Literature DB >> 26629066

CHEK2 mutation and risk of prostate cancer: a systematic review and meta-analysis.

Yue Wang1, Bo Dai1, Dingwei Ye1.   

Abstract

BACKGROUND: CHEK2 encodes for a G2 checkpoint kinase which plays a critical role in DNA repair. Its mutation confers an increased risk of breast cancer. It has also been suggested to increase risks of prostate cancer, but its involvement with this type of cancer has not been confirmed.
METHODS: We performed a systematic review and meta-analysis to clarify the association between CHEK2 1100delC, IVS2+1G>A, I157T mutation and risk of Prostate Cancer. A comprehensive, computerized literature search of PubMed until December 27, 2014 was carried out. Eligible studies were included according to specific inclusion criteria. Pooled hazard ratio was estimated using the fixed effects model or random effects model according to heterogeneity between studies.
RESULTS: Eight eligible studies were included in the analysis, all were retrospective studies. The overall meta-analysis demonstrated that the CHEK2 1100delC mutation (OR 3.29; 95% confidence interval: 1.85-5.85; P = 0.00) and I157T missense mutation (OR 1.80; 95% confidence interval: 1.51-2.14; P = 0.00) was associated with higher risk of Prostate Cancer, and CHEK2 1100delC mutation is irrelevant to familial aggregation phenomenon of prostate cancer (OR 1.59; 95% confidence interval: 0.79-3.20; P = 0.20). The IVS2+1G>A mutation is also irrelevant to Prostate Cancer (OR = 1.59, 95% CI = 0.93-2.71, P = 0.09). None of the single studies materially altered the original results and no evidence of publication bias was found.
CONCLUSION: CHEK2 1100delC mutation and I157T missense mutation in males indicates higher risk of Prostate Cancer, but there's no evidence to prove the CHEK2 1100delC mutation was associated with Familial prostate cancer.

Entities:  

Keywords:  CHEK2 mutation; Prostate cancer; risk of prostate cancer

Year:  2015        PMID: 26629066      PMCID: PMC4658955     

Source DB:  PubMed          Journal:  Int J Clin Exp Med        ISSN: 1940-5901


  27 in total

1.  CHEK2 1100delC and colorectal cancer.

Authors:  O Kilpivaara; P Laiho; L A Aaltonen; H Nevanlinna
Journal:  J Med Genet       Date:  2003-10       Impact factor: 6.318

2.  Homozygosity for a CHEK2*1100delC mutation identified in familial colorectal cancer does not lead to a severe clinical phenotype.

Authors:  Marjo van Puijenbroek; Christi J van Asperen; Anneke van Mil; Peter Devilee; Tom van Wezel; Hans Morreau
Journal:  J Pathol       Date:  2005-06       Impact factor: 7.996

3.  Having pancreatic cancer with tumoral loss of ATM and normal TP53 protein expression is associated with a poorer prognosis.

Authors:  Haeryoung Kim; Burcu Saka; Spencer Knight; Michael Borges; Erica Childs; Alison Klein; Christopher Wolfgang; Joseph Herman; Volkan N Adsay; Ralph H Hruban; Michael Goggins
Journal:  Clin Cancer Res       Date:  2014-01-31       Impact factor: 12.531

4.  Increased risk of breast cancer associated with CHEK2*1100delC.

Authors:  Maren Weischer; Stig Egil Bojesen; Anne Tybjaerg-Hansen; Christen Kirk Axelsson; Børge Grønne Nordestgaard
Journal:  J Clin Oncol       Date:  2006-07-31       Impact factor: 44.544

5.  CHEK2 genomic and proteomic analyses reveal genetic inactivation or endogenous activation across the 60 cell lines of the US National Cancer Institute.

Authors:  G Zoppoli; S Solier; W C Reinhold; H Liu; J W Connelly; A Monks; R H Shoemaker; O D Abaan; S R Davis; P S Meltzer; J H Doroshow; Y Pommier
Journal:  Oncogene       Date:  2011-07-18       Impact factor: 9.867

6.  Linkage of ATM to cell cycle regulation by the Chk2 protein kinase.

Authors:  S Matsuoka; M Huang; S J Elledge
Journal:  Science       Date:  1998-12-04       Impact factor: 47.728

7.  The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families.

Authors:  Rogier A Oldenburg; Karin Kroeze-Jansema; Jaennelle Kraan; Hans Morreau; Jan G M Klijn; Nicoline Hoogerbrugge; Marjolein J L Ligtenberg; Christi J van Asperen; Hans F A Vasen; Carel Meijers; Hanne Meijers-Heijboer; Truuske H de Bock; Cees J Cornelisse; Peter Devilee
Journal:  Cancer Res       Date:  2003-12-01       Impact factor: 12.701

8.  Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts.

Authors:  Daphne W Bell; Sang H Kim; Andrew K Godwin; Taryn A Schiripo; Patricia L Harris; Sara M Haserlat; Doke C R Wahrer; Christopher A Haiman; Mary B Daly; Kristin B Niendorf; Matthew R Smith; Dennis C Sgroi; Judy E Garber; Olufunmilayo I Olopade; Loic Le Marchand; Brian E Henderson; David Altshuler; Daniel A Haber; Matthew L Freedman
Journal:  Int J Cancer       Date:  2007-12-15       Impact factor: 7.396

9.  The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype.

Authors:  Hanne Meijers-Heijboer; Juul Wijnen; Hans Vasen; Marijke Wasielewski; Anja Wagner; Antoinette Hollestelle; Fons Elstrodt; Renate van den Bos; Anja de Snoo; Grace Tjon A Fat; Cecile Brekelmans; Shantie Jagmohan; Patrick Franken; Paul Verkuijlen; Ans van den Ouweland; Pamela Chapman; Carli Tops; Gabriela Möslein; John Burn; Henry Lynch; Jan Klijn; Riccardo Fodde; Mieke Schutte
Journal:  Am J Hum Genet       Date:  2003-04-10       Impact factor: 11.025

10.  CHEK2 variants associate with hereditary prostate cancer.

Authors:  E H Seppälä; T Ikonen; N Mononen; V Autio; A Rökman; M P Matikainen; T L J Tammela; J Schleutker
Journal:  Br J Cancer       Date:  2003-11-17       Impact factor: 7.640

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  12 in total

Review 1.  Inherited pancreatic cancer.

