Volume 123, Issue 10 pp. 847-850
Original Article

Differences in the ARID-1 alpha expressions in squamous and adenosquamous carcinomas of uterine cervix

Dudu Solakoglu Kahraman

Dudu Solakoglu Kahraman

Pathology Laboratory, Tepecik Education and Research Hospital, Izmir, Turkey

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Gulden Diniz

Corresponding Author

Gulden Diniz

Pathology Laboratory, Tepecik Education and Research Hospital, Izmir, Turkey

Gulden Diniz, Pathology Laboratory, Tepecik Education and Research Hospital, Izmir 35220, Turkey. e-mail: [email protected]Search for more papers by this author
Sevil Sayhan

Sevil Sayhan

Pathology Laboratory, Tepecik Education and Research Hospital, Izmir, Turkey

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Duygu Ayaz

Duygu Ayaz

Pathology Laboratory, Tepecik Education and Research Hospital, Izmir, Turkey

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Melek Uncel

Melek Uncel

Pathology Laboratory, Tepecik Education and Research Hospital, Izmir, Turkey

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Tugba Karadeniz

Tugba Karadeniz

Pathology Laboratory, Tepecik Education and Research Hospital, Izmir, Turkey

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Tulay Akman

Tulay Akman

Medical Oncology Clinic, Tepecik Education and Research Hospital, Izmir, Turkey

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Aykut Ozdemir

Aykut Ozdemir

Gynecology and Obstetrics Clinic, Tepecik Education and Research Hospital, Izmir, Turkey

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First published: 25 August 2015
Citations: 3

Abstract

AT-rich interactive domain 1A (ARID1A) is a tumor suppressor gene involved in chromatin remodeling which encodes ARID1A (BAF250a) protein. Recent studies have shown the loss of ARID1A expression in several types of tumors. This retrospective study was designed to evaluate the differences in tissue expressions of ARID1A in a spectrum of cervical neoplasms. Cervical intraepithelial neoplasms, invasive squamous or adenosquamous carcinomas were identified in 100 patients recently diagnosed as cervical neoplasms based on pathology databases. In this series, there were 29 low- and 29 high-grade cervical intraepithelial neoplasms, 27 squamous cell carcinomas, and 15 adenosquamous carcinomas. Mean age of the patients was 47.8 ± 13 years (20–80 years). It was determined that the expression of ARID1A was statistically significantly down-regulated in adenosquamous carcinomas when compared with non-invasive or invasive squamous cell carcinomas (p = 0.015). Lower levels of the ARID1A expression were detected in cases with adenosquamous carcinomas (60%), low- or high-grade squamous intraepithelial lesion (SIL) (31%), and squamous cell carcinomas (18.5%). Our findings have demonstrated the presence of a correlation between ARID1A expression and adenomatous differentiation of uterine squamous cell carcinomas. Therefore, ARID1A gene may suggestively have a role in the pathogenesis of cervical adenosquamous carcinomas.

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