Literature DB >> 24062231

DNA double-strand break repair genotype and phenotype and breast cancer risk within sisters from the New York site of the Breast Cancer Family Registry (BCFR).

Hui-Chen Wu1, Lissette Delgado-Cruzata, Nicola Machella, Qiao Wang, Regina M Santella, Mary Beth Terry.   

Abstract

PURPOSE: We previously observed that poor DNA repair phenotype is associated with increased breast cancer (BC) risk within families. Here, we examined whether genetic variation in double-strand break repair (DSBR) genes is associated with BC risk and if genotypes are related to phenotype in unaffected women.
METHODS: Using data from the New York site of the Breast Cancer Family Registry, we investigated 25 single-nucleotide polymorphism (SNPs) involved in DSBR using biospecimens from 337 BC cases and 410 unaffected sister controls.
RESULTS: Genotypes in XRCC4 were associated with BC risk, with ORs of 1.67 (95 % CI 1.01-2.76) for the combined GA/AA of rs1805377 and 1.69 (95 % CI 1.03-2.77) for rs1056503 TG/GG; these associations were no longer statistically significant in multivariable conditional logistic regression models. When examining the association of SNPs with phenotype, we found that genotypes of XRCC5 rs3834 and rs1051685, which were highly correlated with each other, were associated with end-joining (EJ) capacity; women with the XRCC5 rs3834 GA genotype had better DNA repair as measured by higher levels of EJ capacity (37.8 ± 14.1 % for GA vs. 27.9 ± 11.8 % for GG carriers p = 0.0006). Women with the AA genotype of BRCA1 rs799917 also had higher EJ capacity (35.1 ± 9.2 %) than those with GG (26.4 ± 10.1 %, p = 0.02).
CONCLUSIONS: Overall, we found that selected DSBR genotypes were associated with phenotype, although they were not associated with BC risk itself, suggesting that phenotypic measures are influenced by endogenous and exogenous factors across the life course and may be better markers than genotypic measures for ascertaining BC risk.

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Year:  2013        PMID: 24062231      PMCID: PMC3947831          DOI: 10.1007/s10552-013-0292-z

Source DB:  PubMed          Journal:  Cancer Causes Control        ISSN: 0957-5243            Impact factor:   2.506


  50 in total

1.  Variants in DNA double-strand break repair genes and breast cancer susceptibility.

Authors:  Bettina Kuschel; Annika Auranen; Simon McBride; Karen L Novik; Antonis Antoniou; Julian M Lipscombe; Nicholas E Day; Douglas F Easton; Bruce A J Ponder; Paul D P Pharoah; Alison Dunning
Journal:  Hum Mol Genet       Date:  2002-06-01       Impact factor: 6.150

2.  A role for XRCC4 in age at diagnosis and breast cancer risk.

Authors:  Kristina Allen-Brady; Lisa A Cannon-Albright; Susan L Neuhausen; Nicola J Camp
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2006-07       Impact factor: 4.254

Review 3.  Radiation-induced chromatid breaks and deficient DNA repair in cancer predisposition.

Authors:  R Parshad; K K Sanford
Journal:  Crit Rev Oncol Hematol       Date:  2001-02       Impact factor: 6.312

4.  Homology-directed dna repair, mitomycin-c resistance, and chromosome stability is restored with correction of a Brca1 mutation.

Authors:  M E Moynahan; T Y Cui; M Jasin
Journal:  Cancer Res       Date:  2001-06-15       Impact factor: 12.701

5.  Global DNA methylation levels in white blood cell DNA from sisters discordant for breast cancer from the New York site of the Breast Cancer Family Registry.

Authors:  Lissette Delgado-Cruzata; Hui-Chen Wu; Mary Perrin; Yuyan Liao; Maya A Kappil; Jennifer S Ferris; Julie D Flom; Hulya Yazici; Regina M Santella; Mary Beth Terry
Journal:  Epigenetics       Date:  2012-06-18       Impact factor: 4.528

6.  Genome-wide search for loss of heterozygosity using laser capture microdissected tissue of breast carcinoma: an implication for mutator phenotype and breast cancer pathogenesis.

