to TRAIL-mediated tumor regression. Cancer Cell 6:297–305PubMedCrossRef Luo JL, Maeda S, Hsu LC et al (2004) Inhibition of NF-kappaB in cancer cells converts inflammation-induced tumor growth mediated by TNFalpha to TRAIL-mediated tumor regression. Cancer Cell 6:297–305PubMedCrossRef
120.
Zurück zum Zitat Hsu RY, Chan CH, Spicer JD et al (2011) LPS-induced TLR4 signaling in human colorectal cancer cells increases beta1 integrin-mediated cell adhesion and liver metastasis. Cancer Res 71:1989–1998PubMedCrossRef Hsu RY, Chan CH, Spicer JD et al (2011) LPS-induced TLR4 signaling in human colorectal cancer cells increases beta1 integrin-mediated cell adhesion and liver metastasis. Cancer Res 71:1989–1998PubMedCrossRef
122.
Zurück zum Zitat Li D, Jin Y, Sun Y et al (2014) Knockdown of Toll-like receptor 4 inhibits human NSCLC cancer cell growth and inflammatory cytokine secretion in vitro and in vivo. Int J Oncol 45:813–821PubMedCrossRef Li D, Jin Y, Sun Y et al (2014) Knockdown of Toll-like receptor 4 inhibits human NSCLC cancer cell growth and inflammatory cytokine secretion in vitro and in vivo. Int J Oncol 45:813–821PubMedCrossRef
123.
Zurück zum Zitat Jing YY, Han ZP, Sun K et al (2012) Toll-like receptor 4 signaling promotes epithelial–mesenchymal transition in human hepatocellular carcinoma induced by lipopolysaccharide. BMC Med 10:98PubMedPubMedCentralCrossRef Jing YY, Han ZP, Sun K et al (2012) Toll-like receptor 4 signaling promotes epithelial–mesenchymal transition in human hepatocellular carcinoma induced by lipopolysaccharide. BMC Med 10:98PubMedPubMedCentralCrossRef
124.
Zurück zum Zitat Wang CH, Wang PJ, Hsieh YC et al (2018) Resistin facilitates breast cancer progression via TLR4-mediated induction of mesenchymal phenotypes and stemness properties. Oncogene 37:589–600PubMedCrossRef Wang CH, Wang PJ, Hsieh YC et al (2018) Resistin facilitates breast cancer progression via TLR4-mediated induction of mesenchymal phenotypes and stemness properties. Oncogene 37:589–600PubMedCrossRef
125.
Zurück zum Zitat Park GB, Kim D (2017) TLR4-mediated galectin-1 production triggers epithelial-mesenchymal transition in colon cancer cells through ADAM10- and ADAM17-associated lactate production. Mol Cell Biochem 425:191–202PubMedCrossRef Park GB, Kim D (2017) TLR4-mediated galectin-1 production triggers epithelial-mesenchymal transition in colon cancer cells through ADAM10- and ADAM17-associated lactate production. Mol Cell Biochem 425:191–202PubMedCrossRef
126.
Zurück zum Zitat Duan H, Qu L, Shou C (2014) Mycoplasma hyorhinis induces epithelial–mesenchymal transition in gastric cancer cell MGC803 via TLR4-NF-kappaB signaling. Cancer Lett 354:447–454PubMedCrossRef Duan H, Qu L, Shou C (2014) Mycoplasma hyorhinis induces epithelial–mesenchymal transition in gastric cancer cell MGC803 via TLR4-NF-kappaB signaling. Cancer Lett 354:447–454PubMedCrossRef
127.
Zurück zum Zitat He Z, Deng R, Huang X et al (2015) Lipopolysaccharide enhances OSCC migration by promoting epithelial–mesenchymal transition. J Oral Pathol Med 44:685–692PubMedCrossRef He Z, Deng R, Huang X et al (2015) Lipopolysaccharide enhances OSCC migration by promoting epithelial–mesenchymal transition. J Oral Pathol Med 44:685–692PubMedCrossRef
128.
Zurück zum Zitat Park GB, Kim D (2017) TLR5/7-mediated PI3K activation triggers epithelial-mesenchymal transition of ovarian cancer cells through WAVE3-dependent mesothelin or OCT4/SOX2 expression. Oncol Rep 38:3167–3176PubMedCrossRef Park GB, Kim D (2017) TLR5/7-mediated PI3K activation triggers epithelial-mesenchymal transition of ovarian cancer cells through WAVE3-dependent mesothelin or OCT4/SOX2 expression. Oncol Rep 38:3167–3176PubMedCrossRef
129.
