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DOI 10.1016/j.yexmp.2005.09.011

Медицинская библиотека · Experimental and molecular pathology · 2005

Increased EMMPRIN (CD 147) expression during oral carcinogenesis.

Vigneswaran Nadarajah, Beckers Simone, Waigel Sabine, Mensah John, Wu Jean, Mo Juan, Fleisher Kenneth E, Bouquot Jerry, Sacks Peter G, Zacharias Wolfgang

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Gene expression profiling of oral premalignant (OPM) cells and normal oral epithelial (NOR) cells showed that EMMPRIN expression was markedly upregulated in OPM cells compared to NOR cells. We used an oral squamous cell carcinoma (OSCC) progression model composed of cell lines, organotypic cultures and tissue specimens to characterize EMMPRIN expression patterns by microarray analysis, qRT-PCR, Western blotting and immunohistochemistry. EMMPRIN levels are elevated in OPM and primary and metastatic OSCC cells as compared to NOR. EMMPRIN was detected as high and low glycosylated forms in the OPM and OSCC cellular extracts and was released in the media by OSCC cells but not by OPM cells. EMMPRIN expression in an organotypic culture model of normal and OPM mucosae mirrored the expression patterns in the respective tissues in vivo. EMMPRIN expression was limited to basal cells of normal, benign hyperkeratotic and inflammatory (lichen planus) oral mucosa. EMMPRIN expression is increased in dysplastic leukoplakias spreading to more superficial layers, and its expression levels correlated significantly with the degree of dysplasia. Primary and metastatic OSCC showed strong cell surface expression of EMMPRIN. These results suggest that EMMPRIN overexpression occurs at a very early stage of oral carcinogenesis and plays a contributing role in OSCC tumorigenesis.

Для цитирования: Vigneswaran Nadarajah, Beckers Simone, Waigel Sabine, Mensah John, Wu Jean, Mo Juan, Fleisher Kenneth E, Bouquot Jerry, Sacks Peter G, Zacharias Wolfgang. Increased EMMPRIN (CD 147) expression during oral carcinogenesis.. Experimental and molecular pathology. 2005. DOI: 10.1016/j.yexmp.2005.09.011.

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