Skip to main content
Erschienen in: Clinical and Translational Oncology 10/2023

11.04.2023 | REVIEW ARTICLE

The crosstalk between autophagy and myeloid-derived suppressor cell responses in cancer

verfasst von: Jia Nie, Di Wang, MingJian Li

Erschienen in: Clinical and Translational Oncology | Ausgabe 10/2023

Einloggen, um Zugang zu erhalten

Abstract

The development of cancers is aided by the accumulation of myeloid-derived suppressor cells (MDSCs) within tumors, which are highly effective at suppressing anti-tumor immune responses. Direct cell-to-cell interaction and the production of immunosuppressive mediators have both been proposed as pathways for MDSC-mediated suppression of anti-tumor immune responses. The majority of current cancer treatments focus on altering the development and activity of MDSCs so that they have more of an immunogenic character. Autophagy is a catabolic system that contributes to the breakdown of damaged intracellular material and the recycling of metabolites. However, depending on the stage of tumor growth, autophagy can play both a prophylactic and a therapeutic function in carcinogenesis. However, several indirect lines of research have indicated that autophagy is a significant regulator of MDSC activity. The purpose of this work was to outline the interactions between MDSC and autophagy in cancer.
Literatur
1.
Zurück zum Zitat Meyer C, Sevko A, Ramacher M, Bazhin AV, Falk CS, Osen W, et al. Chronic inflammation promotes myeloid-derived suppressor cell activation blocking antitumor immunity in transgenic mouse melanoma model. Proc Natl Acad Sci. 2011;108(41):17111–6.PubMedPubMedCentralCrossRef Meyer C, Sevko A, Ramacher M, Bazhin AV, Falk CS, Osen W, et al. Chronic inflammation promotes myeloid-derived suppressor cell activation blocking antitumor immunity in transgenic mouse melanoma model. Proc Natl Acad Sci. 2011;108(41):17111–6.PubMedPubMedCentralCrossRef
2.
Zurück zum Zitat Hao Z, Li R, Wang Y, Li S, Hong Z, Han Z. Landscape of Myeloid-derived suppressor cell in tumor immunotherapy. Biomarker Res. 2021;9(1):77.CrossRef Hao Z, Li R, Wang Y, Li S, Hong Z, Han Z. Landscape of Myeloid-derived suppressor cell in tumor immunotherapy. Biomarker Res. 2021;9(1):77.CrossRef
3.
Zurück zum Zitat Tian Y, Xiao H, Yang Y, Zhang P, Yuan J, Zhang W, et al. Crosstalk between 5-methylcytosine and N6-methyladenosine machinery defines disease progression, therapeutic response and pharmacogenomic landscape in hepatocellular carcinoma. Mol Cancer. 2023;22(1):1–25.CrossRef Tian Y, Xiao H, Yang Y, Zhang P, Yuan J, Zhang W, et al. Crosstalk between 5-methylcytosine and N6-methyladenosine machinery defines disease progression, therapeutic response and pharmacogenomic landscape in hepatocellular carcinoma. Mol Cancer. 2023;22(1):1–25.CrossRef
4.
Zurück zum Zitat Yu Y, Wang L, Ni S, Li D, Liu J, Chu HY, et al. Targeting loop3 of sclerostin preserves its cardiovascular protective action and promotes bone formation. Nat Commun. 2022;13(1):4241.PubMedPubMedCentralCrossRef Yu Y, Wang L, Ni S, Li D, Liu J, Chu HY, et al. Targeting loop3 of sclerostin preserves its cardiovascular protective action and promotes bone formation. Nat Commun. 2022;13(1):4241.PubMedPubMedCentralCrossRef
6.
Zurück zum Zitat Parker KH, Horn LA, Ostrand-Rosenberg S. High-mobility group box protein 1 promotes the survival of myeloid-derived suppressor cells by inducing autophagy. J Leucocyte Biol. 2016;100(3):463–70.CrossRef Parker KH, Horn LA, Ostrand-Rosenberg S. High-mobility group box protein 1 promotes the survival of myeloid-derived suppressor cells by inducing autophagy. J Leucocyte Biol. 2016;100(3):463–70.CrossRef
7.
Zurück zum Zitat Samimi Z, Kardideh B, Zafari P, Bahrehmand F, Roghani SA, Taghadosi M. The impaired gene expression of adenosine monophosphate-activated kinase (AMPK), a key metabolic enzyme in leukocytes of newly diagnosed rheumatoid arthritis patients. Mol Biol Rep. 2019;46:6353–60.PubMedCrossRef Samimi Z, Kardideh B, Zafari P, Bahrehmand F, Roghani SA, Taghadosi M. The impaired gene expression of adenosine monophosphate-activated kinase (AMPK), a key metabolic enzyme in leukocytes of newly diagnosed rheumatoid arthritis patients. Mol Biol Rep. 2019;46:6353–60.PubMedCrossRef
8.
Zurück zum Zitat SuiX Z. RSL3 drives ferroptosis through GPX4 inactivation and ROS production in colorectal cancer. FrontPharmacol. 2018;9:1371. SuiX Z. RSL3 drives ferroptosis through GPX4 inactivation and ROS production in colorectal cancer. FrontPharmacol. 2018;9:1371.
