已发表论文

慢性淋巴细胞患者 CD19+ B 细胞中的异常组蛋白修饰

 

Authors Zhou K, Zhang Q, Liu Y, Xiong Y, Wu S, Yang J, Zhou H, Liu X, Wei X, Song Y

Received 2 September 2016

Accepted for publication 9 December 2016

Published 23 February 2017 Volume 2017:10 Pages 1173—1179

DOI https://doi.org/10.2147/OTT.S121301

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Akshita Wason

Peer reviewer comments 2

Editor who approved publication: Dr William Cho

Abstract: The aim of this study was to detect the alterations in histone methylation and acetylation in patients with chronic lymphocytic leukemia (CLL). Global histone H3/H4 acetylation and H3K4/H3K9 methylation were detected by the EpiQuik™ global histone H3/H4 acetylation and H3K4/H3K9 methylation assay kits. The mRNA expression of selected chromatin modifier genes was measured by real-time polymerase chain reaction (RT-PCR). Our results found that the global histone H3/H4 hypoacetylation in the CD19+ B cells of patients with CLL (=0.028 and =0.03, respectively) and the global histone H3K9 methylation in patients with CLL were significantly increased compared with controls (=0.02), while there was no significant difference in the global histone H3K4 methylation between the two groups. The level of SIRT1 and EZH2 mRNA expression was upregulated in patients with CLL (=0.03 and =0.02, respectively), which increased significantly with progression from Binet stage A to stage C (=0.015 and =0.01, respectively) and Rai good to high risk stage (=0.007 and =0.008, respectively). The level of HDAC1 and HDAC7 mRNA expression was significantly increased (=0.02 and =0.008, respectively) and HDAC2 and P300 mRNA expression was reduced in patients with CLL (=0.002 and =0.001, respectively). In conclusion, it is observed that the aberrant histone modification plays an important role in the pathogenesis of CLL.
Keywords: histone methylation, histone acetylation, SIRT1, EZH2, CLL