TY - JOUR
T1 - Stromal galectin-1 expression is associated with long-term survival in resectable pancreatic ductal adenocarcinoma
AU - Chen, Ru
AU - Pan, Sheng
AU - Ottenhof, Niki A.
AU - De Wilde, Roeland F.
AU - Wolfgang, Christopher L.
AU - Lane, Zhaoli
AU - Post, Jane
AU - Bronner, Mary P.
AU - Willmann, Jürgen K.
AU - Maitra, Anirban
AU - Brentnall, Teresa A.
N1 - Funding Information:
We thank Dr Ralph H. Hruban for his assistance with histopathology of the Johns Hopkins cases. We are grateful to the Proteomics Shared Resource Lab at Fred Hutchinson Cancer Research Center for the mass spectrometric analysis. This study was support in part with federal funds from the National Institutes of Health under grants R01CA107209, K07CA116296, K25CA137222, R01DK081368, R21CA161575, R21CA149772, P50CA062924, P01CA134292 and R01CA113669; and funding from Mary Ann Walters Pancreatic Cancer Foundation.
PY - 2012/8
Y1 - 2012/8
N2 - The overall 5-year survival rate for pancreatic ductal adenocarcinoma (i.e., PDAC) is a dismal 5%, although patients that have undergone surgical resection have a somewhat better survival rate of up to 20%. Very long-term survivors of PDAC (defined as patients with ≥ 10 year survival following apparently curative resection), on the other hand, are considerably less frequent. The molecular characteristics of very long-term survivors (VLTS) are poorly understood, but might provide novel insights into prognostication for this disease. In this study, a panel of five VLTS and stage-matched short-term survivors (STS, defined as disease-specific mortality within 14 months of resection) were identified, and quantitative proteomics was applied to comparatively profile tumor tissues from both cohorts. Differentially expressed proteins were identified in cancers from VLTS vs. STS patients. Specifically, the expression of galectin-1 was 2-fold lower in VLTS compared with STS tumors. Validation studies were performed by immunohistochemistry (IHC) in two additional cohorts of resected PDAC, including: (1) an independent cohort of VLTS and (2) a panel of sporadic PDAC with a considerable range of overall survival following surgery. Immunolabeling analysis confirmed that significantly lower expression of stromal galectin-1 was associated with VLTS (p = 0.02) and also correlated with longer survival in sporadic, surgically-treated PDAC cases (hazard ratio = 4.9, p = 0.002). The results from this study provide new insights to better understand the role of galectin-1 in PDAC survival, and might be useful for rendering prognostic information, and developing more effective therapeutic strategies aimed at improving survival.
AB - The overall 5-year survival rate for pancreatic ductal adenocarcinoma (i.e., PDAC) is a dismal 5%, although patients that have undergone surgical resection have a somewhat better survival rate of up to 20%. Very long-term survivors of PDAC (defined as patients with ≥ 10 year survival following apparently curative resection), on the other hand, are considerably less frequent. The molecular characteristics of very long-term survivors (VLTS) are poorly understood, but might provide novel insights into prognostication for this disease. In this study, a panel of five VLTS and stage-matched short-term survivors (STS, defined as disease-specific mortality within 14 months of resection) were identified, and quantitative proteomics was applied to comparatively profile tumor tissues from both cohorts. Differentially expressed proteins were identified in cancers from VLTS vs. STS patients. Specifically, the expression of galectin-1 was 2-fold lower in VLTS compared with STS tumors. Validation studies were performed by immunohistochemistry (IHC) in two additional cohorts of resected PDAC, including: (1) an independent cohort of VLTS and (2) a panel of sporadic PDAC with a considerable range of overall survival following surgery. Immunolabeling analysis confirmed that significantly lower expression of stromal galectin-1 was associated with VLTS (p = 0.02) and also correlated with longer survival in sporadic, surgically-treated PDAC cases (hazard ratio = 4.9, p = 0.002). The results from this study provide new insights to better understand the role of galectin-1 in PDAC survival, and might be useful for rendering prognostic information, and developing more effective therapeutic strategies aimed at improving survival.
KW - Galectin-1/galectin 1
KW - Long-term
KW - Pancreatic ductal adenocarcinoma/PDAC
KW - Prognosis
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=84864549889&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84864549889&partnerID=8YFLogxK
U2 - 10.4161/cbt.20842
DO - 10.4161/cbt.20842
M3 - Article
C2 - 22785208
AN - SCOPUS:84864549889
SN - 1538-4047
VL - 13
SP - 899
EP - 907
JO - Cancer Biology and Therapy
JF - Cancer Biology and Therapy
IS - 10
ER -