Authors:  C Y Shen; J C Yu; Y L Lo; C H Kuo; C T Yue; Y S Jou; C S Huang; J C Lung; C W Wu
Journal:  Cancer Res       Date:  2000-07-15       Impact factor: 12.701

7.  A single mutated BRCA1 allele leads to impaired fidelity of double strand break end-joining.

Authors:  Céline Baldeyron; Emilie Jacquemin; Julianne Smith; Céline Jacquemont; Isabelle De Oliveira; Sophie Gad; Jean Feunteun; Dominique Stoppa-Lyonnet; Dora Papadopoulo
Journal:  Oncogene       Date:  2002-02-21       Impact factor: 9.867

8.  Repetitive element DNA methylation levels in white blood cell DNA from sisters discordant for breast cancer from the New York site of the Breast Cancer Family Registry.

Authors:  Hui-Chen Wu; Lissette Delgado-Cruzata; Julie D Flom; Mary Perrin; Yuyan Liao; Jennifer S Ferris; Regina M Santella; Mary Beth Terry
Journal:  Carcinogenesis       Date:  2012-06-07       Impact factor: 4.944

9.  Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium.

Authors:  Jonine D Figueroa; Montserrat Garcia-Closas; Manjeet Humphreys; Radka Platte; John L Hopper; Melissa C Southey; Carmel Apicella; Fleur Hammet; Marjanka K Schmidt; Annegien Broeks; Rob A E M Tollenaar; Laura J Van't Veer; Peter A Fasching; Matthias W Beckmann; Arif B Ekici; Reiner Strick; Julian Peto; Isabel dos Santos Silva; Olivia Fletcher; Nichola Johnson; Elinor Sawyer; Ian Tomlinson; Michael Kerin; Barbara Burwinkel; Federik Marme; Andreas Schneeweiss; Christof Sohn; Stig Bojesen; Henrik Flyger; Børge G Nordestgaard; Javier Benítez; Roger L Milne; Jose Ignacio Arias; M Pilar Zamora; Hermann Brenner; Heiko Müller; Volker Arndt; Nazneen Rahman; Clare Turnbull; Sheila Seal; Anthony Renwick; Hiltrud Brauch; Christina Justenhoven; Thomas Brüning; Jenny Chang-Claude; Rebecca Hein; Shan Wang-Gohrke; Thilo Dörk; Peter Schürmann; Michael Bremer; Peter Hillemanns; Heli Nevanlinna; Tuomas Heikkinen; Kristiina Aittomäki; Carl Blomqvist; Natalia Bogdanova; Natalia Antonenkova; Yuri I Rogov; Johann Hinrich Karstens; Marina Bermisheva; Darya Prokofieva; Shamil Hanafievich Gantcev; Elza Khusnutdinova; Annika Lindblom; Sara Margolin; Georgia Chenevix-Trench; Jonathan Beesley; Xiaoqing Chen; Arto Mannermaa; Veli-Matti Kosma; Ylermi Soini; Vesa Kataja; Diether Lambrechts; Betül T Yesilyurt; Marie-Rose Chrisiaens; Stephanie Peeters; Paolo Radice; Paolo Peterlongo; Siranoush Manoukian; Monica Barile; Fergus Couch; Adam M Lee; Robert Diasio; Xianshu Wang; Graham G Giles; Gianluca Severi; Laura Baglietto; Catriona Maclean; Ken Offit; Mark Robson; Vijai Joseph; Mia Gaudet; Esther M John; Robert Winqvist; Katri Pylkäs; Arja Jukkola-Vuorinen; Mervi Grip; Irene Andrulis; Julia A Knight; Anna Marie Mulligan; Frances P O'Malley; Louise A Brinton; Mark E Sherman; Jolanta Lissowska; Stephen J Chanock; Maartje Hooning; John W M Martens; Ans M W van den Ouweland; J Margriet Collée; Per Hall; Kamila Czene; Angela Cox; Ian W Brock; Malcolm W R Reed; Simon S Cross; Paul Pharoah; Alison M Dunning; Daehee Kang; Keun-Young Yoo; Dong-Young Noh; Sei-Hyun Ahn; Anna Jakubowska; Jan Lubinski; Katarzyna Jaworska; Katarzyna Durda; Suleeporn Sangrajrang; Valerie Gaborieau; Paul Brennan; James McKay; Chen-Yang Shen; Shian-ling Ding; Huan-Ming Hsu; Jyh-Cherng Yu; Hoda Anton-Culver; Argyrios Ziogas; Alan Ashworth; Anthony Swerdlow; Michael Jones; Nick Orr; Amy Trentham-Dietz; Kathleen Egan; Polly Newcomb; Linda Titus-Ernstoff; Doug Easton; Amanda B Spurdle
Journal:  Hum Mol Genet       Date:  2011-08-18       Impact factor: 6.150

