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|Therapy Name||E7107 + MS023|
|Drug Name||Trade Name||Synonyms||Drug Classes||Drug Description|
|E7107||E7107 is a derivative of Pladienolide D, which inhibits assembly of the spliceosome specifically by binding to SF3B1, thereby inhibiting splicing of pre-mRNA and cell-cycle progression (PMID: 27622333).|
|MS023||MS023 inhibits type I protein arginine methyltransferases (PRMTs), which may lead to anti-tumor activity (PMID: 26598975).|
|Molecular Profile||Indication/Tumor Type||Response Type||Therapy Name||Approval Status||Evidence Type||Efficacy Evidence||References|
|KMT2A - MLLT3||acute myeloid leukemia||sensitive||E7107 + MS023||Preclinical - Cell culture||Actionable||In a preclinical study, MS023 and E7107 synergistically inhibited survival of murine KMT2A-MLLT3 (reported as MLL-AF9)-driven acute myeloid leukemia cells in culture, regardless of SRSF2 mutation status (PMID: 31408619).||31408619|
|Clinical Trial||Phase||Therapies||Title||Recruitment Status|