Indiana University, Gatch Clinical Building, Room 459, 541 N Clinical Dr, Indianapolis, IN 46202-5111, USA.
Semin Oncol. 2010 Oct;37 Suppl 2:S2-14. doi: 10.1053/j.seminoncol.2010.10.007.
Some of the most common cancer types, including breast cancer, prostate cancer, and lung cancer, show a predilection to metastasize to bone. The molecular basis of this preferential growth of cancer cells in the bone microenvironment has been an area of active investigation. Although the precise molecular mechanisms underlying this process remain to be elucidated, it is now increasingly being recognized that the unique characteristics of the bone niche provide homing signals to cancer cells, and create a microenvironment conducive for the cancer cells to colonize. Concomitantly, cancer cells release several regulatory factors that result in abnormal bone destruction and/or formation. This complex bidirectional interplay between tumor cells and bone microenvironment establishes a "vicious cycle" that leads to a selective growth advantage for the cancer cells. The molecular insights gained on the underpinnings of bone metastasis in recent years have also provided us with avenues to devise innovative approaches for therapeutic intervention. The goal of this review is to describe our current understanding of molecular pathophysiology of cancer metastases to bone, as well as its therapeutic implications.
一些最常见的癌症类型,包括乳腺癌、前列腺癌和肺癌,都表现出向骨骼转移的倾向。这种癌细胞在骨骼微环境中优先生长的分子基础一直是一个活跃的研究领域。尽管这一过程的确切分子机制仍有待阐明,但现在越来越多的人认识到,骨骼龛位的独特特征为癌细胞提供了归巢信号,并创造了有利于癌细胞定植的微环境。同时,癌细胞释放出几种调节因子,导致异常的骨破坏和/或形成。肿瘤细胞和骨骼微环境之间的这种复杂的双向相互作用建立了一个“恶性循环”,为癌细胞的选择性生长提供了优势。近年来,在骨骼转移的基础上获得的分子见解也为我们提供了设计创新治疗干预方法的途径。本文的目的是描述我们对癌症骨转移的分子病理生理学及其治疗意义的现有理解。