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首页> 外文期刊>Journal of Translational Medicine >miR-148b reverses cisplatin-resistance in non-small cell cancer cells via negatively regulating DNA (cytosine-5)-methyltransferase 1(DNMT1) expression
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miR-148b reverses cisplatin-resistance in non-small cell cancer cells via negatively regulating DNA (cytosine-5)-methyltransferase 1(DNMT1) expression

机译:miR-148b通过负调控DNA(cytosine-5)-甲基转移酶1(DNMT1)的表达逆转非小细胞癌细胞中的顺铂耐药性

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Background The emergence of drug resistance in cancer patients limits the success rate of clinical chemotherapy. MicroRNAs (miRNAs) may play a role in chemoresistance and may be involved in modulating of some drug resistance-related pathways in cancer cells. In this study, the involvement of microRNA-148b (miR-148b) and its roles in the development of chemoresistance in lung cancer are determined. Methods This study was performed in two lung cancer cell lines (A549 and SPC-A1). The levels of miR-148b and DNMT1 mRNA expression were determined by using Quantitative Real-Time PCR. Proteins of DNMTs are represented by western blot assay. Cell viability was assessed by MTT assay. Cell apoptosis was evaluated using flow cytometry. Results The data showed a down-regulated of miR-148b expression and evaluated methyltransferases (DNMTs) expression in cisplatin-resisted human non-small cell lung cancer (NSCLC) cell line-A549/DDP and SPC-A1/DDP compared with their parental A549 and SPC-A1 cell line. In transfection experiments, miR-148b mimics reduced the DNMT1 expression, as well as enhanced the sensitivity of cells to cisplatin and cisplatin-induced apoptosis in A549/DDP or SPC-A1/DDP cells. While miR-148b inhibitor increased DNMT1 expression, as well as attenuated the sensitivity of cells to cisplatin in A549 and SPC-A1 cells. miR-148b was showed to exert negative effect on DNMT1 expression by targeting its 3′UTR in A549/DDP and A549 cells. Importantly, silenced DNMT1 increases cisplatin sensitivity of A549/DDP cells and over-expressed DNMT1 reverses pro-apoptosis effect of miR-148b mimic. Conclusions miR-148b reverses cisplatin-resistance in non-small cell cancer cells via negatively regulating DNMT1 expression.
机译:背景技术癌症患者中耐药性的出现限制了临床化学疗法的成功率。微小RNA(miRNA)可能在化学抗性中起作用,并且可能参与调节癌细胞中某些与药物抗性相关的途径。在这项研究中,确定了microRNA-148b(miR-148b)的参与及其在肺癌化学耐药性发展中的作用。方法本研究在两种肺癌细胞系(A549和SPC-A1)中进行。通过使用实时定量PCR确定miR-148b和DNMT1 mRNA的表达水平。 DNMT的蛋白质由蛋白质印迹法表示。通过MTT测定评估细胞活力。使用流式细胞仪评估细胞凋亡。结果数据显示,与亲本相比,顺铂耐药的人非小细胞肺癌(NSCLC)细胞系A549 / DDP和SPC-A1 / DDP的miR-148b表达下调并评估了甲基转移酶(DNMT)表达A549和SPC-A1细胞系。在转染实验中,miR-148b模拟物降低了DNMT1的表达,并增强了细胞对顺铂和顺铂诱导的A549 / DDP或SPC-​​A1 / DDP细胞凋亡的敏感性。而miR-148b抑制剂可增加DNMT1的表达,并减弱A549和SPC-A1细胞对顺铂的敏感性。 miR-148b通过靶向A549 / DDP和A549细胞中的3'UTR而对DNMT1表达产生负面影响。重要的是,沉默的DNMT1增加了A549 / DDP细胞的顺铂敏感性,而过表达的DNMT1则逆转了miR-148b模拟物的促凋亡作用。结论miR-148b通过负调节DNMT1的表达逆转非小细胞癌细胞的顺铂耐药性。

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