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乳腺癌骨转移的分子发病机制:已证实的和新出现的治疗靶点。

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

作者信息

Rucci Nadia, Sanità Patrizia, Delle Monache Simona, Alesse Edoardo, Angelucci Adriano

机构信息

Nadia Rucci, Patrizia Sanità, Simona Delle Monache, Edoardo Alesse, Adriano Angelucci, Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, Coppito 67100, L'Aquila, Italy.

出版信息

World J Clin Oncol. 2014 Aug 10;5(3):335-47. doi: 10.5306/wjco.v5.i3.335.

Abstract

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.

摘要

转移的发生是乳腺癌患者死亡的主要原因。高度的亲骨性使乳腺癌成为与转移性骨病相关的最常见原发性肿瘤类型。局限于骨骼系统的转移所具有的特殊临床特征表明,可将这些病例视为预后较好的转移性患者的一个独特亚组。由于骨常常是疾病复发时的首个转移部位,骨转移性疾病治疗方案的下一次改进有可能与乳腺癌患者生存预期和生活质量的改善相关。对骨重塑和乳腺癌亲骨性分子基础的研究已确定了几种参与骨转移形成和进展的治疗候选靶点。这些靶点常常是肿瘤与骨细胞之间正反馈的决定因素,其临床结果是溶骨性病变。在本综述中,我们讨论旨在干扰与乳腺癌转移相关的异常骨重塑的靶向治疗策略所依据的生理病理特征。

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