Author/Authors :
Xia، نويسنده , , Yi and Liu، نويسنده , , Yang and Rocchi، نويسنده , , Palma and Wang، نويسنده , , Menghua and Fan، نويسنده , , Yuting and Qu، نويسنده , , Fanqi and Iovanna، نويسنده , , Juan L. and Peng، نويسنده , , Ling، نويسنده ,
Abstract :
Issued from a lead optimization process, we have identified a novel triazole nucleoside analog which elicits potent anticancer activity on drug-resistant pancreatic cancer. Most importantly, this compound targets heat shock response pathways by down-regulation of heat shock transcription factor 1 and consequential down-regulation of multiple heat shock proteins HSP27, HSP70 and HSP90. Down-regulation of these proteins caused the shut-down of several oncogenic pathways and caspase-dependent apoptosis resulting in a potent anticancer effect in vitro and in vivo. These results demonstrate the potential rewards gained in searching for anticancer candidates with multimodal actions on heat shock response pathways via HSF1 down-regulation.
Keywords :
Heat shock response pathway , pancreatic cancer , Triazole nucleoside , Heat shock factor 1 , Heat Shock Proteins