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Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis

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 As...

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Autores principales: Sato, Go, Shirai, Yuya, Namba, Shinichi, Edahiro, Ryuya, Sonehara, Kyuto, Hata, Tsuyoshi, Uemura, Mamoru, Matsuda, Koichi, Doki, Yuichiro, Eguchi, Hidetoshi, Okada, Yukinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282036/
https://www.ncbi.nlm.nih.gov/pubmed/37340002
http://dx.doi.org/10.1038/s41467-023-39136-7
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author Sato, Go
Shirai, Yuya
Namba, Shinichi
Edahiro, Ryuya
Sonehara, Kyuto
Hata, Tsuyoshi
Uemura, Mamoru
Matsuda, Koichi
Doki, Yuichiro
Eguchi, Hidetoshi
Okada, Yukinori
author_facet Sato, Go
Shirai, Yuya
Namba, Shinichi
Edahiro, Ryuya
Sonehara, Kyuto
Hata, Tsuyoshi
Uemura, Mamoru
Matsuda, Koichi
Doki, Yuichiro
Eguchi, Hidetoshi
Okada, Yukinori
author_sort Sato, Go
collection PubMed
description 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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spelling pubmed-102820362023-06-22 Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis Sato, Go Shirai, Yuya Namba, Shinichi Edahiro, Ryuya Sonehara, Kyuto Hata, Tsuyoshi Uemura, Mamoru Matsuda, Koichi Doki, Yuichiro Eguchi, Hidetoshi Okada, Yukinori Nat Commun Article 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. Nature Publishing Group UK 2023-06-20 /pmc/articles/PMC10282036/ /pubmed/37340002 http://dx.doi.org/10.1038/s41467-023-39136-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sato, Go
Shirai, Yuya
Namba, Shinichi
Edahiro, Ryuya
Sonehara, Kyuto
Hata, Tsuyoshi
Uemura, Mamoru
Matsuda, Koichi
Doki, Yuichiro
Eguchi, Hidetoshi
Okada, Yukinori
Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis
title Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis
title_full Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis
title_fullStr Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis
title_full_unstemmed Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis
title_short Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis
title_sort pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282036/
https://www.ncbi.nlm.nih.gov/pubmed/37340002
http://dx.doi.org/10.1038/s41467-023-39136-7
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