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miR-92b 通过调控 PTEN 影响 A549 非小细胞肺癌细胞的生长和顺铂化疗敏感性

MiR-92b regulates the cell growth, cisplatin chemosensitivity of A549 non small cell lung cancer cell line and target PTEN.

机构信息

Department of Medical Oncology, Shandong Cancer Hospital and Institute, Jinan University, Jinan, Shandong 250117, PR China.

出版信息

Biochem Biophys Res Commun. 2013 Nov 1;440(4):604-10. doi: 10.1016/j.bbrc.2013.09.111. Epub 2013 Oct 4.

Abstract

MicroRNAs (miRNAs) have emerged to play important roles in tumorigenesis and drug resistance of human cancer. Fewer studies were explored the roles of miR-92b on human lung cancer cell growth and resistance to cisplatin (CDDP). In this paper, we utilized real-time PCR to verify miR-92b was significantly up-regulated in non-small cell lung cancer (NSCLC) tissues compared to matched adjacent normal tissues. In vitro assay demonstrated that knock-down of miR-92b inhabits cell growth and sensitized the A549/CDDP cells to CDDP. Furthermore, we found miR-92b could directly target PTEN, a unique tumor suppressor gene, which was downregulated in lung cancer tissues compared to the matched adjacent normal tissues. These data indicate that the miR-92b play an oncogene roles by regulates cell growth, cisplatin chemosensitivity phenotype, and could serve as a novel potential maker for NSCLC therapy.

摘要

微小 RNA(miRNAs)在人类癌症的发生和耐药中发挥着重要作用。关于 miR-92b 在人肺癌细胞生长和对顺铂(CDDP)耐药中的作用的研究较少。在本文中,我们利用实时 PCR 验证 miR-92b 在非小细胞肺癌(NSCLC)组织中明显上调,与配对的相邻正常组织相比。体外试验表明,敲低 miR-92b 抑制细胞生长并使 A549/CDDP 细胞对 CDDP 敏感。此外,我们发现 miR-92b 可以直接靶向 PTEN,一种独特的肿瘤抑制基因,与配对的相邻正常组织相比,肺癌组织中下调。这些数据表明,miR-92b 通过调节细胞生长、顺铂化疗敏感性表型发挥癌基因作用,并可作为 NSCLC 治疗的新的潜在标志物。

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