miRNA-96 Suppresses KRAS and Functions as a Tumor Suppressor Gene in Pancreatic Cancer

被引:281
|
作者
Yu, Shuangni [1 ]
Lu, Zhaohui [1 ]
Liu, Changzheng [2 ]
Meng, Yunxiao [1 ]
Ma, Yihui [1 ]
Zhao, Wugan [1 ]
Liu, Jianping [1 ]
Yu, Jia [2 ,3 ]
Chen, Jie [1 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Pathol, Beijing 100730, Peoples R China
[2] Chinese Acad Med Sci, Dept Biochem, Natl Lab Med Mol Biol, Inst Basic Med Sci, Beijing 100005, Peoples R China
[3] Northwestern Univ, Feinberg Sch Med, Dept Dermatol, Chicago, IL 60611 USA
关键词
K-RAS ONCOGENE; DUCTAL ADENOCARCINOMA; CHROMOSOMAL INSTABILITY; MICRORNA SIGNATURES; CELL-LINES; GROWTH; INHIBITION; ACTIVATION; EXPRESSION; CARCINOMA;
D O I
10.1158/0008-5472.CAN-09-4531
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Therapeutic applications of microRNA (miRNA) in KRAS-driven pancreatic cancers might be valuable, but few studies have explored this area. Here, we report that miR-96 directly targets the KRAS oncogene and functions as a tumor-suppressing miRNA in pancreatic cancer cells. Ectopic expression of miR-96 through a synthetic miRNA precursor inhibited KRAS, dampened Akt signaling, and triggered apoptosis in cells. In human clinical specimens, miR-96 was downregulated or deleted where an association with KRAS elevations was observed. In vitro and in vivo assays established that miR-96 decreased cancer cell invasion and migration and slowed tumor growth in a manner associated with KRAS downregulation. Our findings identify miR-96 as a potent regulator of KRAS, which may provide a novel therapeutic strategy for treatment of pancreatic cancer and other KRAS-driven cancers. Cancer Res; 70(14); 6015-25. (C) 2010 AACR.
引用
收藏
页码:6015 / 6025
页数:11
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