Glypican-3 expression and its relationship with recurrence of HCC after liver transplantation
AIM: To investigate the diagnostic value of glypican-3 (GPC3) and its relationship with hepatocellular carci- noma (HCC) recurrence after liver transplantation. METHODS: HCC tissue samples (n = 31) obtained from patients who had undergone liver transplantation were analyzed. GPC3 mRNA and protein ex...
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Published in | World journal of gastroenterology : WJG Vol. 18; no. 19; pp. 2408 - 2414 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Baishideng Publishing Group Co., Limited
21.05.2012
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Subjects | |
Online Access | Get full text |
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Summary: | AIM: To investigate the diagnostic value of glypican-3 (GPC3) and its relationship with hepatocellular carci- noma (HCC) recurrence after liver transplantation.
METHODS: HCC tissue samples (n = 31) obtained from patients who had undergone liver transplantation were analyzed. GPC3 mRNA and protein expression were analyzed by TaqMan real-time reverse transcription-polymerase chain reaction and immunohistochemistry. Correlation between the GPC3 expression and clinicopathological features was analyzed. The potential prognostic value of GPC3 was investigated by comparing recurrence-free survival between HCC patients with and without GPC3 expression.
RESULTS: Using a cutoff value of 3.5× 10^-2, 20 of 31 cancerous tissues had expression values of 〉 3.5× 10^2, whereas 3 of 31 adjacent non-neoplastic paren-chyma and 0 of 20 control liver tissues had expression values of 〉 3.5 × 10^-2 (P 〈 0.001). GPC3 protein was immunoexpressed in 68% of cancerous tissues, but not in adjacent non-neoplastic parenchyma and control liver tissues. Vascular invasion was significantly related to GPC3 expression (P 〈 0.05). Recurrence-free sur- vival was significantly longer for patients without GPC3 mRNA overexpression (〉 3.5 × 10^2) and those without vascular invasion (P 〈 0.05 for both).
CONCLUSION: GPC3 expression may serve as a valuable diagnostic marker for HCC. GPC3 mRNA overexpression may be an adverse indicator for HCC patients after liver transplantation. |
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Bibliography: | 14-1219/R AIM: To investigate the diagnostic value of glypican-3 (GPC3) and its relationship with hepatocellular carci- noma (HCC) recurrence after liver transplantation. METHODS: HCC tissue samples (n = 31) obtained from patients who had undergone liver transplantation were analyzed. GPC3 mRNA and protein expression were analyzed by TaqMan real-time reverse transcription-polymerase chain reaction and immunohistochemistry. Correlation between the GPC3 expression and clinicopathological features was analyzed. The potential prognostic value of GPC3 was investigated by comparing recurrence-free survival between HCC patients with and without GPC3 expression. RESULTS: Using a cutoff value of 3.5× 10^-2, 20 of 31 cancerous tissues had expression values of 〉 3.5× 10^2, whereas 3 of 31 adjacent non-neoplastic paren-chyma and 0 of 20 control liver tissues had expression values of 〉 3.5 × 10^-2 (P 〈 0.001). GPC3 protein was immunoexpressed in 68% of cancerous tissues, but not in adjacent non-neoplastic parenchyma and control liver tissues. Vascular invasion was significantly related to GPC3 expression (P 〈 0.05). Recurrence-free sur- vival was significantly longer for patients without GPC3 mRNA overexpression (〉 3.5 × 10^2) and those without vascular invasion (P 〈 0.05 for both). CONCLUSION: GPC3 expression may serve as a valuable diagnostic marker for HCC. GPC3 mRNA overexpression may be an adverse indicator for HCC patients after liver transplantation. Liver transplantation; Hepatocellular carci-noma; Glypican-3; mRNA; Recurrence ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Telephone: +86-22-23626622 Fax: +86-22-23626622 Author contributions: Shen ZY designed the study; Wang YL, Teng DH, and Gao W undertook research; Zhu ZJ, and Yao Z analyzed data; Wang YL was responsible for the review of the literature and wrote the manuscript. Correspondence to: Zhong-Yang Shen, MD, PhD, Department of Transplantation Surgery, Tianjin First Central Hospital, Key Laboratory for Critical Care Medicine of the Ministry of Health, Nankai District, 24 Fukang Road, Tianjin 300192, China. zhongyangshen@gmail.com |
ISSN: | 1007-9327 2219-2840 |
DOI: | 10.3748/wjg.v18.i19.2408 |