Abstract
Galectin-3 influences neoangiogenesis, tumor cell adhesion, and tumor-immune-escape mechanisms. Hence, the expression of galectin-3 in pancreatic ductal adenocarcinoma (PDAC) was evaluated. Galectin-3 expression in PDAC cell lines was proven by the presence of intracellular protein and by release into the supernatant. Furthermore, galectin-3 was found in the majority of human tissue samples. Serum concentrations of galectin-3 in PDAC patients did not differ significantly from healthy donors and did not correlate with established tumor markers. In conclusion, galectin-3 is expressed in PDAC tissues suggesting a role in tumor development; however, no relationship between expression and clinical findings could be established.
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Abbreviations
- CEA:
-
Carcinoembryonic antigen
- CPB:
-
Cyclophylin B
- H&E:
-
Haematoxylin and eosin
- IQR:
-
Interquartile range
- PBS:
-
Phosphate-buffered saline
- PDAC:
-
Pancreatic ductal adenocarcinoma
- TMA:
-
Tissue microarray
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Acknowledgements
We thank Birgit Prior, Institute of Immunology, University of Heidelberg and Sarah Messnard, Institute of Pathology, University of Heidelberg for excellent technical support. We also thank Thomas Giese, Institute of Immunology, University of Heidelberg for performing quantitative RT-PCR.
Part of this work has been financially supported by a grant of the “Heidelberg Surgery Foundation” to G.M.H. and M.N.W. All authors declare that they have no conflict of interest to disclose.
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Gaida, M.M., Bach, S.T., Günther, F. et al. Expression of Galectin-3 in Pancreatic Ductal Adenocarcinoma. Pathol. Oncol. Res. 18, 299–307 (2012). https://doi.org/10.1007/s12253-011-9444-1
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DOI: https://doi.org/10.1007/s12253-011-9444-1