Zurück zum Zitat Liu B, Yan S, Jia Y et al (2016) TLR2 promotes human intrahepatic cholangiocarcinoma cell migration and invasion by modulating NF-kappaB pathway-mediated inflammatory responses. FEBS J 283:3839–3850PubMedCrossRef Liu B, Yan S, Jia Y et al (2016) TLR2 promotes human intrahepatic cholangiocarcinoma cell migration and invasion by modulating NF-kappaB pathway-mediated inflammatory responses. FEBS J 283:3839–3850PubMedCrossRef
130.
Zurück zum Zitat Li K, Dan Z, Hu X et al (2013) CD14 regulates gastric cancer cell epithelialmesenchymal transition and invasion in vitro. Oncol Rep 30:2725–2732PubMedCrossRef Li K, Dan Z, Hu X et al (2013) CD14 regulates gastric cancer cell epithelialmesenchymal transition and invasion in vitro. Oncol Rep 30:2725–2732PubMedCrossRef
131.
Zurück zum Zitat Liu YD, Ji CB, Li SB et al (2018) Toll-like receptor 2 stimulation promotes colorectal cancer cell growth via PI3K/Akt and NF-kappaB signaling pathways. Int Immunopharmacol 59:375–383PubMedCrossRef Liu YD, Ji CB, Li SB et al (2018) Toll-like receptor 2 stimulation promotes colorectal cancer cell growth via PI3K/Akt and NF-kappaB signaling pathways. Int Immunopharmacol 59:375–383PubMedCrossRef
132.
Zurück zum Zitat Li D, Gu R, Yang X et al (2014) TLR3 correlated with cervical lymph node metastasis in patients with papillary thyroid cancer. Int J Clin Exp Med 7:5111–5117PubMedPubMedCentral Li D, Gu R, Yang X et al (2014) TLR3 correlated with cervical lymph node metastasis in patients with papillary thyroid cancer. Int J Clin Exp Med 7:5111–5117PubMedPubMedCentral
133.
Zurück zum Zitat Chuang HC, Huang CC, Chien CY, Chuang JH (2012) Toll-like receptor 3-mediated tumor invasion in head and neck cancer. Oral Oncol 48:226–232PubMedCrossRef Chuang HC, Huang CC, Chien CY, Chuang JH (2012) Toll-like receptor 3-mediated tumor invasion in head and neck cancer. Oral Oncol 48:226–232PubMedCrossRef
134.
Zurück zum Zitat Zhang Y, Wang Q, Ma A et al (2014) Functional expression of TLR9 in esophageal cancer. Oncol Rep 31:2298–2304PubMedCrossRef Zhang Y, Wang Q, Ma A et al (2014) Functional expression of TLR9 in esophageal cancer. Oncol Rep 31:2298–2304PubMedCrossRef
135.
Zurück zum Zitat O'Leary DP, Bhatt L, Woolley JF et al (2012) TLR-4 signalling accelerates colon cancer cell adhesion via NF-kappaB mediated transcriptional up-regulation of Nox-1. PLoS ONE 7:e44176PubMedPubMedCentralCrossRef O'Leary DP, Bhatt L, Woolley JF et al (2012) TLR-4 signalling accelerates colon cancer cell adhesion via NF-kappaB mediated transcriptional up-regulation of Nox-1. PLoS ONE 7:e44176PubMedPubMedCentralCrossRef
136.
Zurück zum Zitat Rousseau MC, Hsu RY, Spicer JD et al (2013) Lipopolysaccharide-induced toll-like receptor 4 signaling enhances the migratory ability of human esophageal cancer cells in a selectin-dependent manner. Surgery 154:69–77PubMedCrossRef Rousseau MC, Hsu RY, Spicer JD et al (2013) Lipopolysaccharide-induced toll-like receptor 4 signaling enhances the migratory ability of human esophageal cancer cells in a selectin-dependent manner. Surgery 154:69–77PubMedCrossRef
137.