9.
Zurück zum Zitat Wilson WR, Hay MP. Targeting hypoxia in cancer therapy. Nat Rev Cancer. 2011;11(6):393–410.PubMedCrossRef Wilson WR, Hay MP. Targeting hypoxia in cancer therapy. Nat Rev Cancer. 2011;11(6):393–410.PubMedCrossRef
10.
Zurück zum Zitat Hu S, Hui Z, Lirussi F, Garrido C, Ye X-Y, Xie T. Small molecule DNA-PK inhibitors as potential cancer therapy: a patent review (2010–present). Expert Opin Ther Pat. 2021;31(5):435–52.PubMedCrossRef Hu S, Hui Z, Lirussi F, Garrido C, Ye X-Y, Xie T. Small molecule DNA-PK inhibitors as potential cancer therapy: a patent review (2010–present). Expert Opin Ther Pat. 2021;31(5):435–52.PubMedCrossRef
14.
Zurück zum Zitat Liu S, Li Q, Chen K, Zhang Q, Li G, Zhuo L, et al. The emerging molecular mechanism of m6A modulators in tumorigenesis and cancer progression. Biomed Pharmacother. 2020;127: 110098.PubMedCrossRef Liu S, Li Q, Chen K, Zhang Q, Li G, Zhuo L, et al. The emerging molecular mechanism of m6A modulators in tumorigenesis and cancer progression. Biomed Pharmacother. 2020;127: 110098.PubMedCrossRef
15.
Zurück zum Zitat Levine B, Klionsky DJ. Development by self-digestion: molecular mechanisms and biological functions of autophagy. Dev Cell. 2004;6(4):463–77.PubMedCrossRef Levine B, Klionsky DJ. Development by self-digestion: molecular mechanisms and biological functions of autophagy. Dev Cell. 2004;6(4):463–77.PubMedCrossRef
16.
Zurück zum Zitat Bronte V, Brandau S, Chen S-H, Colombo MP, Frey AB, Greten TF, et al. Recommendations for myeloid-derived suppressor cell nomenclature and characterization standards. Nat Commun. 2016;7(1):12150.PubMedPubMedCentralCrossRef Bronte V, Brandau S, Chen S-H, Colombo MP, Frey AB, Greten TF, et al. Recommendations for myeloid-derived suppressor cell nomenclature and characterization standards. Nat Commun. 2016;7(1):12150.PubMedPubMedCentralCrossRef
17.
Zurück zum Zitat Dolcetti L, Marigo I, Mantelli B, Peranzoni E, Zanovello P, Bronte V. Myeloid-derived suppressor cell role in tumor-related inflammation. Cancer Lett. 2008;267(2):216–25.PubMedCrossRef Dolcetti L, Marigo I, Mantelli B, Peranzoni E, Zanovello P, Bronte V. Myeloid-derived suppressor cell role in tumor-related inflammation. Cancer Lett. 2008;267(2):216–25.PubMedCrossRef
18.
19.
Zurück zum Zitat Solito S, Marigo I, Pinton L, Damuzzo V, Mandruzzato S, Bronte V. Myeloid-derived suppressor cell heterogeneity in human cancers. Ann N Y Acad Sci. 2014;1319(1):47–65.PubMedCrossRef Solito S, Marigo I, Pinton L, Damuzzo V, Mandruzzato S, Bronte V. Myeloid-derived suppressor cell heterogeneity in human cancers. Ann N Y Acad Sci. 2014;1319(1):47–65.PubMedCrossRef
20.
Zurück zum Zitat Weber R, Fleming V, Hu X, Nagibin V, Groth C, Altevogt P, et al. Myeloid-derived suppressor cells hinder the anti-cancer activity of immune checkpoint inhibitors. Front Immunol. 2018;9:1310.PubMedPubMedCentralCrossRef Weber R, Fleming V, Hu X, Nagibin V, Groth C, Altevogt P, et al. Myeloid-derived suppressor cells hinder the anti-cancer activity of immune checkpoint inhibitors. Front Immunol. 2018;9:1310.PubMedPubMedCentralCrossRef
21.
Zurück zum Zitat Nagaraj S, Gupta K, Pisarev V, Kinarsky L, Sherman S, Kang L, et al. Altered recognition of antigen is a mechanism of CD8+ T cell tolerance in cancer. Nat Med. 2007;13(7):828–35.PubMedPubMedCentralCrossRef Nagaraj S, Gupta K, Pisarev V, Kinarsky L, Sherman S, Kang L, et al. Altered recognition of antigen is a mechanism of CD8+ T cell tolerance in cancer. Nat Med. 2007;13(7):828–35.PubMedPubMedCentralCrossRef
22.
Zurück zum Zitat Ashjari D, Karamali N, Rajabinejad M, Hassani SS, Hezarkhani LA, Afshari D, et al. The axis of long non-coding RNA MALAT1/miR-1-3p/CXCR4 is dysregulated in patients with diabetic neuropathy. Heliyon. 2022;8(3): e09178.PubMedPubMedCentralCrossRef Ashjari D, Karamali N, Rajabinejad M, Hassani SS, Hezarkhani LA, Afshari D, et al. The axis of long non-coding RNA MALAT1/miR-1-3p/CXCR4 is dysregulated in patients with diabetic neuropathy. Heliyon. 2022;8(3): e09178.PubMedPubMedCentralCrossRef
23.
Zurück zum Zitat Koike Y, Kanai T, Saeki K, Nakamura Y, Nakano M, Mikami Y, et al. MyD88-dependent interleukin-10 production from regulatory CD11b+ Gr-1high cells suppresses development of acute cerulein pancreatitis in mice. Immunol Lett. 2012;148(2):172–7.PubMedCrossRef Koike Y, Kanai T, Saeki K, Nakamura Y, Nakano M, Mikami Y, et al. MyD88-dependent interleukin-10 production from regulatory CD11b+ Gr-1high cells suppresses development of acute cerulein pancreatitis in mice. Immunol Lett. 2012;148(2):172–7.PubMedCrossRef
