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Erschienen in: International Journal of Clinical Oncology 3/2014

01.06.2014 | Review Article

Update of molecular pathobiology in oral cancer: a review

verfasst von: Tomonori Sasahira, Tadaaki Kirita, Hiroki Kuniyasu

Erschienen in: International Journal of Clinical Oncology | Ausgabe 3/2014

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Abstract

Head and neck cancer including oral squamous cell carcinoma (OSCC) is the sixth most common cancer in the world. OSCC has a high potential for local invasion and nodal metastasis, and the overall 5-year survival rate has not significantly changed during the past 30 years. Recent research has elucidated the detailed molecular mechanisms of carcinogenesis, tumor progression, and metastasis of OSCC. It is generally accepted that OSCC arises from multiple genetic alterations caused by chronic exposure to carcinogens such as alcohol, smoking, viral infections, and inflammation. The molecular mechanisms of carcinogenesis, tumor progression, and metastasis of head and neck cancer have been elucidated by recent advances in molecular biology. However, many unsolved questions remain. In this review, we describe the current molecular biological findings such as human papillomavirus infection, epithelial–mesenchymal transition, microRNA, and our novel molecular pathological findings of OSCC.
Literatur
1.
Zurück zum Zitat Min R, Siyi L, Wenjun Y et al (2012) Toll-like receptor-9 agonists increase cyclin D1 expression partly through activation of activator protein-1 in human oral squamous cell carcinoma cells. Cancer Sci 103(11):1938–1945PubMedCrossRef Min R, Siyi L, Wenjun Y et al (2012) Toll-like receptor-9 agonists increase cyclin D1 expression partly through activation of activator protein-1 in human oral squamous cell carcinoma cells. Cancer Sci 103(11):1938–1945PubMedCrossRef
2.
3.
Zurück zum Zitat Tanaka S, Sobue T (2005) Comparison of oral and pharyngeal cancer mortality in five countries: France, Italy, Japan, UK and USA from the WHO Mortality Database (1960–2000). Jpn J Clin Oncol 35(8):488–491PubMedCrossRef Tanaka S, Sobue T (2005) Comparison of oral and pharyngeal cancer mortality in five countries: France, Italy, Japan, UK and USA from the WHO Mortality Database (1960–2000). Jpn J Clin Oncol 35(8):488–491PubMedCrossRef
4.
Zurück zum Zitat Kurihara M, Kirita T, Sasahira T et al (2013) Protumoral roles of melanoma inhibitory activity 2 in oral squamous cell carcinoma. Br J Cancer 108(7):1460–1469PubMedCentralPubMedCrossRef Kurihara M, Kirita T, Sasahira T et al (2013) Protumoral roles of melanoma inhibitory activity 2 in oral squamous cell carcinoma. Br J Cancer 108(7):1460–1469PubMedCentralPubMedCrossRef
5.
Zurück zum Zitat Dos Reis PP, Bharadwaj RR, Machado J et al (2008) Claudin 1 overexpression increases invasion and is associated with aggressive histological features in oral squamous cell carcinoma. Cancer 113(11):3169–3180PubMedCrossRef Dos Reis PP, Bharadwaj RR, Machado J et al (2008) Claudin 1 overexpression increases invasion and is associated with aggressive histological features in oral squamous cell carcinoma. Cancer 113(11):3169–3180PubMedCrossRef
6.
Zurück zum Zitat Marsh D, Suchak K, Moutasim KA et al (2011) Stromal features are predictive of disease mortality in oral cancer patients. J Pathol 223(4):470–481PubMedCrossRef Marsh D, Suchak K, Moutasim KA et al (2011) Stromal features are predictive of disease mortality in oral cancer patients. J Pathol 223(4):470–481PubMedCrossRef
7.
Zurück zum Zitat Sasahira T, Kurihara M, Bhawal UK et al (2012) Downregulation of miR-126 induces angiogenesis and lymphangiogenesis by activation of VEGF-A in oral cancer. Br J Cancer 107(4):700–706PubMedCentralPubMedCrossRef Sasahira T, Kurihara M, Bhawal UK et al (2012) Downregulation of miR-126 induces angiogenesis and lymphangiogenesis by activation of VEGF-A in oral cancer. Br J Cancer 107(4):700–706PubMedCentralPubMedCrossRef
8.
