miR-127 Regulates Cell Proliferation and Senescence by Targeting BCL6

被引:63
作者
Chen, Jingwen [1 ,2 ]
Wang, Miao [2 ]
Guo, Mingzhou [3 ]
Xie, Yuntao [4 ]
Cong, Yu-Sheng [2 ]
机构
[1] Beijing Normal Univ, Coll Life Sci, Inst Cell Biol, Minist Educ,Key Lab Cell Proliferat & Regulat Bio, Beijing 100875, Peoples R China
[2] Hangzhou Normal Univ, Sch Med, Inst Aging Res, Hangzhou, Zhejiang, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Dept Gastroenterol & Hepatol, Beijing, Peoples R China
[4] Peking Univ, Canc Hosp, Beijing Canc Hosp & Inst, Breast Ctr, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA-DAMAGE; BREAST-CANCER; IN-VIVO; EXPRESSION; MIR-433; P53; MICRORNA-127; PROTEIN;
D O I
10.1371/journal.pone.0080266
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cellular senescence occurs as a response to extracellular and intracellular stresses and contributes to aging and age-related pathologies. Emerging evidence suggests that cellular senescence also acts as a potent tumor suppression mechanism that prevents the oncogenic transformation of primary human cells. Recent reports have indicated that miRNAsact as key modulators of cellular senescence by targeting critical regulators of the senescence pathways. We previously reported that miR-127 is up-regulated in senescent fibroblasts. In this report, we identified miR-127 as a novel regulator of cellular senescence that directly targets BCL6. We further showed that miR-127 is down-regulated in breast cancer tissuesand that this down-regulation is associated with up-regulation of BCL6. Over-expression of miR-127 or depletion of BCL6 inhibits breast cancer cell proliferation. Our data suggest that miR-127 may function as a tumor suppressor that modulates the oncogene BCL6.
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页数:9
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