24.
Zurück zum Zitat Iranshahi N, Assar S, Amiri SM, Zafari P, Fekri A, Taghadosi M. Decreased gene expression of Epstein-Barr Virus-Induced Gene 3 (EBI-3) may contribute to the pathogenesis of rheumatoid arthritis. Immunol Invest. 2019;48(4):367–77.PubMedCrossRef Iranshahi N, Assar S, Amiri SM, Zafari P, Fekri A, Taghadosi M. Decreased gene expression of Epstein-Barr Virus-Induced Gene 3 (EBI-3) may contribute to the pathogenesis of rheumatoid arthritis. Immunol Invest. 2019;48(4):367–77.PubMedCrossRef
25.
Zurück zum Zitat Pan P-Y, Ma G, Weber KJ, Ozao-Choy J, Wang G, Yin B, et al. Immune stimulatory receptor CD40 is required for T-cell suppression and T regulatory cell activation mediated by myeloid-derived suppressor cells in cancer. Can Res. 2010;70(1):99–108.CrossRef Pan P-Y, Ma G, Weber KJ, Ozao-Choy J, Wang G, Yin B, et al. Immune stimulatory receptor CD40 is required for T-cell suppression and T regulatory cell activation mediated by myeloid-derived suppressor cells in cancer. Can Res. 2010;70(1):99–108.CrossRef
26.
Zurück zum Zitat Mao Y, Sarhan D, Steven A, Seliger B, Kiessling R, Lundqvist A. Inhibition of Tumor-Derived Prostaglandin-E2 Blocks the Induction of Myeloid-Derived Suppressor Cells and Recovers Natural Killer Cell ActivityRescue of NK Cells by Blocking the Induction of MDSCs. Clin Cancer Res. 2014;20(15):4096–106.PubMedCrossRef Mao Y, Sarhan D, Steven A, Seliger B, Kiessling R, Lundqvist A. Inhibition of Tumor-Derived Prostaglandin-E2 Blocks the Induction of Myeloid-Derived Suppressor Cells and Recovers Natural Killer Cell ActivityRescue of NK Cells by Blocking the Induction of MDSCs. Clin Cancer Res. 2014;20(15):4096–106.PubMedCrossRef
27.
Zurück zum Zitat Noman MZ, Desantis G, Janji B, Hasmim M, Karray S, Dessen P, et al. PD-L1 is a novel direct target of HIF-1α, and its blockade under hypoxia enhanced MDSC-mediated T cell activation. J Exp Med. 2014;211(5):781–90.PubMedPubMedCentralCrossRef Noman MZ, Desantis G, Janji B, Hasmim M, Karray S, Dessen P, et al. PD-L1 is a novel direct target of HIF-1α, and its blockade under hypoxia enhanced MDSC-mediated T cell activation. J Exp Med. 2014;211(5):781–90.PubMedPubMedCentralCrossRef
28.
Zurück zum Zitat Schreiber RD, Old LJ, Smyth MJ. Cancer immunoediting: integrating immunity’s roles in cancer suppression and promotion. Science. 2011;331(6024):1565–70.PubMedCrossRef Schreiber RD, Old LJ, Smyth MJ. Cancer immunoediting: integrating immunity’s roles in cancer suppression and promotion. Science. 2011;331(6024):1565–70.PubMedCrossRef
29.
Zurück zum Zitat Li Y-J, Lei Y-H, Yao N, Wang C-R, Hu N, Ye W-C, et al. Autophagy and multidrug resistance in cancer. Chin J Cancer. 2017;36(1):1–10.CrossRef Li Y-J, Lei Y-H, Yao N, Wang C-R, Hu N, Ye W-C, et al. Autophagy and multidrug resistance in cancer. Chin J Cancer. 2017;36(1):1–10.CrossRef
30.
Zurück zum Zitat Kishi-Itakura C, Koyama-Honda I, Itakura E, Mizushima N. Ultrastructural analysis of autophagosome organization using mammalian autophagy-deficient cells. J Cell Sci. 2014;127(18):4089–102.PubMed Kishi-Itakura C, Koyama-Honda I, Itakura E, Mizushima N. Ultrastructural analysis of autophagosome organization using mammalian autophagy-deficient cells. J Cell Sci. 2014;127(18):4089–102.PubMed
31.
Zurück zum Zitat Wang H, Gao Y, Vafaei S, Yu Q, Zhang J, Wang L. A chemoresistance lncRNA signature for recurrence risk stratification of colon cancer patients with chemotherapy. Mole Ther-Nucl Acids. 2022;27:427–38.CrossRef Wang H, Gao Y, Vafaei S, Yu Q, Zhang J, Wang L. A chemoresistance lncRNA signature for recurrence risk stratification of colon cancer patients with chemotherapy. Mole Ther-Nucl Acids. 2022;27:427–38.CrossRef
33.
Zurück zum Zitat Dasari SK, Bialik S, Levin-Zaidman S, Levin-Salomon V, Merrill AH, Futerman AH, et al. Signalome-wide RNAi screen identifies GBA1 as a positive mediator of autophagic cell death. Cell Death Differ. 2017;24(7):1288–302.PubMedPubMedCentralCrossRef Dasari SK, Bialik S, Levin-Zaidman S, Levin-Salomon V, Merrill AH, Futerman AH, et al. Signalome-wide RNAi screen identifies GBA1 as a positive mediator of autophagic cell death. Cell Death Differ. 2017;24(7):1288–302.PubMedPubMedCentralCrossRef
34.
