Literature DB >> 22799331

The CHEK2 I157T variant and breast cancer susceptibility: a systematic review and meta-analysis.

Chuan Liu1, Ying Wang, Qing-Shui Wang, Ya-Jie Wang.   

Abstract

BACKGROUND: The cell cycle checkpoint kinase 2 (CHEK2) gene I157T variant may be associated with an increased risk of breast cancer, but it is unclear whether the evidence is sufficient to recommend testing for the mutation in clinical practice.
MATERIALS AND METHODS: We systematically searched PubMed, Embase, Elsevier and Springer for relevant articles published before Nov 2011. Summary odds ratio (OR) and 95% confidence interval (95% CI) incidence rates were calculated using a random-effects model with STATA (version 10.0) software.
RESULTS: A total of fifteen case-control studies, including 19,621 cases and 27,001 controls based on the search criteria, were included for analysis. A significant association was found between carrying the CHEK2 I157T variant and increased risk of unselected breast cancer (OR = 1.48, 95% CI = 1.31-1.66, P < 0.0001), familial breast cancer (OR = 1.48, 95% CI = 1.16-1.89, P < 0.0001), and early-onset breast cancer (OR = 1.47, 95% CI = 1.29-1.66, P < 0.0001). We found an even stronger significant association between the CHEK2 I157T C variant and increased risk of lobular type breast tumors (OR = 4.17, 95% CI = 2.89-6.03, P < 0.0001).
CONCLUSION: Our research indicates that the CHEK2 I157T variant may be another important genetic mutation which increases risk of breast cancer, especially the lobular type.

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Year:  2012        PMID: 22799331     DOI: 10.7314/apjcp.2012.13.4.1355

Source DB:  PubMed          Journal:  Asian Pac J Cancer Prev        ISSN: 1513-7368


  21 in total

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Journal:  CMAJ       Date:  2018-02-05       Impact factor: 8.262

3.  Prevalence of Germline Mutations in Cancer Susceptibility Genes in Patients With Advanced Renal Cell Carcinoma.

Authors:  Maria I Carlo; Semanti Mukherjee; Diana Mandelker; Joseph Vijai; Yelena Kemel; Liying Zhang; Andrea Knezevic; Sujata Patil; Ozge Ceyhan-Birsoy; Kuo-Cheng Huang; Almedina Redzematovic; Devyn T Coskey; Carolyn Stewart; Nisha Pradhan; Angela G Arnold; A Ari Hakimi; Ying-Bei Chen; Jonathan A Coleman; David M Hyman; Marc Ladanyi; Karen A Cadoo; Michael F Walsh; Zsofia K Stadler; Chung-Han Lee; Darren R Feldman; Martin H Voss; Mark Robson; Robert J Motzer; Kenneth Offit
Journal:  JAMA Oncol       Date:  2018-09-01       Impact factor: 31.777

4.  A novel recurrent CHEK2 Y390C mutation identified in high-risk Chinese breast cancer patients impairs its activity and is associated with increased breast cancer risk.

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5.  Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast.

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Journal:  J Clin Oncol       Date:  2021-10-21       Impact factor: 44.544

6.  Differences in Cancer Phenotypes Among Frequent CHEK2 Variants and Implications for Clinical Care-Checking CHEK2.

Authors:  Brittany L Bychkovsky; Nihat B Agaoglu; Carolyn Horton; Jing Zhou; Amal Yussuf; Parichehr Hemyari; Marcy E Richardson; Colin Young; Holly LaDuca; Deborah L McGuinness; Rochelle Scheib; Judy E Garber; Huma Q Rana
Journal:  JAMA Oncol       Date:  2022-09-22       Impact factor: 33.006

7.  Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer.

Authors:  Johanna I Kiiski; Liisa M Pelttari; Sofia Khan; Edda S Freysteinsdottir; Inga Reynisdottir; Steven N Hart; Hermela Shimelis; Sara Vilske; Anne Kallioniemi; Johanna Schleutker; Arto Leminen; Ralf Bützow; Carl Blomqvist; Rosa B Barkardottir; Fergus J Couch; Kristiina Aittomäki; Heli Nevanlinna
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8.  Association of Inherited Pathogenic Variants in Checkpoint Kinase 2 (CHEK2) With Susceptibility to Testicular Germ Cell Tumors.

Authors:  Saud H AlDubayan; Louise C Pyle; Marija Gamulin; Tomislav Kulis; Nathanael D Moore; Amaro Taylor-Weiner; Anis A Hamid; Brendan Reardon; Bradley Wubbenhorst; Rama Godse; David J Vaughn; Linda A Jacobs; Stefanie Meien; Mislav Grgic; Zeljko Kastelan; Sarah C Markt; Scott M Damrauer; Daniel J Rader; Rachel L Kember; Jennifer T Loud; Peter A Kanetsky; Mark H Greene; Christopher J Sweeney; Christian Kubisch; Katherine L Nathanson; Eliezer M Van Allen; Douglas R Stewart; Davor Lessel
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10.  Management of Women With Breast Cancer and Pathogenic Variants in Genes Other Than BRCA1 or BRCA2.

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