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Volumn 324, Issue 5933, 2009, Pages 1457-1461

Inhibition of Hedgehog signaling enhances delivery of chemotherapy in a mouse model of pancreatic cancer

(37)  Olive, Kenneth P a   Jacobetz, Michael A a   Davidson, Christian J b   Gopinathan, Aarthi a,b   McIntyre, Dominick a   Honess, Davina a   Madhu, Basetti a   Goldgraben, Mae A a   Caldwell, Meredith E a   Allard, David a   Frese, Kristopher K a   DeNicola, Gina a,b   Feig, Christine a   Combs, Chelsea b   Winter, Stephen P a   Ireland Zecchini, Heather a   Reichelt, Stefanie a   Howat, William J a   Chang, Alex c   Dhara, Mousumi c   more..


Author keywords

[No Author keywords available]

Indexed keywords

ALPHA SMOOTH MUSCLE ACTIN; CD31 ANTIGEN; CYCLOPAMINE; DOXORUBICIN; GADOLINIUM; GEMCITABINE; IPI 926; LIPOSOME; MESSENGER RNA; PENTETIC ACID; PLANT LECTIN; SMOOTHENED PROTEIN; SONIC HEDGEHOG PROTEIN; UNCLASSIFIED DRUG; VASCULOTROPIN;

EID: 67149143399     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1171362     Document Type: Article
Times cited : (2628)

References (29)
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    • We thank the animal care staffs of the Cambridge Research Institute (CRI, University of Pennsylvania Translational Research Labs, FHCRC, and University Hospital Dresden as well as the histology and genomics cores at CRI, and P. Calses for technical assistance. We also thank B. Bean of Transnetyx Inc. for developing high-throughput genotyping assays for the KPC mice. This research was supported by the Lustgarten Foundation, the University of Cambridge and Cancer Research UK, The Li Ka Shing Foundation and Hutchison Whampoa Limited, the National Institute for Health Research Cambridge Biomedical Research Centre, and NIH grants CA101973, CA111292, CA084291, and CA105490 to D.A.T, K08 CA106610 to C.I.-D, and CA15704 and CA114028 to S.R.H, S.R.H. was supported by a grant from the Mead Foundation. Preliminary studies were supported by a grant from the University of Pennsylvania/GlaxoSmithKline Alternative Drug Discovery Initiative. K.P.O. and K.K.F. were supported by NIH under Ruth L
    • We thank the animal care staffs of the Cambridge Research Institute (CRI), University of Pennsylvania Translational Research Labs, FHCRC, and University Hospital Dresden as well as the histology and genomics cores at CRI, and P. Calses for technical assistance. We also thank B. Bean of Transnetyx Inc. for developing high-throughput genotyping assays for the KPC mice. This research was supported by the Lustgarten Foundation, the University of Cambridge and Cancer Research UK, The Li Ka Shing Foundation and Hutchison Whampoa Limited, the National Institute for Health Research Cambridge Biomedical Research Centre, and NIH (grants CA101973, CA111292, CA084291, and CA105490 to D.A.T.; K08 CA106610 to C.I.-D.; and CA15704 and CA114028 to S.R.H.). S.R.H. was supported by a grant from the Mead Foundation. Preliminary studies were supported by a grant from the University of Pennsylvania/GlaxoSmithKline Alternative Drug Discovery Initiative. K.P.O. and K.K.F. were supported by NIH under Ruth L. Kirschstein National Research Service Awards F32CA123939-02 (K.P.O.) and F32CA123887-01 (K.K.F.). In addition to being an officer of Infinity Pharmaceuticals, J.A. is a member of the Senior Advisory Boards of Constellation Pharma and Auspex Pharma. Cancer Research Technology, which is associated with Cancer Research UK, has filed a U.S. provisional patent application related to this work.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.