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Molecular pathogenesis of bone metastases in breast cancer: Proven and emerging therapeutic targets

机译:乳腺癌骨转移的分子发病机制:业已证明的新兴治疗靶点

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摘要

Metastatic occurrence is the principal cause of death in breast cancer patients. The high osteotropism makes breast cancer the most common primary tumor type associated with metastatic bone disease. The peculiar clinical aspects associated with metastases limited to the skeletal system suggest considering these cases as a distinctive subset of metastatic patients with a better prognosis. Because bone is frequently the first metastatic site in disease relapse, it is feasible that the next improvement in therapeutic options for bone metastatic disease could be associated with an improvement of survival expectation and quality of life in breast cancer patients. Study of the molecular basis of bone remodeling and breast cancer osteotropism has allowed identification of several therapeutic candidates involved in formation and progression of bone metastases. These targets are frequently the determinants of positive feedback between the tumor and bone cells whose clinical outcome is osteolytic lesions. In this review, we discuss the physiopathologic features underlying targeted therapeutic strategies aimed at interfering with the aberrant bone remodeling associated with breast cancer metastases.
机译:转移发生是乳腺癌患者死亡的主要原因。高度向骨性使乳腺癌成为与转移性骨病相关的最常见的原发肿瘤类型。与局限于骨骼系统的转移相关的特殊临床方面提示,应将这些病例视为具有较好预后的转移性患者的独特子集。因为骨经常是疾病复发中的第一个转移部位,所以可行的是,骨转移性疾病的治疗选择的下一个改善可能与乳腺癌患者的生存预期和生活质量的改善有关。对骨骼重塑和乳腺癌骨质疏松症的分子基础的研究已允许鉴定涉及骨转移的形成和进展的几种治疗候选药物。这些靶标通常是肿瘤与骨细胞之间阳性反应的决定因素,而骨细胞的临床结果是溶骨性病变。在这篇综述中,我们讨论了针对性治疗策略的生理病理学特征,这些治疗策略旨在干扰与乳腺癌转移相关的异常骨骼重塑。

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