School of Pharmaceutical Sciences, MVN University 121102, Palwal, Haryana, India.
Amity Institute of Pharmacy, Amity University, Greater Noida 2011308, Uttar Pradesh, India.
Biomed Res Int. 2024 Nov 14;2024:5594542. doi: 10.1155/2024/5594542. eCollection 2024.
The interplay between breast cancer treatment and osteoporosis has important consequences for anticancer therapy and patient bone health. Many breast cancer therapies involve hormonal treatments that lower estrogen levels, which can lead to an increased risk of osteoporosis due to reduced bone mineral density. Aromatase inhibitors, chemotherapy, and surgeries such as oophorectomy can further aggravate bone loss, highlighting the necessity of prioritizing bone health during cancer treatment. This review is aimed at investigating the complex relationship between breast cancer therapies and bone health by examining the molecular and cellular mechanisms through which anticancer treatments lead to bone loss. It also seeks to assess the effects of various treatment options, such as selective estrogen receptor modulators (SERMs) and bisphosphonates, on reducing bone loss and maintaining bone health during cancer therapy. The review explores the mechanisms underlying bone loss in breast cancer patients undergoing treatment, focusing on factors such as estrogen depletion, inflammatory cytokines, and changes in bone remodelling processes. Additionally, it evaluates the efficacy of different therapeutic interventions, including pharmacological treatments like bisphosphonates and third-generation SERMs, in mitigating bone-related side effects. The findings indicate a critical need to balance the effectiveness of breast cancer treatments with the preservation of bone health. Pharmacological treatments like bisphosphonates and denosumab have been identified as essential for managing bone health in breast cancer patients. Furthermore, third-generation SERMs show potential in reducing bone loss associated with cancer therapy.
乳腺癌治疗与骨质疏松症之间的相互作用对癌症治疗和患者骨骼健康具有重要影响。许多乳腺癌治疗方法涉及降低雌激素水平的激素治疗,这可能导致骨密度降低,增加骨质疏松症的风险。芳香化酶抑制剂、化疗和卵巢切除术等手术会进一步加重骨质流失,这凸显了在癌症治疗期间优先考虑骨骼健康的必要性。
本综述旨在通过研究抗癌治疗导致骨质流失的分子和细胞机制,探讨乳腺癌治疗与骨骼健康之间的复杂关系。还评估了各种治疗选择的效果,如选择性雌激素受体调节剂 (SERMs) 和双磷酸盐,以减少骨质流失并维持癌症治疗期间的骨骼健康。
该综述探讨了接受治疗的乳腺癌患者骨质流失的机制,重点关注雌激素耗竭、炎症细胞因子和骨重塑过程变化等因素。此外,还评估了不同治疗干预措施的疗效,包括双磷酸盐和第三代 SERMs 等药物治疗,以减轻与骨骼相关的副作用。
研究结果表明,需要在平衡乳腺癌治疗的有效性与骨骼健康的保护之间取得平衡。双磷酸盐和地舒单抗等药物治疗已被确定为管理乳腺癌患者骨骼健康的重要手段。此外,第三代 SERMs 显示出在减少与癌症治疗相关的骨质流失方面的潜力。