Zurück zum Zitat Leemans CR, Braakhuis BJ, Brakenhoff RH (2011) The molecular biology of head and neck cancer. Nat Rev Cancer 11(1):9–22PubMedCrossRef Leemans CR, Braakhuis BJ, Brakenhoff RH (2011) The molecular biology of head and neck cancer. Nat Rev Cancer 11(1):9–22PubMedCrossRef
9.
Zurück zum Zitat Syrjanen S, Lodi G, von Bultzingslowen I et al (2011) Human papillomaviruses in oral carcinoma and oral potentially malignant disorders: a systematic review. Oral Dis 17(Suppl 1):58–72PubMedCrossRef Syrjanen S, Lodi G, von Bultzingslowen I et al (2011) Human papillomaviruses in oral carcinoma and oral potentially malignant disorders: a systematic review. Oral Dis 17(Suppl 1):58–72PubMedCrossRef
10.
Zurück zum Zitat Kreimer AR, Clifford GM, Boyle P et al (2005) Human papillomavirus types in head and neck squamous cell carcinomas worldwide: a systematic review. Cancer Epidemiol Biomark Prev 14(2):467–475CrossRef Kreimer AR, Clifford GM, Boyle P et al (2005) Human papillomavirus types in head and neck squamous cell carcinomas worldwide: a systematic review. Cancer Epidemiol Biomark Prev 14(2):467–475CrossRef
11.
Zurück zum Zitat D’Souza G, Kreimer AR, Viscidi R et al (2007) Case-control study of human papillomavirus and oropharyngeal cancer. N Engl J Med 356(19):1944–1956PubMedCrossRef D’Souza G, Kreimer AR, Viscidi R et al (2007) Case-control study of human papillomavirus and oropharyngeal cancer. N Engl J Med 356(19):1944–1956PubMedCrossRef
12.
Zurück zum Zitat Begum S, Westra WH (2008) Basaloid squamous cell carcinoma of the head and neck is a mixed variant that can be further resolved by HPV status. Am J Surg Pathol 32(7):1044–1050PubMedCrossRef Begum S, Westra WH (2008) Basaloid squamous cell carcinoma of the head and neck is a mixed variant that can be further resolved by HPV status. Am J Surg Pathol 32(7):1044–1050PubMedCrossRef
13.
Zurück zum Zitat Quan J, Elhousiny M, Johnson NW et al (2013) Transforming growth factor-beta1 treatment of oral cancer induces epithelial–mesenchymal transition and promotes bone invasion via enhanced activity of osteoclasts. Clin Exp Metastasis 30(5):659–670PubMedCentralPubMedCrossRef Quan J, Elhousiny M, Johnson NW et al (2013) Transforming growth factor-beta1 treatment of oral cancer induces epithelial–mesenchymal transition and promotes bone invasion via enhanced activity of osteoclasts. Clin Exp Metastasis 30(5):659–670PubMedCentralPubMedCrossRef
14.
Zurück zum Zitat Heldin CH, Vanlandewijck M, Moustakas A (2012) Regulation of EMT by TGFbeta in cancer. FEBS Lett 586(14):1959–1970PubMedCrossRef Heldin CH, Vanlandewijck M, Moustakas A (2012) Regulation of EMT by TGFbeta in cancer. FEBS Lett 586(14):1959–1970PubMedCrossRef
15.
Zurück zum Zitat Wu BH, Xiong XP, Jia J et al (2011) MicroRNAs: new actors in the oral cancer scene. Oral Oncol 47(5):314–319PubMedCrossRef Wu BH, Xiong XP, Jia J et al (2011) MicroRNAs: new actors in the oral cancer scene. Oral Oncol 47(5):314–319PubMedCrossRef
16.
