Artículos de revistas
Agrin And Perlecan Mediate Tumorigenic Processes In Oral Squamous Cell Carcinoma
Registro en:
Plos One. Public Library Of Science, v. 9, n. 12, p. - , 2014.
19326203
10.1371/journal.pone.0115004
2-s2.0-84918556188
Autor
Kawahara R.
Granato D.C.
Carnielli C.M.
Cervigne N.K.
Oliveria C.E.
Martinez C.A.R.
Yokoo S.
Fonseca F.P.
Lopes M.
Santos-Silva A.R.
Graner E.
Coletta R.D.
Leme A.F.P.
Institución
Resumen
Oral squamous cell carcinoma is the most common type of cancer in the oral cavity, representing more than 90% of all oral cancers. The characterization of altered molecules in oral cancer is essential to understand molecular mechanisms underlying tumor progression as well as to contribute to cancer biomarker and therapeutic target discovery. Proteoglycans are key molecular effectors of cell surface and pericellular microenvironments, performing multiple functions in cancer. Two of the major basement membrane proteoglycans, agrin and perlecan, were investigated in this study regarding their role in oral cancer. Using real time quantitative PCR (qRT-PCR), we showed that agrin and perlecan are highly expressed in oral squamous cell carcinoma. Interestingly, cell lines originated from distinct sites showed different expression of agrin and perlecan. Enzymatically targeting chondroitin sulfate modification by chondroitinase, oral squamous carcinoma cell line had a reduced ability to adhere to extracellular matrix proteins and increased sensibility to cisplatin. Additionally, knockdown of agrin and perlecan promoted a decrease on cell migration and adhesion, and on resistance of cells to cisplatin. Our study showed, for the first time, a negative regulation on oral cancer-associated events by either targeting chondroitin sulfate content or agrin and perlecan levels. 9 12
Argiris, A., Karamouzis, M.V., Raben, D., Ferris, R.L., Head and neck cancer (2008) Lancet, 371, pp. 1695-1709 Belcher, R., Hayes, K., Fedewa, S., Chen, A.Y., Current treatment of head and neck squamous cell cancer (2014) J Surg Oncol Mydlarz, W.K., Hennessey, P.T., Califano, J.A., Advances and Perspectives in the Molecular Diagnosis of Head and Neck Cancer (2010) Expert Opin Med Diagn, 4, pp. 53-65 Da Silva, S.D., Ferlito, A., Takes, R.P., Brakenhoff, R.H., Valentin, M.D., Advances and applications of oral cancer basic research (2011) Oral Oncol, 47, pp. 783-791 Pereira, M.C., Oliveira, D.T., Landman, G., Kowalski, L.P., Histologic subtypes of oral squamous cell carcinoma: Prognostic relevance (2007) J Can Dent Assoc, 73, pp. 339-344 Van Kempen, L.C., Ruiter, D.J., Van Muijen, G.N., Coussens, L.M., The tumor microenvironment: A critical determinant of neoplastic evolution (2003) Eur J Cell Biol, 82, pp. 539-548 Naba, A., Clauser, K.R., Hoersch, S., Liu, H., Carr, S.A., The matrisome: In silico definition and in vivo characterization by proteomics of normal and tumor extracellular matrices (2012) Mol Cell Proteomics, 11, pp. M111+014647 Barash, U., Cohen-Kaplan, V., Dowek, I., Sanderson, R.D., Ilan, N., Proteoglycans in health and disease: New concepts for heparanase function in tumor progression and metastasis (2010) FEBS J, 277, pp. 3890-3903 Theocharis, A.D., Skandalis, S.S., Tzanakakis, G.N., Karamanos, N.K., Proteoglycans in health and disease: Novel roles for proteoglycans in malignancy and their pharmacological targeting (2010) FEBS J, 277, pp. 3904-3923 Iozzo, R.V., Sanderson, R.D., Proteoglycans in cancer biology, tumour microenvironment and angiogenesis (2011) J Cell Mol Med, 15, pp. 1013-1031 Edwards, I.J., Proteoglycans in prostate cancer (2012) Nat Rev Urol, 9, pp. 196-206 Tatrai, P., Dudas, J., Batmunkh, E., Mathe, M., Zalatnai, A., Agrin, a novel basement membrane component in human and rat liver, accumulates in cirrhosis and hepatocellular carcinoma (2006) Lab Invest, 86, pp. 1149-1160 Mundhenke, C., Meyer, K., Drew, S., Friedl, A., Heparan sulfate proteoglycans as regulators of fibroblast growth factor-2 receptor binding in breast carcinomas (2002) Am J Pathol, 160, pp. 185-194 Sharma, B., Handler, M., Eichstetter, I., Whitelock, J.M., Nugent, M.A., Antisense targeting