[No authors listed]
MicroRNAs (miRNAs/miRs) serve important roles in the chemotherapeutic effect of anticancer drugs. To investigate the roles of miRNAs in cisplatinâinduced suppression of lung adenocarcinoma cell proliferation, A549 cells were treated with different concentrations of cisplatin. An MTT assay demonstrated that cisplatin inhibited A549 cell proliferation in a doseâdependent manner. Cisplatin induced cell apoptosis and inhibited cell migration by increasing the levels of miRâ93, miRâ26a and miRâ26b. Furthermore, as an upstream factor, miRâ93 was proposed to regulate cyclin D2 expression in miRâ93âtransfected A549 cells. Cisplatin also induced Bclâ2âassociated X protein expression, and decreased that of Bclâ2 and câMyc in lung adenocarcinoma cells. In vivo analysis further supported that cisplatin inhibited lung adenocarcinoma cell growth by regulating cyclin D2 and miRâ93 expression. In conclusion, our findings demonstrated that cisplatin could effectively inhibit lung adenocarcinoma cell proliferation by decreasing cyclin D2 expression via miRâ93.
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