| Literature DB >> 28822708 |
Yuan Xiang1, Xing-Hua Liao2, Ao Yao1, Huan Qin1, Li-Juan Fan1, Jia-Peng Li1, Peng Hu1, Hui Li1, Wei Guo3, Jun-Yan Li4, Chao-Jiang Gu1, Le-Yuan Bao5, Tong-Cun Zhang6.
Abstract
Breast cancer is the leading cause of cancer death in women worldwide which is closely related to metastasis. Our previous study has shown that MRTF-A promote the migration of MDA-MB-231 cells and WDR1 promotes breast cancer cell migration. But the exact molecular mechanism on metastasis is still not fully understood, we now report that WDR1 enhanced the effect of MRTF-A induced-MDA-MB-231 cell migration by promoting the expression of the EMT markers and migration markers via RhoA-MRTF-A signaling pathway. Importantly, WDR1 promoted the nuclear importion of MRTF-A by affecting the expression of nuclear transport protein importin. But WDR1 did not affect the expression of MRTF-A. Interestingly, MRTF-A promoted the expression of miR-206 via its promoter CArG box but miR-206 inhibits the migration of breast cancer cells through suppressing the expression of WDR1 and MRTF-A via targeted their 3'UTR. Our data thus provide important and novel insights into MRTF-A-miR-206-WDR1 form feedback loop to regulate breast cancer cell migration.Entities:
Keywords: Breast cancer cell migration; EMT; MRTF-A; WDR1; miR-206
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Year: 2017 PMID: 28822708 DOI: 10.1016/j.yexcr.2017.08.023
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905