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c-kit overexpression in neuroendocrine small cell carcinoma of the uterine cervix
1Department of Obstetrics and Gynecology, Jichi Medical School, Kawachi, Tochigi, Japan
2Department of Obstetrics and Gynecology, School of Medicine, Kitasato University, Kitasato, Sagamihara, Japan
3Department of Gynecology, Omiya Medical Center, Jichi Medical School, Omiya, Saitama, Japan
*Corresponding Author(s): M. Suzuki E-mail:
Purpose of investigation: Neuroendocrine small cell carcinoma of the uterine cervix (NESCC) grows aggressively, and is resistant to anticancer agents and radiation, having an extremely poor prognosis. The incidence of c-kit proto-oncogene overexpression is high in gastrointestinal stromal tumors (GISTs) and small cell lung cancer, and tyrosine kinase inhibitors have been used effectively to treat GISTs. Few studies have investigated whether c-kit is overexpressed in NESCC. To investigate whether NESCC can be a target for molecular targeted therapy with tyrosine kinase inhibitors, we examined the expression of c-kit in this tumor.
Methods: Twenty-one NESCCs were examined for c-kit expression by immunohistochemical staining using the labeled streptavidin-biotin complex (LSAB) method. The expression of c-kit was regarded as positive (overexpression) and negative when the membrane and cytoplasm of more or less than 25%, respectively, of tumor cells were stained.
Results: Nine NESCCs (43%) were c-kit-positive (overexpression). No difference in age or clinical stage was noted. No difference in prognosis was observed between the c-kit-positive and -negative patients.
Conclusion: The incidence of c-kit overexpression was high in NESCC; therefore, the patients with this tumor may become a future target for molecular-targeted therapy with tyrosine kinase inhibitors.
c-kit; Neuroendocrine small cell carcinoma; Uterine cervix
M. Ohwada,T. Wada,Y. Saga,S. Tsunoda,T. Jobo,H. Kuramoto,R. Konno,M. Suzuki. c-kit overexpression in neuroendocrine small cell carcinoma of the uterine cervix. European Journal of Gynaecological Oncology. 2006. 27(1);53-55.
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