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Oncotarget. 2016 Jul 5;7(27):42805-42825. doi: 10.18632/oncotarget.8715.

Dysregulation and functional roles of miR-183-96-182 cluster in cancer cell proliferation, invasion and metastasis.

Ma Y1,2, Liang AJ1,2, Fan YP3, Huang YR4, Zhao XM1,2, Sun Y1,2, Chen XF1,2,4.

Author information

1
Center for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
2
Shanghai Key Laboratory for Assisted Reproduction and Reproductive Genetics, Shanghai, China.
3
Reproductive Medicine Center, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, China.
4
Department of Urology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

Abstract

Previous studies have reported aberrant expression of the miR-183-96-182 cluster in a variety of tumors, which indicates its' diagnostic or prognostic value. However, a key characteristic of the miR-183-96-182 cluster is its varied expression levels, and pleomorphic functional roles in different tumors or under different conditions. In most tumor types, the cluster is highly expressed and promotes tumorigenesis, cancer progression and metastasis; yet tumor suppressive effects have also been reported in some tumors. In the present study, we discuss the upstream regulators and the downstream target genes of miR-183-96-182 cluster, and highlight the dysregulation and functional roles of this cluster in various tumor cells. Newer insights summarized in this review will help readers understand the different facets of the miR-183-96-182 cluster in cancer development and progression.

KEYWORDS:

cancer development; cancer progression; metastasis; miR-183-96-182 cluster; prognosis

PMID:
27081087
PMCID:
PMC5173173
DOI:
10.18632/oncotarget.8715
[Indexed for MEDLINE]
Free PMC Article

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