Phenotypes of carriers of two mutated alleles in major cancer susceptibility genes

Author:

Laitman Yael,Niskakoski Anni,Bernstein-Molho Rinal,Koskinen Lotta,Rabina Daniel,Koskenvuo Juha,Friedman EitanORCID

Abstract

Abstract Purpose While cancer phenotypes in carriers of a single mutant allele in most major cancer susceptibility genes are well-established, there is a paucity of data on the phenotype of carriers of two pathogenic variants—double heterozygotes (DH) or homozygous carriers. Here, we describe the phenotype of carriers of homozygous and DH pathogenic sequence variants (PSVs) in major cancer susceptibility genes. Methods Individuals referred for multigene panel testing at Blueprint Genetics laboratory were included. Ethically approved comparison of cancer type and age at diagnosis between DH, homozygous, and single PSV carriers was performed per gene. Results Of 6,685 eligible participants, 928 (13.9%) were single heterozygous PSV carriers, 6 (0.09%) were homozygous PSV carriers, and 17 (0.25%) were DH PSV carriers. Mean age at diagnosis of any cancer among single PSV age was 46.8 ± 14.9 years and among DH PSV carriers 37.6 ± 13.0 years (P < 0.0001). Notably, age at diagnosis for breast cancer among single BRCA1 PSV carriers (n = 59) was 43.8 ± 8.7 years (p = 0.7606), among single BRCA2 PSV carriers (n = 52)—47.9 ± 13.0 years (p = 0.2274) compared with 42.3 ± 13.0 years among DH PSV carriers (n = 10- 9 of whom were carriers of either BRCA1 or BRCA2). Conclusion DH for PSV in two cancer susceptibility genes is a rare event, and the mean age at cancer diagnosis is younger in DH PSV carriers compared with single PSV carriers.

Funder

Tel Aviv University

Publisher

Springer Science and Business Media LLC

Reference18 articles.

1. Fletcher O, Houlston RS (2010) Architecture of inherited susceptibility to common cancer. Nat Rev Cancer 10(5):353–361. https://doi.org/10.1038/nrc2840

2. Foulkes WD (2008) Inherited susceptibility to common cancers. N Engl J Med 359(20):2143–2153. https://doi.org/10.1056/NEJMra0802968

3. Cancer Genetics. (2010) (Cancer Treatment and Research, 155) 2010th Edition. Boris Pasche (Ed), Springer, New York

4. Fanale D, Ottini L, Ricevuto E et al (2021) Hereditary cancers and genetics. In: Russo A, Peeters M, Incorvaia L, Rolfo C (eds) Practical Medical Oncology Textbook. UNIPA Springer Series, Springer, Cham

5. McGuigan A, Whitworth J, Andreou A, Hearn T, Genomics England Research Consortium, Tischkowitz M, Maher ER (2022) Multilocus inherited neoplasia allele syndrome (MINAS): an update. Eur J Hum Genet 30:265–270

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3