Zurück zum Zitat Perez-Sayans M, Pilar GD, Barros-Angueira F et al (2012) Current trends in miRNAs and their relationship with oral squamous cell carcinoma. J Oral Pathol Med 41(6):433–443PubMedCrossRef Perez-Sayans M, Pilar GD, Barros-Angueira F et al (2012) Current trends in miRNAs and their relationship with oral squamous cell carcinoma. J Oral Pathol Med 41(6):433–443PubMedCrossRef
17.
Zurück zum Zitat Park NJ, Zhou H, Elashoff D et al (2009) Salivary microRNA: discovery, characterization, and clinical utility for oral cancer detection. Clin Cancer Res 15(17):5473–5477PubMedCentralPubMedCrossRef Park NJ, Zhou H, Elashoff D et al (2009) Salivary microRNA: discovery, characterization, and clinical utility for oral cancer detection. Clin Cancer Res 15(17):5473–5477PubMedCentralPubMedCrossRef
18.
Zurück zum Zitat Wald AI, Hoskins EE, Wells SI et al (2011) Alteration of microRNA profiles in squamous cell carcinoma of the head and neck cell lines by human papillomavirus. Head Neck 33(4):504–512PubMedCentralPubMedCrossRef Wald AI, Hoskins EE, Wells SI et al (2011) Alteration of microRNA profiles in squamous cell carcinoma of the head and neck cell lines by human papillomavirus. Head Neck 33(4):504–512PubMedCentralPubMedCrossRef
19.
Zurück zum Zitat Li J, Huang H, Sun L et al (2009) MiR-21 indicates poor prognosis in tongue squamous cell carcinomas as an apoptosis inhibitor. Clin Cancer Res 15(12):3998–4008PubMedCrossRef Li J, Huang H, Sun L et al (2009) MiR-21 indicates poor prognosis in tongue squamous cell carcinomas as an apoptosis inhibitor. Clin Cancer Res 15(12):3998–4008PubMedCrossRef
20.
Zurück zum Zitat Liu X, Wang A, Heidbreder CE et al (2010) MicroRNA-24 targeting RNA-binding protein DND1 in tongue squamous cell carcinoma. FEBS Lett 584(18):4115–4120PubMedCentralPubMedCrossRef Liu X, Wang A, Heidbreder CE et al (2010) MicroRNA-24 targeting RNA-binding protein DND1 in tongue squamous cell carcinoma. FEBS Lett 584(18):4115–4120PubMedCentralPubMedCrossRef
21.
Zurück zum Zitat Chang KW, Liu CJ, Chu TH et al (2008) Association between high miR-211 microRNA expression and the poor prognosis of oral carcinoma. J Dent Res 87(11):1063–1068PubMedCrossRef Chang KW, Liu CJ, Chu TH et al (2008) Association between high miR-211 microRNA expression and the poor prognosis of oral carcinoma. J Dent Res 87(11):1063–1068PubMedCrossRef
22.
Zurück zum Zitat Liu CJ, Tsai MM, Hung PS et al (2010) miR-31 ablates expression of the HIF regulatory factor FIH to activate the HIF pathway in head and neck carcinoma. Cancer Res 70(4):1635–1644PubMedCrossRef Liu CJ, Tsai MM, Hung PS et al (2010) miR-31 ablates expression of the HIF regulatory factor FIH to activate the HIF pathway in head and neck carcinoma. Cancer Res 70(4):1635–1644PubMedCrossRef
23.
Zurück zum Zitat Yu ZW, Zhong LP, Ji T et al (2010) MicroRNAs contribute to the chemoresistance of cisplatin in tongue squamous cell carcinoma lines. Oral Oncol 46(4):317–322PubMedCrossRef Yu ZW, Zhong LP, Ji T et al (2010) MicroRNAs contribute to the chemoresistance of cisplatin in tongue squamous cell carcinoma lines. Oral Oncol 46(4):317–322PubMedCrossRef
24.
Zurück zum Zitat Wong TS, Liu XB, Chung-Wai Ho A et al (2008) Identification of pyruvate kinase type M2 as potential oncoprotein in squamous cell carcinoma of tongue through microRNA profiling. Int J Cancer 123(2):251–257PubMedCrossRef Wong TS, Liu XB, Chung-Wai Ho A et al (2008) Identification of pyruvate kinase type M2 as potential oncoprotein in squamous cell carcinoma of tongue through microRNA profiling. Int J Cancer 123(2):251–257PubMedCrossRef
25.
