C-kit protein expression correlated with activating mutations in KIT gene in oral mucosal melanoma |
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Authors: | Rosario S. Rivera Hitoshi Nagatsuka Mehmet Gunduz Beyhan Cengiz Esra Gunduz Chong Huat Siar Hidetsugu Tsujigiwa Ryo Tamamura Kok Ng Han Noriyuki Nagai |
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Affiliation: | (1) Department of Oral Pathology and Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, 2-5-1 Shikata-cho, Okayama 700-8525, Japan;(2) College of Dentistry, University of the East, Manila, Philippines;(3) Department of Oral Pathology, Oral Medicine and Periodontology, Faculty of Dentistry, University of Malaya, Kuala Lampur, Malaysia;(4) Unit of Stomatology, Cancer Research Centre, Institute for Medical Research, Kuala Lumpur, Malaysia |
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Abstract: | C-kit is a trans-membrane receptor tyrosine kinase (RTK) encoded by the proto-oncogene KIT located at 4q11-12. Gain-of-function mutations arising to c-kit activation independent of its ligand were observed in various tumors related to germ cells, mast cells, and interstitial cells of Cajal. C-kit also participates in melanocyte development; hence, its involvement in oral mucosal melanoma (OMM) tumorigenesis was investigated. Immunohistochemistry and mutation analysis were performed using 18 cases of human primary OMM. Results revealed 16 cases positive to c-kit protein. Atypical melanocytes expressed c-kit. All in situ components expressed c-kit, but only four cases exhibited intense expression in the invasive component. Missense mutations were observed in four cases, and two of those correlated with increased protein expression. C-kit expression in atypical melanocytes suggests the role of c-kit in the early stage of OMM tumorigenesis. C-kit protein expression correlated with activating mutations indicating the pertinent role of the proto-oncogene KIT in the tumorigenesis of OMM. |
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Keywords: | Oral mucosal melanoma C-kit mutation Immunohistochemistry |
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