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Clinicopathologic significance of EpCAM expression in squamous cell carcinoma of the tongue and its possibility as a potential target for tongue cancer gene therapy.

Clinicopathologic significance of EpCAM expression in squamous cell carcinoma of the tongue and its possibility as a potential target for tongue cancer gene therapy. Research Abstract Details 

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  • Clinicopathologic significance of EpCAM expression in squamous cell carcinoma of the tongue and its possibility as a potential target for tongue cancer gene therapy. Abstract Text:

    souichi yanamotoSouichi Yanamoto,goro kawasakiGoro Kawasaki,izumi yoshitomiIzumi Yoshitomi,tsutomu iwamotoTsutomu Iwamoto,kazunari hirataKazunari Hirata,akio mizunoAkio Mizuno,souichi yanamotoSouichi Yanamoto,goro kawasakiGoro Kawasaki,izumi yoshitomiIzumi Yoshitomi,tsutomu iwamotoTsutomu Iwamoto,kazunari hirataKazunari Hirata,akio mizunoAkio Mizuno,

    Epithelial adhesion molecule (EpCAM) is a transmembrane glycoprotein involved in intercellular adhesion. In particular, EpCAM appears to be overexpressed by the majority of human epithelial carcinomas, including colorectal, breast, head and neck, and hepatic carcinomas. We therefore hypothesized that EpCAM would be a good molecular target for cancer gene therapy. EpCAM protein expression in 48 primary tongue cancers and 10 normal oral mucosa was evaluated using anti-EpCAM immunohistochemistry, and correlation was examined with the clinicopathologic factors. In four human tongue cancer cell lines (SAS, HSC-2, OSC19 and OSC20), we investigated EpCAM expression by reverse transcription-polymerase chain reaction (RT-PCR). The invasive potential of cancer cells was evaluated using Matrigel invasion assay. Moreover, the effect of EpCAM inhibition was analyzed using RNA interference (RNAi). EpCAM overexpression was detected in 30 of 48 tongue cancers (62.5%), and was significantly higher in primary squamous cell carcinoma (SCC) of the tongue than in normal oral mucosa. The expression of EpCAM was significantly associated with tumor size, regional lymph node metastasis, histological differentiation and invasion pattern. Cancer cell lines with higher EpCAM expression had more invasive potential. Moreover, RNAi-mediated EpCAM reduction decreased the invasion potential and proliferation activity. These results indicated that the overexpression of EpCAM was correlated with a more aggressive phenotype of tongue cancer. Moreover, we suggested that EpCAM could be a molecular target, and that RNAi targeting EpCAM could be useful for tongue cancer gene therapy.

    Clinicopathologic significance of EpCAM expression in squamous cell carcinoma of the tongue and its possibility as a potential target for tongue cancer gene therapy. Publishing Authors By Initials

    s yanamotoS Yanamoto,g kawasakiG Kawasaki,i yoshitomiI Yoshitomi,t iwamotoT Iwamoto,k hirataK Hirata,a mizunoA Mizuno,s yanamotoS Yanamoto,g kawasakiG Kawasaki,i yoshitomiI Yoshitomi,t iwamotoT Iwamoto,k hirataK Hirata,a mizunoA Mizuno,

    For similar abstracts research abstracts see: abstracts research

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    Clinicopathologic significance of EpCAM expression in squamous cell carcinoma of the tongue and its possibility as a potential target for tongue cancer gene therapy. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Oral oncology

    VOLUME: 43

    Page Numbers: 869-77

    Journal Abbreviation: Oral Oncol.

    ISSN: 1368-8375

    DAY: 4

    MONTH: 01

    YEAR: 2007

    Clinicopathologic significance of EpCAM expression in squamous cell carcinoma of the tongue and its possibility as a potential target for tongue cancer gene therapy. Information

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    LANGUAGE: eng

    NlmUniqueID: 9709118

    Clinicopathologic significance of EpCAM expression in squamous cell carcinoma of the tongue and its possibility as a potential target for tongue cancer gene therapy. Keywords Mesh Terms:

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    Grant and Affiliation Information for Clinicopathologic significance of EpCAM expression in squamous cell carcinoma of the tongue and its possibility as a potential target for tongue cancer gene therapy.

    AFFILIATION: Department of Oral and Maxillofacial Surgery, Unit of Translational Medicine, Course of Medical and Dental Sciences, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, Japan. syana@nagasaki-u.ac.jp

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Oral Oncol

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