Zurück zum Zitat Dasari SK, Schejter E, Bialik S, Shkedy A, Levin-Salomon V, Levin-Zaidman S, et al. Death by over-eating: The Gaucher disease associated gene GBA1, identified in a screen for mediators of autophagic cell death, is necessary for developmental cell death in Drosophila midgut. Cell Cycle. 2017;16(21):2003–10.PubMedPubMedCentralCrossRef Dasari SK, Schejter E, Bialik S, Shkedy A, Levin-Salomon V, Levin-Zaidman S, et al. Death by over-eating: The Gaucher disease associated gene GBA1, identified in a screen for mediators of autophagic cell death, is necessary for developmental cell death in Drosophila midgut. Cell Cycle. 2017;16(21):2003–10.PubMedPubMedCentralCrossRef
35.
Zurück zum Zitat Deng G, editor Intervention effect of vitamin D intake and serum 25 (OH) D level on ovarian cancer risk. European Journal of Gynaecological Oncology; 2022: Mre Press 14 Robinson Rd# 08–01a Far East Finance, Singapore, Singapore. Deng G, editor Intervention effect of vitamin D intake and serum 25 (OH) D level on ovarian cancer risk. European Journal of Gynaecological Oncology; 2022: Mre Press 14 Robinson Rd# 08–01a Far East Finance, Singapore, Singapore.
37.
Zurück zum Zitat Azad MB, Chen Y, Gibson SB. Regulation of autophagy by reactive oxygen species (ROS): implications for cancer progression and treatment. Antioxid Redox Signal. 2009;11(4):777–90.PubMedCrossRef Azad MB, Chen Y, Gibson SB. Regulation of autophagy by reactive oxygen species (ROS): implications for cancer progression and treatment. Antioxid Redox Signal. 2009;11(4):777–90.PubMedCrossRef
38.
Zurück zum Zitat Mathew R, Karp CM, Beaudoin B, Vuong N, Chen G, Chen H-Y, et al. Autophagy suppresses tumorigenesis through elimination of p62. Cell. 2009;137(6):1062–75.PubMedPubMedCentralCrossRef Mathew R, Karp CM, Beaudoin B, Vuong N, Chen G, Chen H-Y, et al. Autophagy suppresses tumorigenesis through elimination of p62. Cell. 2009;137(6):1062–75.PubMedPubMedCentralCrossRef
39.
Zurück zum Zitat Burada F, Nicoli ER, Ciurea ME, Uscatu DC, Ioana M, Gheonea DI. Autophagy in colorectal cancer: an important switch from physiology to pathology. World J of Gastrointestinal Oncol. 2015;7(11):271.CrossRef Burada F, Nicoli ER, Ciurea ME, Uscatu DC, Ioana M, Gheonea DI. Autophagy in colorectal cancer: an important switch from physiology to pathology. World J of Gastrointestinal Oncol. 2015;7(11):271.CrossRef
40.
Zurück zum Zitat Karami Fath M, Azargoonjahromi A, Soofi A, Almasi F, Hosseinzadeh S, Khalili S, et al. Current understanding of epigenetics role in melanoma treatment and resistance. Cancer Cell Int. 2022;22(1):1–23.CrossRef Karami Fath M, Azargoonjahromi A, Soofi A, Almasi F, Hosseinzadeh S, Khalili S, et al. Current understanding of epigenetics role in melanoma treatment and resistance. Cancer Cell Int. 2022;22(1):1–23.CrossRef
41.
Zurück zum Zitat Wang H, Fang Z-Z, Zheng Y, Zhou K, Hu C, Krausz KW, et al. Metabolic profiling of praziquantel enantiomers. Biochem Pharmacol. 2014;90(2):166–78.PubMedPubMedCentralCrossRef Wang H, Fang Z-Z, Zheng Y, Zhou K, Hu C, Krausz KW, et al. Metabolic profiling of praziquantel enantiomers. Biochem Pharmacol. 2014;90(2):166–78.PubMedPubMedCentralCrossRef
43.
Zurück zum Zitat Chavez-Dominguez R, Perez-Medina M, Lopez-Gonzalez JS, Galicia-Velasco M, Aguilar-Cazares D. The double-edge sword of autophagy in cancer: from tumor suppression to pro-tumor activity. Front Oncol. 2020;10: 578418.PubMedPubMedCentralCrossRef Chavez-Dominguez R, Perez-Medina M, Lopez-Gonzalez JS, Galicia-Velasco M, Aguilar-Cazares D. The double-edge sword of autophagy in cancer: from tumor suppression to pro-tumor activity. Front Oncol. 2020;10: 578418.PubMedPubMedCentralCrossRef
44.
Zurück zum Zitat Rabbani B, Khorgami M, Dalili M, Zamani N, Mahdieh N, Gollob MH. Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome. Am J Med Genet A. 2021;185(11):3433–45.PubMedCrossRef Rabbani B, Khorgami M, Dalili M, Zamani N, Mahdieh N, Gollob MH. Novel cases of pediatric sudden cardiac death secondary to TRDN mutations presenting as long QT syndrome at rest and catecholaminergic polymorphic ventricular tachycardia during exercise: The TRDN arrhythmia syndrome. Am J Med Genet A. 2021;185(11):3433–45.PubMedCrossRef
45.
Zurück zum Zitat Omidi N, Arabloo J, Rezapour A, Alaeddini F, Bragazzi NL, Pourasghari H, et al. Burden of hypertensive heart disease in Iran during 1990–2017: findings from the Global Burden of Disease study 2017. PLoS ONE. 2021;16(9): e0257617.PubMedPubMedCentralCrossRef Omidi N, Arabloo J, Rezapour A, Alaeddini F, Bragazzi NL, Pourasghari H, et al. Burden of hypertensive heart disease in Iran during 1990–2017: findings from the Global Burden of Disease study 2017. PLoS ONE. 2021;16(9): e0257617.PubMedPubMedCentralCrossRef
