期刊文献+

Expressions of cysteine-rich61,connective tissue growth factor and Nov genes in hepatocellular carcinoma and their clinical significance 被引量:28

Expressions of cysteine-rich61,connective tissue growth factor and Nov genes in hepatocellular carcinoma and their clinical significance
下载PDF
导出
摘要 AIM: To investigate the expression of cysteine-rich61 (Cyr61),connective tissue growth factor (CTGF) and nephroblastomaoverexpressecl gene (Nov) in hepatocellular carcinoma (HCC),and to evaluate the relationship between Cyr61, CTGF and Nov genes expression with invasion and metastasis of HCC.METHODS: Thirty-one HCC specimens were divided into small hepatocellular carcinoma (SHCC), nodular hepatocellular carcinoma (NHCC), solitary large hepatocellular carcinoma (SLHCC) according to their diameter and number of nodes. Reverse transcription polymerse chain reaction (RT-PCR) was used to detect the mRNA expression levels of Cyr61, CTGF and Nov genes in 31 resected specimens of hepatocellular carcinoma and para-cancerous normal liver tissues semi-quantitatively and the relation between their expression levels and clinical pathological parameters were compared.RESULTS: The expressions of Cyr61 and CTGF mRNA in carcinoma tissues were significantly higher than those in para-cancerous normal liver tissues (P<0.01). The expressions of Cyr61 and CTGF mRNA in HCC with venous invasion were higher than those in HCC without venous invasion. CTGF expression in HCC Edmondson's grade Ⅲ-IV was significantly higher than that in HCC Edmondson's grade I-II (P = 0.022). There was no obvious correlation between Nov mRNA and clinical-pathological features.Compared to NHCC, SLHCC had better cell differentiation,easier capsule formation, less microscopic venous invasion,milder liver cirrhosis. The expressions of Cyr61 and CTGF mRNA in NHCC were significantly higher than those in SLHCC and SHCC.CONCLUSION: Cyr61 and CTGF genes may play an important role in hepatocellular carcinogenesis and correlate with recurrence and metastasis of hepatocellular carcinoma.SLHCC has better biological behaviors than NHCC. AIM:To investigate the expression of cysteine-rich61(Cyr61), connective tissue growth factor(CTGF)and nephroblastoma overexpressed gene(Nov)in hepatocellular carcinoma(HCC), and to evaluate the relationship between Cyr61,CTGF and Nov genes expression with invasion and metastasis of HCC. METHODS:Thirty-one HCC specimens were divided into small hepatocellular carcinoma(SHCC),nodular hepatocellular carcinoma(NHCC),solitary large hepatocellular carcinoma (SLHCC)according to their diameter and number of nodes.Reverse transcription polymerse chain reaction (RT-PCR)was used to detect the mRNA expression levels of Cyr61,CTGF and Nov genes in 31 resected specimens of hepatocellular carcinoma and para-cancerous normal liver tissues semi-quantitatively and the relation between their expression levels and clinical pathological parameters were compared. RESULTS:The expressions of Cyr61 and CTGF mRNA in carcinoma tissues were significantly higher than those in para-cancerous normal liver tissues(P<0.01).The expressions of Cyr61 and CTGF mRNA in HCC with venous invasion were higher than those in HCC without venous invasion.CTGF expression in HCC Edmondson's grade Ⅲ- Ⅳ was significantly higher than that in HCC Edmondson's gradeⅠ-Ⅱ(P=0.022).There was no obvious correlation between Nov mRNA and clinical-pathological features. Compared to NHCC,SLHCC had better cell differentiation, easier capsule formation,less microscopic venous invasion, milder liver cirrhosis.The expressions of Cyr61 and CTGF mRNA in NHCC were significantly higher than those in SLHCC and SHCC. CONCLUSION:Cyr61 and CTGF genes may play an important role in hepatocellutar carcinogenesis and correlate with recurrence and metastasis of hepatocellular carcinoma. SLHCC has better biological behaviors than NHCC.
机构地区 LiverCancerLaboratory
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2004年第23期3414-3418,共5页 世界胃肠病学杂志(英文版)
基金 Supported by the National Key Technologies R and D Program,No.2001BA703BO4 and the National Natural Science Foundation of China,No.30371595
  • 相关文献

参考文献3

二级参考文献27

  • 1Stratmann A;Risau W;Plate KH.Cell type-specific expression of angiopoietin-1 and angiopoietin-2 suggests a role in glioblastoma angiogenesis,1998.
  • 2Millauer B;Longhi MP;Plate KH.Dominant-negative inhibition of Flk-1 suppresses the growth of many tumor types in vivo,1996.
  • 3Suzuki K;Hayashi N;Miyamoto Y.Expression of vascular permeability factor/vascular endothelial growth factor in human hepatocellular carcinoma,1996.
  • 4Lauren J;Gunji Y;Alitalo K.Is angiopoietin-2 necessary for the initiation of tumor angiogenesis?,1998.
  • 5Hashizume H,Baluk P,Morikawa S,et al.Openings between defective endothelial cells explain tumor vessel leakiness. American Journal of Pathology . 2000
  • 6Helmlinger G,Yuan F,Dellian M,et al.Interstitial pH and pO2 gradients in solid tumors in vivo: high-resolution measurements reveal a lack of correlation. Nature Medicine . 1997
  • 7Y. Harada,Y. Ogata,K. Shirouzu.Expression of vascular endothelial growth factor and its receptor KDR (kinase domain-containing receptor)/Flk-1 (fetal liver kinase-1) as prognostic factors in human colorectal cancer[J]. International Journal of Clinical Oncology . 2001 (5)
  • 8Gerhard Siemeister,Georg Martiny-Baron,Dieter Marmé.The pivotal role of VEGF in tumor angiogenesis: Molecular facts and therapeutic opportunities[J]. Cancer and Metastasis Reviews . 1998 (2)
  • 9Chen QR,Zhang L,Gasper W, et al.Targeting tumor angiogenesis with gene therapy. Molecular Genetics and Metabolism . 2001
  • 10Siemeister G,Martiny-Baron G,Marme D.The pivotal role of VEGF in tumor angiogenesis: molecular facts and therapeutic opportunities. Cancer and Metastasis Reviews . 1998

共引文献49

同被引文献62

引证文献28

二级引证文献119

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