[No authors listed]
Micro (mi)RNAs are short nonâcoding RNA molecules, which postâtranscriptionally regulate gene expression and exert key roles in cell growth, differentiation and apoptosis. In the present study, the mechanism and the function of miRâ1915â3p in the apoptotic regulation of lung cancer cell lines (NCIâH441 and NCIâH1650) were investigated. The expression analysis confirmed that the expression of miRâ1915â3p was markedly decreased in the apoptotic cells. The overexpression of miRâ1915â3p in the lung cancer cells prevented apoptosis induced by etoposide. Developmentally regulated GTPâbinding protein 2 (DRG2) and preâB cell leukemia homeobox 2 (PBX2) were identified as downstream targets of miRâ1915â3p, which was shown to bind directly to the 3'âuntranslated region of DRG2 and PBX2, subsequently lowering their mRNA and protein expression levels. Coâexpression of miRâ1915â3p and DRG2/PBX2 in the NCIâH441 and NCIâH1650 cells partly circumvented the effect of miRâ1915â3p on apoptosis. The results in the present study revealed that miRâ1915â3p functions as a silencer of apoptosis, which regulates lung cancer apoptosis via targeting DRG2/PBX2, and consequently this miRNA may be a putative therapeutic target in lung cancer.
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