Chemosensitivity enhancement toward arsenic trioxide by inhibition of histone deacetylase in NB4 cell line. (August 2016)

• Record Type: Journal Article
• Authors: Li, Xiaofan; Guan, Xiaoyan; Li, Fang; Chen, Yuanzhong; Li, Nainong
• Is Part Of: Journal of international medical research. Volume 44:Number 4(2016:Aug.)
• Page Start: 882
• Page End: 892
• Publication Date: 2016-08
• Subjects: Histone deacetylase inhibitors; arsenic trioxide; NB4 cell line; apoptosis; all-trans retinoic acid; vorinostat; Medicine -- Periodicals; Pharmacology -- Periodicals; 610.5
• DOI: 10.1177/0300060516646238
• Languages: English
• ISSNs: 0300-0605

Abstract

Objective: To investigate the cytotoxic effects of suberanilohydroxamic acid (vorinostat) in combination with arsenic trioxide (ATO) on the human NB4 cell line in vitro . Methods: The rates of cell proliferation following treatment with vorinostat with or without ATO were measured. Flow cytometry of Annexin-V/propidium iodide double-stained cells was used to measure apoptosis. Acridine Orange and ethidium bromide staining was used to observe morphological changes characteristic of apoptosis. Western blot analysis was used to measure protein levels. Results: Vorinostat and ATO, alone and in combination, inhibited the proliferation of NB4 cells in a time- and dose-dependent manner and the effect was additive. NB4 cells treated with vorinostat + ATO demonstrated greater levels of apoptosis compared with cells treated with either drug alone. Both vorinostat and ATO alone and in combination resulted in lower levels of promyelocytic leukaemia/retinoic acid receptor alpha fusion protein and increased levels of acetyl-histone H3 and acetyl-histone H4 proteins compared with controls. Vorinostat + ATO resulted in lower levels of Akt protein compared with either drug alone. Conclusion: The combination of vorinostat and ATO inhibited cell proliferation, induced apoptosis, and enhanced the chemosensitivity of NB4 cells. The mechanism might be associated with increasing histone acetylation levels as well as downregulation of the Akt signalling pathway.