Related Experiment Video
Updated: Aug 8, 2026

An In Vivo Estrogen Deficiency Mouse Model for Screening Exogenous Estrogen Treatments of Cardiovascular Dysfunction After Menopause
Published on: August 13, 2019
Future perspectives of selective estrogen receptor modulators used alone and in combination with DHEA
1Molecular Endocrinology and Oncology Research Center, Laval University Hospital Research Center (CRCHUL) and Laval University, 2705, Laurier Boulevard, Quebec City, Quebec G1V 4G2, Canada. fernand.labrie@crchul.ulaval.ca
Abstract:
Breast cancer is the most frequently diagnosed and the second cause of cancer death in women, thus making breast cancer a most feared disease. Since breast cancer metastasizes early and it is unlikely that improvements in the treatment of metastatic disease could permit a cure in most cases in the foreseeable future, it is clear that prevention is essential in order practically to eliminate deaths from breast cancer. Tamoxifen is the only selective estrogen receptor modulator (SERM) currently registered for use in breast cancer prevention; the tamoxifen versus raloxifene study should indicate the efficacy of this compound compared with raloxifene. The recent benefits of aromatase inhibitors over tamoxifen indicate the advantages of a blockade of estrogens more complete than the one achieved with tamoxifen, a SERM having some estrogenic activity in the mammary gland and an even higher estrogenic action in the uterus. However, it is unlikely that the general estrogen ablation achieved with aromatase inhibitors will be acceptable for the long-term use required for prevention. It is thus important to develop SERMs with highly potent and pure antagonistic activity in the mammary gland and uterus while possessing estrogen-like activity in tissues of particular importance for women's health, namely the bones and the cardiovascular system. However, it is expected that a SERM alone will not meet all the requirements of women's health at the postmenopause when ovarian estrogen secretion has ceased and peripheral formation of androgens and estrogens from DHEA by intracrine mechanisms is decreased by 60% or more. One possibility is to combine a SERM with DHEA, a precursor of sex steroids that permits, somewhat like SERMs, tissue-specific formation of androgens and/or estrogens according to the level of expression of the steroidogenic and steroid-inactivating enzymes. DHEA could thus compensate for the important loss of androgens that accompanies aging and could also permit sex steroid formation and action in the brain while breast cancer prevention would be achieved by the SERM.
Insights
Preventing breast cancer is crucial. New selective estrogen receptor modulators (SERMs) are needed for potent antagonism in breast and uterus, with estrogenic effects on bone and cardiovascular health. Combining SERMs with DHEA may address postmenopausal health needs.
Area of Science:
- Oncology
- Endocrinology
- Pharmacology
Background:
- Breast cancer is a leading cause of cancer death in women, necessitating effective prevention strategies.
- Current prevention options like tamoxifen have limitations, including estrogenic activity in the uterus.
- Aromatase inhibitors offer more complete estrogen blockade but are unsuitable for long-term preventive use.
Purpose of the Study:
- To explore the development of novel selective estrogen receptor modulators (SERMs) for breast cancer prevention.
- To identify SERMs with potent antagonistic activity in the breast and uterus.
- To investigate SERMs that retain beneficial estrogen-like effects on bone and cardiovascular health.
Main Methods:
- Review of existing breast cancer prevention agents, including tamoxifen and aromatase inhibitors.
- Discussion of the requirements for ideal SERMs for long-term use in postmenopausal women.
- Exploration of combination therapy with SERMs and dehydroepiandrosterone (DHEA).
Main Results:
- Tamoxifen is the only approved SERM for breast cancer prevention, but it has partial estrogenic effects.
- Aromatase inhibitors provide greater estrogen blockade but are not ideal for long-term prevention.
- Novel SERMs are needed that selectively target estrogen receptors in breast and uterine tissues.
- Combination therapy with SERMs and DHEA may address broader postmenopausal health concerns.
Conclusions:
- There is a need for advanced SERMs with pure antagonistic activity in breast and uterine tissues.
- These novel SERMs should possess estrogenic properties beneficial for bone and cardiovascular health.
- Combining SERMs with DHEA presents a potential strategy to meet diverse postmenopausal health requirements, including breast cancer prevention.
Related Concept Videos
Transducer Mechanism: Nuclear Receptors
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
Dose-Response Relationship: Selectivity and Specificity
Modified-Release Drug Delivery Systems: Overview
Hormonal Regulation