冯红超, 宋宇峰, 温玉明. 口腔鳞癌中VEGF表达和肿瘤相关巨噬细胞在血管生成中相互作用的初步研究[J]. 中国肿瘤临床, 2004, 31(8): 435-437.
引用本文: 冯红超, 宋宇峰, 温玉明. 口腔鳞癌中VEGF表达和肿瘤相关巨噬细胞在血管生成中相互作用的初步研究[J]. 中国肿瘤临床, 2004, 31(8): 435-437.
Feng Hong-chao, Song Yu-feng, Wen Yu-min. A Study on the Correlation between Vascular Endothelial Growth Factor and Tumor-associated Macrophages in Tumour Angiogenesis of Human Oral Squamous-cell Carcinomas[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(8): 435-437.
Citation: Feng Hong-chao, Song Yu-feng, Wen Yu-min. A Study on the Correlation between Vascular Endothelial Growth Factor and Tumor-associated Macrophages in Tumour Angiogenesis of Human Oral Squamous-cell Carcinomas[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(8): 435-437.

口腔鳞癌中VEGF表达和肿瘤相关巨噬细胞在血管生成中相互作用的初步研究

A Study on the Correlation between Vascular Endothelial Growth Factor and Tumor-associated Macrophages in Tumour Angiogenesis of Human Oral Squamous-cell Carcinomas

  • 摘要: 目的:探讨口腔鳞癌中血管内皮生长因子(vascular endothelial growth factor VEGF)和肿瘤相关巨噬细胞(tumor-associated macrophages TAMs)在肿瘤血管生成中的关系。方法:采用免疫组化染色,光镜进行高倍视野下巨噬细胞、微血管计数、图像分析,以观察VEGF表达的强度,免疫组化双染观察巨噬细胞内VEGF的表达。结果:在口腔鳞癌中VEGF的表达与微血管计数(P<0.05,γ=0.412)及肿瘤相关巨噬细胞计数(P<0.05,γ=0.376)有关,免疫组化双染显示,TAMs内有VEGF的表达。结论:口腔鳞癌中与TAMs和VEGF表达有关,二者相互作用促进肿瘤的血管生成,参与肿瘤生长和转移。

     

    Abstract: Objective : To study the correlation between vascular endothelial growth factor and tumor-associated macrophages (TAMs) in angiogenesis of human oral squamous-cell carcinomas(OSCC). Methods : After immunohistochemical staining, light microscope was used for counting macrophages and microvessels, and automated image analysis quantification was used to detect VEG F expression. The double staining was also used to detect VEGF expression in TAMs. Results : VEG F expression show a significant positive connection with the counts of microvessels ( P<0.05, r=0.412) and macrophages (P<0.05, r=0.376) in OSCC. TAMs express VEG F in OSCC. Conclusions : VEG F expression, macrophage infiltration and angiogenesis may represents a important synergistic inter-relation between tumor cells and stroma in the micro- environment of OSCC.

     

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