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癌症转移至骨骼所涉及的机制。

Mechanisms involved in the metastasis of cancer to bone.

作者信息

Orr F W, Kostenuik P, Sanchez-Sweatman O H, Singh G

机构信息

Department of Pathology, McMaster University, Hamilton, Ontario, Canada.

出版信息

Breast Cancer Res Treat. 1993;25(2):151-63. doi: 10.1007/BF00662140.

Abstract

The metastasis of cancer to bone is a frequent outcome of common malignancies and is often associated with significant morbidity due to osteolysis. Bone metastasis is also selective in that a disproportionately small number of malignancies account for the majority of tumors which spread to bone. While the mechanisms of bone destruction have been studied, those responsible for the site-specific nature of bone metastasis are poorly understood. As a metastatic target, bone is unique in that it is continuously being remodelled under the influence of local and systemic growth factors, many of which are embedded in the bone matrix. This review summarizes evidence for the hypothesis that the formation of metastatic tumors in bone is the consequence of a unique microenvironment where metastatic cells can alter the metabolism of bone, thereby regulating the release of soluble bone-derived growth factors as a consequence of bone resorption. These, in turn, can modulate the malignant phenotypic properties of receptive cells. Transforming growth factor-beta is one factor which can promote the growth and motility of Walker 256 cells, a rat cell line with a propensity to metastasize spontaneously to bone.

摘要

癌症转移至骨是常见恶性肿瘤的常见结局,常因骨溶解而导致显著的发病率。骨转移具有选择性,即少数恶性肿瘤却占了转移至骨的肿瘤的大部分。虽然骨破坏的机制已得到研究,但导致骨转移部位特异性的机制却知之甚少。作为一个转移靶点,骨具有独特性,因为它在局部和全身生长因子的影响下不断重塑,其中许多生长因子嵌入骨基质中。本综述总结了以下假说的证据:骨中转移性肿瘤的形成是一个独特微环境的结果,在这个微环境中,转移细胞可改变骨的代谢,从而由于骨吸收而调节可溶性骨源性生长因子的释放。反过来,这些因子可调节受体细胞的恶性表型特性。转化生长因子-β是一种可促进Walker 256细胞生长和运动的因子,Walker 256细胞是一种大鼠细胞系,有自发转移至骨的倾向。

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