Abstract
Epigenetic modifications, like histone acetylation, are essential for regulating gene expression within cells. Cancer cells acquire pathological epigenetic modifications resulting in gene expression patterns that facilitate and sustain tumorigenesis. Epigenetic manipulation therefore is emerging as a novel targeted therapy for cancer. Histone Acetylases (HATs) and Histone Deacetylases (HDACs) regulate histone acetylation and hence gene expression. Histone deacetylase (HDAC) inhibitors are well known to affect cancer cell viability and biology and are already in use for the treatment of cancer patients. Immunotherapy can lead to clinical benefit in selected cancer patients, especially in patients with limited disease after tumor debulking. HDAC inhibitors can potentially synergize with immunotherapy by elimination of tumor cells. The direct effects of HDAC inhibitors on immune cell function, however, remain largely unexplored. Initial data have suggested HDAC inhibitors to be predominantly immunosuppressive, but more recent reports have challenged this view. In this review we will discuss the effects of HDAC inhibitors on tumor cells and different immune cell subsets, synergistic interactions and possible mechanisms. Finally, we will address future challenges and potential application of HDAC inhibitors in immunocombination therapy of cancer.
Highlights
Recent reports have demonstrated synergistic effects of Histone Deacetylases (HDACs) inhibitors with cancer immunotherapy
Similar effects have been reported for other panHDAC inhibitors when added to osteosarcoma, leukemia and Ewing sarcoma cell lines in vitro and to primary myeloid leukemia cells ex vivo[53,54,55,56]. These studies collectively show that panHDAC inhibitors can increase the expression of activating NKG2D ligands resulting in enhanced tumor cell recognition and elimination by NK cells
This study elegantly shows that the timing of HDAC inhibitor treatment is essential for the combination with immunotherapy in order to boost anti-tumor immune responses
Summary
Recent reports have demonstrated synergistic effects of HDAC inhibitors with cancer immunotherapy. The mechanisms for the tumor specific induction of NKG2D ligands remained unclear, this study confirms the selective effect of this panHDAC inhibitor on the expression of NK cell activating ligands by malignant cells. These studies collectively show that panHDAC inhibitors can increase the expression of activating NKG2D ligands resulting in enhanced tumor cell recognition and elimination by NK cells.
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