47.
Zurück zum Zitat Chen H-T, Liu H, Mao M-J, Tan Y, Mo X-Q, Meng X-J, et al. Crosstalk between autophagy and epithelial-mesenchymal transition and its application in cancer therapy. Mol Cancer. 2019;18(1):1–19.PubMedPubMedCentralCrossRef Chen H-T, Liu H, Mao M-J, Tan Y, Mo X-Q, Meng X-J, et al. Crosstalk between autophagy and epithelial-mesenchymal transition and its application in cancer therapy. Mol Cancer. 2019;18(1):1–19.PubMedPubMedCentralCrossRef
48.
Zurück zum Zitat Sharif T, Martell E, Dai C, Kennedy BE, Murphy P, Clements DR, et al. Autophagic homeostasis is required for the pluripotency of cancer stem cells. Autophagy. 2017;13(2):264–84.PubMedCrossRef Sharif T, Martell E, Dai C, Kennedy BE, Murphy P, Clements DR, et al. Autophagic homeostasis is required for the pluripotency of cancer stem cells. Autophagy. 2017;13(2):264–84.PubMedCrossRef
49.
Zurück zum Zitat Peng Q, Qin J, Zhang Y, Cheng X, Wang X, Lu W, et al. Autophagy maintains the stemness of ovarian cancer stem cells by FOXA2. J Exp Clin Cancer Res. 2017;36(1):1–12.CrossRef Peng Q, Qin J, Zhang Y, Cheng X, Wang X, Lu W, et al. Autophagy maintains the stemness of ovarian cancer stem cells by FOXA2. J Exp Clin Cancer Res. 2017;36(1):1–12.CrossRef
50.
Zurück zum Zitat Li L, Pan D, Zhang S, Xie D, Zheng X, Chen H. Autophagy regulates chemoresistance of gastric cancer stem cells via the Notch signaling pathway. Eur Rev Med Pharmacol Sci. 2018;22(11):3402–7.PubMed Li L, Pan D, Zhang S, Xie D, Zheng X, Chen H. Autophagy regulates chemoresistance of gastric cancer stem cells via the Notch signaling pathway. Eur Rev Med Pharmacol Sci. 2018;22(11):3402–7.PubMed
51.
Zurück zum Zitat Alissafi T, Hatzioannou A, Mintzas K, Barouni RM, Banos A, Sormendi S, et al. Autophagy orchestrates the regulatory program of tumor-associated myeloid-derived suppressor cells. J Clin Invest. 2018;128(9):3840–52.PubMedPubMedCentralCrossRef Alissafi T, Hatzioannou A, Mintzas K, Barouni RM, Banos A, Sormendi S, et al. Autophagy orchestrates the regulatory program of tumor-associated myeloid-derived suppressor cells. J Clin Invest. 2018;128(9):3840–52.PubMedPubMedCentralCrossRef
52.
Zurück zum Zitat Korolchuk VI, Saiki S, Lichtenberg M, Siddiqi FH, Roberts EA, Imarisio S, et al. Lysosomal positioning coordinates cellular nutrient responses. Nat Cell Biol. 2011;13(4):453–60.PubMedPubMedCentralCrossRef Korolchuk VI, Saiki S, Lichtenberg M, Siddiqi FH, Roberts EA, Imarisio S, et al. Lysosomal positioning coordinates cellular nutrient responses. Nat Cell Biol. 2011;13(4):453–60.PubMedPubMedCentralCrossRef
53.
Zurück zum Zitat Zhao H, Ming T, Tang S, Ren S, Yang H, Liu M, et al. Wnt signaling in colorectal cancer: pathogenic role and therapeutic target. Mol Cancer. 2022;21(1):144.PubMedPubMedCentralCrossRef Zhao H, Ming T, Tang S, Ren S, Yang H, Liu M, et al. Wnt signaling in colorectal cancer: pathogenic role and therapeutic target. Mol Cancer. 2022;21(1):144.PubMedPubMedCentralCrossRef
54.
Zurück zum Zitat Bos R, Sherman LA. CD4+ T-Cell Help in the Tumor Milieu Is required for recruitment and cytolytic Function of CD8+ T LymphocytesMechanisms of Tumor-Specific CD4 Help. Can Res. 2010;70(21):8368–77.CrossRef Bos R, Sherman LA. CD4+ T-Cell Help in the Tumor Milieu Is required for recruitment and cytolytic Function of CD8+ T LymphocytesMechanisms of Tumor-Specific CD4 Help. Can Res. 2010;70(21):8368–77.CrossRef
55.
Zurück zum Zitat Nagaraj S, Nelson A, Youn J-i, Cheng P, Quiceno D, Gabrilovich DI. Antigen-specific CD4+ T Cells Regulate function of myeloid-derived suppressor cells in cancer via retrograde MHC Class II SignalingMDSC and CD4+ T cells. Can Res. 2012;72(4):928–38.CrossRef Nagaraj S, Nelson A, Youn J-i, Cheng P, Quiceno D, Gabrilovich DI. Antigen-specific CD4+ T Cells Regulate function of myeloid-derived suppressor cells in cancer via retrograde MHC Class II SignalingMDSC and CD4+ T cells. Can Res. 2012;72(4):928–38.CrossRef
56.
Zurück zum Zitat Hu Z, Zhao TV, Huang T, Ohtsuki S, Jin K, Goronzy IN, et al. The transcription factor RFX5 coordinates antigen-presenting function and resistance to nutrient stress in synovial macrophages. Nat Metab. 2022;4(6):759–74.PubMedPubMedCentralCrossRef Hu Z, Zhao TV, Huang T, Ohtsuki S, Jin K, Goronzy IN, et al. The transcription factor RFX5 coordinates antigen-presenting function and resistance to nutrient stress in synovial macrophages. Nat Metab. 2022;4(6):759–74.PubMedPubMedCentralCrossRef
