HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

The association between reproductive and hormonal factors and ovarian cancer by estrogen-α and progesterone receptor status.

AbstractOBJECTIVE:
We assessed the association between reproductive and hormonal factors and ovarian cancer incidence characterized by estrogen receptor-α (ERα) and progesterone receptor (PR) status.
METHODS:
Tissue microarrays were used to assess ERα and PR expression among 197 Nurses' Health Study (NHS), 42 NHSII and 76 New England Case-Control Study (NECC) ovarian cancer cases. NHS/NHSII cases were matched to up to 4 controls (n=954) on diagnosis date and birth year. NECC controls (n=725) were frequency matched on age. Cases were considered receptor positive if ≥1% of tumor cells stained positive. Associations by ERα and PR status were assessed using polytomous logistic regression. p-Value for heterogeneity was calculated using a likelihood ratio test.
RESULTS:
45% of ovarian tumors were PR(+), 78% were ERα(+) and 45% were ERα(+)/PR(+), while 22% were ERα(-)/PR(-). Postmenopausal status was associated with an increased risk of PR(-) tumors (OR: 2.07; 95%CI: 1.15-3.75; p-heterogeneity=0.01) and age at natural menopause was inversely associated with PR(-) tumors (OR, per 5years: 0.77; 95%CI: 0.61-0.96; p-het=0.01). Increasing duration of postmenopause was differentially associated by PR status (p-het=0.0009). Number of children and tubal ligation were more strongly associated with ERα(-) versus ERα(+) tumors (p-het=0.002 and 0.05, respectively). No differential associations were observed for oral contraceptive or hormone therapy use.
CONCLUSIONS:
Postmenopausal women have an increased risk of developing PR(-) ovarian tumors compared to premenopausal women. The associations observed for ovarian cancer differ from those seen for breast cancer suggesting that the biology for tumor development through ERα and PR pathways may differ.
AuthorsAmy L Shafrir, Megan S Rice, Mamta Gupta, Kathryn L Terry, Bernard A Rosner, Rulla M Tamimi, Jonathan L Hecht, Shelley S Tworoger
JournalGynecologic oncology (Gynecol Oncol) Vol. 143 Issue 3 Pg. 628-635 (Dec 2016) ISSN: 1095-6859 [Electronic] United States
PMID27720231 (Publication Type: Journal Article)
CopyrightCopyright © 2016 Elsevier Inc. All rights reserved.
Chemical References
  • Contraceptives, Oral
  • ESR1 protein, human
  • Estrogen Receptor alpha
  • Receptors, Progesterone
Topics
  • Adenocarcinoma, Clear Cell (epidemiology, metabolism, pathology)
  • Adult
  • Age Factors
  • Aged
  • Carcinoma, Endometrioid (epidemiology, metabolism, pathology)
  • Case-Control Studies
  • Contraceptives, Oral (therapeutic use)
  • Estrogen Receptor alpha (metabolism)
  • Estrogen Replacement Therapy (statistics & numerical data)
  • Female
  • Humans
  • Logistic Models
  • Menarche
  • Menopause
  • Middle Aged
  • Neoplasm Staging
  • Neoplasms, Cystic, Mucinous, and Serous (epidemiology, metabolism, pathology)
  • Ovarian Neoplasms (epidemiology, metabolism, pathology)
  • Parity
  • Postmenopause
  • Receptors, Progesterone (metabolism)
  • Reproductive History
  • Sterilization, Tubal (statistics & numerical data)
  • Time Factors
  • Tissue Array Analysis
  • United States (epidemiology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: