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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.
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页码:2370 / 2380
页数:11
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