Identification of small molecule inhibitors of USP15
Identification of small molecule inhibitors of USP15
批准号:
10919690
负责人:
Anton Simeonov
金额:
$24.08万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
Biological AssayBiological ProcessDevelopmentDiseaseEukaryotaExcisionFamilyGenesGlioblastomaHumanInflammatoryKnockout MiceLeadMachine LearningMalignant NeoplasmsMalignant neoplasm of ovaryNF-kappa BNeurodegenerative DisordersPathway interactionsPlayPost-Translational Protein ProcessingProteinsRoleSignal PathwayStructureT-Cell ActivationTP53 geneTestingTransforming Growth Factor betaUbiquitinUbiquitinationVirus DiseasesWorkbeta catenincancer immunotherapycancer typecolon cancer cell linehigh throughput screeninghuman diseasein silicoinhibitorinterestmalignant breast neoplasmmelanomamouse modeloverexpressionprospectivescreeningsmall moleculesmall molecule inhibitortumorigenesisubiquitin isopeptidaseubiquitin-specific protease
中文摘要
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英文摘要
Given USP15s role in tumorigenesis and T cell activation, USP15 is a promising target for cancer and cancer immunotherapy. Identification of USP15-specific small-molecule inhibitors through a quantitative high-throughput screening and further development of the lead compound could not only open new strategies to tackle cancer, but allow to better understand biological functions of USP15.
During this period, the project team worked to validate small molecule hits from the previously completed high-throughput screen. Using activity profiles from the orthogonal assays tested against the screening hits, the team employed a machine learning approach to conduct an in silico screen against an additional 100,000 small molecules to extend the number of prospective chemotypes with inhibitory activity against USP15.
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