Zurück zum Zitat Mutallip M, Nohata N, Hanazawa T et al (2011) Glutathione S-transferase P1 (GSTP1) suppresses cell apoptosis and its regulation by miR-133alpha in head and neck squamous cell carcinoma (HNSCC). Int J Mol Med 27(3):345–352PubMed Mutallip M, Nohata N, Hanazawa T et al (2011) Glutathione S-transferase P1 (GSTP1) suppresses cell apoptosis and its regulation by miR-133alpha in head and neck squamous cell carcinoma (HNSCC). Int J Mol Med 27(3):345–352PubMed
26.
Zurück zum Zitat Jiang L, Liu X, Chen Z et al (2010) MicroRNA-7 targets IGF1R (insulin-like growth factor 1 receptor) in tongue squamous cell carcinoma cells. Biochem J 432(1):199–205PubMedCentralPubMedCrossRef Jiang L, Liu X, Chen Z et al (2010) MicroRNA-7 targets IGF1R (insulin-like growth factor 1 receptor) in tongue squamous cell carcinoma cells. Biochem J 432(1):199–205PubMedCentralPubMedCrossRef
27.
Zurück zum Zitat Liu X, Wang C, Chen Z et al (2011) MicroRNA-138 suppresses epithelial–mesenchymal transition in squamous cell carcinoma cell lines. Biochem J 440(1):23–31PubMedCentralPubMedCrossRef Liu X, Wang C, Chen Z et al (2011) MicroRNA-138 suppresses epithelial–mesenchymal transition in squamous cell carcinoma cell lines. Biochem J 440(1):23–31PubMedCentralPubMedCrossRef
28.
Zurück zum Zitat Zidar N, Bostjancic E, Gale N et al (2011) Down-regulation of microRNAs of the miR-200 family and miR-205, and an altered expression of classic and desmosomal cadherins in spindle cell carcinoma of the head and neck–hallmark of epithelial–mesenchymal transition. Hum Pathol 42(4):482–488PubMedCrossRef Zidar N, Bostjancic E, Gale N et al (2011) Down-regulation of microRNAs of the miR-200 family and miR-205, and an altered expression of classic and desmosomal cadherins in spindle cell carcinoma of the head and neck–hallmark of epithelial–mesenchymal transition. Hum Pathol 42(4):482–488PubMedCrossRef
31.
Zurück zum Zitat Slaby O, Redova M, Poprach A et al (2012) Identification of MicroRNAs associated with early relapse after nephrectomy in renal cell carcinoma patients. Genes Chromosom Cancer 51(7):707–716PubMedCrossRef Slaby O, Redova M, Poprach A et al (2012) Identification of MicroRNAs associated with early relapse after nephrectomy in renal cell carcinoma patients. Genes Chromosom Cancer 51(7):707–716PubMedCrossRef
33.
Zurück zum Zitat Sasahira T, Ueda N, Yamamoto K et al (2013) Trks are novel oncogenes involved in the induction of neovascularization, tumor progression, and nodal metastasis in oral squamous cell carcinoma. Clin Exp Metastasis 30(2):165–176PubMedCrossRef Sasahira T, Ueda N, Yamamoto K et al (2013) Trks are novel oncogenes involved in the induction of neovascularization, tumor progression, and nodal metastasis in oral squamous cell carcinoma. Clin Exp Metastasis 30(2):165–176PubMedCrossRef
34.
Zurück zum Zitat Sasahira T, Ueda N, Kurihara M et al (2013) Tropomyosin receptor kinases B and C are tumor progressive and metastatic marker in colorectal carcinoma. Hum Pathol 44(6):1098–1106PubMedCrossRef Sasahira T, Ueda N, Kurihara M et al (2013) Tropomyosin receptor kinases B and C are tumor progressive and metastatic marker in colorectal carcinoma. Hum Pathol 44(6):1098–1106PubMedCrossRef
35.