57.
Zurück zum Zitat Poschke I, Mougiakakos D, Hansson J, Masucci GV, Kiessling R. Immature immunosuppressive CD14+ HLA-DR−/low Cells in melanoma patients are Stat3hi and overexpress CD80, CD83, and DC-SignCharacterization of Melanoma CD14+ HLA-DR−/low MDSC. Can Res. 2010;70(11):4335–45.CrossRef Poschke I, Mougiakakos D, Hansson J, Masucci GV, Kiessling R. Immature immunosuppressive CD14+ HLA-DR−/low Cells in melanoma patients are Stat3hi and overexpress CD80, CD83, and DC-SignCharacterization of Melanoma CD14+ HLA-DR−/low MDSC. Can Res. 2010;70(11):4335–45.CrossRef
58.
Zurück zum Zitat Serafini P, Mgebroff S, Noonan K, Borrello I. Myeloid-derived suppressor cells promote cross-tolerance in B-cell lymphoma by expanding regulatory T cells. Can Res. 2008;68(13):5439–49.CrossRef Serafini P, Mgebroff S, Noonan K, Borrello I. Myeloid-derived suppressor cells promote cross-tolerance in B-cell lymphoma by expanding regulatory T cells. Can Res. 2008;68(13):5439–49.CrossRef
59.
Zurück zum Zitat Wu JS, Li L, Wang SS, Pang X, Wu JB, Sheng SR, et al. Autophagy is positively associated with the accumulation of myeloid-derived suppressor cells in 4-nitroquinoline-1-oxide-induced oral cancer. Oncol Rep. 2018;40(6):3381–91.PubMedPubMedCentral Wu JS, Li L, Wang SS, Pang X, Wu JB, Sheng SR, et al. Autophagy is positively associated with the accumulation of myeloid-derived suppressor cells in 4-nitroquinoline-1-oxide-induced oral cancer. Oncol Rep. 2018;40(6):3381–91.PubMedPubMedCentral
60.
Zurück zum Zitat Thevenot PT, Sierra RA, Raber PL, Al-Khami AA, Trillo-Tinoco J, Zarreii P, et al. The stress-response sensor chop regulates the function and accumulation of myeloid-derived suppressor cells in tumors. Immunity. 2014;41(3):389–401.PubMedPubMedCentralCrossRef Thevenot PT, Sierra RA, Raber PL, Al-Khami AA, Trillo-Tinoco J, Zarreii P, et al. The stress-response sensor chop regulates the function and accumulation of myeloid-derived suppressor cells in tumors. Immunity. 2014;41(3):389–401.PubMedPubMedCentralCrossRef
61.
Zurück zum Zitat Scherz-Shouval R, Elazar Z. Regulation of autophagy by ROS: physiology and pathology. Trends Biochem Sci. 2011;36(1):30–8.PubMedCrossRef Scherz-Shouval R, Elazar Z. Regulation of autophagy by ROS: physiology and pathology. Trends Biochem Sci. 2011;36(1):30–8.PubMedCrossRef
62.
Zurück zum Zitat Parker KH, Sinha P, Horn LA, Clements VK, Yang H, Li J, et al. HMGB1 enhances immune suppression by facilitating the differentiation and suppressive activity of myeloid-derived suppressor cells. Can Res. 2014;74(20):5723–33.CrossRef Parker KH, Sinha P, Horn LA, Clements VK, Yang H, Li J, et al. HMGB1 enhances immune suppression by facilitating the differentiation and suppressive activity of myeloid-derived suppressor cells. Can Res. 2014;74(20):5723–33.CrossRef
63.
65.
Zurück zum Zitat Bellot G, Garcia-Medina R, Gounon P, Chiche J, Roux D, Pouysségur J, et al. Hypoxia-induced autophagy is mediated through hypoxia-inducible factor induction of BNIP3 and BNIP3L via their BH3 domains. Mol Cell Biol. 2009;29(10):2570–81.PubMedPubMedCentralCrossRef Bellot G, Garcia-Medina R, Gounon P, Chiche J, Roux D, Pouysségur J, et al. Hypoxia-induced autophagy is mediated through hypoxia-inducible factor induction of BNIP3 and BNIP3L via their BH3 domains. Mol Cell Biol. 2009;29(10):2570–81.PubMedPubMedCentralCrossRef
66.
Zurück zum Zitat Corzo CA, Condamine T, Lu L, Cotter MJ, Youn JI, Cheng P, et al. HIF-1α regulates function and differentiation of myeloid-derived suppressor cells in the tumor microenvironment. J Exp Med. 2010;207(11):2439–53.PubMedPubMedCentralCrossRef Corzo CA, Condamine T, Lu L, Cotter MJ, Youn JI, Cheng P, et al. HIF-1α regulates function and differentiation of myeloid-derived suppressor cells in the tumor microenvironment. J Exp Med. 2010;207(11):2439–53.PubMedPubMedCentralCrossRef
67.
Zurück zum Zitat Zhang K, Liang F, Qaria MA, Wang H, Lin M, Zhang F. Roles of 630 nm red light-emitting diode in inhibition of RhoA Signal transduction pathway via reducing plekhg5 expression and alleviation of inflammatory response in macrophages. J Biol Regu Homeostatic Agents. 2022;36(5):1419–26. Zhang K, Liang F, Qaria MA, Wang H, Lin M, Zhang F. Roles of 630 nm red light-emitting diode in inhibition of RhoA Signal transduction pathway via reducing plekhg5 expression and alleviation of inflammatory response in macrophages. J Biol Regu Homeostatic Agents. 2022;36(5):1419–26.
68.
