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基于基因集富集分析的控制透明细胞肾细胞癌(ccRCC)发生发展的关键信号通路和基因

Key pathways and genes controlling the development and progression of clear cell renal cell carcinoma (ccRCC) based on gene set enrichment analysis.

作者信息

Huang Haipeng, Tang Yanyan, He Wenwu, Huang Qi, Zhong Jianing, Yang Zhanbin

机构信息

Department of Urinary Surgery, The First Affiliated Hospital, Guangxi Medical University, 6th Shuangyong Road, Nanning, 530021, Guangxi, China.

出版信息

Int Urol Nephrol. 2014 Mar;46(3):539-53. doi: 10.1007/s11255-013-0511-2. Epub 2013 Aug 14.

Abstract

BACKGROUND

Clear-cell renal cell carcinoma (ccRCC) is one of the most common types of kidney cancer in adults; however, its causes are not completely understood. The study was designed to filter the key pathways and genes associated with the occurrence or development of ccRCC, acquaint its pathogenesis at gene and pathway level, to provide more theory evidence and targeted therapy for ccRCC.

METHODS

Gene set enrichment analysis (GSEA) and meta-analysis (Meta) were used to screen the critical pathways and genes which may affect the occurrence and progression of ccRCC on the transcription level. Corresponding pathways of significant genes were obtained with the online website DAVID ( http://david.abcc.ncifcrf.gov/ ).

RESULTS

Thirty seven consistent pathways and key genes in these pathways related to ccRCC were obtained with combined GSEA and meta-analysis. These pathways were mainly involved in metabolism, organismal systems, cellular processes and environmental information processing.

CONCLUSION

The gene pathways that we identified could provide insight concerning the development of ccRCC. Further studies are needed to determine the biological function for the positive genes.

摘要

背景

透明细胞肾细胞癌(ccRCC)是成人中最常见的肾癌类型之一;然而,其病因尚未完全明确。本研究旨在筛选与ccRCC发生或发展相关的关键通路和基因,从基因和通路水平了解其发病机制,为ccRCC提供更多理论依据和靶向治疗方法。

方法

采用基因集富集分析(GSEA)和荟萃分析(Meta)在转录水平筛选可能影响ccRCC发生和进展的关键通路和基因。通过在线网站DAVID(http://david.abcc.ncifcrf.gov/)获得显著基因的相应通路。

结果

通过GSEA和荟萃分析相结合,获得了37条与ccRCC相关的一致通路及这些通路中的关键基因。这些通路主要涉及代谢、机体系统、细胞过程和环境信息处理。

结论

我们鉴定出的基因通路可为ccRCC的发展提供见解。需要进一步研究以确定阳性基因的生物学功能。

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