2. Academic Validation
  3. G9a and DNMT1 inhibition modulates CDKN1A promoter methylation and the cell cycle leading to improvement in kidney fibrosis

G9a and DNMT1 inhibition modulates CDKN1A promoter methylation and the cell cycle leading to improvement in kidney fibrosis

  • Biochim Biophys Acta Gen Subj. 2023 Jun 23;130417. doi: 10.1016/j.bbagen.2023.130417.
Yuanyuan Yang 1,  Zijian Zhou 1,  Lujia Wang 2,  Peng Gao 1,  Zhong Wu 3
Affiliations

Affiliations

  • 1 Department of Urology, Huashan Hospital, Fudan University, Shanghai 200040, China; Institute of Urology, Fudan University, Shanghai 200040, China.
  • 2 Department of Urology, Huashan Hospital, Fudan University, Shanghai 200040, China; Institute of Urology, Fudan University, Shanghai 200040, China; Department of Urology, Huashan Hospital, Fudan University, Shanghai 200040, China.
  • 3 Department of Urology, Huashan Hospital, Fudan University, Shanghai 200040, China; Institute of Urology, Fudan University, Shanghai 200040, China. Electronic address: drzhongwu2020@163.com.
PMID: 37356504 DOI: 10.1016/j.bbagen.2023.130417
Abstract

Background: Epigenetic mechanisms, including histone and DNA methylation, play a key role in kidney fibrosis, but the precise mechanism remains unclear. Concerted action between histone and DNA-methyltransferases like G9a and DNMT1 is a common theme in gene expression regulation. We investigated the role of G9a and DNMT1 in kidney fibrosis pathogenesis and aimed to elucidate key G9a and DNMT1 targets contributing to kidney fibrosis maintenance.

Methods: G9a and DNMT1 were detected in human fibrotic kidneys, UUO mouse kidneys, and TGFβ1-induced HK-2 cells. G9a and DNMT1 expression was knocked down by siRNA or inhibited with CM272 in HK-2 and UUO mouse, and transcriptomic responses to CM272 were examined. Antifibrogenic activity and safety of CM272 were studied in UUO mouse. Cell cycle were analyzed with flow cytometry. Gene expression regulation was analyzed by chromatin immunoprecipitation and methylation-specific PCR.

Results: G9a and DNMT1 were overexpressed in human fibrotic kidneys, UUO mouse kidneys, and TGFβ1-induced HK-2 cells. G9a/DNMT1 inhibition potently alleviated fibrosis in vitro and vivo. G9a/DNMT1 inhibition reduced the expression of E2F targets and altered the methylation status of CDKN1A leading to the attenuated cell-cycle arrest. TGFβ1-induced overexpression of G9a or DNMT1 resulted in the enrichment of H3K9me2 and 5-methylcytosine at CDKN1A promoter.

Conclusions: Our data link G9a and DNMT1 to CDKN1A regulatory function and kidney fibrosis. Combined targeting G9a and DNMT1 could be a promising strategy for the treatment of kidney fibrosis.

Keywords

Cell cycle; DNA methylation; Epigenetic modification; Histone methylation; Kidney fibrosis.

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