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GPC-1 may serve as a predictor of perineural invasion and a prognosticator of survival in pancreatic cancer.

Authors :
Duan L
Hu XQ
Feng DY
Lei SY
Hu GH
Source :
Asian journal of surgery [Asian J Surg] 2013 Jan; Vol. 36 (1), pp. 7-12. Date of Electronic Publication: 2012 Sep 16.
Publication Year :
2013

Abstract

Objective: The purpose of this study was to investigate the expression of glial cell derived neurotrophic factor (GDNF), glypican-1 (GPC-1), and matrix metalloproteinase-9 (MMP-9), and their association with clinicopathologic characteristics as well as prognostic significance in pancreatic cancer.<br />Methods: Immunohistochemical assessment of GDNF, GPC-1, and MMP-9 was performed in 62 cases of surgically resected pancreatic cancer. Perineural invasion in pancreatic cancer was observed by marking nerve fiber with S-100, while 16 normal pancreatic tissues were used as normal control. Correlations of GDNF, GPC-1 and MMP-9 expressions with clinicopathologic parameters were analyzed. A survival analysis was performed to find the prognostic significance.<br />Results: The expressions of GDNF, GPC-1 and MMP-9 in pancreatic cancer tissue were significantly higher than of those in normal pancreatic tissues (41/62 vs. 5/16 for GDNF, 35/62 vs. 2/16 for GPC-1, and 37/62 vs. 3/16 for MMP-9; p<0.01, respectively). The overexpression of GDNF, GPC-1, and MMP-9 in pancreatic cancer tissue was significantly related to the perineural invasion (p<0.05). Although the overexpression of these genes was related to poor survival, GPC-1 had an independent prognostic effect on overall survival.<br />Conclusion: GPC-1 is significantly related to the perineural invasion of pancreatic cancer, holding some prognostic significance in patients with pancreatic cancer.<br /> (Copyright © 2012. Published by Elsevier B.V.)

Details

Language :
English
ISSN :
0219-3108
Volume :
36
Issue :
1
Database :
MEDLINE
Journal :
Asian journal of surgery
Publication Type :
Academic Journal
Accession number :
23270819
Full Text :
https://doi.org/10.1016/j.asjsur.2012.08.001