10.  Association of Rad51 polymorphism with DNA repair in BRCA1 mutation carriers and sporadic breast cancer risk.

Authors:  Luisel J Ricks-Santi; Lara E Sucheston; Yang Yang; Jo L Freudenheim; Claudine J Isaacs; Marc D Schwartz; Ramona G Dumitrescu; Catalin Marian; Jing Nie; Dominica Vito; Stephen B Edge; Peter G Shields
Journal:  BMC Cancer       Date:  2011-06-27       Impact factor: 4.430

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  7 in total

1.  Mismatch Repair Polymorphisms as Markers of Breast Cancer Prevalence in the Breast Cancer Family Registry.

Authors:  Maya Kappil; Mary Beth Terry; Lissette Delgado-Cruzata; Yuyan Liao; Regina M Santella
Journal:  Anticancer Res       Date:  2016-09       Impact factor: 2.480

Review 2.  Association between BRCA1 P871L polymorphism and cancer risk: evidence from a meta-analysis.

Authors:  Limin Miao; Yang Yu; Yefeng Ji; Bo Zhang; Zhiyao Yuan; Yifei Du; Longbiao Zhu; Ruixia Wang; Ning Chen; Hua Yuan
Journal:  Oncotarget       Date:  2017-05-02

3.  Identification and analysis of RNA structural disruptions induced by single nucleotide variants using Riprap and RiboSNitchDB.

Authors:  Jianan Lin; Yang Chen; Yuping Zhang; Zhengqing Ouyang
Journal:  NAR Genom Bioinform       Date:  2020-08-14

4.  DNA Methylation in Breast Tumor from High-risk Women in the Breast Cancer Family Registry.

Authors:  Hui-Chen Wu; Melissa C Southey; Hanina Hibshoosh; Regina M Santella; Mary Beth Terry
Journal:  Anticancer Res       Date:  2017-02       Impact factor: 2.480

5.  Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry.

Authors:  Tú Nguyen-Dumont; Fleur Hammet; Maryam Mahmoodi; Helen Tsimiklis; Zhi L Teo; Roger Li; Bernard J Pope; Mary Beth Terry; Saundra S Buys; Mary Daly; John L Hopper; Ingrid Winship; David E Goldgar; Daniel J Park; Melissa C Southey
Journal:  Breast Cancer Res Treat       Date:  2015-01-10       Impact factor: 4.872

6.  Pubertal development in girls by breast cancer family history: the LEGACY girls cohort.

Authors:  Mary Beth Terry; Theresa H M Keegan; Lauren C Houghton; Mandy Goldberg; Irene L Andrulis; Mary B Daly; Saundra S Buys; Ying Wei; Alice S Whittemore; Angeline Protacio; Angela R Bradbury; Wendy K Chung; Julia A Knight; Esther M John
Journal:  Breast Cancer Res       Date:  2017-06-08       Impact factor: 6.466

7.  The association between BRCA1 gene polymorphism and cancer risk: a meta-analysis.

Authors:  Gui-Ping Xu; Qing Zhao; Ding Wang; Wen-Yue Xie; Li-Jun Zhang; Hua Zhou; Shi-Zhi Chen; Li-Fang Wu
Journal:  Oncotarget       Date:  2018-01-06
  7 in total

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