Zurück zum Zitat Molteni M, Marabella D, Orlandi C, Rossetti C (2006) Melanoma cell lines are responsive in vitro to lipopolysaccharide and express TLR-4. Cancer Lett 235:75–83PubMedCrossRef Molteni M, Marabella D, Orlandi C, Rossetti C (2006) Melanoma cell lines are responsive in vitro to lipopolysaccharide and express TLR-4. Cancer Lett 235:75–83PubMedCrossRef
138.
Zurück zum Zitat Xie W, Huang Y, Xie W et al (2010) Bacteria peptidoglycan promoted breast cancer cell invasiveness and adhesiveness by targeting toll-like receptor 2 in the cancer cells. PLoS ONE 5:e10850PubMedPubMedCentralCrossRef Xie W, Huang Y, Xie W et al (2010) Bacteria peptidoglycan promoted breast cancer cell invasiveness and adhesiveness by targeting toll-like receptor 2 in the cancer cells. PLoS ONE 5:e10850PubMedPubMedCentralCrossRef
139.
Zurück zum Zitat Bondhopadhyay B, Moirangthem A, Basu A (2015) Innate adjuvant receptor Toll-like receptor 3 can promote breast cancer through cell surface. Tumour Biol 36:1261–1271PubMedCrossRef Bondhopadhyay B, Moirangthem A, Basu A (2015) Innate adjuvant receptor Toll-like receptor 3 can promote breast cancer through cell surface. Tumour Biol 36:1261–1271PubMedCrossRef
140.
Zurück zum Zitat Hansen MT, Forst B, Cremers N et al (2015) A link between inflammation and metastasis: serum amyloid A1 and A3 induce metastasis, and are targets of metastasis-inducing S100A4. Oncogene 34:424–435PubMedCrossRef Hansen MT, Forst B, Cremers N et al (2015) A link between inflammation and metastasis: serum amyloid A1 and A3 induce metastasis, and are targets of metastasis-inducing S100A4. Oncogene 34:424–435PubMedCrossRef
141.
143.
Zurück zum Zitat El Rayes T, Catena R, Lee S et al (2015) Lung inflammation promotes metastasis through neutrophil protease-mediated degradation of Tsp-1. Proc Natl Acad Sci USA 112:16000–16005PubMedCrossRefPubMedCentral El Rayes T, Catena R, Lee S et al (2015) Lung inflammation promotes metastasis through neutrophil protease-mediated degradation of Tsp-1. Proc Natl Acad Sci USA 112:16000–16005PubMedCrossRefPubMedCentral
145.
Zurück zum Zitat Yan L, Cai Q, Xu Y (2013) The ubiquitin-CXCR4 axis plays an important role in acute lung infection-enhanced lung tumor metastasis. Clin Cancer Res 19:4706–4716PubMedPubMedCentralCrossRef Yan L, Cai Q, Xu Y (2013) The ubiquitin-CXCR4 axis plays an important role in acute lung infection-enhanced lung tumor metastasis. Clin Cancer Res 19:4706–4716PubMedPubMedCentralCrossRef
147.
Zurück zum Zitat Brown KA, Brain SD, Pearson JD et al (2006) Neutrophils in development of multiple organ failure in sepsis. Lancet 368:157–169PubMedCrossRef Brown KA, Brain SD, Pearson JD et al (2006) Neutrophils in development of multiple organ failure in sepsis. Lancet 368:157–169PubMedCrossRef
148.
Zurück zum Zitat Lieto E, Galizia G, Auricchio A et al (2017) Preoperative neutrophil to lymphocyte ratio and lymphocyte to monocyte ratio are prognostic factors in gastric cancers undergoing surgery. J Gastrointest Surg 21:1–11CrossRef Lieto E, Galizia G, Auricchio A et al (2017) Preoperative neutrophil to lymphocyte ratio and lymphocyte to monocyte ratio are prognostic factors in gastric cancers undergoing surgery. J Gastrointest Surg 21:1–11CrossRef
150.
Zurück zum Zitat McDonald B, Urrutia R, Yipp BG et al (2012) Intravascular neutrophil extracellular traps capture bacteria from the bloodstream during sepsis. Cell Host Microbe 12:324–333PubMedCrossRef McDonald B, Urrutia R, Yipp BG et al (2012) Intravascular neutrophil extracellular traps capture bacteria from the bloodstream during sepsis. Cell Host Microbe 12:324–333PubMedCrossRef
151.
