目的 研究誘導(dǎo)型一氧化氮合酶(iNOS)和p53蛋白在肝細胞癌中的表達及其與腫瘤血管形成的關(guān)系。
方法 采用免疫組化和圖像分析技術(shù)檢測59例肝細胞癌患者腫瘤組織中iNOS和p53蛋白的表達,CD34單克隆抗體免疫組化染色檢測腫瘤組織微血管密度(MVD)。
結(jié)果 ①iNOS和p53蛋白在肝細胞癌組織中表達陽性率分別為81.4%(48/59)和64.4%(38/59),表達強度(IOD值)分別為5 635±1 287和3 352±873。②MVD為32.5±2.73,以腫瘤邊緣和癌旁組織微血管較密集。③iNOS的表達與p53蛋白表達呈顯著正相關(guān)(r=0.65, P<0.05); iNOS的表達與MVD呈顯著正相關(guān)(r=0.75, P<0.05); p53蛋白的表達與MVD呈顯著正相關(guān)(r=0.72, P<0.05)。
結(jié)論 肝細胞癌組織中存在iNOS和p53蛋白的高表達; iNOS和p53可促進肝癌血管形成。
引用本文: 張劍,何生,李茂德. 肝細胞癌中iNOS和p53蛋白的表達及其與腫瘤血管形成的關(guān)系. 中國普外基礎(chǔ)與臨床雜志, 2004, 11(5): 396-398. doi: 復(fù)制
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- 3. Mattern J, Koomagi R, Volm M. Biological characterization of subgroups of squamous cell lung carcinomas [J]. Clin Cancer Res, 1999; 5(6)∶1459.
- 4. Weidner N, Folkman J, Pozza F, et al. Tumor angiogenesis: a new significant and independent prognostic indicator in earlystage breast carcinoma [J]. J Natl Cancer Inst, 1992; 84(24)∶1875.
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- 7. Fujimoto H, Ando Y, Yamashita T, et al. Nitric oxide synthase activity in human lung cancer [J]. Jpn J Cancer Res, 1997; 88(12)∶1190.
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- 9. Chin K, Kurashima Y, Ogura T, et al. Induction of vascular endothelial growth factor by nitric oxide in human glioblastoma and hepatocellular carcinoma cells [J]. Oncogene, 1997; 15(4)∶437.