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Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer.

Publication ,  Journal Article
Schildkraut, JM; Iversen, ES; Wilson, MA; Clyde, MA; Moorman, PG; Palmieri, RT; Whitaker, R; Bentley, RC; Marks, JR; Berchuck, A
Published in: PLoS One
April 8, 2010

BACKGROUND: We analyzed the association between 53 genes related to DNA repair and p53-mediated damage response and serous ovarian cancer risk using case-control data from the North Carolina Ovarian Cancer Study (NCOCS), a population-based, case-control study. METHODS/PRINCIPAL FINDINGS: The analysis was restricted to 364 invasive serous ovarian cancer cases and 761 controls of white, non-Hispanic race. Statistical analysis was two staged: a screen using marginal Bayes factors (BFs) for 484 SNPs and a modeling stage in which we calculated multivariate adjusted posterior probabilities of association for 77 SNPs that passed the screen. These probabilities were conditional on subject age at diagnosis/interview, batch, a DNA quality metric and genotypes of other SNPs and allowed for uncertainty in the genetic parameterizations of the SNPs and number of associated SNPs. Six SNPs had Bayes factors greater than 10 in favor of an association with invasive serous ovarian cancer. These included rs5762746 (median OR(odds ratio)(per allele) = 0.66; 95% credible interval (CI) = 0.44-1.00) and rs6005835 (median OR(per allele) = 0.69; 95% CI = 0.53-0.91) in CHEK2, rs2078486 (median OR(per allele) = 1.65; 95% CI = 1.21-2.25) and rs12951053 (median OR(per allele) = 1.65; 95% CI = 1.20-2.26) in TP53, rs411697 (median OR (rare homozygote) = 0.53; 95% CI = 0.35 - 0.79) in BACH1 and rs10131 (median OR( rare homozygote) = not estimable) in LIG4. The six most highly associated SNPs are either predicted to be functionally significant or are in LD with such a variant. The variants in TP53 were confirmed to be associated in a large follow-up study. CONCLUSIONS/SIGNIFICANCE: Based on our findings, further follow-up of the DNA repair and response pathways in a larger dataset is warranted to confirm these results.

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Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

April 8, 2010

Volume

5

Issue

4

Start / End Page

e10061

Location

United States

Related Subject Headings

  • Tumor Suppressor Protein p53
  • Risk
  • Probability
  • Polymorphism, Single Nucleotide
  • Ovarian Neoplasms
  • Neoplasm Invasiveness
  • Models, Statistical
  • Humans
  • General Science & Technology
  • Female
 

Citation

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Schildkraut, J. M., Iversen, E. S., Wilson, M. A., Clyde, M. A., Moorman, P. G., Palmieri, R. T., … Berchuck, A. (2010). Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer. PLoS One, 5(4), e10061. https://doi.org/10.1371/journal.pone.0010061
Schildkraut, Joellen M., Edwin S. Iversen, Melanie A. Wilson, Merlise A. Clyde, Patricia G. Moorman, Rachel T. Palmieri, Regina Whitaker, Rex C. Bentley, Jeffrey R. Marks, and Andrew Berchuck. “Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer.PLoS One 5, no. 4 (April 8, 2010): e10061. https://doi.org/10.1371/journal.pone.0010061.
Schildkraut JM, Iversen ES, Wilson MA, Clyde MA, Moorman PG, Palmieri RT, et al. Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer. PLoS One. 2010 Apr 8;5(4):e10061.
Schildkraut, Joellen M., et al. “Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer.PLoS One, vol. 5, no. 4, Apr. 2010, p. e10061. Pubmed, doi:10.1371/journal.pone.0010061.
Schildkraut JM, Iversen ES, Wilson MA, Clyde MA, Moorman PG, Palmieri RT, Whitaker R, Bentley RC, Marks JR, Berchuck A. Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer. PLoS One. 2010 Apr 8;5(4):e10061.

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

April 8, 2010

Volume

5

Issue

4

Start / End Page

e10061

Location

United States

Related Subject Headings

  • Tumor Suppressor Protein p53
  • Risk
  • Probability
  • Polymorphism, Single Nucleotide
  • Ovarian Neoplasms
  • Neoplasm Invasiveness
  • Models, Statistical
  • Humans
  • General Science & Technology
  • Female