Riedel F, Götte K, Bergler W, Hörmann K
Department of Otolaryngology, Head and Neck Surgery, University Hospital Mannheim, Germany.
Oncol Rep. 2001 May-Jun;8(3):471-6.
Angiogenesis is essential for tumour growth and metastasis. The induction of tumour vascularization is mediated by the release of angiogenic peptides. Among these factors, basic fibroblast growth factor (bFGF), vascular endothelial growth factor (VEGF) and matrix metalloproteinase-9 (MMP-9) are thought to be the most important. Previous experimental studies indicate that the process of apoptosis, the programme of cell death, may be related to angiogenesis in head and neck carcinogenesis. Therefore, cryostat sections of 49 head and neck squamous cell carcinomas (HNSCC) were investigated immunohistochemically for pro-apoptotic factors caspase-3 and Fas ligand (FasL) using a standard streptavidin-biotin complex procedure. Expression of bFGF, VEGF and MMP-9 served as angiogenic markers. Additionally, intratumoral microvascular density (MVD) was counted by immunostaining of endothelial cells using anti-vWF antibody. Comparing the expression of apoptotic and angiogenic factors, a statistically significant inverse correlation of caspase-3 expression and VEGF and MMP-9 expression was found. Concerning FasL, the correlation of its expression with expression of VEGF, bFGF and MMP-9 was inversely correlated. With respect to vWF-immunostaining, statistical analysis gave a clear inverse correlation between the tumour vascularity and the expression of FasL (p = 0.0008) and caspase-3 (p = 0.0068). Our results suggest that HNSCC tumour angiogenesis contributes to a reduction of apoptosis in tumour cells. This may be explained by the activation of pro-apoptotic factors caused by hypoxia.
血管生成对于肿瘤的生长和转移至关重要。肿瘤血管形成的诱导是由血管生成肽的释放介导的。在这些因子中,碱性成纤维细胞生长因子(bFGF)、血管内皮生长因子(VEGF)和基质金属蛋白酶-9(MMP-9)被认为是最重要的。先前的实验研究表明,细胞凋亡过程,即细胞死亡程序,可能与头颈部癌发生中的血管生成有关。因此,采用标准的链霉亲和素-生物素复合物方法,对49例头颈部鳞状细胞癌(HNSCC)的冷冻切片进行免疫组织化学研究,检测促凋亡因子半胱天冬酶-3和Fas配体(FasL)。bFGF、VEGF和MMP-9的表达作为血管生成标志物。此外,使用抗vWF抗体对内皮细胞进行免疫染色来计数肿瘤内微血管密度(MVD)。比较凋亡因子和血管生成因子的表达,发现半胱天冬酶-3表达与VEGF和MMP-9表达之间存在统计学上显著的负相关。关于FasL,其表达与VEGF、bFGF和MMP-9表达呈负相关。就vWF免疫染色而言,统计分析表明肿瘤血管与FasL(p = 0.0008)和半胱天冬酶-3(p = 0.0068)的表达之间存在明显的负相关。我们的结果表明,HNSCC肿瘤血管生成有助于减少肿瘤细胞中的细胞凋亡。这可能是由缺氧引起的促凋亡因子的激活所解释的。