Literature DB >> 21041712

Clinical experience with Hedgehog pathway inhibitors.

Jennifer A Low1, Frederic J de Sauvage.   

Abstract

The Hedgehog (Hh) signaling pathway is critical for cell growth and differentiation during embryogenesis and early development. While it is mostly quiescent in adults, inappropriate reactivation of the Hh pathway has been shown to be involved in the development of cancer. A number of tumor types rely on overexpression of Hh ligands to activate the pathway in a paracrine manner from the tumor to the surrounding stroma. Alternatively, Hh ligands may act on cancer stem cells in some hematopoietic cancers, such as chronic myelogenous leukemia. However, the role of the Hh pathway is best established in tumors, such as basal cell carcinoma and medulloblastoma, where the pathway is activated via mutations. Understanding the contribution of Hh signaling in these various tumor types will be critical to the development and use of agents targeting this pathway in the clinic. We review here the activity of clinical inhibitors of the Hh pathway, including GDC-0449, a small molecule inhibitor of Smoothened (SMO).

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Year:  2010        PMID: 21041712     DOI: 10.1200/JCO.2010.27.9943

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  78 in total

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4.  High expression of the transcriptional coactivator TAZ is associated with a worse prognosis and affects cell proliferation in patients with medulloblastoma.

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Authors:  Philip W Ingham; Yoshiro Nakano; Claudia Seger
Journal:  Nat Rev Genet       Date:  2011-04-19       Impact factor: 53.242

7.  The Hedgehog pathway effector smoothened exhibits signaling competency in the absence of ciliary accumulation.

Authors:  Chih-Wei Fan; Baozhi Chen; Irene Franco; Jianming Lu; Heping Shi; Shuguang Wei; Changguang Wang; Xiaofeng Wu; Wei Tang; Michael G Roth; Noelle S Williams; Emilio Hirsch; Chuo Chen; Lawrence Lum
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8.  Genome sequencing of SHH medulloblastoma predicts genotype-related response to smoothened inhibition.

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Journal:  Cancer Cell       Date:  2014-03-17       Impact factor: 31.743

9.  p53 modulates the activity of the GLI1 oncogene through interactions with the shared coactivator TAF9.

Authors:  Joon Won Yoon; Marilyn Lamm; Stephen Iannaccone; Nicole Higashiyama; King Fu Leong; Philip Iannaccone; David Walterhouse
Journal:  DNA Repair (Amst)       Date:  2015-08-01

10.  Identification of a novel Smoothened antagonist that potently suppresses Hedgehog signaling.

Authors:  Jiangbo Wang; Robert A Mook; Jiuyi Lu; David M Gooden; Anthony Ribeiro; Anchen Guo; Larry S Barak; H Kim Lyerly; Wei Chen
Journal:  Bioorg Med Chem       Date:  2012-09-23       Impact factor: 3.641

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