MicroRNA-96 Regulates Apoptosis by Targeting PDCD4 in Human Glioma Cells

17Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Glioblastoma multiforme, the most common and aggressive form of primary brain tumor, presents a dismal prognosis. MicroRNAs play a critical role in the initiation, progression, and metastasis of cancer; however, the potential biological role of miRNAs in glioblastoma multiforme remains largely unknown. In our study, we found that microRNA-96 is upregulated in glioma tissues than in normal human brains. Transfection of microRNA-96 mimics into glioma cells significantly decreases apoptosis by suppressing PDCD4, a well-known tumor suppressor that is involved in apoptosis. In contrast, knockdown of microRNA-96 enhanced apoptosis. In vivo, microRNA-96 overexpression inhibits the apoptosis and increases tumor growth. These data suggest that microRNA-96 is a potential molecular target for glioma treatment.

Author supplied keywords

Cite

CITATION STYLE

APA

Ma, Q. Q., Huang, J. T., Xiong, Y. G., Yang, X. Y., Han, R., & Zhu, W. W. (2017). MicroRNA-96 Regulates Apoptosis by Targeting PDCD4 in Human Glioma Cells. Technology in Cancer Research and Treatment, 16(1), 92–98. https://doi.org/10.1177/1533034616629260

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free