MPT0G612, a Novel HDAC6 Inhibitor, Induces Apoptosis and Suppresses IFN-γ-Induced Programmed Death-Ligand 1 in Human Colorectal Carcinoma Cells

Colorectal cancer (CRC) is the third most common cancer and the leading cause of cancer-associated death worldwide. Histone deacetylases (HDACs) have been implicated in regulating complex cellular mechanisms to influence tumor biology and immunogenicity in various types of cancer. The potential of s...

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Bibliographic Details
Published in:Cancers 2019-10, Vol.11 (10), p.1617
Main Authors: Chen, Mei-Chuan, Lin, Yu-Chen, Liao, Yu-Hsuan, Liou, Jing-Ping, Chen, Chun-Han
Format: Article
Language:English
Subjects:
Antitumor activity
Apoptosis
Autophagy
Biomarkers
Cancer therapies
Cell activation
Cell cycle
Cell death
Cell growth
Cell proliferation
Chemotherapy
Colorectal cancer
Colorectal carcinoma
Cytotoxicity
Enzymes
Epigenetics
Histones
Immune checkpoint inhibitors
Immunogenicity
Melanoma
PD-L1 protein
Phagocytosis
Proteins
Solid tumors
Tumors
γ-Interferon
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Summary:Colorectal cancer (CRC) is the third most common cancer and the leading cause of cancer-associated death worldwide. Histone deacetylases (HDACs) have been implicated in regulating complex cellular mechanisms to influence tumor biology and immunogenicity in various types of cancer. The potential of selective inhibition of HDAC6 has been widely discussed for the treatment of hematologic malignancies. We previously identified that MPT0G612 is a novel HDAC6 inhibitor exhibiting a promising antitumor activity against several solid tumors. The purpose of the present study was to evaluate the feasibility and pharmacological mechanisms of MPT0G612 as a potential therapy for CRC patients. Results revealed that MPT0G612 significantly suppresses the proliferation and viability, as well as induces apoptosis in CRC cells. Autophagy activation with LC3B-II formation and p62 degradation was observed, and the inhibition of autophagy by pharmacological inhibitor or Atg5 knockdown enhances MPT0G612-induced cell death. In addition, HDAC6 knockdown reduces MPT0G612-mediated autophagy and further potentiates apoptotic cell death. Furthermore, MPT0G612 downregulates the expression of PD-L1 induced by IFN-γ in CRC cells. These results suggest that MPT0G612 is a potent cell death inducer through inhibiting HDAC6-associated pathway, and a potential agent for combination strategy with immune checkpoint inhibitors for the treatment of CRC.
ISSN:2072-6694
2072-6694
DOI:10.3390/cancers11101617