Literature DB >> 36094610

Cancer risks associated with heterozygous ATM loss of function and missense pathogenic variants based on multigene panel analysis.

Yael Laitman1, Sarah M Nielsen2, Rinat Bernstein-Molho1,3,4, Brandie Heald2, Kathryn E Hatchell2, Edward D Esplin2, Eitan Friedman5,6,7.   

Abstract

PURPOSE: Cancer risks conferred by germline, heterozygous, ATM pathogenic/likely pathogenic variants (PSVs) are yet to be consistently determined. The current study assessed these risks by analysis of a large dataset of ATM heterozygote loss of function (LOF) and missense PSV carriers tested with a multigene panel (MGP).
METHODS: De-identified data of all individuals who underwent ATM sequencing as part of MGP between October 2015 and February 2020 were reviewed. In cancer cases, rates for the six most prevalent variants and for all LOF and missense PSV combined were compared with rates of the same PSV in ethnically matched, healthy population controls. Statistical analysis included Chi-square tests and odds ratios calculations.
RESULTS: For female breast cancer cases, LOF )1794/219,269) and missense (301/219,269) ATM PSVs were seen at higher rates compared to gnomAD non-cancer controls (n = 157/56,001 and n = 27/61,208; p < 0.00001, respectively). Notably, the rate of the c.103C > T variant was higher in controls than in breast cancer cases [p = 0.001; OR 0.31 (95% CI 0.1-0.6)]. For all cancer cases combined, compared with non-cancer population controls, LOF (n = 143) and missense (n = 15) PSVs reported in both datasets were significantly more prevalent in cancer cases [ORLOF 1.7 (95% 1.5-1.9) ORmissense 3.0 (95% CI 2.3-4); p = 0.0001].
CONCLUSION: Both LOF and missense heterozygous ATM PSVs are more frequently detected in cases of several cancer types (breast, ovarian, prostate, lung, pancreatic) compared with healthy population controls. However, not all ATM PSVs confer an increased cancer risk (e.g., breast).
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  ATM heterozygous pathogenic variants; Breast cancer; Cancer risk; Loss of function variants; Missense pathogenic variants

Mesh:

Substances:

Year:  2022        PMID: 36094610     DOI: 10.1007/s10549-022-06723-z

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.624


  12 in total

1.  Cancer risks and mortality in heterozygous ATM mutation carriers.

Authors:  Deborah Thompson; Silvia Duedal; Jennifer Kirner; Lesley McGuffog; James Last; Anne Reiman; Philip Byrd; Malcolm Taylor; Douglas F Easton
Journal:  J Natl Cancer Inst       Date:  2005-06-01       Impact factor: 13.506

2.  Loss-of-function variants in ATM confer risk of gastric cancer.

Authors:  Hannes Helgason; Thorunn Rafnar; Halla S Olafsdottir; Jon G Jonasson; Asgeir Sigurdsson; Simon N Stacey; Adalbjorg Jonasdottir; Laufey Tryggvadottir; Kristin Alexiusdottir; Asgeir Haraldsson; Louise le Roux; Julius Gudmundsson; Hrefna Johannsdottir; Asmundur Oddsson; Arnaldur Gylfason; Olafur T Magnusson; Gisli Masson; Thorvaldur Jonsson; Halla Skuladottir; Daniel F Gudbjartsson; Unnur Thorsteinsdottir; Patrick Sulem; Kari Stefansson
Journal:  Nat Genet       Date:  2015-06-22       Impact factor: 38.330

3.  A Population-Based Study of Genes Previously Implicated in Breast Cancer.

Authors:  Chunling Hu; Steven N Hart; Rohan Gnanaolivu; Hongyan Huang; Kun Y Lee; Jie Na; Chi Gao; Jenna Lilyquist; Siddhartha Yadav; Nicholas J Boddicker; Raed Samara; Josh Klebba; Christine B Ambrosone; Hoda Anton-Culver; Paul Auer; Elisa V Bandera; Leslie Bernstein; Kimberly A Bertrand; Elizabeth S Burnside; Brian D Carter; Heather Eliassen; Susan M Gapstur; Mia Gaudet; Christopher Haiman; James M Hodge; David J Hunter; Eric J Jacobs; Esther M John; Charles Kooperberg; Allison W Kurian; Loic Le Marchand; Sara Lindstroem; Tricia Lindstrom; Huiyan Ma; Susan Neuhausen; Polly A Newcomb; Katie M O'Brien; Janet E Olson; Irene M Ong; Tuya Pal; Julie R Palmer; Alpa V Patel; Sonya Reid; Lynn Rosenberg; Dale P Sandler; Christopher Scott; Rulla Tamimi; Jack A Taylor; Amy Trentham-Dietz; Celine M Vachon; Clarice Weinberg; Song Yao; Argyrios Ziogas; Jeffrey N Weitzel; David E Goldgar; Susan M Domchek; Katherine L Nathanson; Peter Kraft; Eric C Polley; Fergus J Couch
Journal:  N Engl J Med       Date:  2021-01-20       Impact factor: 91.245