Zurück zum Zitat Li W, Tanikawa T, Kryczek I, Xia H, Li G, Wu K, et al. Aerobic Glycolysis controls myeloid-derived suppressor cells and tumor immunity via a specific CEBPB isoform in triple-negative breast cancer. Cell Metab. 2018;28(1):87-103.e6.PubMedPubMedCentralCrossRef Li W, Tanikawa T, Kryczek I, Xia H, Li G, Wu K, et al. Aerobic Glycolysis controls myeloid-derived suppressor cells and tumor immunity via a specific CEBPB isoform in triple-negative breast cancer. Cell Metab. 2018;28(1):87-103.e6.PubMedPubMedCentralCrossRef
69.
Zurück zum Zitat Bianchini G, Balko JM, Mayer IA, Sanders ME, Gianni L. Triple-negative breast cancer: challenges and opportunities of a heterogeneous disease. Nat Rev Clin Oncol. 2016;13(11):674–90.PubMedPubMedCentralCrossRef Bianchini G, Balko JM, Mayer IA, Sanders ME, Gianni L. Triple-negative breast cancer: challenges and opportunities of a heterogeneous disease. Nat Rev Clin Oncol. 2016;13(11):674–90.PubMedPubMedCentralCrossRef
70.
Zurück zum Zitat Harris LN, Ismaila N, McShane LM, Andre F, Collyar DE, Gonzalez-Angulo AM, et al. Use of biomarkers to guide decisions on adjuvant systemic therapy for women with early-stage invasive breast cancer: American society of clinical oncology clinical practice guideline. J Clin Oncol. 2016;34(10):1134.PubMedPubMedCentralCrossRef Harris LN, Ismaila N, McShane LM, Andre F, Collyar DE, Gonzalez-Angulo AM, et al. Use of biomarkers to guide decisions on adjuvant systemic therapy for women with early-stage invasive breast cancer: American society of clinical oncology clinical practice guideline. J Clin Oncol. 2016;34(10):1134.PubMedPubMedCentralCrossRef
74.
Zurück zum Zitat Miao T, Liu Y, (2022) editors. Clinical study of VBA-based diffusion kurtosis imaging technique on cognitive dysfunction of breast cancer patients undergoing chemotherapy. EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY,: MRE PRESS 14 ROBINSON RD# 08–01A FAR EAST FINANCE, SINGAPORE, SINGAPORE. Miao T, Liu Y, (2022) editors. Clinical study of VBA-based diffusion kurtosis imaging technique on cognitive dysfunction of breast cancer patients undergoing chemotherapy. EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY,: MRE PRESS 14 ROBINSON RD# 08–01A FAR EAST FINANCE, SINGAPORE, SINGAPORE.
75.
Zurück zum Zitat Wang W, Kryczek I, Dostál L, Lin H, Tan L, Zhao L, et al. Effector T cells abrogate stroma-mediated chemoresistance in ovarian cancer. Cell. 2016;165(5):1092–105.PubMedPubMedCentralCrossRef Wang W, Kryczek I, Dostál L, Lin H, Tan L, Zhao L, et al. Effector T cells abrogate stroma-mediated chemoresistance in ovarian cancer. Cell. 2016;165(5):1092–105.PubMedPubMedCentralCrossRef
76.
Zurück zum Zitat Liu F, Li X, Lu C, Bai A, Bielawski J, Bielawska A, et al. Ceramide activates lysosomal cathepsin B and cathepsin D to attenuate autophagy and induces ER stress to suppress myeloid-derived suppressor cells. Oncotarget. 2016;7(51):83907–25.PubMedPubMedCentralCrossRef Liu F, Li X, Lu C, Bai A, Bielawski J, Bielawska A, et al. Ceramide activates lysosomal cathepsin B and cathepsin D to attenuate autophagy and induces ER stress to suppress myeloid-derived suppressor cells. Oncotarget. 2016;7(51):83907–25.PubMedPubMedCentralCrossRef
77.
Zurück zum Zitat Wang B, Dong G, Zhang Q, Yan F, Li Z, Li C, et al. The inhibitor of autophagy SBI-0206965 aggravates atherosclerosis through decreasing myeloid-derived suppressor cells. Exp Ther Med. 2020;19(2):1370–8.PubMed Wang B, Dong G, Zhang Q, Yan F, Li Z, Li C, et al. The inhibitor of autophagy SBI-0206965 aggravates atherosclerosis through decreasing myeloid-derived suppressor cells. Exp Ther Med. 2020;19(2):1370–8.PubMed
78.
80.
Zurück zum Zitat Koehn BH, Apostolova P, Haverkamp JM, Miller JS, McCullar V, Tolar J, et al. GVHD-associated, inflammasome-mediated loss of function in adoptively transferred myeloid-derived suppressor cells Blood. J Am Soc Hematol. 2015;126(13):1621–8. Koehn BH, Apostolova P, Haverkamp JM, Miller JS, McCullar V, Tolar J, et al. GVHD-associated, inflammasome-mediated loss of function in adoptively transferred myeloid-derived suppressor cells Blood. J Am Soc Hematol. 2015;126(13):1621–8.
Metadaten
Titel
The crosstalk between autophagy and myeloid-derived suppressor cell responses in cancer
verfasst von
Jia Nie
Di Wang
MingJian Li
Publikationsdatum
11.04.2023
Verlag
Springer International Publishing
Erschienen in
Clinical and Translational Oncology / Ausgabe 10/2023
Print ISSN: 1699-048X
Elektronische ISSN: 1699-3055
DOI
https://doi.org/10.1007/s12094-023-03160-2

