Bone remodeling, normal and abnormal: a biological basis for the understanding of cancer-related bone disease and its treatment.

The Canadian journal of oncology Pub Date : 1995-12-01
A M Parfitt
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Abstract

Remodeling the cyclical replacement of old bone by new, serves to maintain its mechanical and metabolic functions. In each cycle a circumscribed volume of bone is removed by osteoclastic resorption and subsequently replaced by osteoblastic formation at the same location. Remodeling is carried out by elongated structures known as basic multicellular units (BMU) that travel through or across the surface of bone. Each BMU lasts about six months, with continued sequential recruitment of new osteoclasts and osteoblasts. Abnormal bone remodeling involves some combination of loss of directional control, increase in number of remodeling cycles and incomplete replacement. In metastatic bone disease, tumor cells find the hematopoietic bone marrow conducive to their survival and growth, because they can manipulate the local cytokine network to increase recruitment of osteoclasts from local precursors and so increase bone resorption. The effect on bone formation is biphasic; an initial increase is due partly to the normal evolution of the BMU, and partly to the induction of reparative woven bone formation. Later, normal BMU-based bone formation may fall to subnormal levels. In some tumors, a generalized increase in osteoclast recruitment and decline in bone formation are the systemic responses to one or more agents released by tumor cells into the circulation, of which the most frequent is parathyroid hormone-related peptide, but in both metastatic and non-metastatic disease, the cellular events in bone are essentially the same. Cancer-related bone disease is amenable to treatment with drugs that inhibit osteoclast recruitment, of which the bisphosphonates are the most effective. Treatment should be started before there has been irreparable damage to bone structure and before the onset of hypercalcemia. Although bisphosphonates remain in bone for a long time, adverse effects are very unlikely within the patient's lifetime.

骨重塑,正常和异常:了解癌症相关骨病及其治疗的生物学基础。
骨重建是新旧骨的周期性替换,有助于维持其机械和代谢功能。在每个循环中,一定体积的骨被破骨细胞吸收带走,随后在同一位置被成骨细胞取代。骨重塑是由被称为基本多细胞单位(BMU)的细长结构进行的,这些结构穿过或穿过骨表面。每次BMU持续约6个月,新破骨细胞和成骨细胞持续有序募集。骨重构异常包括方向性控制的丧失、骨重构周期的增加和骨置换不完全。在转移性骨病中,肿瘤细胞发现造血骨髓有利于其生存和生长,因为它们可以操纵局部细胞因子网络,增加来自局部前体的破骨细胞的募集,从而增加骨吸收。对骨形成的影响是双期的;最初的增加部分是由于BMU的正常进化,部分是由于诱导修复性编织骨形成。之后,正常的bmu骨形成可能降至亚正常水平。在某些肿瘤中,破骨细胞募集的普遍增加和骨形成的减少是肿瘤细胞释放到循环中的一种或多种药物的全身反应,其中最常见的是甲状旁腺激素相关肽,但在转移性和非转移性疾病中,骨中的细胞事件本质上是相同的。癌症相关的骨病可以用抑制破骨细胞募集的药物治疗,其中双膦酸盐是最有效的。治疗应在骨结构出现不可修复的损伤和出现高钙血症之前开始。虽然双膦酸盐在骨骼中停留很长时间,但在患者的一生中,不良反应是不太可能发生的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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