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首页> 外文期刊>Medical Oncology >Circulating levels of vascular endothelial growth factor (VEGF), matrix metalloproteinase-3 (MMP-3), and BCL-2 in malignant melanoma
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Circulating levels of vascular endothelial growth factor (VEGF), matrix metalloproteinase-3 (MMP-3), and BCL-2 in malignant melanoma

机译:恶性黑色素瘤中血管内皮生长因子(VEGF),基质金属蛋白酶3(MMP-3)和BCL-2的循环水平

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摘要

Vascular endothelial growth factor (VEGF) is a critical regulator of angiogenesis that stimulates proliferation, migration, and metastasis of melanoma. In literature, all studies concerning influences of matrix metalloproteinases (MMPs) and antiapoptotic proteins on VEGF-induced angiogenesis in melanoma patients have been performed in tissue scale in melanoma. The objective of this study was to determine the value of circulating serum VEGF and its possible mechanisms of angiogenesis by circulating VEGF, MMP-3, and Bcl-2 in patients with melanoma. Fifty-one patients with cutaneous melanoma pathologically verified at different stages, and eighteen healthy controls were investigated. Serum VEGF, MMP-3, and Bcl-2 levels were quantitatively analyzed by ELISA. The serum VEGF (P = 0.034) and Bcl-2 (P = 0.005) levels were significantly higher in patients with melanoma than in the control group. However, there was no significant difference in the serum MMP-3 level between melanoma patients and controls (P = 0.51). The serum levels of VEGF were significantly influenced only by Breslow thickness (P = 0.045) and mitosis (0.039) and were not positively correlated with the stage of the disease. Among serum parameters, a significant relationship was found only between serum levels of VEGF and MMP-3 (r = 0.32, P = 0.023). In conclusion, our study demonstrates increased concentrations of VEGF and Bcl-2, but not MMP-3, in serum of melanoma patients regardless of the stage of the disease. VEGF may be a potential endothelial cell growth and survival factor. The mechanism of VEGF regulation of angiogenesis may be in part due to enhanced proliferation and survival of endothelial cells by differential expression of antiapoptotic genes and in part by activation of MMPs.
机译:血管内皮生长因子(VEGF)是刺激黑色素瘤增殖,迁移和转移的重要血管生成调节剂。在文献中,所有关于基质金属蛋白酶(MMPs)和抗凋亡蛋白对黑色素瘤患者中VEGF诱导的血管生成的影响的研究均已在黑色素瘤的组织范围内进行。这项研究的目的是确定黑色素瘤患者中循环血清VEGF的价值及其通过循环VEGF,MMP-3和Bcl-2进行血管生成的可能机制。对五十一个皮肤黑色素瘤患者在不同阶段进行了病理检查,并对十八名健康对照者进行了调查。通过ELISA定量分析血清VEGF,MMP-3和Bcl-2水平。黑色素瘤患者的血清VEGF(P = 0.034)和Bcl-2(P = 0.005)水平显着高于对照组。但是,黑色素瘤患者和对照组之间的血清MMP-3水平没有显着差异(P = 0.51)。 VEGF的血清水平仅受Breslow厚度(P = 0.045)和有丝分裂(0.039)的显着影响,与疾病的分期没有正相关。在血清参数之间,仅在VEGF和MMP-3的血清水平之间发现显着的相关性(r = 0.32,P = 0.023)。总之,我们的研究表明,黑色素瘤患者血清中的VEGF和Bcl-2浓度升高,而MMP-3则不升高,而与疾病的分期无关。 VEGF可能是潜在的内皮细胞生长和存活因子。 VEGF调节血管生成的机制可能部分归因于抗凋亡基因的差异表达增强了内皮细胞的增殖和存活,也部分归因于MMP的激活。

著录项

  • 来源
    《Medical Oncology》 |2008年第4期|431-436|共6页
  • 作者单位

    Institute of Oncology Istanbul University Capa 34390 Istanbul Turkey;

    Institute of Oncology Istanbul University Capa 34390 Istanbul Turkey;

    Institute of Oncology Istanbul University Capa 34390 Istanbul Turkey;

    Institute of Oncology Istanbul University Capa 34390 Istanbul Turkey;

    Institute of Oncology Istanbul University Capa 34390 Istanbul Turkey;

    Institute of Oncology Istanbul University Capa 34390 Istanbul Turkey;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Bcl-2; Melanoma; MMP-3; Serum; VEGF;

    机译:Bcl-2;黑素瘤;MMP-3;血清;VEGF;

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