Weitere Artikel der Ausgabe 10/2023

Clinical and Translational Oncology 10/2023 Zur Ausgabe

Erhöhte Mortalität bei postpartalem Brustkrebs

07.05.2024 Mammakarzinom Nachrichten

Auch für Trägerinnen von BRCA-Varianten gilt: Erkranken sie fünf bis zehn Jahre nach der letzten Schwangerschaft an Brustkrebs, ist das Sterberisiko besonders hoch.

Hypertherme Chemotherapie bietet Chance auf Blasenerhalt

07.05.2024 Harnblasenkarzinom Nachrichten

Eine hypertherme intravesikale Chemotherapie mit Mitomycin kann für Patienten mit hochriskantem nicht muskelinvasivem Blasenkrebs eine Alternative zur radikalen Zystektomie darstellen. Kölner Urologen berichten über ihre Erfahrungen.

Ein Drittel der jungen Ärztinnen und Ärzte erwägt abzuwandern

07.05.2024 Medizinstudium Nachrichten

Extreme Arbeitsverdichtung und kaum Supervision: Dr. Andrea Martini, Sprecherin des Bündnisses Junge Ärztinnen und Ärzte (BJÄ) über den Frust des ärztlichen Nachwuchses und die Vorteile des Rucksack-Modells.

Bessere Prognose mit links- statt rechtsseitigem Kolon-Ca.

06.05.2024 Kolonkarzinom Nachrichten

Menschen mit linksseitigem Kolonkarzinom leben im Mittel zweieinhalb Jahre länger als solche mit rechtsseitigem Tumor. Auch aktuell ist das Sterberisiko bei linksseitigen Tumoren US-Daten zufolge etwa um 11% geringer als bei rechtsseitigen.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.