Cancer Res Treat. 2002 Feb;34(1):41-5. doi: 10.4143/crt.2002.34.1.41.
There are increasing evidences that angiogenesis enhances tumor growth and biological aggressiveness in gastric carcinoma. Mast cells have been implicated in the angiogenic process, by secreting angiogenic factors including vascular endothelial growth factor (VEGF), or enzymes that degrade extracellular matrices. However, the exact nature of mast cells in relation to cancer is contradictory so we conducted retrospective studies, to find the significance of mast cell densities, and microvessel counts in each clinicopathologic factors, including VEGF expression, in proper muscle (PM) gastric carcinoma.
52 specimens, obtained from patients with PM gastric carcinoma, were studied using the immunohistochemical methods, monoclonal antibodies for mast cell tryptase, factor VIII-related antigen and VEGF.
Mast cell densities were significantly increased in diffuse histologic type (p=0.042), infiltrating margins (p<0.0001) and VEGF positive (p=0.010) tumors.Microvessel counts were significantly higher in patients over 55 years old (p=0.024), with tumor sizes larger than >3 cm (p=0.015), diffuse histologic type (p=0.038) and lymph node metastasis (p=0.001). Similarly there were significantly increased densities in VEGF positive tumors (p<0.0001). Pearson's correlation analysis revealed a significant relationship between mast cell densities and microvessel counts (r=0.614, p<0.01), indicating a high vascular grade with increased number of mast cells.
We demonstrated a close relationship between mast cell densities, microvessel counts and VEGF expression. These results suggest that mast cells and VEGF are important regulators of tumor angiogenesis and cooperatively induce the formation of vascular stroma in PM gastric carcinomas.
越来越多的证据表明血管生成可增强胃癌的肿瘤生长和生物学侵袭性。肥大细胞可通过分泌血管内皮生长因子(VEGF)或降解细胞外基质的酶等血管生成因子参与血管生成过程。然而,关于肥大细胞与癌症的确切关系存在争议,因此我们进行了回顾性研究,以确定肥大细胞密度与 VEGF 表达在每种临床病理因素中的意义,包括在固有肌层(PM)胃癌中。
采用免疫组化方法,用抗肥大细胞类胰蛋白酶、VIII 因子相关抗原和 VEGF 的单克隆抗体,对 52 例 PM 胃癌患者的标本进行研究。
肥大细胞密度在弥漫型组织学类型(p=0.042)、浸润边缘(p<0.0001)和 VEGF 阳性(p=0.010)肿瘤中显著增加。微血管计数在年龄>55 岁(p=0.024)、肿瘤大小>3cm(p=0.015)、弥漫型组织学类型(p=0.038)和淋巴结转移(p=0.001)的患者中显著升高。VEGF 阳性肿瘤中的密度也显著升高(p<0.0001)。Pearson 相关分析显示,肥大细胞密度与微血管计数之间存在显著相关性(r=0.614,p<0.01),表明血管等级较高,肥大细胞数量增加。
我们证明了肥大细胞密度、微血管计数与 VEGF 表达之间存在密切关系。这些结果表明,肥大细胞和 VEGF 是肿瘤血管生成的重要调节因子,并协同诱导 PM 胃癌中血管基质的形成。