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Use of bisphosphonates for the treatment of bone metastasis in experimental animal models
1Division of Endocrinology and Metabolism, Department of Medicine, The University of Texas Health Science Center at San Antonio, San Antonio, Texas 78284-7877, USA.
Abstract:
Therapeutic effectiveness of bisphosphonates (BP) on bone metastases in patients with cancers including those of the breast and prostate has been well documented. However, there are still many important questions that remain unsolved or controversial. To obtain answers for these questions that are not readily addressed in a well-controlled manner in clinical studies, we have developed two animal models of bone metastasis (orthotopic and experimental). Using these models, we studied the effects of BP alone or in combination with anti-cancer agents on the metastasis of breast cancer to bone and visceral organs. In addition, we also determined the effects of BP on osteosclerotic metastases. We found that BP impaired the progression of bone metastases primarily through enhancing apoptosis in osteoclasts and breast cancer cells colonized in bone. In some situations, however, BP alone increased metastases in visceral organs including liver and adrenal glands. However, combination of BP with anti-cancer agents enhanced the suppression of tumour in both bone and visceral organs, leading to prolonged survival of tumour-bearing animals. Of potential importance, preventative administration of BP inhibited the development of eventual osteosclerotic bone metastases. These results suggest that BP exhibits diverse beneficial effects on osteolytic and osteoblastic bone metastasis and non-bone organ metastasis in breast cancer when administered appropriately. They also suggest that the animal models of bone metastasis described here allow us to produce clinically- relevant information that is useful for the design of optimal regimens of BP for the treatment of breast cancer patients with bone and visceral metastases.
Insights
Bisphosphonates (BP) show varied effects on bone and visceral metastases in breast cancer. Combination therapy with anti-cancer agents improves tumor suppression and survival, suggesting optimized BP use is crucial.
Area of Science:
- Oncology
- Pharmacology
- Cancer Metastasis Research
Background:
- Bisphosphonates (BP) are established treatments for bone metastases in breast and prostate cancers.
- Unresolved questions and controversies persist regarding BP's comprehensive therapeutic role.
- Clinical studies face limitations in addressing complex aspects of BP effectiveness.
Purpose of the Study:
- To investigate the effects of bisphosphonates (BP) alone and in combination with anti-cancer agents on breast cancer bone and visceral metastases.
- To evaluate BP's impact on osteosclerotic bone metastases.
- To develop and utilize novel animal models for clinically relevant metastasis research.
Main Methods:
- Development of orthotopic and experimental animal models for bone metastasis.
- Administration of BP alone and in combination with anti-cancer agents.
- Assessment of BP effects on osteolytic, osteoblastic, and visceral metastases, including apoptosis and survival.
Main Results:
- BP impaired bone metastasis progression by enhancing apoptosis in osteoclasts and cancer cells.
- BP alone sometimes increased visceral metastases (liver, adrenal glands).
- Combination therapy significantly suppressed tumors in bone and visceral organs, prolonging survival.
- Preventative BP administration inhibited osteosclerotic bone metastases development.
Conclusions:
- Bisphosphonates demonstrate diverse benefits for osteolytic, osteoblastic, and visceral metastases in breast cancer when used appropriately.
- Developed animal models provide clinically relevant data for optimizing BP treatment regimens.
- Combination therapy with anti-cancer agents enhances efficacy and survival in metastatic breast cancer.