Inhibition of the acetyltransferases p300 and CBP reveals a targetable function for p300 in the survival and invasion pathways of prostate cancer cell lines
Santer,F.R.; Höschele,P.P.; Oh,S.J.; Erb,H.H.; Bouchal,J.; Cavarretta,I.T.; Parson,W.; Meyers,D.J.; Cole,P.A.; Culig,Z.;
Inhibitors of histone deacetylases have been approved for clinical application in cancer treatment. On the other hand, histone acetyltransferase (HAT) inhibitors have been less extensively investigated for their potential use in cancer therapy. In prostate cancer, the HATs and coactivators p300 and CBP are upregulated and may induce transcription of androgen receptor (AR)-responsive genes, even in the absence or presence of low levels of AR.
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