Disruption of TFIIH activities generates a stress gene expression response and reveals possible new targets against cancer.
Ontology highlight
ABSTRACT: Disruption of the enzymatic activities of the transcription factor TFIIH by the small molecules Triptolide (TPL) or THZ1 could be used against cancer. Here, we used the MCF10A-ErSrc oncogenesis model to compare the effect of TFIIH inhibitors between transformed cells and their progenitors. We report that tumour cells exhibited highly increased sensitivity to TPL or THZ1 and that the combination of both had a synergic effect. TPL affects the interaction between XPB and p52, causing a reduction in the levels of XPB, p52 and p8, but not other TFIIH subunits. RNA-Seq and RNAPII-ChIP-Seq experiments showed that although the levels of many transcripts were reduced, the levels of a significant number were increased after TPL treatment, with maintained or increased RNAPII promoter occupancy. A sig
SUBMITTER: Uriostegui-Arcos M
PROVIDER: S-EPMC7333893 | biostudies-literature | 2020 Jun
REPOSITORIES: biostudies-literature
ACCESS DATA