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沉默调节蛋白4通过抑制JAK2/STAT3信号通路促进肝癌SMCC7721细胞衰老

Facilitation of liver cancer SMCC7721 cell aging by sirtuin 4 via inhibiting JAK2/STAT3 signal pathway.

作者信息

Xia X-H, Xiao C-J, Shan H

机构信息

Interventional Radiology Institute, Sun Yat-sen University, Guangzhou, Guangdong, China.

出版信息

Eur Rev Med Pharmacol Sci. 2017 Mar;21(6):1248-1253.

Abstract

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.

摘要

目的

肝癌严重威胁公众健康。分子靶向治疗是癌症治疗的进一步发展。沉默相关酶4(sirtuin 4)在肝癌治疗中的功能作用仍需进一步研究。本研究旨在阐明sirtuin 4对SMCC7721肝癌细胞系衰老的影响、潜在分子机制及临床潜在应用。

材料与方法

在SMCC7721肝癌细胞系上建立阿霉素诱导的衰老模型。转染sirtuin 4过表达或siRNA质粒。通过β-半乳糖苷酶法检测细胞衰老。采用蛋白质免疫印迹法对衰老相关蛋白P53和P16进行定量分析,并检测Janus激酶2(JAK2)信号通路的激活情况。使用CP-690550抑制JAK2信号通路以检测SMCC7721细胞的衰老状态。

结果

在衰老的SMCC7721细胞中,sirtuin 4上调,同时P53和P16蛋白水平升高,伴随JAK2/STAT3信号通路激活。转染sirtuin 4过表达质粒或siRNA可使sirtuin 4表达增加或减少。阿霉素诱导的衰老在sirtuin 4上调或下调的细胞中分别增强或受到抑制,同时JAK2信号通路分别受到抑制或增强。使用JAK2信号抑制剂CP-690550可增强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,从而提供了一种新的抗癌策略。

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