Riedel F, Götte K, Schwalb J, Bergler W, Hörmann K
Universitäts-Hals-Nasen-Ohrenklinik Mannheim.
Laryngorhinootologie. 2000 Dec;79(12):730-5. doi: 10.1055/s-2000-9131.
Angiogenesis is crucial for tumor growth and metastasis. In several tumors, microvascular density has been shown to correlate with metastasis and aggressiveness. Vascular endothelial growth factor (VEGF) and basic Fibroblast Growth Factor (bFGF) are known to have potent angiogenic activity. Their expression has been identified in a wide variety of malignancies including head and neck squamous cell carcinoma (HNSCC). Aim of our study was to investigate the role of co-expression of VEGF and bFGF for angiogenesis in HNSCC.
Cryostat sections of 51 primary HNSCC were immunostained for VEGF and bFGF using a standard streptavidin-biotin complex procedure. To evaluate angiogenesis, endothelial cells were stained immunohistochemically using anti-vWF polyclonal antibody. Microvessels were quantified by counting vessels in a x200 field in the most vascular area of the tumor.
25/51 (49%) of the investigated carcinomas showed co-expression of both factors (VEGF+/bFGF+), while 6/51 (11.7%) carcinomas only expressed VEGF and 13/51 (25.5%) carcinomas expressed bFGF. 7/51 (13.7%) tumors showed no expression of these factors (VEGF-/bFGF-). Carcinomas with a co-expression of VEGF and bFGF showed a significantly increased mean microvessel density (88.3 +/- 24.4) compared to tumors expressing only VEGF (77 +/- 16.8) or bFGF (71.1 +/- 15.8) (p = 0.022) or tumors with no expression of both factors (51.1 +/- 13.4) (p < 0.001). The association of VEGF and bFGF expression level was not significant (p = 0.178).
The positive correlation of the co-expression of angiogenic VEGF and bFGF with increased microvessel density underlines the importance of both factors for tumor angiogenesis in HNSCC. VEGF and bFGF might act cooperatively in the process of neovascularization in human head and neck cancer.
血管生成对于肿瘤的生长和转移至关重要。在多种肿瘤中,微血管密度已被证明与转移和侵袭性相关。血管内皮生长因子(VEGF)和碱性成纤维细胞生长因子(bFGF)具有强大的血管生成活性。它们的表达已在包括头颈部鳞状细胞癌(HNSCC)在内的多种恶性肿瘤中被发现。本研究的目的是探讨VEGF和bFGF共表达在HNSCC血管生成中的作用。
采用标准的链霉亲和素-生物素复合物法对51例原发性HNSCC的冷冻切片进行VEGF和bFGF免疫染色。为评估血管生成,使用抗vWF多克隆抗体对内皮细胞进行免疫组织化学染色。通过在肿瘤血管最丰富区域的200倍视野下计数血管来量化微血管。
25/51(49%)的研究癌组织显示两种因子共表达(VEGF+/bFGF+),而6/51(11.7%)的癌组织仅表达VEGF,13/51(25.5%)的癌组织表达bFGF。7/51(13.7%)的肿瘤未显示这些因子的表达(VEGF-/bFGF-)。与仅表达VEGF(77±16.8)或bFGF(71.1±15.8)的肿瘤(p = 0.022)或两种因子均不表达的肿瘤(51.1±13.4)(p < 0.001)相比,VEGF和bFGF共表达的癌组织平均微血管密度显著增加(88.3±24.4)。VEGF和bFGF表达水平的相关性不显著(p = 0.178)。
血管生成性VEGF和bFGF的共表达与微血管密度增加呈正相关,突出了这两种因子在HNSCC肿瘤血管生成中的重要性。VEGF和bFGF可能在人类头颈部癌的新生血管形成过程中协同作用。