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Molecular changes in pancreatic cancer : implications for molecular targeting therapy

Journal Volume 75 - 2012
Issue Fasc.2 - Case series
Author(s) P. Demetter, R. Maréchal, L. Verset, I. Salmon, J.-B. Bachet, J.-L. Van Laethem
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Departments of (1) Pathology and (2) Gastroenterology, Erasme University Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium ; (3) Department of Gastroenterology, Hôpital Pitié Salpêtrière, Paris, France.

Pancreatic ductal adenocarcinoma has a high mortality rate, which is generally related to the initial diagnosis coming at late stage disease combined with a lack of effective treatment options. Gemcitabine has been the most commonly used drug over the past decade and is still the cornerstone of therapy in adjuvant and metastatic settings. Intrinsic or acquired resistance of tumours to gemcitabine is, however, a major clinical problem. New therapeu- tic strategies are urgently needed whereas we also need to identify new prognostic and predictive biomarkers. This article focuses on gemcitabine resistance, on the role of chemokines and chemokine receptors in pancreatic carcinoma initiation and progression, and on stellate cells as partners in crime with neoplastic epithelial cells. (Acta gastroenterol. belg., 2012, 75, 210-214).

© Acta Gastro-Enterologica Belgica.
PMID 22870784