Literature DB >> 23381647

Association between the NBS1 Glu185Gln polymorphism and breast cancer risk: a meta-analysis.

Fan Yao1, Yue Fang, Bo Chen, Feng Jin, Shubao Wang.   

Abstract

Nijmegen breakage syndrome 1 (NBS1), a vital DNA repair protein in the homologous recombination repair pathway and a signal modifier in the intra-S phase checkpoint, plays a critical role in cellular response to DNA damages and the maintenance of genomic stability. The NBS1 Glu185Gln (NBS1 E185Q, NBS1 8360G>C, rs1805794) polymorphism has been indicated to be involved in the development of cancer, but results of previous individual studies on the association between NBS1 Glu185Gln polymorphism and breast cancer risk remain controversial and inconclusive. Our meta-analysis investigated this association for the first time by pooling the odds ratios with corresponding 95 % confidence intervals (95 % CIs) of all individual publications available to date. Overall, 14 separate studies with 6,642 cases and 7,138 controls were finally included into the present meta-analysis after a comprehensive literature search of the PubMed, Embase, Web of Science, and China National Knowledge Infrastructure databases up to October 21, 2012. Overall analysis and subgroup analyses by ethnicity and source of controls were performed. Meta-analysis of total studies showed that the NBS1 Glu185Gln variant carriers were not susceptible to breast cancer (ORGln vs. Glu = 1.05, 95 % CI 0.80-1.39, P OR = 0.719; OR Gln/Gln vs. Glu/Glu = 0.82, 95 % CI 0.62-1.08, P OR = 0.154; OR Glu/Gln vs. Glu/Glu = 1.00, 95 % CI 0.90-1.13, P OR = 0.939; ORGln/Gln + Glu/Gln vs. Glu/Glu = 0.96, 95 % CI 0.83-1.11, P OR = 0.551; ORGln/Gln vs. Glu/Glu + Glu/Gln = 0.84, 95 % CI 0.67-1.05, P OR = 0.134). Similar results were observed in heterogeneity-adjusted meta-analysis of all studies. Furthermore, subgroup analyses by ethnicity and source of controls did not identify any appreciable relationship of the NBS1 Glu185Gln polymorphism with breast cancer susceptibility in any populations. Sensitivity analysis by sequentially omitting individual studies confirmed the stability and reliability of our results. Our meta-analysis of currently available data shows no association between the NBS1 Glu185Gln polymorphism and breast cancer risk.

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Year:  2013        PMID: 23381647     DOI: 10.1007/s13277-013-0668-4

Source DB:  PubMed          Journal:  Tumour Biol        ISSN: 1010-4283


  40 in total

1.  Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex.

Authors:  Shinya Matsuura; Junya Kobayashi; Hiroshi Tauchi; Kenshi Komatsu
Journal:  Adv Biophys       Date:  2004

2.  Constitutional short telomeres are strong genetic susceptibility markers for bladder cancer.

Authors:  Karin Broberg; Jonas Björk; Karin Paulsson; Mattias Höglund; Maria Albin
Journal:  Carcinogenesis       Date:  2005-03-03       Impact factor: 4.944

Review 3.  Breast cancer screening in women at average risk and high risk.

Authors:  Jennifer L Griffin; Mark D Pearlman
Journal:  Obstet Gynecol       Date:  2010-12       Impact factor: 7.661

4.  The comparison of percentages in matched samples.

Authors:  W G COCHRAN
Journal:  Biometrika       Date:  1950-12       Impact factor: 2.445