Zurück zum Zitat Najmeh S, Cools-Lartigue J, Rayes RF et al (2017) Neutrophil extracellular traps sequester circulating tumor cells via beta1-integrin mediated interactions. Int J Cancer 140:2321–2330PubMedCrossRef Najmeh S, Cools-Lartigue J, Rayes RF et al (2017) Neutrophil extracellular traps sequester circulating tumor cells via beta1-integrin mediated interactions. Int J Cancer 140:2321–2330PubMedCrossRef
152.
Zurück zum Zitat Tohme S, Yazdani HO, Al-Khafaji AB et al (2016) Neutrophil extracellular traps promote the development and progression of liver metastases after surgical stress. Cancer Res 76:1367–1380PubMedPubMedCentralCrossRef Tohme S, Yazdani HO, Al-Khafaji AB et al (2016) Neutrophil extracellular traps promote the development and progression of liver metastases after surgical stress. Cancer Res 76:1367–1380PubMedPubMedCentralCrossRef
153.
Zurück zum Zitat Park J, Wysocki RW, Amoozgar Z et al (2016) Cancer cells induce metastasis-supporting neutrophil extracellular DNA traps. Sci Transl Med 8:361ra138PubMedPubMedCentralCrossRef Park J, Wysocki RW, Amoozgar Z et al (2016) Cancer cells induce metastasis-supporting neutrophil extracellular DNA traps. Sci Transl Med 8:361ra138PubMedPubMedCentralCrossRef
154.
Zurück zum Zitat Albrengues J, Shields MA, Ng D et al (2018) Neutrophil extracellular traps produced during inflammation awaken dormant cancer cells in mice. Science 361:eaao4227PubMedPubMedCentralCrossRef Albrengues J, Shields MA, Ng D et al (2018) Neutrophil extracellular traps produced during inflammation awaken dormant cancer cells in mice. Science 361:eaao4227PubMedPubMedCentralCrossRef
155.
156.
Zurück zum Zitat Huhta H, Helminen O, Lehenkari PP et al (2016) Toll-like receptors 1, 2, 4 and 6 in esophageal epithelium, Barrett's esophagus, dysplasia and adenocarcinoma. Oncotarget 7:23658–23667PubMedPubMedCentralCrossRef Huhta H, Helminen O, Lehenkari PP et al (2016) Toll-like receptors 1, 2, 4 and 6 in esophageal epithelium, Barrett's esophagus, dysplasia and adenocarcinoma. Oncotarget 7:23658–23667PubMedPubMedCentralCrossRef
157.
Zurück zum Zitat Lan F, Yue X, Ren G et al (2015) miR-15a/16 enhances radiation sensitivity of non-small cell lung cancer cells by targeting the TLR1/NF-kappaB signaling pathway. Int J Radiat Oncol Biol Phys 91:73–81PubMedCrossRef Lan F, Yue X, Ren G et al (2015) miR-15a/16 enhances radiation sensitivity of non-small cell lung cancer cells by targeting the TLR1/NF-kappaB signaling pathway. Int J Radiat Oncol Biol Phys 91:73–81PubMedCrossRef
158.
Zurück zum Zitat Ayari C, Bergeron A, LaRue H et al (2011) Toll-like receptors in normal and malignant human bladders. J Urol 185:1915–1921PubMedCrossRef Ayari C, Bergeron A, LaRue H et al (2011) Toll-like receptors in normal and malignant human bladders. J Urol 185:1915–1921PubMedCrossRef
159.
Zurück zum Zitat Pimentel-Nunes P, Afonso L, Lopes P et al (2011) Increased expression of toll-like receptors (TLR) 2, 4 and 5 in gastric dysplasia. Pathol Oncol Res 17:677–683PubMedCrossRef Pimentel-Nunes P, Afonso L, Lopes P et al (2011) Increased expression of toll-like receptors (TLR) 2, 4 and 5 in gastric dysplasia. Pathol Oncol Res 17:677–683PubMedCrossRef
160.
Zurück zum Zitat Szczepanski M, Stelmachowska M, Stryczynski L et al (2007) Assessment of expression of toll-like receptors 2, 3 and 4 in laryngeal carcinoma. Eur Arch Otorhinolaryngol 264:525–530PubMedCrossRef Szczepanski M, Stelmachowska M, Stryczynski L et al (2007) Assessment of expression of toll-like receptors 2, 3 and 4 in laryngeal carcinoma. Eur Arch Otorhinolaryngol 264:525–530PubMedCrossRef
161.