Authors:  Fei Chen; Nicholas J Roberts; Alison P Klein
Journal:  Chin Clin Oncol       Date:  2017-12

2.  Validation of a Semiautomated Natural Language Processing-Based Procedure for Meta-Analysis of Cancer Susceptibility Gene Penetrance.

Authors:  Zhengyi Deng; Kanhua Yin; Yujia Bao; Victor Diego Armengol; Cathy Wang; Ankur Tiwari; Regina Barzilay; Giovanni Parmigiani; Danielle Braun; Kevin S Hughes
Journal:  JCO Clin Cancer Inform       Date:  2019-08

3.  A Clinical Decision Support Tool to Predict Cancer Risk for Commonly Tested Cancer-Related Germline Mutations.

Authors:  Danielle Braun; Jiabei Yang; Molly Griffin; Giovanni Parmigiani; Kevin S Hughes
Journal:  J Genet Couns       Date:  2018-03-02       Impact factor: 2.537

4.  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

5.  Progression inference for somatic mutations in cancer.

Authors:  Leif E Peterson; Tatiana Kovyrshina
Journal:  Heliyon       Date:  2017-04-11

6.  Is CHEK2 a moderate-risk breast cancer gene or the younger sister of Li-Fraumeni?

Authors:  Dilanka L De Silva; Ingrid Winship
Journal:  BMJ Case Rep       Date:  2020-09-07

Review 7.  CHEK2 Germline Variants in Cancer Predisposition: Stalemate Rather than Checkmate.

Authors:  Lenka Stolarova; Petra Kleiblova; Marketa Janatova; Jana Soukupova; Petra Zemankova; Libor Macurek; Zdenek Kleibl
Journal:  Cells       Date:  2020-12-12       Impact factor: 6.600

Review 8.  Hereditary Predisposition to Prostate Cancer: From Genetics to Clinical Implications.

Authors:  Andreia Brandão; Paula Paulo; Manuel R Teixeira
Journal:  Int J Mol Sci       Date:  2020-07-16       Impact factor: 5.923

9.  Implementation of Germline Testing for Prostate Cancer: Philadelphia Prostate Cancer Consensus Conference 2019.

Authors:  Veda N Giri; Karen E Knudsen; William K Kelly; Heather H Cheng; Kathleen A Cooney; Michael S Cookson; William Dahut; Scott Weissman; Howard R Soule; Daniel P Petrylak; Adam P Dicker; Saud H AlDubayan; Amanda E Toland; Colin C Pritchard; Curtis A Pettaway; Mary B Daly; James L Mohler; J Kellogg Parsons; Peter R Carroll; Robert Pilarski; Amie Blanco; Ashley Woodson; Alanna Rahm; Mary-Ellen Taplin; Thomas J Polascik; Brian T Helfand; Colette Hyatt; Alicia K Morgans; Felix Feng; Michael Mullane; Jacqueline Powers; Raoul Concepcion; Daniel W Lin; Richard Wender; James Ryan Mark; Anthony Costello; Arthur L Burnett; Oliver Sartor; William B Isaacs; Jianfeng Xu; Jeffrey Weitzel; Gerald L Andriole; Himisha Beltran; Alberto Briganti; Lindsey Byrne; Anne Calvaresi; Thenappan Chandrasekar; David Y T Chen; Robert B Den; Albert Dobi; E David Crawford; James Eastham; Scott Eggener; Matthew L Freedman; Marc Garnick; Patrick T Gomella; Nathan Handley; Mark D Hurwitz; Joseph Izes; R Jeffrey Karnes; Costas Lallas; Lucia Languino; Stacy Loeb; Ana Maria Lopez; Kevin R Loughlin; Grace Lu-Yao; S Bruce Malkowicz; Mark Mann; Patrick Mille; Martin M Miner; Todd Morgan; Jose Moreno; Lorelei Mucci; Ronald E Myers; Sarah M Nielsen; Brock O'Neil; Wayne Pinover; Peter Pinto; Wendy Poage; Ganesh V Raj; Timothy R Rebbeck; Charles Ryan; Howard Sandler; Matthew Schiewer; E Michael D Scott; Brittany Szymaniak; William Tester; Edouard J Trabulsi; Neha Vapiwala; Evan Y Yu; Charnita Zeigler-Johnson; Leonard G Gomella
Journal:  J Clin Oncol       Date:  2020-06-09       Impact factor: 44.544

10.  The evolving role of germline genetic testing and management in prostate cancer: Report from the Princess Margaret Cancer Centre international retreat.

Authors:  Roderick Clark; Miran Kenk; Kristen McAlpine; Emily Thain; Kirsten M Farncombe; Colin C Pritchard; Robert Nussbaum; Alexander W Wyatt; Johann de Bono; Danny Vesprini; Yvonne Bombard; Justin Lorentz; Steven Narod; Raymond Kim; Neil Fleshner
Journal:  Can Urol Assoc J       Date:  2021-12       Impact factor: 1.862

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