5.  Associations between NBS1 polymorphisms, haplotypes and smoking-related cancers.

Authors:  Sungshim L Park; Delara Bastani; Binh Y Goldstein; Shen-Chih Chang; Wendy Cozen; Lin Cai; Carlos Cordon-Cardo; Baoguo Ding; Sander Greenland; Na He; Shehnaz K Hussain; Qingwu Jiang; Yuan-Chin A Lee; Simin Liu; Ming-Lan Lu; Thomas M Mack; Jenny T Mao; Hal Morgenstern; Li-Na Mu; Sam S Oh; Allan Pantuck; Jeanette C Papp; Jianyu Rao; Victor E Reuter; Donald P Tashkin; Hua Wang; Nai-Chieh Y You; Shun-Zhang Yu; Jin-Kou Zhao; Zuo-Feng Zhang
Journal:  Carcinogenesis       Date:  2010-05-17       Impact factor: 4.944

6.  Bias in meta-analysis detected by a simple, graphical test. Asymmetry detected in funnel plot was probably due to true heterogeneity.

Authors:  A E Stuck; L Z Rubenstein; D Wieland
Journal:  BMJ       Date:  1998-02-07

7.  Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome.

Authors:  R Varon; C Vissinga; M Platzer; K M Cerosaletti; K H Chrzanowska; K Saar; G Beckmann; E Seemanová; P R Cooper; N J Nowak; M Stumm; C M Weemaes; R A Gatti; R K Wilson; M Digweed; A Rosenthal; K Sperling; P Concannon; A Reis
Journal:  Cell       Date:  1998-05-01       Impact factor: 41.582

8.  Direct activation of the ATM protein kinase by the Mre11/Rad50/Nbs1 complex.

Authors:  Ji-Hoon Lee; Tanya T Paull
Journal:  Science       Date:  2004-04-02       Impact factor: 47.728

9.  PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.

Authors:  Nazneen Rahman; Sheila Seal; Deborah Thompson; Patrick Kelly; Anthony Renwick; Anna Elliott; Sarah Reid; Katarina Spanova; Rita Barfoot; Tasnim Chagtai; Hiran Jayatilake; Lesley McGuffog; Sandra Hanks; D Gareth Evans; Diana Eccles; Douglas F Easton; Michael R Stratton
Journal:  Nat Genet       Date:  2006-12-31       Impact factor: 38.330

10.  Association between the NBS1 E185Q polymorphism and cancer risk: a meta-analysis.

Authors:  Meixia Lu; Jiachun Lu; Xiaobo Yang; Miao Yang; Hao Tan; Bai Yun; Luyuan Shi
Journal:  BMC Cancer       Date:  2009-04-24       Impact factor: 4.430

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  9 in total

1.  Genetic variations in the homologous recombination repair pathway genes modify risk of glioma.

Authors:  Haishi Zhang; Yanhong Liu; Keke Zhou; Chengcheng Zhou; Renke Zhou; Chunxia Cheng; Qingyi Wei; Daru Lu; Liangfu Zhou
Journal:  J Neurooncol       Date:  2015-10-29       Impact factor: 4.130

2.  Association between vitamin D receptor gene Cdx2 polymorphism and breast cancer susceptibility.

Authors:  Zhu-Chao Zhou; Jie Wang; Zi-Hao Cai; Qun-hua Zhang; Zhen-Xin Cai; Jian-Hua Wu
Journal:  Tumour Biol       Date:  2013-07-03

3.  The impact of functional LIG4 polymorphism on platinum-based chemotherapy response and survival in non-small cell lung cancer.

Authors:  You-Hua Jiang; Xiao-Ling Xu; Hai-Hong Ruan; Wei-Zhen Xu; Dan Li; Jian-Guo Feng; Qian-Bo Han; Wei-Min Mao
Journal:  Med Oncol       Date:  2014-04-11       Impact factor: 3.064

4.  Association between vitamin D receptor poly(A) polymorphism and breast cancer risk: a meta-analysis.

Authors:  Jinjiang Xu; Hongyu Li; Lixue Gu; Xiaoping Zhou
Journal:  Tumour Biol       Date:  2013-09-15

5.  Associations between NBS1 Polymorphisms and Colorectal Cancer in Chinese Population.

Authors:  Jing-Tao Li; Bao-Yuan Zhong; Hui-Hui Xu; Sheng-Yan Qiao; Gui Wang; Jing Huang; Hui-Zhen Fan; Hong-Chuan Zhao
Journal:  PLoS One       Date:  2015-07-17       Impact factor: 3.240

6.  Homologous Recombination Repair Polymorphisms and the Risk for Osteosarcoma.

Authors:  Katja Goričar; Viljem Kovač; Janez Jazbec; Janez Lamovec; Vita Dolžan
Journal:  J Med Biochem       Date:  2015-03-03       Impact factor: 3.402

7.  rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk.

