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Original Research

Open Access

Immunohistochemical c-kit expression in uterine serous carcinoma tissue

  • J. Menczer1,*,
  • L. Schreiber2
  • E. Berger2
  • T. Levy1

1Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, E. Wolfson Medical Center, Holon, Tel Aviv University, Sackler Faculty of Medicine, Tel Aviv, Israel

2Department of Pathology, E. Wolfson Medical Center, Holon, Tel Aviv University, Sackler Faculty of Medicine, Tel Aviv, Israel

DOI: 10.12892/ejgo3382.2017 Vol.38,Issue 2,April 2017 pp.207-208

Published: 10 April 2017

*Corresponding Author(s): J. Menczer E-mail: joseph12@internet-zahav.net

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Abstract

Aim: Uterine serous carcinoma (USC) is an aggressive tumor that represents only 10% of endometrial cancer cases but accounts for a disproportionate number of deaths due to uterine cancer. Advances in the development of specific c-kit receptor-targeted drugs have promoted its potential therapeutic application as a target in tumor-related diseases. The aim of the present study was to evaluate imunohistochemical expression of c-kit in USC tissue in order to assess whether positive cases can be candidates for targeted therapy. Materials and Methods: C-kit expression assessment by immunohistochemistry was performed on deparaffinized sections of paraffin-embedded tissue blocks of confirmed consecutive available USC uterine specimens of patients diagnosed from 2000 to 2014. Sections of gastrointestinal stromal tumor (GIST) tissue known to contain c-kit served as positive controls. Results: Immunohistochemical c-kit staining was not observed in any of 31 USC tissue samples examined. Intense staining was observed in the sections of GIST tissue. Conclusion: The present results may indicate that primary USC is not a candidate for c-kit targeted therapy.

Keywords

C-kit tissue expression; Uterine serous carcinoma; Targeted therapy.

Cite and Share

J. Menczer, L. Schreiber, E. Berger, T. Levy. Immunohistochemical c-kit expression in uterine serous carcinoma tissue. European Journal of Gynaecological Oncology. 2017; 38(2): 207-208. doi: 10.12892/ejgo3382.2017

References

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