Researchers found different outcomes on the advancement of breast cancer on comparing four types of progestins used in hormone replacement therapies.
Researchers found different outcomes on the advancement of breast cancer on comparing four types of progestins used in hormone replacement therapies. Progestins are used in hormone replacement therapies to counteract the negative effects of estrogen on the uterus and reduce the risk of uterine cancer. However, evidence in recent studies and clinical trials has demonstrated that progestins increase the risk of breast cancer.
But it is now that theUniversity of Missouri researchers have come to the above conclusion.
"Synthetic progestins have different biological effects, due to differences in their structure, stability and how they interact in the body. Clinical use of progestins requires caution. These powerful steroids should only be prescribed when a person has no latent, or dormant, cancer and does not have a family history of cancer. However, it is difficult to diagnose latent tumor cells in women since there are no symptoms," said Salman Hyder, the Zalk Endowed Professor in Tumor Angiogenesis and professor of biomedical sciences in the College of Veterinary Medicine and the Dalton Cardiovascular Research Center.
In the study, researchers compared the effects of four clinically relevant progestins on breast cancer tumors in an animal model.
The progestins used in the study were the synthetic progestin medroxporgresterone acetate (MPA), norgesterel (N-EL), norethindrone (N-ONE) and megestrol acetate (MGA). In the United States, most women on hormone replacement therapy are treated with MPA, the progestin in Prempro, said Hyder.
"Although previous studies using an animal model for breast cancer found that MPA functions as a tumor promoter, this study show that N-EL and N-One, when administrated using the same protocol as used for MPA, strongly inhibited tumor development," said Hyder.
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The study has been published in the September issue of Cancer Prevention Research from the American Association for Cancer Research.
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