首页> 外文期刊>Tumour biology : >Knockdown of RLIP76 expression by RNA interference inhibits proliferation, enhances apoptosis, and increases chemosensitivity to daunorubicin in U937 leukemia cells.
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Knockdown of RLIP76 expression by RNA interference inhibits proliferation, enhances apoptosis, and increases chemosensitivity to daunorubicin in U937 leukemia cells.

机译:RNA干扰抑制RLIP76表达可抑制增殖,增强细胞凋亡并增加U937白血病细胞对柔红霉素的化学敏感性。

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RLIP76 is known to play a role in cell growth, division, apoptosis, and chemosensitivity in various malignant cancer cells. However, few studies have been done on the role of RLIP76 in leukemia. In this study, human leukemia cell line U937 was transiently transfected with a RLIP76-targeted short hairpin RNA (shRNA) to investigate the effects of RLIP76 on cellular functions. Real-time PCR and western blot analysis revealed that the expression levels of RLIP76 mRNA and protein in U937 cells were significantly suppressed after transfection with shRNA-containing vector. Knockdown of RLIP76 significantly inhibited cell growth and decreased the colony formation rate, as assessed by trypan blue exclusion and colony formation assay. Flow cytometry analysis showed that reduced RLIP76 expression resulted in cell cycle arrest at G1 phase and induced apoptosis. Meanwhile, western blot analysis demonstrated that RLIP76 knockdown increased expression of Bax, cleaved caspase-3/-9, and cleaved poly (ADP-ribose) polymerase (PARP) but reduced the expression of cyclin D1, cyclin E, and Bcl-2 in U937 cells. Finally, knockdown of RLIP76 in U937 cells also enhanced their chemosensitivity to daunorubicin. Taken together, this study suggests that RLIP76 is a potential target for developing novel therapeutic strategies for leukemia.
机译:已知RLIP76在各种恶性癌细胞中的细胞生长,分裂,凋亡和化学敏感性中起作用。但是,关于RLIP76在白血病中的作用的研究很少。在这项研究中,用靶向RLIP76的短发夹RNA(shRNA)瞬时转染了人类白血病细胞系U937,以研究RLIP76对细胞功能的影响。实时荧光定量PCR和蛋白质印迹分析表明,转染含shRNA的载体后,U937细胞中RLIP76 mRNA和蛋白的表达水平被显着抑制。通过台盼蓝排除法和菌落形成试验评估,敲低RLIP76可以显着抑制细胞生长并降低菌落形成速率。流式细胞仪分析表明,降低的RLIP76表达导致细胞周期停滞在G1期并诱导凋亡。同时,蛋白质印迹分析表明,RLIP76敲低可增加Bax的表达,裂解的caspase-3 / -9和裂解的多聚(ADP-核糖)聚合酶(PARP),但降低cyclin D1,cyclin E和Bcl-2的表达。 U937细胞。最后,敲除U937细胞中的RLIP76也增强了其对柔红霉素的化学敏感性。两者合计,这项研究表明RLIP76是开发新的白血病治疗策略的潜在目标。

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