吉西他滨
胰腺癌
化疗
癌症研究
间质细胞
药物输送
癌症
刺猬
刺猬信号通路
药品
胰腺导管腺癌
腺癌
内科学
医学
药理学
生物
信号转导
化学
细胞生物学
有机化学
作者
Kenneth P. Olive,Michael A. Jacobetz,Christian J. Davidson,Aarthi Gopinathan,Dominick J. O. McIntyre,Davina J. Honess,Basetti Madhu,Mae A. Goldgraben,Meredith E. Caldwell,David Allard,Kristopher K. Frese,Gina M. DeNicola,Christine Feig,Chelsea Combs,Stephen P. Winter,Heather Ireland‐Zecchini,Stefanie Reichelt,William Howat,Alex Chang,Mousumi Dhara
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2009-05-21
卷期号:324 (5933): 1457-1461
被引量:3134
标识
DOI:10.1126/science.1171362
摘要
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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