Liver Cancer
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Oct 1, 2004; 10(19): 2785-2790
Published online Oct 1, 2004. doi: 10.3748/wjg.v10.i19.2785
Are gap junction gene connexins 26, 32 and 43 of prognostic values in hepatocellular carcinoma? A prospective study
I-Shyan Sheen, Kuo-Shyang Jeng, Po-Chuan Wang, Shou-Chuan Shih, Wen-Hsing Chang, Horng-Yuan Wang, Chung-Chu Chen, Li-Rung Shyung
I-Shyan Sheen, Division of Hepatogastroenterology, Chang Gung Memorial Hospital, Taipei, Taiwan, China
Kuo-Shyang Jeng, Departments of Surgery, Mackay Memorial Hospital, Taipei, Taiwan, China
Po-Chuan Wang, Shou-Chuan Shih, Wen-Hsing Chang, Horng-Yuan Wang, Chung-Chu Chen, Li-Rung Shyung, Department of Internal Medicine, Mackay Memorial Hospital, Taipei, Taiwan, China
Kuo-Shyang Jeng, Mackay Junior School of Nursing, Taipei, Taiwan, China
Author contributions: All authors contributed equally to the work.
Supported by grants from Department of Health, National Science Council, Executive Yuan, Taiwan, China NSC-89-2314-B-195-027
Correspondence to: Kuo-Shyang Jeng, M.D, F.A.C.S, Department of Surgery, Mackay Memorial Hospital, No.92, Sec 2,Chung-San North Road, Taipei, Taiwan, China. issheen.jks@msa.hinet.net
Telephone: +886-2-25433535 Fax: +886-2-27065704
Received: February 2, 2004
Revised: February 16, 2004
Accepted: February 23, 2004
Published online: October 1, 2004
Abstract

AIM: To investigate the prognostic value of the expression of connexin (Cx) 26, 32 and 43 messenger RNA (mRNA) in hepatocellular carcinoma (HCC) tissues.

METHODS: Using a reverse-transcriptase polymerase chain reaction (RT-PCR), Cx 26, Cx 32 and Cx 43 mRNAs were determined in the liver tissues of 15 controls and in HCC tissues of 25 patients undergoing curative hepatic resection. The patients were followed up clinically.

RESULTS: Cx 26 and Cx 32 mRNAs were significantly lower in HCC tissues compared with controls (both P < 0.01). By multivariate analysis, a lower level of Cx 26 and Cx 32 mRNA correlated significantly with a risk of HCC recurrence (P = 0.033) and recurrence-related mortality (P = 0.031, P = 0.031). Cx 43 mRNA was higher in HCC tissues compared with controls but did not correlate with postoperative recurrence or recurrence-related mortality. Other significant predictors of HCC recurrence included cellular dedifferentiation (P = 0.033), less encapsulation (P = 0.050), vascular permeation (P = 0.046), and daughter nodules (P = 0.046). Significant variables related to recurrence-related mortality consisted of cell dedifferentiation (P = 0.031), vascular permeation (P = 0.048), and daughter nodules (P = 0.048). The levels of Cx 26 and Cx 32 mRNAs correlated significantly with cell differentiation (P = 0.031).

CONCLUSION: A low expression of Cx 26 and Cx 32 mRNAs in HCC tissues is predictive of postoperative recurrence of HCCs.

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