GRB10附近的基因变异与犬类和人类的骨骼生长和骨肉瘤风险有关。

IF 2.4 3区 医学 Q3 ONCOLOGY Cancer Epidemiology Pub Date : 2024-06-12 DOI:10.1016/j.canep.2024.102599
{"title":"GRB10附近的基因变异与犬类和人类的骨骼生长和骨肉瘤风险有关。","authors":"","doi":"10.1016/j.canep.2024.102599","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Canine and human osteosarcoma are similar in clinical presentation and tumor genomics. Giant breed dogs experience elevated osteosarcoma incidence, and taller stature remains a consistent risk factor for human osteosarcoma. Whether evolutionarily conserved genes contribute to both human and canine osteosarcoma predisposition merits evaluation.</p></div><div><h3>Methods</h3><p>A multi-center sample of childhood osteosarcoma patients and controls underwent genome-wide genotyping and imputation. Ancestry-adjusted SNP associations were calculated within each dataset using logistic regression, then meta-analyzed across the three datasets, totaling 1091 patients and 3026 controls. Ten regions previously associated with canine osteosarcoma risk were mapped to the human genome, spanning ∼6 Mb. We prioritized association testing of 5985 human SNPs mapping to candidate osteosarcoma risk regions detected in Irish wolfhounds, the largest dog breed studied. Secondary analyses explored 6289 additional human SNPs mapping to candidate osteosarcoma risk regions identified in Rottweilers and greyhounds.</p></div><div><h3>Results</h3><p>Fourteen SNPs were associated with human osteosarcoma risk after adjustment for multiple comparisons, all within a 42 kb region of human Chromosome 7p12.1. The lead variant was rs17454681 (OR=1.25, 95 %CI: 1.12–1.39; P=4.1×10<sup>−5</sup>), and independent risk variants were not observed in conditional analyses. While the associated region spanned 2.1 Mb and contained eight genes in Irish wolfhounds, associations were localized to a 50-fold smaller region of the human genome and strongly implicate <em>GRB10</em> (growth factor receptor-bound protein 10) in canine and human osteosarcoma predisposition. PheWAS analysis in UK Biobank data identified noteworthy associations of the rs17454681 risk allele with varied measures of height and pubertal timing.</p></div><div><h3>Conclusions</h3><p>Our comparative oncology analysis identified a novel human osteosarcoma risk allele near <em>GRB10</em>, a growth inhibitor that suppresses activated receptor tyrosine kinases including IGF1R, PDGFRB, and EGFR. Epidemiologists may benefit from leveraging cross-species comparisons to identify haplotypes in highly susceptible but genetically homogenous populations of domesticated animals, then fine-mapping these associations in diverse human populations.</p></div>","PeriodicalId":56322,"journal":{"name":"Cancer Epidemiology","volume":"92 ","pages":"Article 102599"},"PeriodicalIF":2.4000,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S187778212400078X/pdfft?md5=19622a51d52db1824060f77c4375677c&pid=1-s2.0-S187778212400078X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Genetic variation near GRB10 associated with bone growth and osteosarcoma risk in canine and human populations\",\"authors\":\"\",\"doi\":\"10.1016/j.canep.2024.102599\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Canine and human osteosarcoma are similar in clinical presentation and tumor genomics. Giant breed dogs experience elevated osteosarcoma incidence, and taller stature remains a consistent risk factor for human osteosarcoma. Whether evolutionarily conserved genes contribute to both human and canine osteosarcoma predisposition merits evaluation.</p></div><div><h3>Methods</h3><p>A multi-center sample of childhood osteosarcoma patients and controls underwent genome-wide genotyping and imputation. Ancestry-adjusted SNP associations were calculated within each dataset using logistic regression, then meta-analyzed across the three datasets, totaling 1091 patients and 3026 controls. Ten regions previously associated with canine osteosarcoma risk were mapped to the human genome, spanning ∼6 Mb. We prioritized association testing of 5985 human SNPs mapping to candidate osteosarcoma risk regions detected in Irish wolfhounds, the largest dog breed studied. Secondary analyses explored 6289 additional human SNPs mapping to candidate osteosarcoma risk regions identified in Rottweilers and greyhounds.</p></div><div><h3>Results</h3><p>Fourteen SNPs were associated with human osteosarcoma risk after adjustment for multiple comparisons, all within a 42 kb region of human Chromosome 7p12.1. The lead variant was rs17454681 (OR=1.25, 95 %CI: 1.12–1.39; P=4.1×10<sup>−5</sup>), and independent risk variants were not observed in conditional analyses. While the associated region spanned 2.1 Mb and contained eight genes in Irish wolfhounds, associations were localized to a 50-fold smaller region of the human genome and strongly implicate <em>GRB10</em> (growth factor receptor-bound protein 10) in canine and human osteosarcoma predisposition. PheWAS analysis in UK Biobank data identified noteworthy associations of the rs17454681 risk allele with varied measures of height and pubertal timing.</p></div><div><h3>Conclusions</h3><p>Our comparative oncology analysis identified a novel human osteosarcoma risk allele near <em>GRB10</em>, a growth inhibitor that suppresses activated receptor tyrosine kinases including IGF1R, PDGFRB, and EGFR. Epidemiologists may benefit from leveraging cross-species comparisons to identify haplotypes in highly susceptible but genetically homogenous populations of domesticated animals, then fine-mapping these associations in diverse human populations.</p></div>\",\"PeriodicalId\":56322,\"journal\":{\"name\":\"Cancer Epidemiology\",\"volume\":\"92 \",\"pages\":\"Article 102599\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2024-06-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S187778212400078X/pdfft?md5=19622a51d52db1824060f77c4375677c&pid=1-s2.0-S187778212400078X-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer Epidemiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S187778212400078X\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer Epidemiology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S187778212400078X","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景:犬骨肉瘤和人类骨肉瘤在临床表现和肿瘤基因组学方面非常相似。巨型犬的骨肉瘤发病率较高,而身材高大仍是人类骨肉瘤的一致风险因素。进化上保守的基因是否有助于人类和犬类骨肉瘤的易感性值得评估:方法:对儿童骨肉瘤患者和对照组的多中心样本进行了全基因组基因分型和估算。使用逻辑回归法计算了每个数据集的祖先调整SNP关联,然后对三个数据集(共1091名患者和3026名对照)进行了元分析。以前与犬骨肉瘤风险相关的 10 个区域被映射到人类基因组中,跨度达 6 Mb。我们优先对 5985 个人类 SNPs 进行了关联测试,这些 SNPs 映射到在爱尔兰猎狼犬(所研究的最大犬种)中检测到的候选骨肉瘤风险区域。我们还对另外 6289 个与在罗威纳犬和灰猎犬中发现的候选骨肉瘤风险区域相对应的人类 SNP 进行了二次分析:结果:经多重比较调整后,14 个 SNP 与人类骨肉瘤风险有关,它们都位于人类染色体 7p12.1 的 42 kb 区域内。主要变异为 rs17454681(OR=1.25,95 %CI:1.12-1.39;P=4.1×10-5),条件分析中未观察到独立的风险变异。爱尔兰猎狼犬的相关区域横跨 2.1 Mb,包含 8 个基因,而人类基因组的相关区域则小了 50 倍,而且 GRB10(生长因子受体结合蛋白 10)与犬和人类的骨肉瘤易感性密切相关。对英国生物库数据进行的PheWAS分析发现,rs17454681风险等位基因与身高和青春期时间的不同测量值存在显著关联:我们的肿瘤学比较分析在 GRB10 附近发现了一个新的人类骨肉瘤风险等位基因,GRB10 是一种生长抑制剂,可抑制活化的受体酪氨酸激酶,包括 IGF1R、PDGFRB 和 EGFR。流行病学家可以利用跨物种比较来确定高度易感但基因同源的驯养动物群体中的单倍型,然后在不同的人类群体中精细绘制这些关联图,从而从中获益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Genetic variation near GRB10 associated with bone growth and osteosarcoma risk in canine and human populations

