| Literature DB >> 27325686 |
Allison E Cherry1, Brian R Haas1, Alipi V Naydenov2, Susan Fung2, Cong Xu1, Katie Swinney1, Michael Wagenbach3, Jennifer Freeling4, David A Canton5, Jonathan Coy1, Eric A Horne1, Barry Rickman6, Juan Jesus Vicente3, John D Scott5, Rodney J Y Ho4, Denny Liggitt6, Linda Wordeman3, Nephi Stella7.
Abstract
Glioblastoma multiforme is a devastating and intractable type of cancer. Current antineoplastic drugs do not improve the median survival of patients diagnosed with glioblastoma multiforme beyond 14 to 15 months, in part because the blood-brain barrier is generally impermeable to many therapeutic agents. Drugs that target microtubules (MT) have shown remarkable efficacy in a variety of cancers, yet their use as glioblastoma multiforme treatments has also been hindered by the scarcity of brain-penetrant MT-targeting compounds. We have discovered a new alkylindole compound, ST-11, that acts directly on MTs and rapidly attenuates their rate of assembly. Accordingly, ST-11 arrests glioblastoma multiforme cells in prometaphase and triggers apoptosis. In vivo analyses reveal that unlike current antitubulin agents, ST-11 readily crosses the blood-brain barrier. Further investigation in a syngeneic orthotopic mouse model of glioblastoma multiforme shows that ST-11 activates caspase-3 in tumors to reduce tumor volume without overt toxicity. Thus, ST-11 represents the first member of a new class of brain-penetrant antitubulin therapeutic agents. Mol Cancer Ther; 15(9); 2018-29. ©2016 AACR. ©2016 American Association for Cancer Research.Entities:
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Year: 2016 PMID: 27325686 PMCID: PMC5010991 DOI: 10.1158/1535-7163.MCT-15-0800
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.261