Liver Cancer
Copyright ©The Author(s) 2005. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 14, 2005; 11(38): 5931-5937
Published online Oct 14, 2005. doi: 10.3748/wjg.v11.i38.5931
Expressions of inducible nitric oxide synthase and matrix metalloproteinase-9 and their effects on angiogenesis and progression of hepatocellular carcinoma
Min-Hua Sun, Xi-Chun Han, Ming-Ku Jia, Wei-Dong Jiang, Min Wang, Hong Zhang, Gang Han, Yi Jiang
Min-Hua Sun, Xi-Chun Han, Ming-Ku Jia, Wei-Dong Jiang, Min Wang, Hong Zhang, Gang Han, Yi Jiang, Department of General Surgery, Second Hospital, Jilin University, Changchun 130041, Jilin Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Professor Xi-Chun Han, Department of General Surgery, Second Hospital, Jilin University, Changchun 130041, Jilin Province, China. hanxichun@medmail.com.cn
Telephone: +86-431-8796988 Fax: +86-431-8934741
Received: March 12, 2004
Revised: April 1, 2005
Accepted: April 2, 2005
Published online: October 14, 2005
Abstract

AIM: To determine the expressions of inducible nitric oxide synthase (iNOS) and matrix metalloproteinase-9 (MMP-9) in hepatocellular carcinoma (HCC) and to investigate the relationship between iNOS and MMP-9 expression and their effects on angiogenesis and progression of HCC.

METHODS: In this study, we examined iNOS, MMP-9, and CD34 expression in specimens surgically removed from 32 HCC patients and 7 normal liver tissues by immunohistochemical staining. Meanwhile, microvessel density (MVD) was determined as a marker of angiogenesis by counting CD34-positive cells.

RESULTS: The positive rates of iNOS and MMP-9 expression were 71.88% (23/32) and 78.13% (25/32) in HCC. MMP-9 expression was significantly correlated with tumor size, capsule status, TNM stage, and risk of HCC recurrence (P = 0.032, P = 0.033, P = 0.007, and P = 0.001, respectively). There was also a significant relationship between iNOS expression and capsule status and risk of HCC recurrence (P = 0.049 and P = 0.004, respectively), but no correlation between iNOS expression and tumor size and TNM stage. There was a positive association between MVD and TNM stage and risk of HCC recurrence (P = 0.037 and P = 0.000, respectively). The count of MVD was significantly different in different iNOS and MMP-9 immunoreactivity groups (F = 17.713 and 17.097, P = 0.000 and P = 0.000, respectively). The examination of Spearman’s rank correlation coefficient showed that there was a

significant positive correlation between MVD and iNOS, MMP-9 immunoreactivity (r = 0.754 and 0.751, P = 0.000 and P=0.000, respectively). There was also a significant association between MMP-9 and iNOS expression in HCC (P = 0.010).

CONCLUSION: Nitric oxide (NO) produced by iNOS could modulate MMP-9 production and therefore contribute to tumor cell angiogenesis and invasion and metastasis in HCC. The strong expression of iNOS and MMP-9 in HCC may be helpful in evaluating the recurrence of HCC, predicting poor prognosis. For patients with strong expression of MMP-9 and iNOS, the optimal treatment scheme needs to be selected.

Keywords: Inducible nitric oxide synthase; Matrix metalloproteinase-9; Angiogenesis; Hepatocellular carcinoma