Zurück zum Zitat Davidson B, Reich R, Lazarovici P et al (2003) Expression and activation of the nerve growth factor receptor TrkA in serous ovarian carcinoma. Clin Cancer Res 9(6):2248–2259PubMed Davidson B, Reich R, Lazarovici P et al (2003) Expression and activation of the nerve growth factor receptor TrkA in serous ovarian carcinoma. Clin Cancer Res 9(6):2248–2259PubMed
36.
Zurück zum Zitat Yu X, Liu L, Cai B et al (2008) Suppression of anoikis by the neurotrophic receptor TrkB in human ovarian cancer. Cancer Sci 99(3):543–552PubMedCrossRef Yu X, Liu L, Cai B et al (2008) Suppression of anoikis by the neurotrophic receptor TrkB in human ovarian cancer. Cancer Sci 99(3):543–552PubMedCrossRef
37.
Zurück zum Zitat Bouzas-Rodriguez J, Cabrera JR, Delloye-Bourgeois C et al (2010) Neurotrophin-3 production promotes human neuroblastoma cell survival by inhibiting TrkC-induced apoptosis. J Clin Invest 120(3):850–858PubMedCentralPubMedCrossRef Bouzas-Rodriguez J, Cabrera JR, Delloye-Bourgeois C et al (2010) Neurotrophin-3 production promotes human neuroblastoma cell survival by inhibiting TrkC-induced apoptosis. J Clin Invest 120(3):850–858PubMedCentralPubMedCrossRef
38.
Zurück zum Zitat Nakagawara A, Arima-Nakagawara M, Scavarda NJ et al (1993) Association between high levels of expression of the TRK gene and favorable outcome in human neuroblastoma. N Engl J Med 328(12):847–854PubMedCrossRef Nakagawara A, Arima-Nakagawara M, Scavarda NJ et al (1993) Association between high levels of expression of the TRK gene and favorable outcome in human neuroblastoma. N Engl J Med 328(12):847–854PubMedCrossRef
39.
Zurück zum Zitat Yamashiro DJ, Liu XG, Lee CP et al (1997) Expression and function of Trk-C in favourable human neuroblastomas. Eur J Cancer 33(12):2054–2057PubMedCrossRef Yamashiro DJ, Liu XG, Lee CP et al (1997) Expression and function of Trk-C in favourable human neuroblastomas. Eur J Cancer 33(12):2054–2057PubMedCrossRef
40.
Zurück zum Zitat Satoh F, Mimata H, Nomura T et al (2001) Autocrine expression of neurotrophins and their receptors in prostate cancer. Int J Urol 8(7):S28–S34PubMedCrossRef Satoh F, Mimata H, Nomura T et al (2001) Autocrine expression of neurotrophins and their receptors in prostate cancer. Int J Urol 8(7):S28–S34PubMedCrossRef
41.
Zurück zum Zitat Chuang LS, Ito K, Ito Y (2013) RUNX family: regulation and diversification of roles through interacting proteins. Int J Cancer 132(6):1260–1271PubMedCrossRef Chuang LS, Ito K, Ito Y (2013) RUNX family: regulation and diversification of roles through interacting proteins. Int J Cancer 132(6):1260–1271PubMedCrossRef
42.
Zurück zum Zitat Sasahira T, Kurihara M, Yamamoto K et al (2011) Downregulation of runt-related transcription factor 3 associated with poor prognosis of adenoid cystic and mucoepidermoid carcinomas of the salivary gland. Cancer Sci 102(2):492–497PubMedCrossRef Sasahira T, Kurihara M, Yamamoto K et al (2011) Downregulation of runt-related transcription factor 3 associated with poor prognosis of adenoid cystic and mucoepidermoid carcinomas of the salivary gland. Cancer Sci 102(2):492–497PubMedCrossRef
43.
Zurück zum Zitat Sasahira T, Akama Y, Fujii K et al (2005) Expression of receptor for advanced glycation end products and HMGB1/amphoterin in colorectal adenomas. Virchows Arch 446(4):411–415PubMedCrossRef Sasahira T, Akama Y, Fujii K et al (2005) Expression of receptor for advanced glycation end products and HMGB1/amphoterin in colorectal adenomas. Virchows Arch 446(4):411–415PubMedCrossRef
44.