of perlecan blocks tumor growth and angiogenesis in vivo (1998) J Clin Invest, 102, pp. 1599-1608 Savore, C., Zhang, C., Muir, C., Liu, R., Wyrwa, J., Perlecan knockdown in metastatic prostate cancer cells reduces heparin-binding growth factor responses in vitro and tumor growth in vivo (2005) Clin Exp Metastasis, 22, pp. 377-390 Iozzo, R.V., Cohen, I.R., Grassel, S., Murdoch, A.D., The biology of perlecan: The multifaceted heparan sulphate proteoglycan of basement membranes and pericellular matrices (1994) Biochem J, 302, pp. 625-639 Noonan, D.M., Fulle, A., Valente, P., Cai, S., Horigan, E., The complete sequence of perlecan, a basement membrane heparan sulfate proteoglycan, reveals extensive similarity with laminin A chain, low density lipoprotein-receptor, and the neural cell adhesion molecule (1991) J Biol Chem, 266, pp. 22939-22947 Murdoch, A.D., Liu, B., Schwarting, R., Tuan, R.S., Iozzo, R.V., Widespread expression of perlecan proteoglycan in basement membranes and extracellular matrices of human tissues as detected by a novel monoclonal antibody against domain III and by in situ hybridization (1994) J Histochem Cytochem, 42, pp. 239-249 Mishra, M., Chandavarkar, V., Naik, V.V., Kale, A.D., An immunohistochemical study of basement membrane heparan sulfate proteoglycan (perlecan) in oral epithelial dysplasia and squamous cell carcinoma (2013) J Oral Maxillofac Pathol, 17, pp. 31-35 Ida-Yonemochi, H., Ikarashi, T., Nagata, M., Hoshina, H., Takagi, R., The basement membrane-type heparan sulfate proteoglycan (perlecan) in ameloblastomas: Its intercellular localization in stellate reticulum-like foci and biosynthesis by tumor cells in culture (2002) Virchows Arch, 441, pp. 165-173 Ikarashi, T., Ida-Yonemochi, H., Ohshiro, K., Cheng, J., Saku, T., Intraepithelial expression of perlecan, a basement membrane-type heparan sulfate proteoglycan reflects dysplastic changes of the oral mucosal epithelium (2004) J Oral Pathol Med, 33, pp. 87-95 Iozzo, R.V., Zoeller, J.J., Nystrom, A., Basement membrane proteoglycans: Modulators Par Excellence of cancer growth and angiogenesis (2009) Mol Cells, 27, pp. 503-513 Winzen, U., Cole, G.J., Halfter, W., Agrin is a chimeric proteoglycan with the attachment sites for heparan sulfate/chondroitin sulfate located in two multiple serine-glycine clusters (2003) J Biol Chem, 278, pp. 30106-30114 Somoracz, A., Tatrai, P., Horvath, G., Kiss, A., Kupcsulik, P., Agrin immunohistochemistry facilitates the determination of primary versus metastatic origin of liver carcinomas (2010) Hum Pathol, 41, pp. 1310-1319 Batmunkh, E., Tatrai, P., Szabo, E., Lodi, C., Holczbauer, A., Comparison of the expression of agrin, a basement membrane heparan sulfate proteoglycan, in cholangiocarcinoma and hepatocellular carcinoma (2007) Hum Pathol, 38, pp. 1508-1515 Agostini, M., Almeida, L.Y., Bastos, D.C., Ortega, R.M., Moreira, F.S., The Fatty Acid synthase inhibitor orlistat reduces the growth and metastasis of orthotopic tongue oral squamous cell carcinomas (2014) Mol Cancer Ther, 13, pp. 585-595 Aragao, A.Z., Belloni, M., Simabuco, F.M., Zanetti, M.R., Yokoo, S., Novel processed form of syndecan-1 shed from SCC-9 cells plays a role in cell migration (2012) PLoS One, 7, p. e43521 Silva, H., Frezard, F., Peterson, E.J., Kabolizadeh, P., Ryan, J.J., Heparan sulfate proteoglycan-mediated entry pathway for charged tri-platinum compounds: Differential cellular accumulation mechanisms for platinum (2012) Mol Pharm, 9, pp. 1795-1802 Terp, M.G., Lund, R.R., Jensen, O.N., Leth-Larsen, R., Ditzel, H.J., Identification of markers associated with highly aggressive metastatic phenotypes using quantitative comparative proteomics (2012) Cancer Genomics Proteomics, 9, pp. 265-273 Noguti, J., De Moura, C.F., De Jesus, G.P., Da Silva, V.H., Hossaka, T.A., Metastasis from oral cancer: An overview (2012) Cancer Genomics Proteomics, 9, pp. 329-335 O'Donnell, R.K., Kupferman, M., Wei, S.J., Singhal, S., Weber, R., Gene expression signature predicts lymphatic metastasis in squamous cell carcinoma of the oral cavity (2005) Oncogene, 24, pp. 1244-1251 