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Expression and Effects of JMJD2A Histone Demethylase in Endometrial Carcinoma

  • Wang, Hong-Li (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University) ;
  • Liu, Mei-Mei (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University) ;
  • Ma, Xin (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University) ;
  • Fang, Lei (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University) ;
  • Zhang, Zong-Feng (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University) ;
  • Song, Tie-Fang (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University) ;
  • Gao, Jia-Yin (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University) ;
  • Kuang, Ye (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University) ;
  • Jiang, Jing (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University) ;
  • Li, Lin (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University) ;
  • Wang, Yang-Yang (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University) ;
  • Li, Pei-Ling (Department of Obstetrics and Gynaecology, Second Affiliated Hospital of Harbin Medical University)
  • Published : 2014.04.01

Abstract

Previous studies have demonstrated that JMJD2A is a potential oncogene and is overexpressed in human tumors. However, its role in the endometrial carcinoma remains largely unknown. In this study, we discovered that JMJD2A was overexpressed in endometrial carcinoma, using immunohistochemistry, quantitative realtime polymerase chain reaction, and western blotting. Downregulation of JMJD2A led to reduced endometrial carcinoma RL95-2 and ISK cell proliferation, invasion and metastasis as asessed with cell counting kit-8, cell migration and invasive assays. Collectively, our results support that JMJD2A is a promoter of endometrial carcinoma cell proliferation and survival, and is a potential novel drug target.

Keywords

JMJD2A;endometrial carcinoma;cell proliferation;tumor migration;tumor invasion

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