4.  Breast and other cancers in families with ataxia-telangiectasia.

Authors:  M Swift; P J Reitnauer; D Morrell; C L Chase
Journal:  N Engl J Med       Date:  1987-05-21       Impact factor: 91.245

5.  Mice heterozygous for mutation in Atm, the gene involved in ataxia-telangiectasia, have heightened susceptibility to cancer.

Authors:  Kevin Spring; Farida Ahangari; Shaun P Scott; Paul Waring; David M Purdie; Philip C Chen; Kevin Hourigan; Jonathan Ramsay; Peter J McKinnon; Michael Swift; Martin F Lavin
Journal:  Nat Genet       Date:  2002-08-26       Impact factor: 38.330

6.  Incidence of cancer in 161 families affected by ataxia-telangiectasia.

Authors:  M Swift; D Morrell; R B Massey; C L Chase
Journal:  N Engl J Med       Date:  1991-12-26       Impact factor: 91.245

7.  Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.

Authors:  Mary B Daly; Tuya Pal; Michael P Berry; Saundra S Buys; Patricia Dickson; Susan M Domchek; Ahmed Elkhanany; Susan Friedman; Michael Goggins; Mollie L Hutton; Beth Y Karlan; Seema Khan; Catherine Klein; Wendy Kohlmann; Allison W Kurian; Christine Laronga; Jennifer K Litton; Julie S Mak; Carolyn S Menendez; Sofia D Merajver; Barbara S Norquist; Kenneth Offit; Holly J Pederson; Gwen Reiser; Leigha Senter-Jamieson; Kristen Mahoney Shannon; Rebecca Shatsky; Kala Visvanathan; Jeffrey N Weitzel; Myra J Wick; Kari B Wisinski; Matthew B Yurgelun; Susan D Darlow; Mary A Dwyer
Journal:  J Natl Compr Canc Netw       Date:  2021-01-06       Impact factor: 11.908

8.  Rare variants in the ATM gene and risk of breast cancer.

Authors:  David E Goldgar; Sue Healey; James G Dowty; Leonard Da Silva; Xiaoqing Chen; Amanda B Spurdle; Mary Beth Terry; Mary J Daly; Saundra M Buys; Melissa C Southey; Irene Andrulis; Esther M John; Kum Kum Khanna; John L Hopper; Peter J Oefner; Sunil Lakhani; Georgia Chenevix-Trench
Journal:  Breast Cancer Res       Date:  2011-07-25       Impact factor: 6.466

9.  Prevalence of pathogenic germline cancer risk variants in high-risk urothelial carcinoma.

Authors:  Amin H Nassar; Sarah Abou Alaiwi; Saud H AlDubayan; Huma Q Rana; Guru Sonpavde; Nicholas Moore; Kent W Mouw; David J Kwiatkowski; Toni K Choueiri; Catherine Curran; Jacob E Berchuck; Lauren C Harshman; Pier V Nuzzo; Nieves Martinez Chanza; Eliezer Van Allen; Edward D Esplin; Shan Yang; Thomas Callis; Judy E Garber
Journal:  Genet Med       Date:  2019-12-17       Impact factor: 8.822

10.  Comparison of Universal Genetic Testing vs Guideline-Directed Targeted Testing for Patients With Hereditary Cancer Syndrome.

Authors:  N Jewel Samadder; Douglas Riegert-Johnson; Lisa Boardman; Deborah Rhodes; Myra Wick; Scott Okuno; Katie L Kunze; Michael Golafshar; Pedro L S Uson; Luke Mountjoy; Natalie Ertz-Archambault; Neej Patel; Eduardo A Rodriguez; Blanca Lizaola-Mayo; Michael Lehrer; Cameron S Thorpe; Nathan Y Yu; Edward D Esplin; Robert L Nussbaum; Richard R Sharp; Cindy Azevedo; Margaret Klint; Megan Hager; Sarah Macklin-Mantia; Alan H Bryce; Tanios S Bekaii-Saab; Aleksandar Sekulic; A Keith Stewart
Journal:  JAMA Oncol       Date:  2021-02-01       Impact factor: 31.777

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.