Abstract

Ubiquitin-like with PHD and RING finger domains 1 (UHRF1) is an epigenetic regulator that plays critical roles in tumours. However, the DNA methylation alteration patterns driven by UHRF1 and the related differentially expressed tumour-related genes remain unclear. In this study, a UHRF1-shRNA MCF-7 cell line was constructed, and whole-genome bisulfite sequencing and RNA sequencing were performed. The DNA methylation alteration landscape was elucidated, and DNA methylation-altered regions (DMRs) were found to be distributed in both gene bodies and adjacent regions. The DMRs were annotated and categorized into 488 hypermethylated/1696 hypomethylated promoters and 1149 hypermethylated/5501 hypomethylated gene bodies. Through an integrated analysis with the RNA sequencing data, 217 methylation-regulated upregulated genes and 288 downregulated genes were identified, and these genes were primarily enriched in nervous system development and cancer signalling pathways. Further analysis revealed 21 downregulated oncogenes and 15 upregulated TSGs. We also showed that UHRF1 silencing inhibited cell proliferation and migration and suppressed tumour growth in vivo. Our study suggested that UHRF1 and the oncogenes or TSGs it regulates might serve as biomarkers and targets for breast cancer treatment.

Details

Title
Identification of differentially expressed tumour-related genes regulated by UHRF1-driven DNA methylation
Author
Dong, Qincai 1 ; Gong, Chunxue 2 ; Jiang, Qian 2 ; Liu, Yue 1 ; Hu, Yong 1 ; Wang, Di 1 ; Liu, Hainan 1 ; Zheng, Tong 1 ; Song, Caiwei 1 ; Wang, Tingting 2 ; Ju, Ruixia 1 ; Wang, Chen 2 ; Song, Dengcen 1 ; Liu, Zijing 1 ; Liu, Yuting 1 ; Lu, Yuwei 1 ; Fan, Jinlian 1 ; Liu, Mengzi 1 ; Gao, Ting 1 ; An, Ziqian 1 ; Zhang, Jiaxin 1 ; Li, Ping 1 ; Cao, Cheng 1 ; Liu, Xuan 1 

 Beijing Institute of Biotechnology, Beijing, China (GRID:grid.418873.1) 
 Anhui University, Institute of Health Sciences, Hefei, China (GRID:grid.252245.6) (ISNI:0000 0001 0085 4987) 
Pages
18371
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3090091255
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.