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

Schmidt TJ, Klempnauer K-H.

Research article (journal) | Peer reviewed

Abstract

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 about the publication

JournalMolecules
Volume27
StatusPublished
Release year2022
Language in which the publication is writtenEnglish
DOI10.3390/molecules27072077
Link to the full texthttps://www.mdpi.com/1420-3049/27/7/2077/html
Keywordstranscription factor; MYB; C/EBPβ; p300; cancer; leukemia; natural product; sesquiterpene lactone; withanolide; withaferin A; celastrol; naphthoquinone; plumbagin

Authors from the University of Münster

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