Background

Canine and human osteosarcoma are similar in clinical presentation and tumor genomics. Giant breed dogs experience elevated osteosarcoma incidence, and taller stature remains a consistent risk factor for human osteosarcoma. Whether evolutionarily conserved genes contribute to both human and canine osteosarcoma predisposition merits evaluation.

Methods

A multi-center sample of childhood osteosarcoma patients and controls underwent genome-wide genotyping and imputation. Ancestry-adjusted SNP associations were calculated within each dataset using logistic regression, then meta-analyzed across the three datasets, totaling 1091 patients and 3026 controls. Ten regions previously associated with canine osteosarcoma risk were mapped to the human genome, spanning ∼6 Mb. We prioritized association testing of 5985 human SNPs mapping to candidate osteosarcoma risk regions detected in Irish wolfhounds, the largest dog breed studied. Secondary analyses explored 6289 additional human SNPs mapping to candidate osteosarcoma risk regions identified in Rottweilers and greyhounds.

Results

Fourteen SNPs were associated with human osteosarcoma risk after adjustment for multiple comparisons, all within a 42 kb region of human Chromosome 7p12.1. The lead variant was rs17454681 (OR=1.25, 95 %CI: 1.12–1.39; P=4.1×10−5), and independent risk variants were not observed in conditional analyses. While the associated region spanned 2.1 Mb and contained eight genes in Irish wolfhounds, associations were localized to a 50-fold smaller region of the human genome and strongly implicate GRB10 (growth factor receptor-bound protein 10) in canine and human osteosarcoma predisposition. PheWAS analysis in UK Biobank data identified noteworthy associations of the rs17454681 risk allele with varied measures of height and pubertal timing.

Conclusions

Our comparative oncology analysis identified a novel human osteosarcoma risk allele near GRB10, a growth inhibitor that suppresses activated receptor tyrosine kinases including IGF1R, PDGFRB, and EGFR. Epidemiologists may benefit from leveraging cross-species comparisons to identify haplotypes in highly susceptible but genetically homogenous populations of domesticated animals, then fine-mapping these associations in diverse human populations.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Cancer Epidemiology
Cancer Epidemiology 医学-肿瘤学
CiteScore
4.50
自引率
3.80%
发文量
200
审稿时长
39 days
期刊介绍: Cancer Epidemiology is dedicated to increasing understanding about cancer causes, prevention and control. The scope of the journal embraces all aspects of cancer epidemiology including: • Descriptive epidemiology • Studies of risk factors for disease initiation, development and prognosis • Screening and early detection • Prevention and control • Methodological issues The journal publishes original research articles (full length and short reports), systematic reviews and meta-analyses, editorials, commentaries and letters to the editor commenting on previously published research.
期刊最新文献
Editorial Board Years of life lost due to cancer in Ecuador Trends in incidence and survival of the four most common cancers by stage at diagnosis in Cyprus: A population-based study from 2004 to 2017 Measuring healthy life expectancy and determinants of poor perceived health: A population-based study among a subset of rare and common cancer survivors Colorectal cancer survival in Mexico: Leveraging a national health insurance database
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1