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Combined CRISPRi/a-Based Chemical Genetic Screens Reveal that Rigosertib Is a Microtubule-Destabilizing Agent.

Molecular cell | 2017

Chemical libraries paired with phenotypic screens can now readily identify compounds with therapeutic potential. A central limitation to exploiting these compounds, however, has been in identifying their relevant cellular targets. Here, we present a two-tiered CRISPR-mediated chemical-genetic strategy for target identification: combined genome-wide knockdown and overexpression screening as well as focused, comparative chemical-genetic profiling. Application of these strategies to rigosertib, a drug in phase 3 clinical trials for high-risk myelodysplastic syndrome whose molecular target had remained controversial, pointed singularly to microtubules as rigosertib's target. We showed that rigosertib indeed directly binds to and destabilizes microtubules using cell biological, in vitro, and structural approaches. Finally, expression of tubulin with a structure-guided mutation in the rigosertib-binding pocket conferred resistance to rigosertib, establishing that rigosertib kills cancer cells by destabilizing microtubules. These results demonstrate the power of our chemical-genetic screening strategies for pinpointing the physiologically relevant targets of chemical agents.

Pubmed ID: 28985505 RIS Download

Associated grants

  • Agency: NCI NIH HHS, United States
    Id: U01 CA217882
  • Agency: NCI NIH HHS, United States
    Id: R00 CA204602
  • Agency: NCI NIH HHS, United States
    Id: K99 CA204602
  • Agency: NIBIB NIH HHS, United States
    Id: T32 EB009383
  • Agency: Howard Hughes Medical Institute, United States
  • Agency: NCI NIH HHS, United States
    Id: U01 CA168370
  • Agency: NCI NIH HHS, United States
    Id: K99 CA181494
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM007618
  • Agency: NIGMS NIH HHS, United States
    Id: F32 GM116331
  • Agency: NIGMS NIH HHS, United States
    Id: P50 GM102706
  • Agency: NIDA NIH HHS, United States
    Id: R01 DA036858

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