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由阴阳1转录激活的RNA聚合酶I亚基D促进结肠癌细胞的细胞增殖和血管生成。

RNA polymerase I subunit D activated by Yin Yang 1 transcription promote cell proliferation and angiogenesis of colorectal cancer cells.

作者信息

Shan Jianfeng, Liang Yuanxiao, Yang Zhili, Chen Wenshan, Chen Yun, Sun Ke

机构信息

Department of Colorectal Surgery, Xinchang People's Hospital, Xinchang, Zhejiang 312500, China.

出版信息

Korean J Physiol Pharmacol. 2024 May 1;28(3):265-273. doi: 10.4196/kjpp.2024.28.3.265.

Abstract

This study aims to explore possible effect of RNA polymerase I subunit D (POLR1D) on proliferation and angiogenesis ability of colorectal cancer (CRC) cells and mechanism herein. The correlation of POLR1D and Yin Yang 1 (YY1) expressions with prognosis of CRC patients in TCGA database was analyzed. Quantitative realtime polymerase chain reaction (qRT-PCR) and Western blot were applied to detect expression levels of POLR1D and YY1 in CRC cell lines and CRC tissues. SW480 and HT- 29 cells were transfected with si-POLR1D or pcDNA3.1-POLR1D to achieve POLR1D suppression or overexpression before cell migration, angiogenesis of human umbilical vein endothelial cells were assessed. Western blot was used to detect expressions of p38 MAPK signal pathway related proteins and interaction of YY1 with POLR1D was confirmed by dual luciferase reporter gene assay and chromatin immunoprecipitation (ChIP). TCGA data showed that both POLR1D and YY1 expressions were up-regulated in CRC patients. High expression of POLR1D was associated with poor prognosis of CRC patients. The results showed that POLR1D and YY1 were highly expressed in CRC cell lines. Inhibition or overexpression of POLR1D can respectively suppress or enhance proliferation and angiogenesis of CRC cells. YY1 inhibition can suppress CRC progression and deactivate p38 MAPK signal pathway, which can be counteracted by POLR1D overexpression. JASPAR predicted YY1 can bind with POLR1D promoter, which was confirmed by dual luciferase reporter gene assay and ChIP. YY1 transcription can up-regulate POLR1D expression to activate p38 MAPK signal pathway, thus promoting proliferation and angiogenesis ability of CRC cells.

摘要

本研究旨在探讨RNA聚合酶I亚基D(POLR1D)对结直肠癌(CRC)细胞增殖和血管生成能力的可能影响及其机制。分析了TCGA数据库中POLR1D和阴阳1(YY1)表达与CRC患者预后的相关性。应用定量实时聚合酶链反应(qRT-PCR)和蛋白质免疫印迹法检测CRC细胞系和CRC组织中POLR1D和YY1的表达水平。在评估人脐静脉内皮细胞的细胞迁移、血管生成之前,用si-POLR1D或pcDNA3.1-POLR1D转染SW480和HT-29细胞以实现POLR1D的抑制或过表达。采用蛋白质免疫印迹法检测p38 MAPK信号通路相关蛋白的表达,并通过双荧光素酶报告基因检测和染色质免疫沉淀(ChIP)证实YY1与POLR1D的相互作用。TCGA数据显示,CRC患者中POLR1D和YY1的表达均上调。POLR1D高表达与CRC患者的不良预后相关。结果表明,POLR1D和YY1在CRC细胞系中高表达。抑制或过表达POLR1D可分别抑制或增强CRC细胞的增殖和血管生成。抑制YY1可抑制CRC进展并使p38 MAPK信号通路失活,而POLR1D过表达可抵消这种作用。JASPAR预测YY1可与POLR1D启动子结合,双荧光素酶报告基因检测和ChIP证实了这一点。YY1转录可上调POLR1D表达以激活p38 MAPK信号通路,从而促进CRC细胞的增殖和血管生成能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a8/11058543/8ed86afd07da/kjpp-28-3-265-f1.jpg

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