Zurück zum Zitat Saint-Jean M, Knol AC, Nguyen JM et al (2011) TLR expression in human melanoma cells. Eur J Dermatol 21:899–905PubMedCrossRef Saint-Jean M, Knol AC, Nguyen JM et al (2011) TLR expression in human melanoma cells. Eur J Dermatol 21:899–905PubMedCrossRef
162.
Zurück zum Zitat Ng LK, Rich AM, Hussaini HM et al (2011) Toll-like receptor 2 is present in the microenvironment of oral squamous cell carcinoma. Br J Cancer 104:460–463PubMedCrossRef Ng LK, Rich AM, Hussaini HM et al (2011) Toll-like receptor 2 is present in the microenvironment of oral squamous cell carcinoma. Br J Cancer 104:460–463PubMedCrossRef
163.
Zurück zum Zitat Zhou M, McFarland-Mancini MM, Funk HM et al (2009) Toll-like receptor expression in normal ovary and ovarian tumors. Cancer Immunol Immunother 58:1375–1385PubMedCrossRef Zhou M, McFarland-Mancini MM, Funk HM et al (2009) Toll-like receptor expression in normal ovary and ovarian tumors. Cancer Immunol Immunother 58:1375–1385PubMedCrossRef
164.
Zurück zum Zitat Gonzalez-Reyes S, Marin L, Gonzalez L et al (2010) Study of TLR3, TLR4 and TLR9 in breast carcinomas and their association with metastasis. BMC Cancer 10:665PubMedPubMedCentralCrossRef Gonzalez-Reyes S, Marin L, Gonzalez L et al (2010) Study of TLR3, TLR4 and TLR9 in breast carcinomas and their association with metastasis. BMC Cancer 10:665PubMedPubMedCentralCrossRef
165.
Zurück zum Zitat Sheyhidin I, Nabi G, Hasim A et al (2011) Overexpression of TLR3, TLR4, TLR7 and TLR9 in esophageal squamous cell carcinoma. World J Gastroenterol 17:3745–3751PubMedPubMedCentralCrossRef Sheyhidin I, Nabi G, Hasim A et al (2011) Overexpression of TLR3, TLR4, TLR7 and TLR9 in esophageal squamous cell carcinoma. World J Gastroenterol 17:3745–3751PubMedPubMedCentralCrossRef
166.
Zurück zum Zitat Eiro N, Ovies C, Fernandez-Garcia B et al (2013) Expression of TLR3, 4, 7 and 9 in cutaneous malignant melanoma: relationship with clinicopathological characteristics and prognosis. Arch Dermatol Res 305:59–67PubMedCrossRef Eiro N, Ovies C, Fernandez-Garcia B et al (2013) Expression of TLR3, 4, 7 and 9 in cutaneous malignant melanoma: relationship with clinicopathological characteristics and prognosis. Arch Dermatol Res 305:59–67PubMedCrossRef
167.
Zurück zum Zitat Gonzalez-Reyes S, Fernandez JM, Gonzalez LO et al (2011) Study of TLR3, TLR4, and TLR9 in prostate carcinomas and their association with biochemical recurrence. Cancer Immunol Immunother 60:217–226PubMedCrossRef Gonzalez-Reyes S, Fernandez JM, Gonzalez LO et al (2011) Study of TLR3, TLR4, and TLR9 in prostate carcinomas and their association with biochemical recurrence. Cancer Immunol Immunother 60:217–226PubMedCrossRef
168.
Zurück zum Zitat Schmausser B, Andrulis M, Endrich S et al (2005) Toll-like receptors TLR4, TLR5 and TLR9 on gastric carcinoma cells: an implication for interaction with Helicobacter pylori. Int J Med Microbiol 295:179–185PubMedCrossRef Schmausser B, Andrulis M, Endrich S et al (2005) Toll-like receptors TLR4, TLR5 and TLR9 on gastric carcinoma cells: an implication for interaction with Helicobacter pylori. Int J Med Microbiol 295:179–185PubMedCrossRef
169.
Zurück zum Zitat MacRedmond R, Greene C, Taggart CC et al (2005) Respiratory epithelial cells require Toll-like receptor 4 for induction of human beta-defensin 2 by lipopolysaccharide. Respir Res 6:116PubMedPubMedCentralCrossRef MacRedmond R, Greene C, Taggart CC et al (2005) Respiratory epithelial cells require Toll-like receptor 4 for induction of human beta-defensin 2 by lipopolysaccharide. Respir Res 6:116PubMedPubMedCentralCrossRef
170.
