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Identification of differentially expressed genes in oral squamous cell carcinoma
Author(s) -
Arora Shilpi,
Matta Ajay,
Shukla Nootan Kumar,
Deo S.V.S.,
Ralhan Ranju
Publication year - 2005
Publication title -
molecular carcinogenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.254
H-Index - 97
eISSN - 1098-2744
pISSN - 0899-1987
DOI - 10.1002/mc.20048
Subject(s) - biology , carcinogenesis , differential display , cancer research , gene , cancer , cell , angiogenesis , cell growth , gene expression , microbiology and biotechnology , genetics
Abstract Rapid advances in multimodality therapy have not significantly improved the overall 5‐yr survival of oral cancer patients in the past two decades, thereby underscoring the need for molecular therapeutics. The development of new treatment strategies for more effective management of oral cancer requires identification of novel biological targets. Therefore, the aim of this study was to identify novel genes associated with oral tumorigenesis by comparing gene expression profile of oral squamous cell carcinomas (OSCCs) and matched nonmalignant oral epithelial tissues with differential display. Of the 180 differentially expressed cDNAs isolated, reamplified, and cloned into pGEMT‐Easy Vector, 26 cDNAs were confirmed to be upregulated in OSCCs by reverse Northern blot analysis. The differentially expressed genes included components of immune system, signaling pathways, angiogenesis, cell structure, proliferation, apoptosis, cell‐adhesion, and cellular metabolism. Reverse transcription (RT)‐polymerase chain reaction (PCR) analysis of 15 OSCCs and matched nonmalignant oral tissues provided the first evidence that 14‐3‐3‐zeta, melanoma metastasizing clone D (MEMD), KIAA0471, sperm protein 17 (SP17), TC21, and anti‐TNF α antibody are upregulated in OSCCs. Immunohistochemical analysis confirmed overexpression of 14‐3‐3‐zeta and TC21 protein, a member of the Ras family, in OSCCs as compared to histologically normal oral tissues validating the differential display analysis. Identification of six novel differentially expressed genes in oral tumors adds to the repertoire of genes associated with oral carcinogenesis and provides candidate potential biological targets for diagnosis and/or therapy. Further characterization of the 14 unknown differentially expressed cDNAs identified in this study may provide significant clues for understanding the molecular mechanisms underlying oral tumorigenesis. © 2004 Wiley‐Liss, Inc.

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