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Heterogeneity Mapping of Protein Expression in Tumors using Quantitative Immunofluorescence
Published on: October 25, 2011
Immunohistochemical evaluation of KIT expression in sarcomas of the gynecologic region
Masato Nakayama1, Tomoko Mitsuhashi, Yoshihiko Shimizu
1Department of Pathology, Saitama Medical School, Saitama, Japan.
Abstract:
KIT is expressed in most gastrointestinal stromal tumors, and they usually show c-kit aberrations (most frequently deletions or deletions coexisting with a single or multiple point mutations). Recently, several studies regarding KIT expression in gynecologic tumors have been reported; however, their outcomes were not consistent. In this study, we immunohistochemically examined KIT expression in sarcomas of the female genital tract and studied the existence of c-kit aberrations to elucidate the characteristics of KIT-positive tumors in the gynecologic region. Formalin-fixed, paraffin-embedded tissues from 25 surgically resected and 1 biopsy specimen from 26 patients were used. Histological diagnoses included 14 uterine leiomyosarcomas, 6 carcinosarcomas, 5 endometrial stromal sarcomas, and 1 vaginal epithelioid sarcoma. Immunohistochemical studies were performed using anti-KIT polyclonal antibody. Only four of the above tumors (15%) were positive for KIT, all of which were carcinosarcomas. Specific KIT immunoreactivity was observed in the only carcinomatous components in one case, in the only sarcomatous component in two cases, and in the both components in one case. However, none of the cases showed c-kit aberrations in exons 9, 11, 13, and 17. Judicious decision is mandatory before applying Imatinib therapy to KIT-positive gynecologic tumors.
Insights
KIT expression in gynecologic sarcomas is rare, with only 15% of tumors showing positivity, predominantly in carcinosarcomas. Aberrations in c-kit were not detected, suggesting caution with targeted therapies.
Area of Science:
- Oncology
- Pathology
- Gynecologic Oncology
Background:
- KIT (CD117) is a key marker in gastrointestinal stromal tumors (GISTs), often exhibiting c-kit aberrations.
- KIT expression in gynecologic tumors is inconsistently reported, necessitating further investigation.
Purpose of the Study:
- To investigate KIT protein expression and c-kit gene aberrations in female genital tract sarcomas.
- To characterize KIT-positive gynecologic tumors and inform potential therapeutic strategies.
Main Methods:
- Immunohistochemistry using anti-KIT antibody on 26 formalin-fixed, paraffin-embedded gynecologic sarcoma specimens.
- Analysis of c-kit gene aberrations in exons 9, 11, 13, and 17.
Main Results:
- KIT expression was detected in only 4 out of 26 tumors (15%), exclusively in carcinosarcomas.
- KIT immunoreactivity varied between carcinomatous and sarcomatous components in these cases.
- No c-kit aberrations were identified in the analyzed exons across all tested tumors.
Conclusions:
- KIT expression is infrequent in female genital tract sarcomas, primarily occurring in carcinosarcomas.
- The absence of detectable c-kit aberrations suggests that KIT positivity alone may not predict response to therapies targeting these mutations.
- Clinical decisions regarding Imatinib therapy in KIT-positive gynecologic tumors require careful consideration.
