MicroRNA-200b targets protein kinase Cα and suppresses triple-negative breast cancer metastasis

Brock Humphries, Zhishan Wang, Aaron L.Oom, Theresa Fisher, Dongfeng Tan, Yuehua Cui, Yiguo Jiang, Chengfeng Yang

Research output: Contribution to journalArticlepeer-review

92 Scopus citations

Abstract

Triple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer with poor prognosis and lacks effective targeted therapies. The microRNA-200 (miR-200) family is found to inhibit or promote breast cancer metastasis; however, the underlying mechanism is not well understood. This study was performed to investigate the effect and mechanism of miR-200b on TNBC metastasis and identify targets for developing more efficient treatment for TNBC. We found that miR-200 family expression levels are significantly lower in highly migratory TNBC cells and metastatic TNBC tumors than other types of breast cancer cells and tumors. Ectopically expressing a single member (miR-200b) of the miR-200 family drastically reduces TNBC cell migration and inhibits tumor metastasis in an orthotopic mouse mammary xenograft tumor model. We identified protein kinase Ca (PKCα) as a new direct target of miR-200b and found that PKCα protein levels are inversely correlated with miR-200b levels in 12 kinds of breast cancer cells. Inhibiting PKCα activity or knocking down PKCα levels significantly reduces TNBC cell migration. In contrast, forced expression of PKCa impairs the inhibitory effect of miR-200b on cell migration and tumor metastasis. Further mechanistic studies revealed that PKCα downregulation by miR-200b results in a significant decrease of Rac1 activation in TNBC cells. These results show that loss of miR-200b expression plays a crucial role in TNBC aggressiveness and that miR-200b suppresses TNBC cell migration and tumor metastasis by targeting PKCα. Our findings suggest that miR-200b and PKCα may serve as promising therapeutic targets for metastatic TNBC.

Original languageEnglish
Pages (from-to)2254-2263
Number of pages10
JournalCarcinogenesis
Volume35
Issue number10
DOIs
StatePublished - Oct 2014

Bibliographical note

Funding Information:
National Institutes of Health (R01ES017777 to C.Y.) and National Science Foundation (DMS-1209112 to Y.C.).

Publisher Copyright:
© The Author 2014. Published by Oxford University Press. All rights reserved.

ASJC Scopus subject areas

  • Cancer Research

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