Zurück zum Zitat Kusume A, Sasahira T, Luo Y et al (2009) Suppression of dendritic cells by HMGB1 is associated with lymph node metastasis of human colon cancer. Pathobiology 76(4):155–162PubMedCrossRef Kusume A, Sasahira T, Luo Y et al (2009) Suppression of dendritic cells by HMGB1 is associated with lymph node metastasis of human colon cancer. Pathobiology 76(4):155–162PubMedCrossRef
45.
Zurück zum Zitat Kuniyasu H, Sasaki T, Sasahira T et al (2004) Depletion of tumor-infiltrating macrophages is associated with amphoterin expression in colon cancer. Pathobiology 71(3):129–136PubMedCrossRef Kuniyasu H, Sasaki T, Sasahira T et al (2004) Depletion of tumor-infiltrating macrophages is associated with amphoterin expression in colon cancer. Pathobiology 71(3):129–136PubMedCrossRef
46.
Zurück zum Zitat Sasahira T, Sasaki T, Kuniyasu H (2005) Interleukin-15 and transforming growth factor alpha are associated with depletion of tumor-associated macrophages in colon cancer. J Exp Clin Cancer Res 24(1):69–74PubMed Sasahira T, Sasaki T, Kuniyasu H (2005) Interleukin-15 and transforming growth factor alpha are associated with depletion of tumor-associated macrophages in colon cancer. J Exp Clin Cancer Res 24(1):69–74PubMed
47.
Zurück zum Zitat Rauvala H, Huttunen HJ, Fages C et al (2000) Heparin-binding proteins HB-GAM (pleiotrophin) and amphoterin in the regulation of cell motility. Matrix Biol 19(5):377–387PubMedCrossRef Rauvala H, Huttunen HJ, Fages C et al (2000) Heparin-binding proteins HB-GAM (pleiotrophin) and amphoterin in the regulation of cell motility. Matrix Biol 19(5):377–387PubMedCrossRef
48.
Zurück zum Zitat Taguchi A, Blood DC, del Toro G et al (2000) Blockade of RAGE-amphoterin signalling suppresses tumour growth and metastases. Nature 405(6784):354–360PubMedCrossRef Taguchi A, Blood DC, del Toro G et al (2000) Blockade of RAGE-amphoterin signalling suppresses tumour growth and metastases. Nature 405(6784):354–360PubMedCrossRef
49.
Zurück zum Zitat Kuniyasu H, Oue N, Wakikawa A et al (2002) Expression of receptors for advanced glycation end-products (RAGE) is closely associated with the invasive and metastatic activity of gastric cancer. J Pathol 196(2):163–170PubMedCrossRef Kuniyasu H, Oue N, Wakikawa A et al (2002) Expression of receptors for advanced glycation end-products (RAGE) is closely associated with the invasive and metastatic activity of gastric cancer. J Pathol 196(2):163–170PubMedCrossRef
50.
Zurück zum Zitat Kuniyasu H, Chihara Y, Takahashi T (2003) Co-expression of receptor for advanced glycation end products and the ligand amphoterin associates closely with metastasis of colorectal cancer. Oncol Rep 10(2):445–448PubMed Kuniyasu H, Chihara Y, Takahashi T (2003) Co-expression of receptor for advanced glycation end products and the ligand amphoterin associates closely with metastasis of colorectal cancer. Oncol Rep 10(2):445–448PubMed
51.
Zurück zum Zitat Sasahira T, Kirita T, Bhawal UK et al (2007) Receptor for advanced glycation end products (RAGE) is important in the prediction of recurrence in human oral squamous cell carcinoma. Histopathology 51(2):166–172PubMedCrossRef Sasahira T, Kirita T, Bhawal UK et al (2007) Receptor for advanced glycation end products (RAGE) is important in the prediction of recurrence in human oral squamous cell carcinoma. Histopathology 51(2):166–172PubMedCrossRef
52.
