Natural Products with Antitumor Potential targeting the MYB-C/EBPbeta-p300 Transcription Module

Schmidt TJ, Klempnauer K-H.

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

The transcription factor MYB is expressed predominantly in hematopoietic progenitor cells, where it plays an essential role in the development of most lineages of the hematopoietic system. In the myeloid lineage, MYB is known to cooperate with members of the CCAAT box/enhancer binding protein (C/EBP) family of transcription factors. MYB and C/EBPs interact with the co-activator p300 or its paralog CREB-binding protein (CBP), to form a transcriptional module involved in myeloid-specific gene expression. Recent work has demonstrated that MYB is involved in the development of human leukemia, especially in acute T-cell leukemia (T-ALL) and acute myeloid leukemia (AML). Chemical entities that inhibit the transcriptional activity of the MYB-C/EBPβ-p300 transcription module may therefore be of use as potential anti-tumour drugs. In searching for small molecule inhibitors, studies from our group over the last 10 years have identified natural products belonging to different structural classes, including various sesquiterpene lactones, a steroid lactone, quinone methide triterpenes and naphthoquinones that interfere with the activity of this transcriptional module in different ways. This review gives a comprehensive overview on the various classes of inhibitors and the inhibitory mechanisms by which they affect the MYB-C/EBPβ-p300 transcriptional module as a potential anti-tumor target. We also focus on the current knowledge on structure-activity relationships underlying these biological effects and on the potential of these compounds for further development.

Details zur Publikation

FachzeitschriftMolecules
Jahrgang / Bandnr. / Volume27
StatusVeröffentlicht
Veröffentlichungsjahr2022
Sprache, in der die Publikation verfasst istEnglisch
DOI10.3390/molecules27072077
Link zum Volltexthttps://www.mdpi.com/1420-3049/27/7/2077/html
Stichwörtertranscription factor; MYB; C/EBPβ; p300; cancer; leukemia; natural product; sesquiterpene lactone; withanolide; withaferin A; celastrol; naphthoquinone; plumbagin

Autor*innen der Universität Münster

Klempnauer, Karl-Heinz
Professur für Biochemie (Prof. Klempnauer)
Schmidt, Thomas
Professur für Pharmazeutische Biologie und Phytochemie (Prof. Schmidt)