Literature DB >> 10849328

Expression of urokinase-type plasminogen activator, urokinase-type plasminogen activator receptor, and plasminogen activator inhibitor-1 and -2 in hepatocellular carcinoma.

L Zhou1, Y Hayashi, T Itoh, W Wang, J Rui, H Itoh.   

Abstract

It has become more and more clear in recent decades that the plasminogen activation system, which includes urokinase-type plasminogen activator (uPA), urokinase-type plasminogen activator receptor (uPAR), plasminogen activator inhibitor (PAI)-1 and PAI-2, plays a very important role in the aggressiveness of cancer. Using immunohistochemistry and enzyme-linked immunosorbent assay (ELISA), the expression of these four components of the uPA system was analyzed in 19 cases of hepatocellular carcinoma (HCC) and 18 cases of the adjacent non-cancer tissues which all had chronic active hepatitis with liver fibrosis or liver cirrhosis. Four cases of normal liver tissues, as controls for immunohistochemical stains, were obtained from the hepatectomized liver of patients with metastatic cancer in the liver. The positive rates of uPA, uPAR, PAI-1 and PAI-2 for immunohistochemical stains in cancer tissues were 78.9, 68.4, 57.9 and 31.6%, respectively. Positive signals were mainly distributed in the cytoplasm of the cancer and in stromal cells. Moreover, the strong stains were chiefly located in the invasive front of the cancer cells. No specific stain was detected in four cases of normal liver tissues. In ELISA, there were significant differences between cancer and non-cancer tissues in concentration of uPA, uPAR and PAI-1 (P < 0.0003, 0.0024 and 0.01, respectively), but there was no significant difference in that of PAI-2 (P = 0.37). These results suggest that uPA, uPAR and PAI-1 are related to invasion of HCC.

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Year:  2000        PMID: 10849328     DOI: 10.1046/j.1440-1827.2000.01059.x

Source DB:  PubMed          Journal:  Pathol Int        ISSN: 1320-5463            Impact factor:   2.534


  6 in total

1.  Overexpression of hepatic plasminogen activator inhibitor type 1 mRNA in rabbits with fatty liver.

Authors:  J G Fan; L H Chen; Z J Xu; M D Zeng
Journal:  World J Gastroenterol       Date:  2001-10       Impact factor: 5.742

2.  Analysis of gene expression profile of pancreatic carcinoma using cDNA microarray.

Authors:  Zhi-Jun Tan; Xian-Gui Hu; Gui-Song Cao; Yan Tang
Journal:  World J Gastroenterol       Date:  2003-04       Impact factor: 5.742

3.  Low expression of PAI-2 as a novel marker of portal vein tumor thrombosis and poor prognosis in hepatocellular carcinoma.

Authors:  Li Zhou; Ye Jin; Quan-Cai Cui; Ke-Min Jin; Wei-Xun Zhou; Bao-Cai Xing
Journal:  World J Surg       Date:  2013-03       Impact factor: 3.352

4.  The Clinicopathological and Prognostic Significance of the Gross Classification of Hepatocellular Carcinoma.

Authors:  Yangkyu Lee; Hyunjin Park; Hyejung Lee; Jai Young Cho; Yoo-Seok Yoon; Young-Rok Choi; Ho-Seong Han; Eun Sun Jang; Jin-Wook Kim; Sook-Hyang Jeong; Soomin Ahn; Haeryoung Kim
Journal:  J Pathol Transl Med       Date:  2017-11-24

5.  Functional Modulation of Gene Expression by Ultraconserved Long Non-coding RNA TUC338 during Growth of Human Hepatocellular Carcinoma.

Authors:  Hui-Ju Wen; Michael P Walsh; Irene K Yan; Kenji Takahashi; Alan Fields; Tushar Patel
Journal:  iScience       Date:  2018-04-27

6.  SERPINA11 Inhibits Metastasis in Hepatocellular Carcinoma by Suppressing MEK/ERK Signaling Pathway.

Authors:  Ye Song; Zhuo Li; Lei Li; Houming Zhou; Ting-Ting Zeng; Chuan Jin; Jin-Rong Lin; Sha Gao; Yan Li; Xin-Yuan Guan; Ying-Hui Zhu
Journal:  J Hepatocell Carcinoma       Date:  2021-07-06
  6 in total

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