Open AccessPharmacological or transcriptional inhibition of both HDAC 1 and 2 leads to cell cycle blockage and apoptosis via p21 Waf1/Cip1 and p19 INK4d upregulation in hepatocellular carcinoma
Author(s) -
Zhou Hengyu,
Cai Ying,
Liu Dina,
Li Menghui,
Sha Yu,
Zhang Wenlu,
Wang Kai,
Gong Jianping,
Tang Ni,
Huang Ailong,
Xia Jie
Publication year - 2018
Publication title -
cell proliferation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.647
H-Index - 74
eISSN - 1365-2184
pISSN - 0960-7722
DOI - 10.1111/cpr.12447
Subject(s) - downregulation and upregulation , cell cycle , apoptosis , cell growth , vorinostat , cancer research , cell cycle checkpoint , growth inhibition , cdk inhibitor , cyclin dependent kinase , chemistry , histone deacetylase , microbiology and biotechnology , biology , histone , biochemistry , gene
Objectives Histone deacetylases ( HDAC s) are commonly dysregulated in cancer and represent promising therapeutic targets. However, global HDAC inhibitors have shown limited efficacy in the treatment of solid tumours, including hepatocellular carcinoma ( HCC ). In this study, we investigated the therapeutic effect of selectively inhibiting HDAC 1 and 2 in HCC . Methods HDAC 1 inhibitor Tacedinaline ( CI 994), HDAC 2 inhibitor Santacruzamate A ( CAY 10683), HDAC 1/2 common inhibitor Romidepsin ( FK 228) and global HDAC inhibitor Vorinostat ( SAHA ) were used to treat HCC cells. Cell cycle, apoptosis and the protein levels of CDK s and CDKN s were performed to evaluate HCC cell growth. Inhibition of HDAC 1/2 by RNA i was further investigated. Results Combined inhibition of HDAC 1/2 led to HCC cell morphology changes, growth inhibition, cell cycle blockage and apoptosis in vitro and suppressed the growth of subcutaneous HCC xenograft tumours in vivo. p21 Waf1/Cip1 and p19 INK 4d , which play roles in cell cycle blockage and apoptosis induction, were upregulated. Inhibition of HDAC 1/2 by si RNA further demonstrated that HDAC 1 and 2 cooperate in blocking the cell cycle and inducing apoptosis via p19 INK 4d and p21 Waf1/Cip1 upregulation. Finally, H3K18, H3K56 and H4K12 in the p19 INK 4d and p21 Waf1/Cip1 promoter regions were found to be targets of HDAC 1/2. Conclusions Pharmacological or transcriptional inhibition of HDAC 1/2 increases p19 INK 4d and p21 Waf1/Cip1 expression, decreases CDK expression and arrests HCC growth. These results indicated a potential pharmacological mechanism of selective HDAC 1/2 inhibitors in HCC therapy.