Department of Pathology, Tanta University, Egypt.
Ann Diagn Pathol. 2010 Oct;14(5):321-7. doi: 10.1016/j.anndiagpath.2009.12.011. Epub 2010 Feb 8.
Vascular endothelial growth factor (VEGF) and basic fibroblastic growth factor (b-FGF) have been described as essential cytokines in the regulation of angiogenesis. Their elevation has been associated with an unfavorable outcome in different neoplasms. However, their role in angiogenesis and proliferation in B-cell non-Hodgkin's lymphoma (B-NHL) is unclear. Seventy cases of B-NHL besides 5 cases with reactive lymphadenitis were collected randomly and classified according to World Health Organization classification, Ann Arbor staging. They were subjected to immunostaining using VEGF, b-FGF, CD34, and Ki67 markers. There were a positive correlation between the proliferation and aggressiveness of the tumor as measured with Ki67 and both VEGF and b-FGF, and this was reflected on the stromal increase in microvessel density as measured by CD34. In conclusion, as the tumor becomes more aggressive, it also becomes independent of stromal paracrine factors by the establishment of an autocrine VEGF and b-FGF stimulation that can increase its angiogenesis and proliferation.
血管内皮生长因子 (VEGF) 和碱性成纤维细胞生长因子 (b-FGF) 已被描述为调节血管生成的重要细胞因子。它们的升高与不同肿瘤的不良预后相关。然而,它们在 B 细胞非霍奇金淋巴瘤 (B-NHL) 中的血管生成和增殖中的作用尚不清楚。本研究随机收集了 70 例 B-NHL 病例和 5 例反应性淋巴结炎病例,根据世界卫生组织分类和 Ann Arbor 分期进行分类。使用 VEGF、b-FGF、CD34 和 Ki67 标志物进行免疫染色。Ki67 与 VEGF 和 b-FGF 之间呈正相关,Ki67 可衡量肿瘤的增殖和侵袭性,VEGF 和 b-FGF 可衡量肿瘤的血管生成和增殖,这反映在 CD34 测量的基质中微血管密度增加。总之,随着肿瘤变得更具侵袭性,它也通过建立自分泌 VEGF 和 b-FGF 刺激而变得独立于基质旁分泌因子,这可以增加其血管生成和增殖。