An estrogen receptor genetic polymorphism and a history of spontaneous abortion ? Correlation in women with estrogen receptor positive breast cancer but not in women with estrogen receptor negative breast cancer or in women without cancer
Abstract:We previously identified a polymorphism in the human estrogen receptor gene. In a preliminary study on women with estrogen receptor positive (ER+) breast tumors, we found that the presence of the rarer of the two alleles, the B' allele, is correlated with a history of spontaneous abortion. Because that study evaluated only women with estrogen receptor positive (ER+) breast cancer, it was unknown whether the observed correlation was restricted to the cancer group or was independent of breast cancer. We have now… Show more
“…In women with ER‐positive breast cancer, history of spontaneous abortions was associated with presence of the b allele of the ER. This association could not be shown in women with ER‐negative breast cancer or women without breast cancer (27–29) . Furthermore, no associations have been shown between G 261 ‐C and incidence of breast cancer (30,46) .…”
Section: Discussionmentioning
confidence: 89%
“…In human mammary tumors the polymorphism affects the binding of estrogen to the receptor (25) . This polymorphism has been found to be associated with recurrent abortions and breast cancer in some studies (26,27) . Other studies could not confirm these findings (28–30) …”
“…In women with ER‐positive breast cancer, history of spontaneous abortions was associated with presence of the b allele of the ER. This association could not be shown in women with ER‐negative breast cancer or women without breast cancer (27–29) . Furthermore, no associations have been shown between G 261 ‐C and incidence of breast cancer (30,46) .…”
Section: Discussionmentioning
confidence: 89%
“…In human mammary tumors the polymorphism affects the binding of estrogen to the receptor (25) . This polymorphism has been found to be associated with recurrent abortions and breast cancer in some studies (26,27) . Other studies could not confirm these findings (28–30) …”
“…Probably this difference is due to chance. Furthermore, women with the B¢ allele were more often nulliparous compared to women homozygous for the BB genotype, which could be due to the fact the the B¢ allele has been associated with a higher risk of spontaneous abortions [38].…”
The results of this study suggest that the PvuII polymorphism in the ER-alpha, or another mutation in linkage disequilibrium with PvuII, in combination with high E2 levels increases breast cancer risk in postmenopausal women.
“…Unlike mutations, polymorphisms are not directly linked to a certain disease. However, they are useful tools in the study of multifactorial disorders (16,17). Polymorphism is related with the leiomyoma development, including AR (18), estrogen receptor (19), and insulin-like growth factor II gene polymorphisms (20).…”
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