Revealing the functions of clonal driver gene mutations in patients based on evolutionary dependencies

IF 3.3 2区 医学 Q2 GENETICS & HEREDITY
Human Mutation Pub Date : 2022-10-11 DOI:10.1002/humu.24484
Yujia Lan, Wei Liu, Xiaobo Hou, Shuai Wang, Hao Wang, Menglan Deng, Guiyu Wang, Yanyan Ping, Xinxin Zhang
{"title":"Revealing the functions of clonal driver gene mutations in patients based on evolutionary dependencies","authors":"Yujia Lan,&nbsp;Wei Liu,&nbsp;Xiaobo Hou,&nbsp;Shuai Wang,&nbsp;Hao Wang,&nbsp;Menglan Deng,&nbsp;Guiyu Wang,&nbsp;Yanyan Ping,&nbsp;Xinxin Zhang","doi":"10.1002/humu.24484","DOIUrl":null,"url":null,"abstract":"<p>The clonal mutations in driver genes enable cells to gradually acquire growth advantage in tumor development. Therefore, revealing the functions of clonal driver gene mutations is important. Here, we proposed the method FCMP that considered evolutionary dependencies to analyze the functions of clonal driver gene mutations in a single patient. Applying our method to five cancer types from The Cancer Genome Atlas, we identified specific functions and common functions of clonal driver gene mutations. We found that the clonal driver gene mutations in the same patient played multiple functions. We also found that clonal mutations in the same driver gene performed different functions in different patients. These findings suggested that the clonal driver gene mutations showed strong tumor heterogeneity. In the pan-cancer analysis, the immune-related functions for clonal driver gene mutations were shared by multiple cancer types. In addition, clonal mutations in some driver genes predicted the survival of patients in cancers.</p>","PeriodicalId":13061,"journal":{"name":"Human Mutation","volume":"43 12","pages":"2187-2204"},"PeriodicalIF":3.3000,"publicationDate":"2022-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Mutation","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/humu.24484","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

The clonal mutations in driver genes enable cells to gradually acquire growth advantage in tumor development. Therefore, revealing the functions of clonal driver gene mutations is important. Here, we proposed the method FCMP that considered evolutionary dependencies to analyze the functions of clonal driver gene mutations in a single patient. Applying our method to five cancer types from The Cancer Genome Atlas, we identified specific functions and common functions of clonal driver gene mutations. We found that the clonal driver gene mutations in the same patient played multiple functions. We also found that clonal mutations in the same driver gene performed different functions in different patients. These findings suggested that the clonal driver gene mutations showed strong tumor heterogeneity. In the pan-cancer analysis, the immune-related functions for clonal driver gene mutations were shared by multiple cancer types. In addition, clonal mutations in some driver genes predicted the survival of patients in cancers.

Abstract Image

基于进化依赖揭示克隆驱动基因突变在患者中的功能
驱动基因的克隆性突变使细胞在肿瘤发展过程中逐渐获得生长优势。因此,揭示克隆驱动基因突变的功能具有重要意义。在此,我们提出了考虑进化依赖性的FCMP方法来分析克隆驱动基因突变在单个患者中的功能。将我们的方法应用于癌症基因组图谱中的五种癌症类型,我们确定了克隆驱动基因突变的特定功能和共同功能。我们发现同一患者的克隆驱动基因突变具有多种功能。我们还发现,同一驱动基因的克隆突变在不同的患者中发挥不同的功能。这些结果表明克隆驱动基因突变具有很强的肿瘤异质性。在泛癌症分析中,克隆驱动基因突变的免疫相关功能在多种癌症类型中是共享的。此外,一些驱动基因的克隆突变预测了癌症患者的生存。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Human Mutation
Human Mutation 医学-遗传学
CiteScore
8.40
自引率
5.10%
发文量
190
审稿时长
2 months
期刊介绍: Human Mutation is a peer-reviewed journal that offers publication of original Research Articles, Methods, Mutation Updates, Reviews, Database Articles, Rapid Communications, and Letters on broad aspects of mutation research in humans. Reports of novel DNA variations and their phenotypic consequences, reports of SNPs demonstrated as valuable for genomic analysis, descriptions of new molecular detection methods, and novel approaches to clinical diagnosis are welcomed. Novel reports of gene organization at the genomic level, reported in the context of mutation investigation, may be considered. The journal provides a unique forum for the exchange of ideas, methods, and applications of interest to molecular, human, and medical geneticists in academic, industrial, and clinical research settings worldwide.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信