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|Therapy Name||BAZ2-ICR + JQ1|
|Drug Name||Trade Name||Synonyms||Drug Classes||Drug Description|
|BAZ2-ICR||BAZ2-ICR is a selective BAZ2A and BAZ2B bromodomain inhibitor, which has potential antitumor activity (PMID: 25719566, PMID: 31000582).|
|JQ1||JQ-1||BET Inhibitor (Pan) 30||JQ1 is a BET bromodomain inhibitor with greatest specificity towards BRD4, resulting in decreased Myc expression, increased cell death, reduced macrophage immunosuppression, and inhibition of tumor growth (PMID: 24231268, PMID: 31018997, PMID: 30906568, PMID: 32800944).|
|Molecular Profile||Indication/Tumor Type||Response Type||Therapy Name||Approval Status||Evidence Type||Efficacy Evidence||References|
|Unknown unknown||triple-receptor negative breast cancer||not applicable||BAZ2-ICR + JQ1||Preclinical - Cell culture||Actionable||In a preclinical study, BAZ2-ICR and JQ1 combination treatment inhibited Rb1 phosphorylation, and induced moderate growth inhibition and cellular senescence in triple-negative breast cancer cell lines in culture (PMID: 31000582).||31000582|
|Clinical Trial||Phase||Therapies||Title||Recruitment Status|