Zurück zum Zitat Sasahira T, Kirita T, Bhawal UK et al (2007) The expression of receptor for advanced glycation end products is associated with angiogenesis in human oral squamous cell carcinoma. Virchows Arch 450(3):287–295PubMedCrossRef Sasahira T, Kirita T, Bhawal UK et al (2007) The expression of receptor for advanced glycation end products is associated with angiogenesis in human oral squamous cell carcinoma. Virchows Arch 450(3):287–295PubMedCrossRef
53.
Zurück zum Zitat Yamamoto K, Kitayama W, Denda A et al (2006) Expression of receptor for advanced glycation end products during rat tongue carcinogenesis by 4-nitroquinoline 1-oxide and effect of a selective cyclooxygenase-2 inhibitor, etodolac. Pathobiology 73(6):317–324PubMedCrossRef Yamamoto K, Kitayama W, Denda A et al (2006) Expression of receptor for advanced glycation end products during rat tongue carcinogenesis by 4-nitroquinoline 1-oxide and effect of a selective cyclooxygenase-2 inhibitor, etodolac. Pathobiology 73(6):317–324PubMedCrossRef
54.
Zurück zum Zitat Bosserhoff AK, Moser M, Buettner R (2004) Characterization and expression pattern of the novel MIA homolog TANGO. Gene Expr Patterns 4(4):473–479PubMedCrossRef Bosserhoff AK, Moser M, Buettner R (2004) Characterization and expression pattern of the novel MIA homolog TANGO. Gene Expr Patterns 4(4):473–479PubMedCrossRef
55.
Zurück zum Zitat Bosserhoff AK, Buettner R (2002) Expression, function and clinical relevance of MIA (melanoma inhibitory activity). Histol Histopathol 17(1):289–300PubMed Bosserhoff AK, Buettner R (2002) Expression, function and clinical relevance of MIA (melanoma inhibitory activity). Histol Histopathol 17(1):289–300PubMed
56.
Zurück zum Zitat Arndt S, Bosserhoff AK (2006) TANGO is a tumor suppressor of malignant melanoma. Int J Cancer 119(12):2812–2820PubMedCrossRef Arndt S, Bosserhoff AK (2006) TANGO is a tumor suppressor of malignant melanoma. Int J Cancer 119(12):2812–2820PubMedCrossRef
57.
Zurück zum Zitat Arndt S, Bosserhoff AK (2007) Reduced expression of TANGO in colon and hepatocellular carcinomas. Oncol Rep 18(4):885–891PubMed Arndt S, Bosserhoff AK (2007) Reduced expression of TANGO in colon and hepatocellular carcinomas. Oncol Rep 18(4):885–891PubMed
58.
Zurück zum Zitat Koehler MR, Bosserhoff A, von Beust G et al (1996) Assignment of the human melanoma inhibitory activity gene (MIA) to 19q13.32–q13.33 by fluorescence in situ hybridization (FISH). Genomics 35(1):265–267PubMedCrossRef Koehler MR, Bosserhoff A, von Beust G et al (1996) Assignment of the human melanoma inhibitory activity gene (MIA) to 19q13.32–q13.33 by fluorescence in situ hybridization (FISH). Genomics 35(1):265–267PubMedCrossRef
59.
Zurück zum Zitat Bosserhoff AK, Stoll R, Sleeman JP et al (2003) Active detachment involves inhibition of cell-matrix contacts of malignant melanoma cells by secretion of melanoma inhibitory activity. Lab Invest 83(11):1583–1594PubMedCrossRef Bosserhoff AK, Stoll R, Sleeman JP et al (2003) Active detachment involves inhibition of cell-matrix contacts of malignant melanoma cells by secretion of melanoma inhibitory activity. Lab Invest 83(11):1583–1594PubMedCrossRef
60.
