Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/201931
Type: Artigo de periódico
Title: Agrin And Perlecan Mediate Tumorigenic Processes In Oral Squamous Cell Carcinoma.
Author: Kawahara, Rebeca
Granato, Daniela C
Carnielli, Carolina M
Cervigne, Nilva K
Oliveria, Carine E
Martinez, César A R
Yokoo, Sami
Fonseca, Felipe P
Lopes, Marcio
Santos-Silva, Alan R
Graner, Edgard
Coletta, Ricardo D
Paes Leme, Adriana Franco
Abstract: 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.
Rights: aberto
Identifier DOI: 10.1371/journal.pone.0115004
Address: http://www.ncbi.nlm.nih.gov/pubmed/25506919
Date Issue: 2014
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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