<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Feris EJ</submitter><funding>NCI NIH HHS</funding><pagination>2147-2157</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8522838</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(21)</volume><pubmed_abstract>Mechanism-based targeted therapies have exhibited remarkable success in treating otherwise untreatable or unresectable cancers. Novel targeted therapies that correct dysregulated transcriptional programs in cancer are an unmet medical need. The transcription factor MYC is the most frequently amplified gene in human cancer and is overexpressed because of mutations in an array of oncogenic signaling pathways. The fact that many cancer cells cannot survive without MYC - a phenomenon termed "MYC addiction" - provides a compelling case for the development of MYC-specific targeted therapies. We propose a new strategy to inhibit MYC function by disrupting its essential interaction with TRRAP using small molecules. To achieve our goal, we developed a platform using luminescence complementation for</pubmed_abstract><journal>Oncotarget</journal><pubmed_title>Luminescence complementation technology for the identification of MYC:TRRAP inhibitors.</pubmed_title><pmcid>PMC8522838</pmcid><funding_grant_id>P30 CA023108</funding_grant_id><funding_grant_id>R01 CA055248</funding_grant_id><pubmed_authors>Feris EJ</pubmed_authors><pubmed_authors>Cole MD</pubmed_authors><pubmed_authors>Hinds JW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Luminescence complementation technology for the identification of MYC:TRRAP inhibitors.</name><description>Mechanism-based targeted therapies have exhibited remarkable success in treating otherwise untreatable or unresectable cancers. Novel targeted therapies that correct dysregulated transcriptional programs in cancer are an unmet medical need. The transcription factor MYC is the most frequently amplified gene in human cancer and is overexpressed because of mutations in an array of oncogenic signaling pathways. The fact that many cancer cells cannot survive without MYC - a phenomenon termed "MYC addiction" - provides a compelling case for the development of MYC-specific targeted therapies. We propose a new strategy to inhibit MYC function by disrupting its essential interaction with TRRAP using small molecules. To achieve our goal, we developed a platform using luminescence complementation for</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2026-05-10T00:48:31.166Z</modification><creation>2025-04-04T12:03:19.757Z</creation></dates><accession>S-EPMC8522838</accession><cross_references><pubmed>34676047</pubmed><doi>10.18632/oncotarget.28078</doi></cross_references></HashMap>