Authors:  Jingjing Liu; Ivona Lončar; J Margriet Collée; Manjeet K Bolla; Joe Dennis; Kyriaki Michailidou; Qin Wang; Irene L Andrulis; Monica Barile; Matthias W Beckmann; Sabine Behrens; Javier Benitez; Carl Blomqvist; Bram Boeckx; Natalia V Bogdanova; Stig E Bojesen; Hiltrud Brauch; Paul Brennan; Hermann Brenner; Annegien Broeks; Barbara Burwinkel; Jenny Chang-Claude; Shou-Tung Chen; Georgia Chenevix-Trench; Ching Y Cheng; Ji-Yeob Choi; Fergus J Couch; Angela Cox; Simon S Cross; Katarina Cuk; Kamila Czene; Thilo Dörk; Isabel Dos-Santos-Silva; Peter A Fasching; Jonine Figueroa; Henrik Flyger; Montserrat García-Closas; Graham G Giles; Gord Glendon; Mark S Goldberg; Anna González-Neira; Pascal Guénel; Christopher A Haiman; Ute Hamann; Steven N Hart; Mikael Hartman; Sigrid Hatse; John L Hopper; Hidemi Ito; Anna Jakubowska; Maria Kabisch; Daehee Kang; Veli-Matti Kosma; Vessela N Kristensen; Loic Le Marchand; Eunjung Lee; Jingmei Li; Artitaya Lophatananon; Arto Mannermaa; Keitaro Matsuo; Roger L Milne; Susan L Neuhausen; Heli Nevanlinna; Nick Orr; Jose I A Perez; Julian Peto; Thomas C Putti; Katri Pylkäs; Paolo Radice; Suleeporn Sangrajrang; Elinor J Sawyer; Marjanka K Schmidt; Andreas Schneeweiss; Chen-Yang Shen; Martha J Shrubsole; Xiao-Ou Shu; Jacques Simard; Melissa C Southey; Anthony Swerdlow; Soo H Teo; Daniel C Tessier; Somchai Thanasitthichai; Ian Tomlinson; Diana Torres; Thérèse Truong; Chiu-Chen Tseng; Celine Vachon; Robert Winqvist; Anna H Wu; Drakoulis Yannoukakos; Wei Zheng; Per Hall; Alison M Dunning; Douglas F Easton; Maartje J Hooning; Ans M W van den Ouweland; John W M Martens; Antoinette Hollestelle
Journal:  Sci Rep       Date:  2016-11-15       Impact factor: 4.379

8.  Germline variants in MRE11/RAD50/NBN complex genes in childhood leukemia.

Authors:  Maria Mosor; Iwona Ziółkowska-Suchanek; Karina Nowicka; Agnieszka Dzikiewicz-Krawczyk; Danuta Januszkiewicz-Lewandowska; Jerzy Nowak
Journal:  BMC Cancer       Date:  2013-10-05       Impact factor: 4.430

9.  Micronuclei Formation upon Radioiodine Therapy for Well-Differentiated Thyroid Cancer: The Influence of DNA Repair Genes Variants.

Authors:  Luís S Santos; Octávia M Gil; Susana N Silva; Bruno C Gomes; Teresa C Ferreira; Edward Limbert; José Rueff
Journal:  Genes (Basel)       Date:  2020-09-17       Impact factor: 4.096

  9 in total

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