Chang, K.P., Yu, J.S., Chien, K.Y., Lee, C.W., Liang, Y., Identification of PRDX4 and P4HA2 as metastasis-associated proteins in oral cavity squamous cell carcinoma by comparative tissue proteomics of microdissected specimens using iTRAQ technology (2011) J Proteome Res, 10, pp. 4935-4947 Chai, Y.D., Zhang, L., Yang, Y., Su, T., Charugundla, P., Discovery of potential serum protein biomarkers for lymph-node metastasis in oral cancer (2014) Head Neck Feller, L.L.J., Oral Squamous Cell Carcinoma: Epidemiology, Clinical Presentation and Treatment (2012) Journal of Cancer Therapy, 3, pp. 263-268 Afratis, N., Gialeli, C., Nikitovic, D., Tsegenidis, T., Karousou, E., Glycosaminoglycans: Key players in cancer cell biology and treatment (2012) FEBS J, 279, pp. 1177-1197 Fuster, M.M., Esko, J.D., The sweet and sour of cancer: Glycans as novel therapeutic targets (2005) Nat Rev Cancer, 5, pp. 526-542 Vlodavsky, I., Friedmann, Y., Molecular properties and involvement of heparanase in cancer metastasis and angiogenesis (2001) J Clin Invest, 108, pp. 341-347 Goldshmidt, O., Zcharia, E., Abramovitch, R., Metzger, S., Aingorn, H., Cell surface expression and secretion of heparanase markedly promote tumor angiogenesis and metastasis (2002) Proc Natl Acad Sci U S A, 99, pp. 10031-10036 Pantazaka, E., Papadimitriou, E., Chondroitin sulfate-cell membrane effectors as regulators of growth factor-mediated vascular and cancer cell migration (2014) Biochim Biophys Acta, 1840, pp. 2643-2650 Cattaruzza, S., Perris, R., Proteoglycan control of cell movement during wound healing and cancer spreading (2005) Matrix Biol, 24, pp. 400-417 Zhou, Z., Wang, J., Cao, R., Morita, H., Soininen, R., Impaired angiogenesis, delayed wound healing and retarded tumor growth in perlecan heparan sulfate-deficient mice (2004) Cancer Res, 64, pp. 4699-4702 Whitelock, J.M., Graham, L.D., Melrose, J., Murdoch, A.D., Iozzo, R.V., Human perlecan immunopurified from different endothelial cell sources has different adhesive properties for vascular cells (1999) Matrix Biol, 18, pp. 163-178 Klein, G., Conzelmann, S., Beck, S., Timpl, R., Muller, C.A., Perlecan in human bone marrow: A growth-factor-presenting, but anti-adhesive, extracellular matrix component for hematopoietic cells (1995) Matrix Biol, 14, pp. 457-465 Bix, G., Iozzo, R.V., Matrix revolutions: Tail of basement-membrane components with angiostatic functions (2005) Trends Cell Biol, 15, pp. 52-60 Hayashi, K., Madri, J.A., Yurchenco, P.D., Endothelial cells interact with the core protein of basement membrane perlecan through beta 1 and beta 3 integrins: An adhesion modulated by glycosaminoglycan (1992) J Cell Biol, 119, pp. 945-959 Martin, P.T., Sanes, J.R., Integrins mediate adhesion to agrin and modulate agrin signaling (1997) Development, 124, pp. 3909-3917 Yip, G.W., Smollich, M., Gotte, M., Therapeutic value of glycosaminoglycans in cancer (2006) Mol Cancer Ther, 5, pp. 2139-2148 Zhang, J.S., Anraku, M., Kadowaki, D., Imai, T., Suenaga, A., Spectroscopic studies of interactions of chondroitin sulfates with cisplatin (2011) Carbohydr Res, 346, pp. 631-637 Rabik, C.A., Dolan, M.E., Molecular mechanisms of resistance and toxicity associated with platinating agents (2007) Cancer Treat Rev, 33, pp. 9-23 Galluzzi, L., Senovilla, L., Vitale, I., Michels, J., Martins, I., Molecular mechanisms of cisplatin resistance (2012) Oncogene, 31, pp. 1869-1883 Dasari, S., Bernard Tchounwou, P., Cisplatin in Cancer therapy: Molecular mechanisms of action (2014) Eur J Pharmacol Barr, M.P., Gray, S.G., Hoffmann, A.C., Hilger, R.A., Thomale, J., Generation and characterisation of cisplatin-resistant non-small cell lung cancer cell lines displaying a stem-like signature (2013) PLoS One, 8, p. e54193 Eberle, K.E., Sansing, H.A., Szaniszlo, P., Resto, V.A., Berrier, A.L., Carcinoma matrix controls resistance to cisplatin through talin regulation of NF-kB (2011) PLoS One, 6, p. e21496 Teng, P.N., Wang, G., Hood, B.L., Conrads, K.A., Hamilton, C.A., Identification of candidate circulating cisplatin-resistant biomarkers from epithelial ovarian carcinoma cell secretomes (2014) Br J Cancer, 110, pp. 123-132