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• W1821596905 abstract "The aldo-keto reductase 1C3 (AKR1C3) has been heavily implicated in the propagation of prostate malignancy. AKR1C3 protein is elevated within prostate cancer tissue, it contributes to the formation of androgens and downstream stimulation of the androgen receptor (AR). Elevated expression of AKR1C3 is also reported in acute myeloid leukemia but the target nuclear receptors have been identified as members of the peroxisome-proliferator activated receptor (PPARs) subfamily. Thus, AKR1C3 cancer biology is likely to be tissue dependent and hormonally linked to the availability of ligands for both the steroidogenic and non-steroidogenic nuclear receptors. In the current study we investigated the potential for AKR1C3 to regulate the availability of prostaglandin-derived ligands for PPARg mainly, prostaglandin J2 (PGJ2). Using prostate cancer cell lines with stably reduced AKR1C3 levels we examined the impact of AKR1C3 upon proliferation mediated by PPAR ligands. These studies revealed knockdown of AKR1C3 had no effect upon the sensitivity of androgen receptor independent prostate cancer cells towards PPAR ligands. However, the reduction of levels of AKR1C3 was accompanied by a significantly reduced mRNA expression of a range of HDACs, transcriptional co-regulators, and increased sensitivity towards SAHA, a clinically approved histone deacetylase inhibitor. These results suggest a hitherto unidentified link between AKR1C3 levels and the epigenetic status in prostate cancer cells. This raises an interesting possibility of a novel rational to target AKR1C3, the utilization of AKRIC3 selective inhibitors in combination with HDAC inhibition as part of novel epigenetic therapies in androgen deprivation therapy recurrent prostate cancer." @default.
• W1821596905 created "2016-06-24" @default.
• W1821596905 creator A5015137207 @default.
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• W1821596905 date "2016-01-01" @default.
• W1821596905 modified "2023-10-15" @default.
• W1821596905 title "Knockdown of AKR1C3 exposes a potential epigenetic susceptibility in prostate cancer cells" @default.
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• W1821596905 doi "https://doi.org/10.1016/j.jsbmb.2015.09.037" @default.
• W1821596905 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5391256" @default.
• W1821596905 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26429394" @default.
• W1821596905 hasPublicationYear "2016" @default.
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