MRTF-A and STAT3 synergistically promote breast cancer cell migration

被引:37
|
作者
Liao, Xing-Hua [1 ,2 ,3 ]
Wang, Nan [1 ,2 ]
Liu, Long-Yue [1 ,2 ]
Zheng, Li [1 ,2 ]
Xing, Wen-Jing [1 ,2 ]
Zhao, Dong-Wei [1 ,2 ]
Sun, Xue-Guang [1 ,2 ]
Hu, Peng [3 ]
Dong, Jian [3 ]
Zhang, Tong-Cun [1 ,2 ,3 ]
机构
[1] Tianjin Univ Sci & Technol, Minishy Educ, Key Lab Ind Fermentat Microbiol, Tianjin 300457, Peoples R China
[2] Tianjin Univ Sci & Technol, Coll Biotechnol, Tianjin 300457, Peoples R China
[3] Wuhan Univ Sci & Technol, Inst Biol & Med, Wuhan 430000, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
MRTF-A; STAT3; Myl-9; Cyr-61; Breast cancer cell migration; TRANSCRIPTION FACTORS; SIGNAL TRANSDUCERS; ACTIVATORS; MOTILITY; TARGETS; FAMILY;
D O I
10.1016/j.cellsig.2014.07.023
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Breast cancer is the leading cause of cancer death in women worldwide which is closely related to metastasis. But the exact molecular mechanism on metastasis is still not fully understood; we now report that both MRTF-A and STAT3 play important role in breast cancer migration of MDA-MB-231 cells. Moreover, MRTF-A and STAT3 synergistically increased MDA-MB-231 cell migration by promoting the expression of migration markers Myl-9 and Cyr-61. Importantly, we identified a detailed molecular mechanism of MDA-MB-231 cell migration controlled via physical interaction between MRTF-A and STAT3, which synergistically promote the transactivity of the migration marker Myl-9 and Cyr-61 by CArG box binding. Interestingly, the two signaling pathways RhoA-MRTF-A and JAK-STAT3 across talk to regulate MDA-MB-231 cell migration. Our data thus provide important and novel insights into the roles of MRTF-A and STAT3 in regulating MDA-MB-231 cell migration. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:2370 / 2380
页数:11
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