MiR-195 suppresses non-small cell lung cancer by targeting CHEK1
Metrics: PDF 1737 views | HTML 1769 views | ?
Ben Liu1,*, Jinli Qu1,*, Fangxiu Xu1, Yan Guo1, Yu Wang1, Herbert Yu2, Biyun Qian1,3
1Department of Epidemiology and Biostatistics, Key Laboratory of Breast Cancer Prevention and Therapy, Ministry of Education, Key Laboratory of Cancer Prevention and Therapy, Tianjin, National Clinical Research Center of Cancer, Tianjin Medical University Cancer Institute and Hospital, Tianjin 300060, China
2Cancer Epidemiology Program, University of Hawaii Cancer Center, Honolulu, HI 96813, USA
3Hongqiao International Institute of Medicine, Shanghai Tongren Hospital and Faculty of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China
*These authors have contributed equally to this work
Biyun Qian, e-mail: firstname.lastname@example.org
Keywords: non-small cell lung cancer, miR-195, CHEK1, prognosis, cell cycle
Received: December 08, 2014 Accepted: January 31, 2015 Published: March 25, 2015
MiR-195 suppresses tumor growth and is associated with better survival outcomes in several malignancies including non-small cell lung cancer (NSCLC). Our previous study showed high miR-195 plasma levels associated with favorable overall survival of non-smoking women with lung adenocarcinoma. To further elucidate role of miR-195 in NSCLC, we conducted in vitro experiment as well as clinical studies in a cohort of 299 NSCLC samples. We demonstrated that miR-195 expression was lower in tumor tissues and was associated with poor survival outcome. Overexpression of miR-195 suppressed tumor cell growth, migration and invasion. We discovered that CHEK1 was a direct target of miR-195, which decreased CHEK1 expression in lung cancer cells. High expression of CHEK1 in lung tumors was associated with poor overall survival. Our results suggest that miR-195 suppresses NSCLC and predicts lung cancer prognosis.
All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.