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首页> 外文期刊>Oncology letters >Ruxolitinib induces apoptosis of human colorectal cancer cells by downregulating the JAK1/2-STAT1-Mcl-1 axis
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Ruxolitinib induces apoptosis of human colorectal cancer cells by downregulating the JAK1/2-STAT1-Mcl-1 axis

机译:通过下调JAK1 / 2-STAT1-MCL-1轴来诱导人结肠直肠癌细胞的凋亡

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Under pathological conditions, the Janus kinase (JAK)/STAT signaling pathway can regulate the proliferation, differentiation and migration of tumor cells, including colorectal cancer (CRC). CRC is the third major types of cancer among males and the second among females worldwide. In China, CRC is the fifth common cancer among both males and females. Western blotting, flow cytometry, RNA interference, immunoprecipitation, xenografts models, and immunohistochemical staining were carried out to evaluate the possible mechanisms of acton of ruxolitinib. The present data suggested that ruxolitinib can suppress CRC cell proliferation by inducing apoptosis. Firstly, JAK1/2-STAT1 was identified as the target of ruxolitinib. Then, ruxolitinib downregulated myeloid cell leukemia-1 (Mcl-1) mRNA level and decreased its protein level, which enabled Bak to trigger CRC apoptosis. Furthermore, ruxolitinib exerted potent activity against CRC xenograft growth in vivo. High expression of phosphorylated STAT1 (S727) was also confirmed in 44 pairs of human colon carcinoma and adjacent normal tissues. Taken together, the results showed that ruxolitinib decreased JAK1/2-STAT1-Mcl-1 protein level and effectively suppressed CRC cell proliferation in vitro and in vivo. Therefore, ruxolitinib could be a promising anticancer agent for CRC treatment.
机译:在病理条件下,Janus激酶(JAK)/STAT信号通路可以调节包括结直肠癌(CRC)在内的肿瘤细胞的增殖、分化和迁移。大肠癌是全世界第三大男性癌症,第二大女性癌症。在中国,大肠癌是男性和女性的第五大常见癌症。通过免疫印迹、流式细胞术、RNA干扰、免疫沉淀、异种移植物模型和免疫组织化学染色来评估鲁索利替尼阿克顿的可能机制。目前的数据表明,鲁索利替尼可以通过诱导凋亡来抑制大肠癌细胞的增殖。首先,JAK1/2-STAT1被确定为鲁索利替尼的靶点。然后,鲁索利替尼下调髓细胞白血病-1(Mcl-1)mRNA水平并降低其蛋白质水平,这使Bak能够触发CRC凋亡。此外,ruxolitinib在体内对CRC异种移植物生长具有强大的活性。磷酸化STAT1(S727)在44对人结肠癌和癌旁正常组织中也被证实高表达。总之,结果表明,在体外和体内,鲁索利替尼降低了JAK1/2-STAT1-Mcl-1蛋白水平,并有效抑制了结直肠癌细胞的增殖。因此,鲁索利替尼有望成为治疗大肠癌的一种有前途的抗癌药物。

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