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Updated: Jun 29, 2026

Orthotopic Transplantation of Breast Tumors as Preclinical Models for Breast Cancer
Published on: May 18, 2020
Laboratory models of breast and endometrial cancer to develop strategies for antiestrogen therapy
R M O'Regan1, G M England, J I Macgregor
1Robert H. Lurie Comprehensive Cancer Center, Northwestern University Medical School, Chicago, IL 60611, USA.
Abstract:
Laboratory models for breast and endometrial cancer have had an enormous impact on the clinical development of antiestrogens. Results from the DMBA-induced rat mammary cancer model has provided the scientific principles required to evaluate long-term adjuvant tamoxifen therapy. Similarly, the athymic mouse model allowed the identification of clinically relevant mechanisms of drug resistance to tamoxifen and a model system to test new agents for cross resistance. Additionally, the endometrial cancer model has allowed the identification of agents that cause a slight increase in the risk of endometrial cancer long before the data would have be available from clinical studies. However, it should be stressed that this model is really only relevant for agents to be tested as preventives in normal women. The risks of developing endometrial cancer during tamoxifen therapy are slight compared with the survival benefit in controlling breast cancer.Finally the discovery of the carcinogenic potential of tamoxifen in the rat liver, 20 years after it was first introduced into clinical practice, raises an interesting issue. If the studies of liver carcinogenicity had been completed and published in the early 1970's there would be no tamoxifen and tens of thousands of women with breast cancer would have died prematurely. In fact there would have been no incentive to develop new agents as alternatives to tamoxifen or following tamoxifen failure. Most importantly, we would not have any knowledge about the target-site or selective actions of antiestrogens. All the current interest in selective estrogen receptor modulators (SERMs) is based on the huge clinical data base obtained by studying tamoxifen. The success of tamoxifen as an agent that preserves bone density, lowers cholesterol and prevents contralateral breast cancer(43) has become a classic example of a multimechanistic drug. These concepts have acted as a catalyst to develop new agents for new applications. The laboratory studies of raloxifene(44-46)) provided the scientific rationale for the use of raloxifene as a preventive for osteoporosis(47)) but with the goal of preventing breast cancer in post-menopausal women(48,49)) (Fig 5). It is clear that the close collaboration between laboratory and clinical research has revolutionized the prospects for women's health care in the 21st century.
Insights
Laboratory models have been crucial in developing antiestrogen therapies like tamoxifen for breast and endometrial cancers. These models inform drug evaluation, resistance mechanisms, and risk assessment, revolutionizing women's health.
Area of Science:
- Oncology
- Pharmacology
- Women's Health
Background:
- Antiestrogen therapies, particularly tamoxifen, have significantly impacted breast and endometrial cancer treatment.
- Laboratory models have been instrumental in understanding these drugs' efficacy and side effects.
Purpose of the Study:
- To highlight the critical role of laboratory models in advancing antiestrogen drug development and clinical application.
- To demonstrate how preclinical studies inform the evaluation of drug resistance and potential risks.
Main Methods:
- Utilizing DMBA-induced rat mammary cancer models to assess long-term tamoxifen therapy.
- Employing athymic mouse models to investigate tamoxifen resistance mechanisms.
- Using endometrial cancer models to identify agents affecting cancer risk.
Main Results:
- Laboratory models provided scientific principles for evaluating tamoxifen therapy and identifying resistance mechanisms.
- Endometrial cancer models identified agents with potential risks before clinical data was available.
- Studies on tamoxifen's carcinogenicity informed the development of newer agents and understanding of selective estrogen receptor modulators (SERMs).
Conclusions:
- The close collaboration between laboratory and clinical research has revolutionized women's healthcare prospects.
- Tamoxifen's success paved the way for developing multimechanistic drugs like raloxifene for osteoporosis and breast cancer prevention.
- Preclinical models are essential for evaluating drug safety, efficacy, and guiding the development of novel therapeutic strategies.
