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Correlation of the expression of vascular endothelial growth factor and its receptors with microvessel density in ovarian cancer

机译:卵巢癌中血管内皮生长因子及其受体的表达与微血管密度的相关性

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摘要

The present study aimed to investigate the correlation between the expression of vascular endothelial growth factor (VEGF) and its receptors, the Flt-1 and KDR proteins, with clinical pathology and microvessel density (MVD) in ovarian cancer tissue. The protein expression levels of VEGF and its receptors, Flt-1 and KDR/Flk-1, were detected in 48 cases of ovarian cancer using the streptavidin-biotin complex (SABC) immunohistochemical method, and tumor MVD was evaluated using F8 factor (FVIII-RA). The expression of the VEGF, Flt-1 and KDR proteins was not significantly associated with the pathological type, extent of differentiation or clinical stage of ovarian cancer. However, the co-expression of VEGF and Flt-1 was markedly correlated with differentiation and clinical stage (P<0.01). The co-expression levels of VEGF and receptor Flt-1 in malignant neoplasms with lymph node metastasis was significantly higher compared with malignant neoplasms without lymph node metastasis (P<0.05). The expression level of KDR in patients with hepatic metastasis was significantly higher compared with patients without hepatic metastasis (P<0.05). The co-expression level of VEGF and KDR in patients with hepatic metastasis was significantly higher compared with patients without hepatic metastasis (P<0.05) and the Flt-1 expression level in patients with ascites <1,000 ml was significantly lower than that in patients with ascites ≥1000 ml (P<0.05). The mean MVD of VEGF- and KDR-positive patients was significantly higher compared with VEGF- and KDR-negative patients (P<0.05). The expression of VEGF and its receptors is involved in the malignant transformation of ovarian tumors, tumor progression and metastasis, as well as ascites formation and angiogenesis.
机译:本研究旨在研究卵巢癌组织中血管内皮生长因子(VEGF)及其受体Flt-1和KDR蛋白的表达与临床病理和微血管密度(MVD)之间的相关性。使用链霉亲和素-生物素复合物(SABC)免疫组织化学方法检测48例卵巢癌中VEGF及其受体Flt-1和KDR / Flk-1的蛋白表达水平,并使用F8因子(FVIII)评价肿瘤MVD -RA)。 VEGF,Flt-1和KDR蛋白的表达与卵巢癌的病理类型,分化程度或临床分期无关。然而,VEGF和Flt-1的共表达与分化和临床分期显着相关(P <0.01)。伴有淋巴结转移的恶性肿瘤中VEGF和受体Flt-1的共表达水平明显高于无淋巴结转移的恶性肿瘤(P <0.05)。肝转移患者的KDR表达水平明显高于无肝转移患者(P <0.05)。肝转移患者的VEGF和KDR共表达水平明显高于无肝转移患者(P <0.05),腹水<1,000 ml患者的Flt-1表达水平明显低于肝转移患者。腹水≥1000ml(P <0.05)。 VEGF和KDR阳性患者的平均MVD显着高于VEGF和KDR阴性患者(P <0.05)。 VEGF及其受体的表达与卵巢肿瘤的恶性转化,肿瘤的进展和转移以及腹水的形成和血管生成有关。

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