Zurück zum Zitat Jachimczak P, Apfel R, Bosserhoff AK et al (2005) Inhibition of immunosuppressive effects of melanoma-inhibiting activity (MIA) by antisense techniques. Int J Cancer 113(1):88–92PubMedCrossRef Jachimczak P, Apfel R, Bosserhoff AK et al (2005) Inhibition of immunosuppressive effects of melanoma-inhibiting activity (MIA) by antisense techniques. Int J Cancer 113(1):88–92PubMedCrossRef
61.
Zurück zum Zitat Sasahira T, Kirita T, Oue N et al (2008) High mobility group box-1-inducible melanoma inhibitory activity is associated with nodal metastasis and lymphangiogenesis in oral squamous cell carcinoma. Cancer Sci 99(9):1806–1812PubMed Sasahira T, Kirita T, Oue N et al (2008) High mobility group box-1-inducible melanoma inhibitory activity is associated with nodal metastasis and lymphangiogenesis in oral squamous cell carcinoma. Cancer Sci 99(9):1806–1812PubMed
62.
Zurück zum Zitat Sasahira T, Kirita T, Kurihara M et al (2010) MIA-dependent angiogenesis and lymphangiogenesis are closely associated with progression, nodal metastasis and poor prognosis in tongue squamous cell carcinoma. Eur J Cancer 46(12):2285–2294PubMedCrossRef Sasahira T, Kirita T, Kurihara M et al (2010) MIA-dependent angiogenesis and lymphangiogenesis are closely associated with progression, nodal metastasis and poor prognosis in tongue squamous cell carcinoma. Eur J Cancer 46(12):2285–2294PubMedCrossRef
63.
Zurück zum Zitat Bosserhoff AK, Moser M, Scholmerich J et al (2003) Specific expression and regulation of the new melanoma inhibitory activity-related gene MIA2 in hepatocytes. J Biol Chem 278(17):15225–15231PubMedCrossRef Bosserhoff AK, Moser M, Scholmerich J et al (2003) Specific expression and regulation of the new melanoma inhibitory activity-related gene MIA2 in hepatocytes. J Biol Chem 278(17):15225–15231PubMedCrossRef
64.
Zurück zum Zitat Hellerbrand C, Bataille F, Schlegel J et al (2005) In situ expression patterns of melanoma inhibitory activity 2 in healthy and diseased livers. Liver Int 25(2):357–366PubMedCrossRef Hellerbrand C, Bataille F, Schlegel J et al (2005) In situ expression patterns of melanoma inhibitory activity 2 in healthy and diseased livers. Liver Int 25(2):357–366PubMedCrossRef
65.
Zurück zum Zitat Hellerbrand C, Amann T, Schlegel J et al (2008) The novel gene MIA2 acts as a tumour suppressor in hepatocellular carcinoma. Gut 57(2):243–251PubMedCrossRef Hellerbrand C, Amann T, Schlegel J et al (2008) The novel gene MIA2 acts as a tumour suppressor in hepatocellular carcinoma. Gut 57(2):243–251PubMedCrossRef
66.
Zurück zum Zitat Biomarkers Definitions Working Group (2001) Biomarkers and surrogate endpoints: preferred definitions and conceptual framework. Clin Pharmacol Ther 69(3):89–95CrossRef Biomarkers Definitions Working Group (2001) Biomarkers and surrogate endpoints: preferred definitions and conceptual framework. Clin Pharmacol Ther 69(3):89–95CrossRef
67.
Zurück zum Zitat Wu JY, Yi C, Chung HR et al (2010) Potential biomarkers in saliva for oral squamous cell carcinoma. Oral Oncol 46(4):226–231PubMedCrossRef Wu JY, Yi C, Chung HR et al (2010) Potential biomarkers in saliva for oral squamous cell carcinoma. Oral Oncol 46(4):226–231PubMedCrossRef
Metadaten
Titel
Update of molecular pathobiology in oral cancer: a review
verfasst von
Tomonori Sasahira
Tadaaki Kirita
Hiroki Kuniyasu
Publikationsdatum
01.06.2014
Verlag
Springer Japan
Erschienen in
International Journal of Clinical Oncology / Ausgabe 3/2014
Print ISSN: 1341-9625
Elektronische ISSN: 1437-7772
DOI
https://doi.org/10.1007/s10147-014-0684-4

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