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首页> 外文期刊>European review for medical and pharmacological sciences. >Facilitation of liver cancer SMCC7721 cell aging by sirtuin 4 via inhibiting JAK2/STAT3 signal pathway
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Facilitation of liver cancer SMCC7721 cell aging by sirtuin 4 via inhibiting JAK2/STAT3 signal pathway

机译:sirtuin 4通过抑制JAK2 / STAT3信号通路促进肝癌SMCC7721细胞衰老

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OBJECTIVE: Liver cancer severely threatens public health. Molecular targeted treatment is the further of cancer treatment. The functional role of Sir-related enzymes 4 (sirtuin 4) in treating liver cancer still requires further investigation. This study aimed to elucidate the effect of sirtuin 4 on aging of SMCC7721 liver cancer cell line, to underlying molecular mechanism and potential application in clinics. MATERIALS AND METHODS: Adriamycin-induced aging model was established on SMCC7721 liver cancer cell line. Sirtuin 4 over-expression or siRNA plasmid was transfected. Cell aging was measured by β-galactosidase approach. Aging-related proteins P53 and P16 were quantified in Western blot, which also examined activation of Janus kinase 2 (JAK2) signal pathway. CP-690550 was used to suppress JAK2 signal pathway for measuring aging status of SMCC7721 cells. RESULTS: In aged SMCC7721 cells, sirtuin 4 was up-regulated, whilst P53 and P16 protein levels were elevated, in accompanied with JAK2/STAT3 signal pathway. Transfection of sirtuin 4 over-expression plasmid or siRNA increased or decreased sirtuin 4 expression. Adriamycin-induced aging was enhanced or suppressed, accompanied with inhibited or potentiated JAK2 signal pathway in sirtuin 4 up-regulation or down-regulation cells, respectively. The usage of JAK2 signal inhibitor, CP-690550, enhanced Adriamycin-induced cell aging. CONCLUSIONS: Sirtuin 4 facilitates Adriamycin-induced aging of SMCC7721 liver cancer cells via inhibiting JAK2/STAT3 signal pathway, thus providing one novel anti-cancer strategy.
机译:目的:肝癌严重威胁公共健康。分子靶向治疗是癌症治疗的进一步方法。 Sir相关酶4(sirtuin 4)在治疗肝癌中的功能作用仍需进一步研究。这项研究旨在阐明Sirtuin 4对SMCC7721肝癌细胞系衰老的影响,潜在的分子机制以及在临床中的潜在应用。材料与方法:建立了阿霉素诱导的SMCC7721肝癌细胞系衰老模型。 Sirtuin 4过表达或siRNA质粒被转染。通过β-半乳糖苷酶方法测量细胞衰老。衰老相关蛋白P53和P16在Western blot中定量,该蛋白还检查了Janus激酶2(JAK2)信号通路的激活。 CP-690550用于抑制JAK2信号通路,以测量SMCC7721细胞的衰老状态。结果:在老年SMCC7721细胞中,Sirtuin 4被上调,而P53和P16蛋白水平升高,并伴有JAK2 / STAT3信号通路。 sirtuin 4过表达质粒或siRNA的转染增加或减少了sirtuin 4的表达。阿霉素诱导的衰老被增强或抑制,并伴随着沉默调节蛋白4上调或下调细胞中JAK2信号通路的抑制或增强。 JAK2信号抑制剂CP-690550的使用增强了阿霉素诱导的细胞衰老。结论:Sirtuin 4通过抑制JAK2 / STAT3信号通路促进阿霉素诱导的SMCC7721肝癌细胞衰老,从而提供了一种新颖的抗癌策略。

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