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Published in: Cellular Oncology 6/2011

01-12-2011 | Original Paper

Characterization of human pancreatic orthotopic tumor xenografts suitable for drug screening

Authors: Sandra Pérez-Torras, Anna Vidal-Pla, Rosa Miquel, Vanessa Almendro, Laureano Fernández-Cruz, Salvador Navarro, Joan Maurel, Neus Carbó, Pere Gascón, Adela Mazo

Published in: Cellular Oncology | Issue 6/2011

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Abstract

Background

Efforts to identify novel therapeutic options for human pancreatic ductal adenocarcinoma (PDAC) have failed to result in a clear improvement in patient survival to date. Pancreatic cancer requires efficient therapies that must be designed and assayed in preclinical models with improved predictor ability. Among the available preclinical models, the orthotopic approach fits with this expectation, but its use is still occasional.

Methods

An in vivo platform of 11 orthotopic tumor xenografts has been generated by direct implantation of fresh surgical material. In addition, a frozen tumorgraft bank has been created, ensuring future model recovery and tumor tissue availability.

Results

Tissue microarray studies allow showing a high degree of original histology preservation and maintenance of protein expression patterns through passages. The models display stable growth kinetics and characteristic metastatic behavior. Moreover, the molecular diversity may facilitate the identification of tumor subtypes and comparison of drug responses that complement or confirm information obtained with other preclinical models.

Conclusions

This panel represents a useful preclinical tool for testing new agents and treatment protocols and for further exploration of the biological basis of drug responses.
Appendix
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Metadata
Title
Characterization of human pancreatic orthotopic tumor xenografts suitable for drug screening
Authors
Sandra Pérez-Torras
Anna Vidal-Pla
Rosa Miquel
Vanessa Almendro
Laureano Fernández-Cruz
Salvador Navarro
Joan Maurel
Neus Carbó
Pere Gascón
Adela Mazo
Publication date
01-12-2011
Publisher
Springer Netherlands
Published in
Cellular Oncology / Issue 6/2011
Print ISSN: 2211-3428
Electronic ISSN: 2211-3436
DOI
https://doi.org/10.1007/s13402-011-0049-1

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