期刊文献+

PPI基因对在癌症中的共表达分析 被引量:1

Coexpression Analysis of Gene Pairs with Protein-Protein Interaction in Cancers
在线阅读 下载PDF
导出
摘要 蛋白质-蛋白质相互作用(PPI)可通过基因表达量之间的相关系数来反映.研究癌细胞或组织中全局的PPI,有利于了解基因型和表型之间的关系,更好地发掘正常与异常细胞或组织之间的癌症发生发展机制.文中利用TCGA数据库中11种癌症5726个样本的mRNA表达数据和临床信息,结合STRING和HPRD数据库中的PPI基因对,使用皮尔逊相关系数计算癌症组织特异PPI基因对在正常样本和癌症不同时期样本的相关系数,筛选得到癌症紊乱及癌症特异的PPI基因对.通过基因差异表达与生存分析,得到可能影响癌症发生发展的关键PPI基因对.结果表明:PPI基因对在癌症样本中的相关性要显著低于正常样本.癌症紊乱PPI基因对有2812对,其中LRSAM 1、ATXN 1、SMARCC 2与SMARCA 2等基因出现在多个癌症中并通过相互作用聚类成网络模块,可能在癌症中发挥重要作用;癌症特异PPI基因对有31对,其中BMP 1与COL1A 1在癌症中的相互作用很可能促进癌细胞的迁移和浸润转移,对癌症产生、发展产生重要的影响.此外,在癌症紊乱及特异中筛选了113对具有差异表达的PPI基因对,其中有16对显著差异PPI基因对在7个癌症中具有生存显著差异. The relativity of protein-protein interaction(PPI)can be reflected by the gene coexpression correlation.The study of global PPIs in cancer cells or tissues will facilitate the understanding of the relationship between genotypes and phenotypes,as well as the mechanisms of cancer development in normal and abnormal cells or tissues.The mRNA expression profile data and clinical information was collected from the Cancer Genome Atlas(TCGA),including 5726 samples across 11 human cancers type.Combining with PPI gene pairs of Human from STRING and HPRD databases,Pearson correlation coefficients(PCC)was used to calculate the gene coexpression coefficients of tissue-specific PPIs in normal samples and cancer samples at different stages,and then the cancer-disordered and cancer-specific PPI gene pairs were obtained.With the different gene expression and survival analysis,PPI gene pairs which may affect the development of cancer were found out.Result shows that:the gene coexpression coefficient of PPI gene pairs in cancer samples is significantly lower than normal samples.There are 2812 pairs of can-cer-disordered PPI genes,among which LRSAM1,ATXN1,SMARCC2 and SMARCA2 appear in multiple cancers interacted and clustered into a network module,and they may play an important role in caner.There are 31 pairs of cancer-specific PPI genes,among which BMP1 and COL1A1 may interact to promote tumorous migration and infiltration.In addition,113 pairs of PPI genes with differential expression were selected from cancer-disordered and cancer-specific genes.Among them,16 pairs show significantly survival difference in 7 cancers.
作者 蒙裕欢 白云梦 崔莹 杜红丽 MENG Yuhuan;BAI Yunmeng;CUI Ying;DU Hongli(School of Biological Science and Engineering,South China University of Technology,Guangzhou 510006,Guangdong,China)
出处 《华南理工大学学报(自然科学版)》 EI CAS CSCD 北大核心 2019年第11期78-88,共11页 Journal of South China University of Technology(Natural Science Edition)
基金 中国博士后科学基金资助项目(2018M633045)。
关键词 癌症 TCGA 蛋白质-蛋白质相互作用 基因共表达 cancer TCGA protein-protein interaction gene coexpression
  • 相关文献

参考文献7

二级参考文献134

  • 1庞广昌.中华饮食文化和食品科学探源[J].食品科学,2009,30(3):11-20. 被引量:12
  • 2仲小敏,何敬东,陈小飞,喻晓娟.新型钙离子通道蛋白TRPV6在胃癌组织中的表达及其临床意义[J].中国肿瘤生物治疗杂志,2015,22(1):73-78. 被引量:3
  • 3庞广昌,陈庆森,胡志和.食品是如何通过细胞因子网络控制人类健康的(I)[J].食品科学,2006,27(5):258-264. 被引量:31
  • 4[23]McGurk KA, Brierley CH, Burchell B. Drug glucuronidation by human renal UDP-glucuronosyltransferases. Biochem Pharmacol,1998;55:1005~1012
  • 5[24]Lampe JW, Bigler J, Bush AC, et al. Prevalence of polymorphisms in the human UDP-glucuronosyltransferase 2B family: UGT2B4(D458E), UGT2B7(H268Y), and UGT2B15(D85Y). Cancer Epidemiol Biomarkers Prey,2000; 9:329~333.
  • 6[25]Levesque E, Beaulieu M, Green MD, et al. Isolation and characterization of UGT2B 15(Y85): a UDP-glucuronosyltransferase encoded by a polymorphic gene.Pharmacogenetics,1997; 7: 317~325.
  • 7[26]Belanger A, Hum DW, Beaulieu M, et al. Characterization and regulation of UDP-glucuronosyltransferases in steroid target tissues.J Steroid Biochem Mol Bio1,1998; 65: 301~310.
  • 8[27]Brown SY, Garland WA, Fukuda EK. Isolation and characterization of an unusual glucuronide conjugate of rimantadine. Drug Metab Dispos, 1990; 18: 546~547.
  • 9[28]Burchell B and Coughtrie MWH. UDP-glucuronosyltransferases.Pharm Ther, 1989:261~289.
  • 10[29]Bock KW, Gschaidmeier H, Heel H, et al. Functions and transcriptional regulation of PAH-inducible human UDP-glucuronosyltransferases. Drug Metabolism Reviews, 1999;31:411~422.

共引文献46

同被引文献7

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部