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长链非编码RNA PVT1通过招募EZH2调节肝癌细胞的增殖和凋亡。

Long noncoding RNA PVT1 modulates hepatocellular carcinoma cell proliferation and apoptosis by recruiting EZH2.

作者信息

Guo Jianping, Hao Chong, Wang Congcong, Li Luo

机构信息

Department of Oncology, Maternal and Child Health Care Hospital of Zibo, Zibo, 255029 Shandong China.

Scientific Research Office, Zibo Central Hospital, No. 54 West Gongqingtuan Road, Zhangdian District, Zibo, 255000 Shandong China.

出版信息

Cancer Cell Int. 2018 Jul 11;18:98. doi: 10.1186/s12935-018-0582-3. eCollection 2018.

Abstract

BACKGROUND

We aimed to figure out the molecular network of PVT1 and EZH2 on hepatocellular carcinoma (HCC) cells growth. We also explored the interaction between PVT1, EZH2, MDM2 and P53.

METHODS

Microarray analysis was performed to screen for abnormally expressed genes in HCC tissues and PVT1 was identified as one gene significantly upregulated in HCC. CCK-8 assay, colony formation assay, and flow cytometry detected cell vitality, proliferation and apoptosis, respectively. RIP and RNA pull-down assays were employed to examine the connection between PVT1 and EZH2. The effect of PVT1 on the stability of EZH2 protein and the impact of EZH2 on MDM2 were detected by ELISA. Co-immunoprecipitation assay was used to evaluate the relationship between MDM2 and EZH2. Western blot detected the expression of EZH2, MDM2 and P53.

RESULTS

Up-regulated PVT1 was detected in HCC. Knockdown of PVT1 inhibited HCC cell propagation and promoted apoptotic cells. PVT1 could improve EZH2 protein stability by binding to EZH2 protein but have no significant impact on mRNA expression. EZH2 protein stabilized MDM2 protein expression by binding to MDM2 protein. PVT1 enhanced the protein expression of EZH2 and MDM2 as well as inhibited P53 protein expression.

CONCLUSIONS

PVT1 promoted HCC cell propagation and inhibited apoptotic cells by recruiting EZH2, stabilizing MDM2 protein expression and restraining P53 expression.

摘要

背景

我们旨在弄清楚PVT1和EZH2在肝癌(HCC)细胞生长中的分子网络。我们还探讨了PVT1、EZH2、MDM2和P53之间的相互作用。

方法

进行微阵列分析以筛选HCC组织中异常表达的基因,PVT1被鉴定为HCC中显著上调的一个基因。CCK-8测定、集落形成测定和流式细胞术分别检测细胞活力、增殖和凋亡。采用RIP和RNA下拉测定法检测PVT1与EZH2之间的联系。通过ELISA检测PVT1对EZH2蛋白稳定性的影响以及EZH2对MDM2的影响。采用免疫共沉淀测定法评估MDM2与EZH2之间的关系。蛋白质印迹法检测EZH2、MDM2和P53的表达。

结果

在HCC中检测到PVT1上调。敲低PVT1可抑制HCC细胞增殖并促进凋亡细胞生成。PVT1可通过与EZH2蛋白结合来提高EZH2蛋白稳定性,但对mRNA表达无显著影响。EZH2蛋白通过与MDM2蛋白结合来稳定MDM2蛋白表达。PVT1增强了EZH2和MDM2的蛋白表达,并抑制了P53蛋白表达。

结论

PVT1通过招募EZH2、稳定MDM2蛋白表达和抑制P53表达来促进HCC细胞增殖并抑制凋亡细胞生成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/6042336/c0b87aa5c6dd/12935_2018_582_Fig1_HTML.jpg

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