TY - JOUR
T1 - Is the expression of γ-glutamyl transpeptidase messenger RNA an indicator of biological behavior in recurrent hepatocellular carcinoma?
AU - Sheen, I. Shyan
AU - Jeng, Kuo Shyang
AU - Tsai, Yi Chun
PY - 2003/3/1
Y1 - 2003/3/1
N2 - Aim: To investigate the correlation between gamma-glutamyl transpeptidase (γ-GTP) expression in the primary HCC and post-resection recurrence and its biological behaviors. Methods: Forty consecutive patients having curative resection for HCC were included in this study. The primers for reverse-transcription polymerase chain reaction (RT-PCR) were corresponding to the 5′-noncoding human γ-GTP mRNA of fetal liver (type A), HepG2 cells (type B), and placenta (type C). Both thetancef and non-cancerous tissues of the resected liver were analyzed. The correlations between the expression of γ-GTP and the clinicopathological variables and outcomes (recurrence and survival) were studied. Results: Those with type B γ-GTP mRNA in cancer had significant higher recurrence rate than those without it (63.6 % vs 14.3 %). Both those with type B in cancer and in non-cancer died significantly more than those without it (45.5 % vs 0 % and 53.6 % vs 0 %, respectively). By multivariate analysis, the significant predictors of recurrence included high serum AFP (P=0.0108), vascular permeation (P=0.0084), and type B γ-GTP mRNA in non-cancerous liver (P=0.0107). The significant predictors of post-recurrence death included high serum AFP (P=0.0141), vascular permeation (P=0.0130), and daughter nodules (P=0.0053). As to the manifestations (recurrent number ≧2, recurrent extent ≧2 segments, extra-hepatic metastasis, and death) in recurrent patient, there were no statistical significant differences between those with type B in the primary tumor and those without it. The difference between those with type B in non-cancerous liver and those without it also was not significant. Conclusion: Patients of HCC with type B γ-GTP mRNA both in cancer and in non-cancerous tissue had a worse outcome, earlier recurrence, and more post-recurrence death.
AB - Aim: To investigate the correlation between gamma-glutamyl transpeptidase (γ-GTP) expression in the primary HCC and post-resection recurrence and its biological behaviors. Methods: Forty consecutive patients having curative resection for HCC were included in this study. The primers for reverse-transcription polymerase chain reaction (RT-PCR) were corresponding to the 5′-noncoding human γ-GTP mRNA of fetal liver (type A), HepG2 cells (type B), and placenta (type C). Both thetancef and non-cancerous tissues of the resected liver were analyzed. The correlations between the expression of γ-GTP and the clinicopathological variables and outcomes (recurrence and survival) were studied. Results: Those with type B γ-GTP mRNA in cancer had significant higher recurrence rate than those without it (63.6 % vs 14.3 %). Both those with type B in cancer and in non-cancer died significantly more than those without it (45.5 % vs 0 % and 53.6 % vs 0 %, respectively). By multivariate analysis, the significant predictors of recurrence included high serum AFP (P=0.0108), vascular permeation (P=0.0084), and type B γ-GTP mRNA in non-cancerous liver (P=0.0107). The significant predictors of post-recurrence death included high serum AFP (P=0.0141), vascular permeation (P=0.0130), and daughter nodules (P=0.0053). As to the manifestations (recurrent number ≧2, recurrent extent ≧2 segments, extra-hepatic metastasis, and death) in recurrent patient, there were no statistical significant differences between those with type B in the primary tumor and those without it. The difference between those with type B in non-cancerous liver and those without it also was not significant. Conclusion: Patients of HCC with type B γ-GTP mRNA both in cancer and in non-cancerous tissue had a worse outcome, earlier recurrence, and more post-recurrence death.
UR - http://www.scopus.com/inward/record.url?scp=0037347973&partnerID=8YFLogxK
U2 - 10.3748/wjg.v9.i3.468
DO - 10.3748/wjg.v9.i3.468
M3 - 文章
C2 - 12632499
AN - SCOPUS:0037347973
SN - 1007-9327
VL - 9
SP - 468
EP - 473
JO - World Journal of Gastroenterology
JF - World Journal of Gastroenterology
IS - 3
ER -