Essential role of HDAC6 in the regulation of PD-L1 in melanoma.
Histone deacetylases (HDACs), originally described as histone modifiers, have more recently been demonstrated to target a variety of other proteins unrelated to the chromatin environment. In this context, our present work demonstrates that the pharmacological or genetic abrogation of HDAC6 in primary melanoma samples and cell lines, down-regulates the expression ... of PD-L1, an important co-stimulatory molecule expressed in cancer cells, which activates the inhibitory regulatory pathway PD-1 in T-cells. Our data suggests that this novel mechanism of PD-L1 regulation is mainly mediated by the influence of HDAC6 over the recruitment and activation of STAT3. Additionally, we observed that selective HDAC6 inhibitors impairs tumor growth and reduce the in vivo expression of several inhibitory check-point molecules and other regulatory pathways involved in immunosurveillance. Most importantly, these results provide a key pre-clinical rationale and justification to further study isotype selective HDAC6 inhibitors as potential immuno-modulatory agents in cancer.
Mesh Terms:
Animals, B7-H1 Antigen, Cell Line, Tumor, Cytokines, Gene Expression Regulation, Neoplastic, Gene Knockdown Techniques, Histone Deacetylase 6, Histone Deacetylases, Humans, Melanoma, Mice, Inbred C57BL, Promoter Regions, Genetic, STAT3 Transcription Factor, Signal Transduction, Skin, Skin Neoplasms
Animals, B7-H1 Antigen, Cell Line, Tumor, Cytokines, Gene Expression Regulation, Neoplastic, Gene Knockdown Techniques, Histone Deacetylase 6, Histone Deacetylases, Humans, Melanoma, Mice, Inbred C57BL, Promoter Regions, Genetic, STAT3 Transcription Factor, Signal Transduction, Skin, Skin Neoplasms
Mol Oncol
Date: Dec. 01, 2015
PubMed ID: 26775640
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