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芦可替尼通过下调JAK1/2-STAT1-Mcl-1轴诱导人结肠癌细胞凋亡。

Ruxolitinib induces apoptosis of human colorectal cancer cells by downregulating the JAK1/2-STAT1-Mcl-1 axis.

作者信息

Li Xia, Wang Zhe, Zhang Shengjie, Yao Qinghua, Chen Wei, Liu Feiyan

机构信息

College of Life Sciences, Zhejiang University, Hangzhou, Zhejiang 310058, P.R. China.

Institute of Cancer and Basic Medicine, Chinese Academy of Sciences, Hangzhou, Zhejiang 310022, P.R. China.

出版信息

Oncol Lett. 2021 May;21(5):352. doi: 10.3892/ol.2021.12613. Epub 2021 Mar 4.

DOI:10.3892/ol.2021.12613
PMID:33747209
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7967999/
Abstract

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 . 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 and . Therefore, ruxolitinib could be a promising anticancer agent for CRC treatment.

摘要

在病理条件下,Janus激酶(JAK)/信号转导和转录激活因子(STAT)信号通路可调节肿瘤细胞的增殖、分化和迁移,包括结直肠癌(CRC)。CRC是全球男性中第三大主要癌症类型,女性中第二大主要癌症类型。在中国,CRC是男性和女性中第五大常见癌症。进行了蛋白质免疫印迹法、流式细胞术、RNA干扰、免疫沉淀、异种移植模型和免疫组织化学染色,以评估鲁索替尼的可能作用机制。目前的数据表明,鲁索替尼可通过诱导凋亡来抑制CRC细胞增殖。首先,JAK1/2-STAT1被确定为鲁索替尼的靶点。然后,鲁索替尼下调髓样细胞白血病-1(Mcl-1)的mRNA水平并降低其蛋白水平,这使得Bak能够触发CRC凋亡。此外,鲁索替尼对CRC异种移植瘤生长具有强大的抑制作用。在44对人结肠癌和癌旁正常组织中也证实了磷酸化STAT1(S727)的高表达。综上所述,结果表明鲁索替尼降低了JAK1/2-STAT1-Mcl-1蛋白水平,并有效抑制了CRC细胞增殖。因此,鲁索替尼可能是一种有前景的用于CRC治疗的抗癌药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fdb/7967999/570f80d83a39/ol-21-05-12613-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fdb/7967999/9a00ffc75f97/ol-21-05-12613-g00.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fdb/7967999/72236edb0038/ol-21-05-12613-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fdb/7967999/db426831bec3/ol-21-05-12613-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fdb/7967999/d29bb892d720/ol-21-05-12613-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fdb/7967999/570f80d83a39/ol-21-05-12613-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fdb/7967999/9a00ffc75f97/ol-21-05-12613-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fdb/7967999/20b0b55e6f9a/ol-21-05-12613-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fdb/7967999/9e8d9d67c019/ol-21-05-12613-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fdb/7967999/72236edb0038/ol-21-05-12613-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fdb/7967999/db426831bec3/ol-21-05-12613-g04.jpg
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