Suppr超能文献

全基因组关联研究在肤色和皮肤癌中的应用:综述与荟萃分析。

Genome-wide association studies of pigmentation and skin cancer: a review and meta-analysis.

机构信息

Genetic Epidemiology Branch/Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD, USA.

出版信息

Pigment Cell Melanoma Res. 2010 Oct;23(5):587-606. doi: 10.1111/j.1755-148X.2010.00730.x. Epub 2010 Jul 16.

Abstract

Recent genome-wide association studies (GWAS) identified genetic loci associated with pigmentation, nevi, and skin cancer. We performed a review and meta-analysis of GWAS results, grouping them into four categories: (i) loci associated with pigmentation (hair, eye, and/or skin color), cutaneous UV-response (sun sensitivity and/or freckling), and skin cancer; (ii) loci associated with nevi and melanoma; (iii) loci associated with pigmentation and/or cutaneous UV-response but not skin cancer; and (iv) loci associated distinctly with skin cancer, mostly basal cell carcinoma, but not pigmentation or cutaneous UV-response. These findings suggest at least two pathways for melanoma development (via pigmentation and via nevi), and two pathways for basal cell carcinoma development (via pigmentation and independent of pigmentation). However, further work is necessary to separate the association with skin cancer from the association with pigmentation. As with any GWAS, the identified loci may not include the causal variants and may need confirmation by direct genome sequencing.

摘要

最近的全基因组关联研究 (GWAS) 确定了与色素沉着、痣和皮肤癌相关的遗传位点。我们对 GWAS 结果进行了综述和荟萃分析,将它们分为四类:(i) 与色素沉着(头发、眼睛和/或皮肤颜色)、皮肤对紫外线的反应(日晒敏感性和/或雀斑)和皮肤癌相关的位点;(ii) 与痣和黑色素瘤相关的位点;(iii) 与色素沉着和/或皮肤对紫外线的反应相关但与皮肤癌无关的位点;(iv) 与皮肤癌(主要是基底细胞癌)相关但与色素沉着或皮肤对紫外线的反应无关的位点。这些发现表明黑色素瘤的发展至少有两种途径(通过色素沉着和通过痣),基底细胞癌的发展也有两种途径(通过色素沉着和独立于色素沉着)。然而,需要进一步的工作来将与皮肤癌的关联与与色素沉着的关联区分开来。与任何 GWAS 一样,所确定的位点可能不包括因果变异,并且可能需要通过直接基因组测序来确认。

相似文献

1
Genome-wide association studies of pigmentation and skin cancer: a review and meta-analysis.
Pigment Cell Melanoma Res. 2010 Oct;23(5):587-606. doi: 10.1111/j.1755-148X.2010.00730.x. Epub 2010 Jul 16.
4
Interaction between p53 codon 72 polymorphism and melanocortin 1 receptor variants on suntan response and cutaneous melanoma risk.
Br J Dermatol. 2008 Aug;159(2):314-21. doi: 10.1111/j.1365-2133.2008.08624.x. Epub 2008 May 28.
5
Current opportunities and challenges: genome-wide association studies on pigmentation and skin cancer.
Pigment Cell Melanoma Res. 2012 Sep;25(5):612-7. doi: 10.1111/j.1755-148X.2012.01023.x. Epub 2012 Jul 12.
6
A germline variant in the interferon regulatory factor 4 gene as a novel skin cancer risk locus.
Cancer Res. 2011 Mar 1;71(5):1533-9. doi: 10.1158/0008-5472.CAN-10-1818. Epub 2011 Jan 26.
7
Genetics of pigmentation and melanoma predisposition.
G Ital Dermatol Venereol. 2010 Feb;145(1):37-45.
9
Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma.
PLoS One. 2017 Oct 3;12(10):e0185730. doi: 10.1371/journal.pone.0185730. eCollection 2017.

引用本文的文献

1
The Genetics and Evolution of Human Pigmentation.
Biology (Basel). 2025 Aug 10;14(8):1026. doi: 10.3390/biology14081026.
2
A Comprehensive Review of GWASs of Human Hair Traits.
J Invest Dermatol. 2025 Aug 19. doi: 10.1016/j.jid.2025.07.004.
3
Polygenic Risk Score Analysis of 37 SNPs Associated with Melanoma Risk in Colombian Population.
Int J Mol Sci. 2025 May 14;26(10):4674. doi: 10.3390/ijms26104674.
4
Global and Local Ancestry and its Importance: A Review.
Curr Genomics. 2024;25(4):237-260. doi: 10.2174/0113892029298909240426094055. Epub 2024 May 9.
6
A Comprehensive Analysis of Cutaneous Melanoma Patients in Greece Based on Multi-Omic Data.
Cancers (Basel). 2023 Jan 28;15(3):815. doi: 10.3390/cancers15030815.
9
Genome-Wide Association Study for Screening and Identifying Potential Shin Color Loci in Ducks.
Genes (Basel). 2022 Aug 4;13(8):1391. doi: 10.3390/genes13081391.
10
Genome-Wide Analysis Identifies Candidate Genes Encoding Beak Color of Duck.
Genes (Basel). 2022 Jul 18;13(7):1271. doi: 10.3390/genes13071271.

本文引用的文献

1
Rare variants create synthetic genome-wide associations.
PLoS Biol. 2010 Jan 26;8(1):e1000294. doi: 10.1371/journal.pbio.1000294.
3
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
Am J Hum Genet. 2009 Nov;85(5):679-91. doi: 10.1016/j.ajhg.2009.09.012. Epub 2009 Oct 15.
4
Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma.
J Invest Dermatol. 2010 Feb;130(2):520-8. doi: 10.1038/jid.2009.258. Epub 2009 Aug 27.
5
Genome-wide association study identifies five susceptibility loci for glioma.
Nat Genet. 2009 Aug;41(8):899-904. doi: 10.1038/ng.407. Epub 2009 Jul 5.
7
Genome-wide association study identifies three loci associated with melanoma risk.
Nat Genet. 2009 Aug;41(8):920-5. doi: 10.1038/ng.411. Epub 2009 Jul 5.
8
New common variants affecting susceptibility to basal cell carcinoma.
Nat Genet. 2009 Aug;41(8):909-14. doi: 10.1038/ng.412. Epub 2009 Jul 5.
9
Relationship between interferon regulatory factor 4 genetic polymorphisms, measures of sun sensitivity and risk for non-Hodgkin lymphoma.
Cancer Causes Control. 2009 Oct;20(8):1291-302. doi: 10.1007/s10552-009-9348-5. Epub 2009 Apr 28.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验