| Literature DB >> 27073562 |
Fang Huang1, Yaofeng Jin2, Yafeng Wei1.
Abstract
MicroRNAs (miRs) are endogenous non-coding RNAs that serve key functions in a wide range of biological processes, including cell growth, development, apoptosis and carcinogenesis. However, the association between miR-187 and B-cell lymphoma 6 (BCL6) has yet to be fully investigated in lymphoma cell apoptosis. The present study hypothesized that a post-translational mechanism may exist for BCL6 expression, which is regulated by miR-187 in lymphoma cells. The present study demonstrated that the expression of miR-187 in diffuse large B-cell lymphoma (DLBCL) cells was significantly decreased, and its expression was negatively correlated with BCL6 expression. It was also observed that miR-187 directly binds to the 3'-untranslated region of BCL6 mRNA and subsequently suppresses the expression of BCL6. Additionally, the induced expression of miR-187 significantly promoted DLBCL cell apoptosis in vitro. The drug sensitivity of human DLBCL SUDHL2 cells was increased following induction of miR-187 overexpression via an miR-187 mimic. In conclusion, the results of the present study suggest that the modulation of miR-187 expression in DLBCL cells may improve the sensitivity of chemotherapy through BCL6 targeting.Entities:
Keywords: B-cell lymphoma 6; apoptosis; diffuse large B-cell lymphoma; miRNA-187; multidrug resistance
Year: 2016 PMID: 27073562 PMCID: PMC4812283 DOI: 10.3892/ol.2016.4313
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967