4.8 Article

Inhibition of Hedgehog Signaling Enhances Delivery of Chemotherapy in a Mouse Model of Pancreatic Cancer

Journal

SCIENCE
Volume 324, Issue 5933, Pages 1457-1461

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1171362

Keywords

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Funding

  1. Lustgarten Foundation
  2. University of Cambridge
  3. Cancer Research UK
  4. The Li Ka Shing Foundation
  5. Hutchison Whampoa Limited
  6. National Institute for Health Research Cambridge Biomedical Research Centre
  7. NIH [CA101973, CA111292, CA084291, CA105490, K08 CA106610, CA15704, CA114028, F32CA123939-02, F32CA123887-01]
  8. Mead Foundation
  9. University of Pennsylvania GlaxoSmithKline Alternative Drug Discovery Initiative

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Pancreatic ductal adenocarcinoma (PDA) is among the most lethal human cancers in part because it is insensitive to many chemotherapeutic drugs. Studying a mouse model of PDA that is refractory to the clinically used drug gemcitabine, we found that the tumors in this model were poorly perfused and poorly vascularized, properties that are shared with human PDA. We tested whether the delivery and efficacy of gemcitabine in the mice could be improved by coadministration of IPI-926, a drug that depletes tumor-associated stromal tissue by inhibition of the Hedgehog cellular signaling pathway. The combination therapy produced a transient increase in intratumoral vascular density and intratumoral concentration of gemcitabine, leading to transient stabilization of disease. Thus, inefficient drug delivery may be an important contributor to chemoresistance in pancreatic cancer.

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