Knockdown of JARID2 inhibits the proliferation and invasion of ovarian cancer through the PI3K/Akt signaling pathway

被引:24
作者
Cao, Jian [1 ]
Li, Huiling [2 ]
Liu, Guangquan [1 ]
Han, Suping [3 ]
Xu, Pengfei [4 ]
机构
[1] Nanjing Med Univ, Dept Obstet & Gynecol, Obstet & Gynecol Hosp, Nanjing 210004, Jiangsu, Peoples R China
[2] Peking Univ, Hosp 3, Dept Obstet & Gynecol, Beijing 100191, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp 1, Dept Obstet & Gynecol, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Obstet & Gynecol Hosp, Nanjing Maternal & Child Hlth Inst, 123 Mochou Rd, Nanjing 210004, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
protein Jumonji; ovarian cancer; proliferation; invasion; CELLS; DIFFERENTIATION; LINES; EMT;
D O I
10.3892/mmr.2017.7024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Protein Jumonji (JARID2), a member of the family of JmjC domain-containing proteins, has been reported to serve an important role in tumor growth and metastasis. However, the expression pattern and role of JARID2 in ovarian cancer remains unclear. Therefore, in the present study, the role of JARID2 in ovarian cancer was investigated, as well as the underlying mechanisms. The results of the present study demonstrated that the expression of JARID2 is upregulated in human ovarian cancer cell lines. Furthermore, downregulation of JARID2 significantly suppressed proliferation, migration, invasion and epithelial-mesenchymal transition in human ovarian cancer cells. Mechanistically, downregulation of JARID2 decreased the protein expression levels of phosphorylated phosphoinositide 3-kinase (PI3K) and protein kinase B (Akt) in ovarian cancer cells. In conclusion the observations suggested that knockdown of JARID2 inhibited proliferation, migration and invasion in vitro through the inactivation of the PI3K/Akt signaling pathway. Therefore, JARID2 may represent a potential therapeutic target for the treatment of ovarian cancer.
引用
收藏
页码:3600 / 3605
页数:6
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