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Breast cancer risk varies among different progestins used in hormone replacement therapy, study finds

Date:
August 12, 2010
Source:
University of Missouri-Columbia
Summary:
New research has found that progestins used in hormone replacement therapies to counteract the negative effects of estrogen on the uterus and reduce the risk of uterine cancer may increase the risk of breast cancer.

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. Now, University of Missouri researchers have compared four types of progestins used in hormone replacement therapies and found significantly different outcomes on the progression of breast cancer in an animal model depending on the type of progestins used.

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"Synthetic progestins have different biological effects, due to differences in their structure, stability and how they interact in the body," 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. "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."

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, Hyder said.

"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," Hyder said. "Thus progestins seem to have tumor-stage specific effects, which determine whether these will function as tumor promoters or tumor suppressors. Progestins, such as N-EL and N-ONE, may have potential as preventive agents in women with no history of breast disease or family history of breast cancer. These progestins may also have a preventive role in post-menopausal women who are at an increased risk for developing breast cancer due to ingestion of combined estrogen/progestin (MPA) hormone replacement therapy and may have early stage disease."

The study is published in the September issue of Cancer Prevention Research from the American Association for Cancer Research.


Story Source:

The above story is based on materials provided by University of Missouri-Columbia. Note: Materials may be edited for content and length.


Journal Reference:

  1. Indira Benakanakere, Cynthia Besch-Williford, Candace E. Carroll, and Salman M. Hyder. Synthetic Progestins Differentially Promote or Prevent 7,12-Dimethylbenz(a)anthracene%u2013Induced Mammary Tumors in Sprague-Dawley Rats. Cancer Prevention Research, 2010; DOI: 10.1158/1940-6207.CAPR-10-0064

Cite This Page:

University of Missouri-Columbia. "Breast cancer risk varies among different progestins used in hormone replacement therapy, study finds." ScienceDaily. ScienceDaily, 12 August 2010. <www.sciencedaily.com/releases/2010/08/100810163506.htm>.
University of Missouri-Columbia. (2010, August 12). Breast cancer risk varies among different progestins used in hormone replacement therapy, study finds. ScienceDaily. Retrieved November 27, 2014 from www.sciencedaily.com/releases/2010/08/100810163506.htm
University of Missouri-Columbia. "Breast cancer risk varies among different progestins used in hormone replacement therapy, study finds." ScienceDaily. www.sciencedaily.com/releases/2010/08/100810163506.htm (accessed November 27, 2014).

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