MiR-497 decreases cisplatin resistance in ovarian cancer cells by targeting mTOR/P70S6K1

被引:73
|
作者
Xu, Shaohua [1 ]
Fu, Guang-Bo [2 ]
Tao, Zhen [4 ]
OuYang, Jun [5 ]
Kong, Fanfei [1 ]
Jiang, Bing-Hua [6 ,7 ]
Wan, Xiaoping [1 ]
Chen, Ke [3 ]
机构
[1] Tongji Univ, Sch Med, Shanghai Maten & Infant Hosp 1, Dept Obstet & Gynecol, Shanghai 200092, Peoples R China
[2] Nanjing Med Univ, Huaian Peoples Hosp 1, Dept Urol & Pathol, Huaian, Peoples R China
[3] Huazhong Univ Sci & Technol, Union Hosp, Ctr Canc, Wuhan 430074, Peoples R China
[4] Tianjin Med Univ, Canc Hosp & Inst, Dept Radiat Oncol, Dept Sci & Technol, Tianjin, Peoples R China
[5] Nanjing Med Univ, Changzhou Maternal & Child Hlth Hosp, Changzhou, Peoples R China
[6] Nanjing Med Univ, Ctr Canc, State Key Lab Reprod Med, Nanjing, Jiangsu, Peoples R China
[7] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
基金
美国国家卫生研究院;
关键词
miR-497; mTOR; p70S6K1; cisplatin resistance; ovarian cancer; MICRORNA EXPRESSION; PROSTATE-CANCER; DOWN-REGULATION; SENSITIVITY; CARCINOMA; IDENTIFICATION; INHIBITORS; APOPTOSIS; ANTIGENS; RECEPTOR;
D O I
10.18632/oncotarget.4762
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The mechanism of cisplatin resistance in ovarian cancer is not clearly understood. In the present investigation, we found that the expression levels of miR-497 were reduced in chemotherapy-resistant ovarian cancer cells and tumor tissues due to hypermethylation of miR-497 promoter. Low miR-497 expression levels were associated with chemo-resistant phonotype of ovarian cancer. By analyzing the expression levels of miR-497, mTOR and p70S6K1 in a clinical gene-expression array dataset, we found that mTOR and p70S6K1, two proteins correlated to chemotherapy-resistance in multiple types of human cancers, were inversely correlated with miR-497 levels in ovarian cancer tissues. By using an orthotopic ovarian tumor model and a Tet-On inducible miR-497 expression system, our results demonstrated that overexpression of miR-497 sensitizes the resistant ovarian tumor to cisplatin treatment. Therefore, we suggest that miR-497 might be used as a therapeutic supplement to increase ovarian cancer treatment response to cisplatin.
引用
收藏
页码:26457 / 26471
页数:15
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