全基因组联合分析发现,ATM:C.1564_1565del 变体与共济失调-特朗吉特氏病和乳腺癌存在分离关系。

IF 1.4 4区 医学 Q4 GENETICS & HEREDITY
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引用次数: 0

摘要

ATM基因的杂合状态与乳腺癌的发病有关,而共济失调-毛细血管扩张症(A-T)的同型或复合杂合状态则与乳腺癌的发病有关。共济失调-毛细血管扩张症(A-T)是一种罕见的小脑共济失调综合征,表现为进行性神经功能损害、毛细血管扩张以及白血病和淋巴瘤风险增加。尽管 ATM 在 A-T 和乳腺癌中的作用已得到充分证实,但对同一家族中同时出现这两种表型的 ATM 变异进行研究的数量有限。在这里,我们利用联合分析和全基因组测序,调查了一个家族中的 ATM c.1564_1565del,该家族中有一名同基因成员患有 A-T(OMIM # 208900),还有三名杂合成员,其中一人患有乳腺癌(OMIM #114480)。据我们所知,这是首次对同一家族中同时出现 A-T 和乳腺癌表型的 ATM c.1564_1565del 基因分离进行研究。这项研究强调,在对A-T家族中的ATM杂合子携带者进行适当的癌症风险管理时,需要采用全面的基因组学方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Whole genome joint analysis reveals ATM:C.1564_1565del variant segregating with Ataxia-Telangiectasia and breast cancer

ATM gene is implicated in the development of breast cancer in the heterozygous state, and Ataxia-telangiectasia (A-T) in a homozygous or compound heterozygous state. Ataxia-telangiectasia (A-T) is a rare cerebellar ataxia syndrome presenting with progressive neurologic impairment, telangiectasia, and an increased risk of leukemia and lymphoma.

Although the role of ATM, separately, in association with A-T and breast cancer is well documented, there is a limited number of studies investigating ATM variants when segregating with both phenotypes in the same family. Here, using joint analysis and whole genome sequencing, we investigated ATM c.1564_1565del in a family with one homozygous member presenting with A-T (OMIM # 208900) and three heterozygous members, of whom one had breast cancer (OMIM #114480). To our knowledge, this is the first study of ATM c.1564_1565del segregation with both A-T and breast cancer phenotypes within the same kindred. This study highlights the need for a comprehensive genomic approach in the appropriate cancer risk management of heterozygote carriers of ATM in families with A-T.

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来源期刊
Cancer Genetics
Cancer Genetics ONCOLOGY-GENETICS & HEREDITY
CiteScore
3.20
自引率
5.30%
发文量
167
审稿时长
27 days
期刊介绍: The aim of Cancer Genetics is to publish high quality scientific papers on the cellular, genetic and molecular aspects of cancer, including cancer predisposition and clinical diagnostic applications. Specific areas of interest include descriptions of new chromosomal, molecular or epigenetic alterations in benign and malignant diseases; novel laboratory approaches for identification and characterization of chromosomal rearrangements or genomic alterations in cancer cells; correlation of genetic changes with pathology and clinical presentation; and the molecular genetics of cancer predisposition. To reach a basic science and clinical multidisciplinary audience, we welcome original full-length articles, reviews, meeting summaries, brief reports, and letters to the editor.
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