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巴西亚马逊地区原住民中与遗传性乳腺癌相关基因的变异(rs11571707、rs144848和rs11571769)鉴定

Identification of Variants (rs11571707, rs144848, and rs11571769) in the Gene Associated with Hereditary Breast Cancer in Indigenous Populations of the Brazilian Amazon.

作者信息

Dobbin Elizabeth Ayres Fragoso, Medeiros Jéssyca Amanda Gomes, Costa Marta Solange Camarinha Ramos, Rodrigues Juliana Carla Gomes, Guerreiro João Farias, Kroll José Eduardo, Souza Sandro José de, de Assumpção Paulo Pimentel, Ribeiro-Dos-Santos Ândrea, Santos Sidney Emanuel Batista Dos, Burbano Rommel Mario Rodríguez, Fernandes Marianne Rodrigues, Santos Ney Pereira Carneiro Dos

机构信息

Núcleo de Pesquisas em Oncologia, Universidade Federal do Pará, Belém 66075-110, Brazil.

Laboratório de Genética Humana e Médica, Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém 66075-110, Brazil.

出版信息

Genes (Basel). 2021 Jan 22;12(2):142. doi: 10.3390/genes12020142.

Abstract

Estimates show that 5-10% of breast cancer cases are hereditary, caused by genetic variants in autosomal dominant genes; of these, 16% are due to germline mutations in the and genes. The comprehension of the mutation profile of these genes in the Brazilian population, particularly in Amazonian Amerindian groups, is scarce. We investigated fifteen polymorphisms in the and genes in Amazonian Amerindians and compared the results with the findings of global populations publicly available in the 1000 Genomes Project database. Our study shows that three variants (rs11571769, rs144848, and rs11571707) of the gene, commonly associated with hereditary breast cancer, had a significantly higher allele frequency in the Amazonian Amerindian individuals in comparison with the African, American, European, and Asian groups analyzed. These data outline the singular genetic profiles of the indigenous population from the Brazilian Amazon region. The knowledge about and variants is critical to establish public policies for hereditary breast cancer screening in Amerindian groups and populations admixed with them, such as the Brazilian population.

摘要

据估计,5%至10%的乳腺癌病例是遗传性的,由常染色体显性基因的基因变异引起;其中,16%是由于 和 基因的种系突变。在巴西人群中,尤其是在亚马逊印第安人群体中,对这些基因的突变谱的了解很少。我们研究了亚马逊印第安人中 和 基因的15个多态性,并将结果与1000基因组计划数据库中公开的全球人群的研究结果进行了比较。我们的研究表明,与遗传性乳腺癌通常相关的 基因的三个变体(rs11571769、rs144848和rs11571707),在亚马逊印第安个体中的等位基因频率明显高于所分析的非洲、美洲、欧洲和亚洲群体。这些数据勾勒出了巴西亚马逊地区土著居民独特的基因图谱。了解 和 变体对于制定针对印第安人群体以及与他们混血的人群(如巴西人群)进行遗传性乳腺癌筛查的公共政策至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7e7/7911168/ab594e0b3bf6/genes-12-00142-g001.jpg

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