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Heparanase and vascular endothelial growth factor expression in the progression of oral mucosal melanoma

机译:口腔粘膜黑色素瘤进展中乙酰肝素酶和血管内皮生长因子的表达

摘要

Oral mucosal melanoma is an aggressive neoplasm with poor prognosis. Heparanase is an endo-beta-d-glucuronidase, which cleaves heparan sulphate chains. The vascular endothelial growth factor (VEGF) is the most potent angiogenic mitogen and interaction with its receptor (VEGFR) has been associated with angiogenesis. We investigated the expression of these molecules in the progression of oral mucosal melanoma. Immunohistochemistry was carried out in 15 oral melanotic macules and 19 oral melanomas using heparanase, VEGF, VEGFR-2, CD34 and Ki-67. Microvessel density was determined and subjected to statistical analysis. Heparanase and VEGFR-2 were not expressed in the oral melanotic macule. Atypical melanocytes and melanoma cells expressed heparanase, VEGF and VEGFR-2. An intense expression was noted in the early invasive phase, which marks the crucial transition from in situ to the invasive phase. In the invasive component, heparanase was intense but selective in the invasive fronts and at the periphery of nests unlike the extensive expression of VEGF and VEGFR-2. However, hot spots were only observed at the periphery of the nests. In conclusion, melanoma cells expressed heparanase, VEGF and VEGFR-2. The coexpression of these molecules in atypical melanocytes and melanoma cells suggests their function in cell migration and invasion. Moreover, the intense expression in the crucial transition from in situ to the invasive phase suggests their role in the progression of the tumor. The role of VEGF and VEGFR-2 in angiogenesis was evident only at the periphery of the nests in the invasive components.
机译:口腔粘膜黑色素瘤是一种侵袭性肿瘤,预后较差。乙酰肝素酶是一种内切β-d-葡萄糖醛酸酶,可裂解硫酸乙酰肝素链。血管内皮生长因子(VEGF)是最有效的血管生成促有丝分裂原,与其受体(VEGFR)的相互作用与血管生成有关。我们调查了这些分子在口腔粘膜黑色素瘤进展中的表达。使用乙酰肝素酶,VEGF,VEGFR-2,CD34和Ki-67在15个口腔黑色素斑和19个口腔黑色素瘤中进行免疫组织化学。确定微血管密度并进行统计分析。肝素酶和VEGFR-2在口腔黑色素斑中不表达。非典型黑素细胞和黑素瘤细胞表达乙酰肝素酶,VEGF和VEGFR-2。在早期侵入阶段注意到强烈的表达,这标志着从原位到侵入阶段的关键过渡。在侵袭性成分中,乙酰肝素酶是强烈的,但是在侵袭性前沿和巢周边具有选择性,这与VEGF和VEGFR-2的广泛表达不同。然而,仅在巢的外围观察到热点。总之,黑色素瘤细胞表达乙酰肝素酶,VEGF和VEGFR-2。这些分子在非典型黑素细胞和黑色素瘤细胞中的共表达提示它们在细胞迁移和侵袭中的功能。而且,在从原位到侵入期的关键过渡中的强烈表达表明它们在肿瘤进展中的作用。 VEGF和VEGFR-2在血管生成中的作用仅在侵袭性成分巢的外围可见。

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