| Literature DB >> 24684846 |
Marie Morfouace1, Anang Shelat2, Megan Jacus3, Burgess B Freeman4, David Turner3, Sarah Robinson1, Frederique Zindy1, Yong-Dong Wang5, David Finkelstein5, Olivier Ayrault6, Laure Bihannic6, Stephanie Puget7, Xiao-Nan Li8, James M Olson9, Giles W Robinson10, R Kiplin Guy2, Clinton F Stewart3, Amar Gajjar10, Martine F Roussel11.
Abstract
We devised a high-throughput, cell-based assay to identify compounds to treat Group3 medulloblastoma (G3 MB). Mouse G3 MBs neurospheres were screened against a library of approximately 7,000 compounds including US Food and Drug Administration-approved drugs. We found that pemetrexed and gemcitabine preferentially inhibited G3 MB proliferation in vitro compared to control neurospheres and substantially inhibited G3 MB proliferation in vivo. When combined, these two drugs significantly increased survival of mice bearing cortical implants of mouse and human G3 MBs that overexpress MYC compared to each agent alone, while having little effect on mouse MBs of the sonic hedgehog subgroup. Our findings strongly suggest that combination therapy with pemetrexed and gemcitabine is a promising treatment for G3 MBs.Entities:
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Year: 2014 PMID: 24684846 PMCID: PMC3994669 DOI: 10.1016/j.ccr.2014.02.009
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743