期刊文献+

P16和VEGF在胃癌组织中的表达及临床意义 被引量:1

Expression of P16 and VEGF in Gastric Carcinoma and Its Clinical Significance
下载PDF
导出
摘要 目的研究抑癌基因P16和血管内皮生长因子(VEGF)在胃癌组织中的表达及与临床病理学参数之间的关系。方法采用链霉素抗生物素蛋白-过氧化物酶(streptaridin peroxidase,SP)免疫组织化学方法及形态定量分析方法,检测胃癌78例、胃良性病变15例组织中P16蛋白及VEGF的表达情况。结果胃癌标本VEGF阳性表达率高于胃良性病变,VEGF主要表达于肿瘤细胞胞浆或胞膜,与胃癌淋巴结转移、临床分期有关(P<0.01);胃癌中的P16蛋白阳性表达率低于胃良性病变,P16蛋白主要表达于肿瘤细胞胞核,其表达与胃癌淋巴结转移、临床分期有关(P<0.05);胃癌中P16蛋白的低表达与VEGF的高表达具有显著相关性(P<0.01)。结论VEGF促进肿瘤血管生成,VEGF表达上调或P16蛋白表达下调对胃癌发生、发展及转移起重要作用,为判定肿瘤的生物学行为和转移潜能提供了重要指标。 Objective To research the behaviour of P16-cancer suppressor gene and Vascular endothelial growth factor (VEGF) in Gastric cancer tissue and the relationship between it and Clinical pathology parameters. Methods The expression of P16 and VEGF in 78 specimens of gastric carcinoma and 15 specimens of benign lesion of stomach were detected by S-P immunohistochemieal method and the morphometry quantitative method. Results The positive expression rate of VEGF in gastric carcinoma was taller than in benign lesion of stomach and VEGF main express in tumour cytoplasm or membrane, and it related with lymph node metastasis of gastric cancer and clinical stage( P 〈 0.01) .The positive expression rate of P16 in gastric carcinoma was lower than in benign lesion of stomach and P16 main express in turnout nuclear, and it related with lymph node metastasis of gastric cancer and clinical stage( P 〈 0.05). P16 high expression notability related with VEGF low expression( P 〈 0.01 ). Conduslon VEGF promote tumor angiogenesis. Up regulation of VEGF expression or down regulation of P16 expression is very important role to the occurrence, development and transfer of gastric carcinoma, and it provide a very important indicator for biological behavior and metastasis in patients of tumour.
出处 《中国实验诊断学》 2008年第12期1543-1545,共3页 Chinese Journal of Laboratory Diagnosis
基金 吉林省科技发展计划(20060908-02)资助项目
关键词 胃癌 P16蛋白 血管内皮生长因子 免疫组织化学 Gastric carcinoma P16 VEGF Immunohistochemical
  • 相关文献

参考文献5

  • 1Ferrara N, HenzelW J. Pituitary follicular cells secrete a novel heparinbinding growth factor specific for vascular endothelial cells[J]. Biochem- Biophys Res Commun, 1989,161:8512581. 被引量:1
  • 2Folkman J,Clinical app lications of research on angiogenesis[J]. N EngJ Med, 1995,333:17572831. 被引量:1
  • 3Cabrilovich DJ, Chen HL, Girgis KR, et al. Production of vascular endothelial growth factor by human turmors inhibits the functional maturationof dendritic cells[J]. NatMed, 1996,2(10) : 109621031. 被引量:1
  • 4Liotta LA,StrackeML.Tumor invasion and metastasis[J]. Cell Mol Biol, 1998;2231. 被引量:1
  • 5赵维,张录民,刘国津.p16和VEGF在老年肺癌组织中的表达及临床意义[J].中国老年学杂志,2006,26(1):41-43. 被引量:2

二级参考文献7

  • 1Kamb A, Gruis NA, Weaver-Feldhaus J, et al, A cell cycle regulator potentially involved in genesis of many tumor types[ J]. Science, 1994 ,264 :436. 被引量:1
  • 2David CS, Lisa V, Characterization of chromosome in human ovarian neoplasm identifies frequent genetic imbalance on 9q and rare alterations involving 9q, including CDKN2 [ J], Cancer Res, 1995 ; 15 (55) :2150. 被引量:1
  • 3Ferrara N, Henzel W J. Pituitary follicular cells secrete a novel heparin-binding growth factor specific for vascular endothelial cells[ J]: Biochem Biophys Res Commun, 1989 ; 161:851-58. 被引量:1
  • 4Folkman J, Clinical applications of research on angiogenesis[ J ]. N Engl J Med, 1995 1333 : 1757-83. 被引量:1
  • 5Cabrilovich DJ, Chen HL, Girgis KR, et al. Production of vascular endothelial growth factor by human turmors inhibits the functional maturation of dendritic cells [ J]. Nat Med, 1996 ;2 (10) : 1096-103. 被引量:1
  • 6Liotta LA, Stracke ML Tumor invasion and metastasis [ J ]. Cell Mol Bi-ol, 1998 ;223,. 被引量:1
  • 7Douck N. p53 and angiogenesis[ J]. Biochem Biophys Acta, 1996;1287(1):63-6. 被引量:1

共引文献1

同被引文献8

  • 1申兴斌,王瑞婷,赵晓明,于再东.P16在胃癌组织中的表达及临床意义[J].承德医学院学报,2004,21(3):187-188. 被引量:2
  • 2邱文生,张彦,岳麓,任德玲,张红军,梁军.医学教育中应用多媒体技术的利弊分析[J].青岛大学医学院学报,2006,42(4):363-365. 被引量:19
  • 3Kamb A,Gruis N,Jane WF,et al.A cell cycle regulator potentially involved in genesis of many tumor types[J].Science,1994,264(5157):436-440. 被引量:1
  • 4Nobori T,Miura K,Wu DJ,et al.Deletions of the cyclin dependent kinase 4-inhibitor gene in multiple human carcinomas[J].Nature,1994,368(6473):753-756. 被引量:1
  • 5Serrano M,Hannon GJ,Beach D.A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4[J].Nature,1993,367(3667):704-707. 被引量:1
  • 6Allay JA,Steiner MS,Zhang Y,et al.Adenovirus p16 gene therapy for prostate cancer[J].World J Urol,2000,18(2):111-120. 被引量:1
  • 7Steiner MS,Zhang Y,Farooq F,et al.Adenoviral vector containing wild-type p16 suppresses prostate carcinoma growth and prolongs survival by inducing cell senescence[J].Carcinoma Gene Ther,2000,7(3):360-372. 被引量:1
  • 8Lukas J,Parry D,Aagaard I,et al.Retinoblastoma protein dependent cell-cycle inhibition by the tumor suppressor P16[J].Nature,1995,369(6531):503-506. 被引量:1

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部