Genetic variation near GRB10 associated with bone growth and osteosarcoma risk in canine and human populations

IF 2.4 3区 医学 Q3 ONCOLOGY
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Abstract

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.

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。
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。
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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.
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