全基因组关联研究
生物
生命银行
癌变
癌症
遗传学
前列腺癌
遗传关联
乳腺癌
人口
遗传力
计算生物学
肿瘤科
单核苷酸多态性
医学
基因
基因型
环境卫生
作者
Go Sato,Yuya Shirai,Shinichi Namba,Ryuya Edahiro,Kyuto Sonehara,Tsuyoshi Hata,Mamoru Uemura,Yuji Yamanashi,Yoichi Furukawa,Takayuki Morisaki,Yoshinori Murakami,Yoichiro Kamatani,Kaori Muto,Akiko Nagai,Wataru Obara,Ken Yamaji,Kazuhisa Takahashi,Satoshi Asai,Yasuo Takahashi,Takao Suzuki
标识
DOI:10.1038/s41467-023-39136-7
摘要
Abstract Integrating genomic data of multiple cancers allows de novo cancer grouping and elucidating the shared genetic basis across cancers. Here, we conduct the pan-cancer and cross-population genome-wide association study (GWAS) meta-analysis and replication studies on 13 cancers including 250,015 East Asians (Biobank Japan) and 377,441 Europeans (UK Biobank). We identify ten cancer risk variants including five pleiotropic associations (e.g., rs2076295 at DSP on 6p24 associated with lung cancer and rs2525548 at TRIM4 on 7q22 nominally associated with six cancers). Quantifying shared heritability among the cancers detects positive genetic correlations between breast and prostate cancer across populations. Common genetic components increase the statistical power, and the large-scale meta-analysis of 277,896 breast/prostate cancer cases and 901,858 controls identifies 91 newly genome-wide significant loci. Enrichment analysis of pathways and cell types reveals shared genetic backgrounds across said cancers. Focusing on genetically correlated cancers can contribute to enhancing our insights into carcinogenesis.
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