Zurück zum Zitat Huang B, Zhao J, Li H et al (2005) Toll-like receptors on tumor cells facilitate evasion of immune surveillance. Cancer Res 65:5009–5014PubMedCrossRef Huang B, Zhao J, Li H et al (2005) Toll-like receptors on tumor cells facilitate evasion of immune surveillance. Cancer Res 65:5009–5014PubMedCrossRef
171.
Zurück zum Zitat Zhang YB, He FL, Fang M et al (2009) Increased expression of Toll-like receptors 4 and 9 in human lung cancer. Mol Biol Rep 36:1475–1481PubMedCrossRef Zhang YB, He FL, Fang M et al (2009) Increased expression of Toll-like receptors 4 and 9 in human lung cancer. Mol Biol Rep 36:1475–1481PubMedCrossRef
172.
Zurück zum Zitat Song C, Chen LZ, Zhang RH et al (2006) Functional variant in the 3′-untranslated region of Toll-like receptor 4 is associated with nasopharyngeal carcinoma risk. Cancer Biol Ther 5:1285–1291PubMedCrossRef Song C, Chen LZ, Zhang RH et al (2006) Functional variant in the 3′-untranslated region of Toll-like receptor 4 is associated with nasopharyngeal carcinoma risk. Cancer Biol Ther 5:1285–1291PubMedCrossRef
173.
Zurück zum Zitat Fan P, Zhang JJ, Wang B et al (2012) Hypoxia-inducible factor-1 up-regulates the expression of Toll-like receptor 4 in pancreatic cancer cells under hypoxic conditions. Pancreatology 12:170–178PubMedCrossRef Fan P, Zhang JJ, Wang B et al (2012) Hypoxia-inducible factor-1 up-regulates the expression of Toll-like receptor 4 in pancreatic cancer cells under hypoxic conditions. Pancreatology 12:170–178PubMedCrossRef
174.
Zurück zum Zitat Cai Z, Sanchez A, Shi Z et al (2011) Activation of Toll-like receptor 5 on breast cancer cells by flagellin suppresses cell proliferation and tumor growth. Cancer Res 71:2466–2475PubMedPubMedCentralCrossRef Cai Z, Sanchez A, Shi Z et al (2011) Activation of Toll-like receptor 5 on breast cancer cells by flagellin suppresses cell proliferation and tumor growth. Cancer Res 71:2466–2475PubMedPubMedCentralCrossRef
175.
Zurück zum Zitat Kim WY, Lee JW, Choi JJ et al (2008) Increased expression of Toll-like receptor 5 during progression of cervical neoplasia. Int J Gynecol Cancer 18:300–305PubMedCrossRef Kim WY, Lee JW, Choi JJ et al (2008) Increased expression of Toll-like receptor 5 during progression of cervical neoplasia. Int J Gynecol Cancer 18:300–305PubMedCrossRef
176.
Zurück zum Zitat Rhee SH, Im E, Pothoulakis C (2008) Toll-like receptor 5 engagement modulates tumor development and growth in a mouse xenograft model of human colon cancer. Gastroenterology 135:518–528PubMedCrossRef Rhee SH, Im E, Pothoulakis C (2008) Toll-like receptor 5 engagement modulates tumor development and growth in a mouse xenograft model of human colon cancer. Gastroenterology 135:518–528PubMedCrossRef
177.
Zurück zum Zitat Song EJ, Kang MJ, Kim YS et al (2011) Flagellin promotes the proliferation of gastric cancer cells via the Toll-like receptor 5. Int J Mol Med 28:115–119PubMed Song EJ, Kang MJ, Kim YS et al (2011) Flagellin promotes the proliferation of gastric cancer cells via the Toll-like receptor 5. Int J Mol Med 28:115–119PubMed
178.
Zurück zum Zitat Chen SK, Chung CA, Cheng YC et al (2014) Toll-like receptor 6 and connective tissue growth factor are significantly upregulated in mitomycin-C-treated urothelial carcinoma cells under hydrostatic pressure stimulation. Genet Test Mol Biomark 18:410–416CrossRef Chen SK, Chung CA, Cheng YC et al (2014) Toll-like receptor 6 and connective tissue growth factor are significantly upregulated in mitomycin-C-treated urothelial carcinoma cells under hydrostatic pressure stimulation. Genet Test Mol Biomark 18:410–416CrossRef
179.
