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非洲人群乳腺癌的遗传学:文献综述

Genetics of breast cancer in African populations: a literature review.

作者信息

Abbad A, Baba H, Dehbi H, Elmessaoudi-Idrissi M, Elyazghi Z, Abidi O, Radouani F

机构信息

Laboratoire d'écologie et d'environnement- Faculté des Sciences Ben M'sik, Université Hassan II de Casablanca, Casablanca, Morocco.

Virologie Médicale et Laboratoire de BSL-3, Institut Pasteur du Maroc, Casablanca, Morocco.

出版信息

Glob Health Epidemiol Genom. 2018 May 11;3:e8. doi: 10.1017/gheg.2018.8. eCollection 2018.

DOI:10.1017/gheg.2018.8
PMID:30263132
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6152487/
Abstract

Breast cancer (BC) is one of the most complex, diverse and leading cause of death in women worldwide. The present investigation aims to explore genes panel associated with BC in different African regions, and compare them to those studied worldwide. We extracted relevant information from 43 studies performed in Africa using the following criteria: case-control study, association between genetic variations and BC risk. Data were provided on mutations and polymorphisms associated with BC without fixing a specific date. Case-only studies and clinical trials were excluded. Our study revealed that the majority of African BC genetic studies remain restricted to the investigation of BRCA1 and BRCA2 genes and differences in their mutations spectrum. Therefore, it is necessary to encourage African researchers to characterize more genes involved in BC using methods generating global information such as next-generation sequencing in order to guide specific and more effective therapeutic strategies for the African community.

摘要

乳腺癌(BC)是全球女性中最复杂、最多样化且主要的死因之一。本研究旨在探索不同非洲地区与乳腺癌相关的基因面板,并将其与全球范围内研究的基因进行比较。我们使用以下标准从在非洲进行的43项研究中提取了相关信息:病例对照研究、基因变异与乳腺癌风险之间的关联。提供了与乳腺癌相关的突变和多态性数据,未设定具体日期。仅病例研究和临床试验被排除。我们的研究表明,大多数非洲乳腺癌基因研究仍局限于对BRCA1和BRCA2基因及其突变谱差异的调查。因此,有必要鼓励非洲研究人员使用能生成全局信息的方法,如下一代测序,来鉴定更多与乳腺癌相关的基因,以便为非洲社区制定具体且更有效的治疗策略提供指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4fd/6152487/5196e3c3a177/S2054420018000088_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4fd/6152487/50ed7d5a38a1/S2054420018000088_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4fd/6152487/5196e3c3a177/S2054420018000088_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4fd/6152487/50ed7d5a38a1/S2054420018000088_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4fd/6152487/5196e3c3a177/S2054420018000088_fig2.jpg

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Hum Mol Genet. 2018 Mar 1;27(5):853-859. doi: 10.1093/hmg/ddy005.
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Breast Cancer Survival of BRCA1/BRCA2 Mutation Carriers in a Hospital-Based Cohort of Young Women.基于医院队列的年轻女性中 BRCA1/BRCA2 突变携带者的乳腺癌生存情况。
J Natl Cancer Inst. 2017 Aug 1;109(8). doi: 10.1093/jnci/djw329.
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Exome Sequencing in a Family with Luminal-Type Breast Cancer Underpinned by Variation in the Methylation Pathway.
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More recent insights into the breast cancer burden across BRICS-Plus: Health consequences in key nations with emerging economies using the global burden of disease study 2019.关于“金砖+”国家乳腺癌负担的最新见解:利用2019年全球疾病负担研究对新兴经济体主要国家的健康影响
Front Oncol. 2023 Jan 24;13:1100300. doi: 10.3389/fonc.2023.1100300. eCollection 2023.
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