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Neovascular Prostate-Specific Membrane Antigen Expression Is Associated with Improved Overall Survival under Palliative Chemotherapy in Patients with Pancreatic Ductal Adenocarcinoma

Authors :
Rebekka Wiesch
Konrad Steinestel
Jan Sperveslage
Marcel Trautmann
Wolfgang Hartmann
Sebastian Huss
Jan-Henrik Mikesch
Nora Beller
Jan Rehkämper
Birthe Heitkötter
Katharina Stock
Eva Wardelmann
Anna Hansmeier
Source :
BioMed Research International, Vol 2017 (2017), BioMed Research International
Publication Year :
2017
Publisher :
Hindawi Limited, 2017.

Abstract

Aims. Expression of PSMA (prostate-specific membrane antigen) has been demonstrated in various cancers, including pancreatic ductal adenocarcinoma (PDAC). However, PSMA expression in PDAC-associated neovasculature has so far not been systematically analyzed.Methods and Results. We analyzed PSMA expression in 81 PDAC tissue samples from 61 patients. Microvessel density (MVD) was assessed by software-based image analysis and showed a mean MVD of 63.7 microvessels/0.785 mm2. PSMA was practically absent in tumor tissue (5.3%) and PDAC cell lines (0/7) but could be detected in tumor-associated neovasculature in 53.2% of cases. There was no association between neovascular PSMA expression and clinicopathological tumor characteristics. Samples with PSMA+ neovasculature showed increased MVD; however, this result was not statistically significant (p>0.05). Presence of PSMA+ neovessels correlated with overall survival under palliative chemotherapy (894 versus 400 days; HR 0.42; 95% CI: 0.12 to 0.87;p<0.05).Conclusion. PSMA expression in tumor-associated neovasculature is a common feature and associated with improved overall survival under palliative chemotherapy in PDAC. Our results point towards a possible association between PSMA expression and response to therapy which might be based on enhanced intratumoral bioavailability of systemic chemotherapy.

Details

ISSN :
23146141 and 23146133
Volume :
2017
Database :
OpenAIRE
Journal :
BioMed Research International
Accession number :
edsair.doi.dedup.....13bbd2a126ab6d5178df59f2b7fe2b53