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ARID1A mutation in endometrial cancer: a review

  • Ye Yang1
  • Xiaowei Xi1,*,

1Department of Obstetrics and Gynecology, Shanghai General Hospital of Shanghai Jiaotong University, Shanghai (China)

DOI: 10.12892/ejgo4274.2018 Vol.39,Issue 5,October 2018 pp.705-709

Published: 10 October 2018

*Corresponding Author(s): Xiaowei Xi E-mail: xixiaowei1966@126.com

Abstract

Endometrial carcinoma is the most frequent gynecological malignancy and a leading cause of cancer death in women worldwide. ARID1A, a gene participated in chromatin remodeling, is an emerging tumor suppressor gene. Accumulating evidence has reported somatic inactivating mutations of ARID1A and loss of its expression in many types of human cancers, especially in endometrium-derived tumors. The high prevalence of somatic mutations in endometrial cancers indicates a pivotal role of ARID1A in their development. Understanding the roles of ARID1A in the pathogenesis of endometrial carcinoma is fundamental for future translational studies aimed at designing new diagnostic tests for early detection and identifying critical molecular targets for new therapeutic interventions.

Keywords

ARID1A; Mutation; Endometrial cancer; ARID1B.

Cite and Share

Ye Yang,Xiaowei Xi. ARID1A mutation in endometrial cancer: a review. European Journal of Gynaecological Oncology. 2018. 39(5);705-709.

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