多发性骨髓瘤中的血管生成。

Chemical immunology and allergy Pub Date : 2014-01-01 Epub Date: 2013-10-17 DOI:10.1159/000353312
Angelo Vacca, Roberto Ria, Antonia Reale, Domenico Ribatti
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引用次数: 27

摘要

血管生成是多发性骨髓瘤进展的一个恒定标志,并具有预后潜力。多发性骨髓瘤细胞与周围宿主细胞和细胞外基质相互作用,这种串扰影响了原发性和继发性肿瘤部位恶性表型的最重要方面。多发性骨髓瘤诱导的血管生成的病理生理包括血浆细胞直接产生血管生成细胞因子和骨髓微环境细胞诱导血管生成细胞因子。骨髓巨噬细胞和肥大细胞直接参与血管生成模拟,从而与循环内皮细胞和内皮前体细胞一起促进多发性骨髓瘤新生血管的形成。宿主细胞或生态位微环境和细胞外基质的作用代表了一个激烈的研究领域,最终实现了对完整肿瘤实体(即恶性细胞和微环境)的病理生理修饰的更好理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Angiogenesis in multiple myeloma.

Angiogenesis is a constant hallmark of multiple myeloma progression and has prognostic potential. Multiple myeloma cells interact with surrounding host cells and extracellular matrix, this crosstalk affecting the most important aspects of the malignant phenotype, both at primary and secondary tumor sites. The pathophysiology of multiple myeloma-induced angiogenesis involves both direct production of angiogenic cytokines by plasma cells and their induction within the bone marrow microenvironment cells. A direct involvement of bone marrow macrophages and mast cells in vasculogenic mimicry has been demonstrated, thus contributing together with circulating endothelial cells and endothelial precursor cells to the multiple myeloma neovascularization. The role of host cells or the niche microenvironment and extracellular matrix represents an intense area of research, finalized at a better understanding of the pathophysiological modifications of the complete tumor entity, i.e. malignant cells and microenvironment.

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