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Cyclin E overexpression in epithelial ovarian cancer characterizes an etiologic subgroup.

Publication ,  Journal Article
Schildkraut, JM; Moorman, PG; Bland, AE; Halabi, S; Calingaert, B; Whitaker, R; Lee, PS; Elkins-Williams, T; Bentley, RC; Marks, JR; Berchuck, A
Published in: Cancer Epidemiol Biomarkers Prev
March 2008

BACKGROUND: The objective of this study was to determine whether cyclin E overexpression defines an etiologically distinct subgroup of ovarian cancer. METHODS: We analyzed data from 538 epithelial ovarian cancer cases and 629 controls enrolled in a population-based case-control study. Cyclin E protein overexpression was assessed using immunohistochemistry. Case-control and case-case comparisons were done to evaluate the relationship between cyclin E overexpression and epidemiologic risk factors. Logistic regression models were used to estimate odds ratios (OR) and 95% confidence intervals (95% CI) while adjusting for potential confounders. RESULTS: Case-control comparisons showed ovarian cancers with and without cyclin E overexpression have different associations with several epidemiologic risk factors. A dose-response relationship was observed between lifetime ovulatory cycles (LOC) and ovarian cancer that overexpressed cyclin E [OR, 1.8; 95% CI, 1.1-3.0 for moderately high LOC (265-390 cycles) and OR, 2.7; 95% CI, 1.6-4.5 for high LOC (>390 cycles) compared with low LOC (<265 cycles)], but no relationship was seen with cancers that lacked overexpression. The most important components of the LOC variable contributing to the differences in the association with the cyclin E subgroups of ovarian cancer were months of oral contraceptive use and months pregnant. CONCLUSIONS: Cyclin E overexpression is associated with a high number of LOC, largely influenced by oral contraceptive use and pregnancy. This suggests that cyclin E overexpression is a molecular signature characteristic of ovarian cancer cases that may arise via a pathway that involves ovulation-induced alterations.

Duke Scholars

Published In

Cancer Epidemiol Biomarkers Prev

DOI

ISSN

1055-9965

Publication Date

March 2008

Volume

17

Issue

3

Start / End Page

585 / 593

Location

United States

Related Subject Headings

  • Surveys and Questionnaires
  • Risk Factors
  • Registries
  • Ovarian Neoplasms
  • North Carolina
  • Neoplasm Staging
  • Middle Aged
  • Immunohistochemistry
  • Humans
  • Female
 

Citation

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Schildkraut, J. M., Moorman, P. G., Bland, A. E., Halabi, S., Calingaert, B., Whitaker, R., … Berchuck, A. (2008). Cyclin E overexpression in epithelial ovarian cancer characterizes an etiologic subgroup. Cancer Epidemiol Biomarkers Prev, 17(3), 585–593. https://doi.org/10.1158/1055-9965.EPI-07-0596
Schildkraut, Joellen M., Patricia G. Moorman, Amy E. Bland, Susan Halabi, Brian Calingaert, Regina Whitaker, Paula S. Lee, et al. “Cyclin E overexpression in epithelial ovarian cancer characterizes an etiologic subgroup.Cancer Epidemiol Biomarkers Prev 17, no. 3 (March 2008): 585–93. https://doi.org/10.1158/1055-9965.EPI-07-0596.
Schildkraut JM, Moorman PG, Bland AE, Halabi S, Calingaert B, Whitaker R, et al. Cyclin E overexpression in epithelial ovarian cancer characterizes an etiologic subgroup. Cancer Epidemiol Biomarkers Prev. 2008 Mar;17(3):585–93.
Schildkraut, Joellen M., et al. “Cyclin E overexpression in epithelial ovarian cancer characterizes an etiologic subgroup.Cancer Epidemiol Biomarkers Prev, vol. 17, no. 3, Mar. 2008, pp. 585–93. Pubmed, doi:10.1158/1055-9965.EPI-07-0596.
Schildkraut JM, Moorman PG, Bland AE, Halabi S, Calingaert B, Whitaker R, Lee PS, Elkins-Williams T, Bentley RC, Marks JR, Berchuck A. Cyclin E overexpression in epithelial ovarian cancer characterizes an etiologic subgroup. Cancer Epidemiol Biomarkers Prev. 2008 Mar;17(3):585–593.

Published In

Cancer Epidemiol Biomarkers Prev

DOI

ISSN

1055-9965

Publication Date

March 2008

Volume

17

Issue

3

Start / End Page

585 / 593

Location

United States

Related Subject Headings

  • Surveys and Questionnaires
  • Risk Factors
  • Registries
  • Ovarian Neoplasms
  • North Carolina
  • Neoplasm Staging
  • Middle Aged
  • Immunohistochemistry
  • Humans
  • Female