Zurück zum Zitat Garau G, Rocca PC, Manca A et al (2015) Preliminary study on the expression of Toll-like receptors 7 and 8 in bladder urothelial tumors. Urologia 82:226–228PubMedCrossRef Garau G, Rocca PC, Manca A et al (2015) Preliminary study on the expression of Toll-like receptors 7 and 8 in bladder urothelial tumors. Urologia 82:226–228PubMedCrossRef
180.
Zurück zum Zitat Grimm M, Kim M, Rosenwald A et al (2010) Toll-like receptor (TLR) 7 and TLR8 expression on CD133+ cells in colorectal cancer points to a specific role for inflammation-induced TLRs in tumourigenesis and tumour progression. Eur J Cancer 46:2849–2857PubMedCrossRef Grimm M, Kim M, Rosenwald A et al (2010) Toll-like receptor (TLR) 7 and TLR8 expression on CD133+ cells in colorectal cancer points to a specific role for inflammation-induced TLRs in tumourigenesis and tumour progression. Eur J Cancer 46:2849–2857PubMedCrossRef
181.
Zurück zum Zitat Wang F, Jin R, Zou BB et al (2016) Activation of Toll-like receptor 7 regulates the expression of IFN-lambda1, p53, PTEN, VEGF, TIMP-1 and MMP-9 in pancreatic cancer cells. Mol Med Rep 13:1807–1812PubMedCrossRef Wang F, Jin R, Zou BB et al (2016) Activation of Toll-like receptor 7 regulates the expression of IFN-lambda1, p53, PTEN, VEGF, TIMP-1 and MMP-9 in pancreatic cancer cells. Mol Med Rep 13:1807–1812PubMedCrossRef
182.
Zurück zum Zitat Zhang Y, Yang H, Barnie PA et al (2014) The expression of Toll-like receptor 8 and its relationship with VEGF and Bcl-2 in cervical cancer. Int J Med Sci 11:608–613PubMedPubMedCentralCrossRef Zhang Y, Yang H, Barnie PA et al (2014) The expression of Toll-like receptor 8 and its relationship with VEGF and Bcl-2 in cervical cancer. Int J Med Sci 11:608–613PubMedPubMedCentralCrossRef
183.
Zurück zum Zitat Berger R, Fiegl H, Goebel G et al (2010) Toll-like receptor 9 expression in breast and ovarian cancer is associated with poorly differentiated tumors. Cancer Sci 101:1059–1066PubMedCrossRef Berger R, Fiegl H, Goebel G et al (2010) Toll-like receptor 9 expression in breast and ovarian cancer is associated with poorly differentiated tumors. Cancer Sci 101:1059–1066PubMedCrossRef
184.
Zurück zum Zitat Lee JW, Choi JJ, Seo ES et al (2007) Increased toll-like receptor 9 expression in cervical neoplasia. Mol Carcinog 46:941–947PubMedCrossRef Lee JW, Choi JJ, Seo ES et al (2007) Increased toll-like receptor 9 expression in cervical neoplasia. Mol Carcinog 46:941–947PubMedCrossRef
185.
Zurück zum Zitat Ronkainen H, Hirvikoski P, Kauppila S et al (2011) Absent Toll-like receptor-9 expression predicts poor prognosis in renal cell carcinoma. J Exp Clin Cancer Res 30:84PubMedPubMedCentralCrossRef Ronkainen H, Hirvikoski P, Kauppila S et al (2011) Absent Toll-like receptor-9 expression predicts poor prognosis in renal cell carcinoma. J Exp Clin Cancer Res 30:84PubMedPubMedCentralCrossRef
Metadaten
Titel
Toll-like receptors: exploring their potential connection with post-operative infectious complications and cancer recurrence
verfasst von
S. D. Gowing
J. J. Cool-Lartigue
J. D. Spicer
A. J. E. Seely
L. E. Ferri
Publikationsdatum
23.01.2020
Verlag
Springer Netherlands
Erschienen in
Clinical & Experimental Metastasis / Ausgabe 2/2020
Print ISSN: 0262-0898
Elektronische ISSN: 1573-7276
DOI
https://doi.org/10.1007/s10585-020-10018-2

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