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首页> 外文期刊>Molecular medicine reports >Downregulation of the expression of B-cell lymphoma-extra large by RNA interference induces apoptosis and enhances the radiosensitivity of non-small cell lung cancer cells
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Downregulation of the expression of B-cell lymphoma-extra large by RNA interference induces apoptosis and enhances the radiosensitivity of non-small cell lung cancer cells

机译:RNA干扰下调超大B细胞淋巴瘤的表达诱导细胞凋亡并增强非小细胞肺癌细胞的放射敏感性

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摘要

B-cell lymphoma-extra large (Bcl-xL), an important member of anti-apoptotic Bcl-2 family, is involved in tumor progression and development. The overexpression of Bcl-xL is associated with radioresistance of human malignancies. The present study aimed to investigate the inhibitory effect of small interfering RNA (siRNA) on the expression of Bcl-xL in the A549 non-small lung cancer (NSCLC) cell line, and its role in inducing the apoptosis and increasing the radiosensitivity of A549 cells. An siRNA expression vector, pSilencer4-CMVneo-short hairpin (sh)RNA, was constructed and stably transfected into A549 cells. The effects of Bcl-xL-shRNA on cell proliferation, apoptosis and the protein expression levels of associated proteins were assessed in vitro in the A549 cells. The radiosensitivity of the A549 cells was evaluated using a clonogenic cell survival assay. The results demonstrated that the sequence-specific siRNA targeting Bcl-xL efficiently and specifically downregulated the mRNA and protein expression levels of Bcl-xL. The RNA interference-mediated downregulation in the expression of Bcl-xL inhibited cell proliferation, induced apoptosis and reduced the radioresistance of the NSCLC cells. These findings suggested that Bcl-xL may be a promising therapeutic approach for the treatment of NSCLC.
机译:B细胞超大淋巴瘤(Bcl-xL)是抗凋亡Bcl-2家族的重要成员,参与肿瘤的进展和发展。 Bcl-xL的过表达与人类恶性肿瘤的放射抵抗有关。本研究旨在探讨小干扰RNA(siRNA)对A549非小肺癌(NSCLC)细胞系中Bcl-xL表达的抑制作用及其在诱导A549细胞凋亡和增加放射敏感性中的作用。细胞。构建了siRNA表达载体pSilencer4-CMVneo-短发夹(sh)RNA,并将其稳定转染到A549细胞中。在体外在A549细胞中评估了Bcl-xL-shRNA对细胞增殖,凋亡和相关蛋白的蛋白表达水平的影响。使用克隆细胞存活测定法评估A549细胞的放射敏感性。结果表明,针对Bcl-xL的序列特异性siRNA有效且特异性地下调了Bcl-xL的mRNA和蛋白质表达水平。 RNA干扰介导的Bcl-xL表达下调抑制了细胞增殖,诱导了细胞凋亡并降低了NSCLC细胞的抗辐射性。这些发现表明,Bcl-xL可能是治疗NSCLC的有前途的治疗方法。

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