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首页> 外文期刊>American Journal of Pathology >Microvessel Density and Expression of Vascular Endothelial Growth Factor and Its Receptors in Diffuse Large B-Cell Lymphoma Subtypes
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Microvessel Density and Expression of Vascular Endothelial Growth Factor and Its Receptors in Diffuse Large B-Cell Lymphoma Subtypes

机译:弥漫性大B细胞淋巴瘤亚型的微血管密度和血管内皮生长因子及其受体的表达

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摘要

Angiogenesis is known to play a major role in neoplasia, including hematolymphoid neoplasia. We assessed the relationships among angiogenesis and expression of vascular endothelial growth factor and its receptors in the context of clinically and biologically relevant subtypes of diffuse large B-cell lymphoma using immunohistochemical evaluation of tissue microarrays. We found that diffuse large B-cell lymphoma specimens showing higher local vascular endothelial growth factor expression showed correspondingly higher microvessel density, implying that lymphoma cells induce local tumor angiogenesis. In addition, local vascular endothelial growth factor expression was higher in those specimens showing higher expression of the receptors of the growth factor, suggesting an autocrine growth-promoting feedback loop. The germinal center-like and nongerminal center-like subtypes of diffuse large B-cell lymphoma were biologically and prognostically distinct. Interestingly, only in the more clinically aggressive nongerminal center-like subtype were microvessel densities significantly higher in specimens showing higher vascular endothelial growth factor expression; the same was true for the finding of higher vascular endothelial growth factor receptor-1 expression in conjunction with higher vascular endothelial growth factor expression. These differences may have important implications for the responsiveness of the two diffuse large B-cell lymphoma subtypes to anti-vascular endothelial growth factor and anti-angiogenic therapies.
机译:已知血管生成在包括血淋巴样赘生物在内的赘生物中起主要作用。我们使用组织芯片的免疫组织化学评估,在弥散性大B细胞淋巴瘤的临床和生物学相关亚型的背景下,评估了血管生成与血管内皮生长因子及其受体表达之间的关系。我们发现弥漫性大B细胞淋巴瘤标本显示较高的局部血管内皮生长因子表达显示相应较高的微血管密度,这意味着淋巴瘤细胞可诱导局部肿瘤血管生成。另外,在那些显示出生长因子受体的较高表达的标本中,局部血管内皮生长因子的表达较高,表明存在促进自分泌生长的反馈环。弥漫性大B细胞淋巴瘤的生发中心样和非胚芽样中心亚型在生物学和预后上均不同。有趣的是,只有在临床上更具侵略性的非生殖器中心样亚型中,血管内皮生长因子表达较高的标本中的微血管密度才显着升高。对于发现更高的血管内皮生长因子受体-1表达与更高的血管内皮生长因子表达相结合的情况也是如此。这些差异可能对两种弥漫性大B细胞淋巴瘤亚型对抗血管内皮生长因子和抗血管生成疗法的反应性具有重要意义。

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