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肝细胞癌VEGF 、bFGF 与凋亡相关蛋白表达的关系[J]. 肿瘤防治研究, 2005, 32(05): 276-278. DOI: 10.3971/j.issn.1000-8578.2475
引用本文: 肝细胞癌VEGF 、bFGF 与凋亡相关蛋白表达的关系[J]. 肿瘤防治研究, 2005, 32(05): 276-278. DOI: 10.3971/j.issn.1000-8578.2475
Correlation between the Expressions of VEGF, bFGF and Some Apoptosis Proteins in Hapatocellular Carcinoma[J]. Cancer Research on Prevention and Treatment, 2005, 32(05): 276-278. DOI: 10.3971/j.issn.1000-8578.2475
Citation: Correlation between the Expressions of VEGF, bFGF and Some Apoptosis Proteins in Hapatocellular Carcinoma[J]. Cancer Research on Prevention and Treatment, 2005, 32(05): 276-278. DOI: 10.3971/j.issn.1000-8578.2475

肝细胞癌VEGF 、bFGF 与凋亡相关蛋白表达的关系

Correlation between the Expressions of VEGF, bFGF and Some Apoptosis Proteins in Hapatocellular Carcinoma

  • 摘要: 目的 探讨肝细胞癌(hepatocellular carcinoma,HCC)组织中血管内皮生长因子(vascular endothelial growth factor,VEGF)、碱性成纤维细胞生长因子(basic fibroblast growth factor,bFGF)以及凋亡相关蛋白Fas、bax、bcl-2和bcl-xl之间的关系。方法 对经病理证实的肝细胞癌38例共40个癌灶进行分析,用免疫组化SP法检测癌组织中VEGF、bFGF、Fas、bax、bcl-2和bcl-Xl的表达情况,分析它们之间的相互关系。结果 VEGF、bFGF、Fas、bax、bcl-2和bcl-xl的阳性表达率分别为77.5%(31/40)、75%(30/40)、20%(8/40)、25%(10/40)、27.5%(11/40)和50%(20/40)。VEGF与bFGF、bcl-2与bcl-xl之间明显相关(P<0.01),bax与bcl-2、VEGF与bcl-2、bax与bFGF之间也存在一定的相关性(P<0.05)。结论 VEGF、bFGF和凋亡相关蛋白共同调控HCC的血管生成和细胞凋亡。

     

    Abstract: Objective  To explore the correlation between the expressions of vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF) and some apoptosis proteins including Fas, bax, bcl-2 and bcl-xl in hepatocellular carcinoma ( HCC) . Methods  Thirty2eight cases (40 lesions) of HCC verified by histopathology were studied. The expressions of VEGF, bFGF, Fas, bax, bcl-2 and bcl-xl were detected with immunohistochemical SP method, and the relationships among these proteins were analyzed. Results  The positive rate of VEGF, bFGF, Fas, bax, bcl-2 and bcl-xl was 77. 5%(31/40), 75 %(30/40), 20 %(8/40), 25 %(10/40), 27. 5 %(11/40) and 50%(20/40) in HCC respectively. The positive correlations between VEGF and bFGF, bcl-2 and bcl-xl were found ( P < 0. 01 respectively) . The same results were also found between bax and bcl-2, VEGF and bcl2-2 、bax and bFGF ( P < 0. 05 respectively) . Conclusion  The angiogenesis and cell apoptosis in HCC may be regulated by the expressions of VEGF, bFGF, Fas, bax, bcl-2 and bcl-xl.

     

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