Mechanism of KMT2D-mediated epigenetic modification in IL-1β-induced nucleus pulposus cell degeneration.

KMT2D promoted miR-133a-5p expression through H3K4me2 methylation, thereby promoting the binding of miR-133a-5p to PFKFB2, reducing the mRNA level of PFKFB2, promoting inflammation and apoptosis of IL-1β-induced NPCs, and inhibiting NPC proliferation.

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Publication Details

Journal
PubMed
Published
2025-05-01
DOI
https://doi.org/10.14670/hh-18-813
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
0.00
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article

Mechanism of KMT2D-mediated epigenetic modification in IL-1β-induced nucleus pulposus cell degeneration.

Hongjiang Liu, Hai‐Quan Liu, Zuyu Meng, Wensheng Zhang
PubMed
Epigenetics and DNA Methylation
article

Mechanism of KMT2D-mediated epigenetic modification in IL-1β-induced nucleus pulposus cell degeneration.

Hongjiang Liu, Hai‐Quan Liu, Zuyu Meng, Wensheng Zhang
article en

Abstract

KMT2D promoted miR-133a-5p expression through H3K4me2 methylation, thereby promoting the binding of miR-133a-5p to PFKFB2, reducing the mRNA level of PFKFB2, promoting inflammation and apoptosis of IL-1β-induced NPCs, and inhibiting NPC proliferation.

PubMedVol. 40(5)
Guangzhou University of Chinese Medicine (CN), Jinan University (CN), Third Affiliated Hospital of Guangzhou Medical University (CN), The Third Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine (CN), Huizhou Central People's Hospital (CN), Guangzhou Medical University (CN), Huizhou University (CN)
Openalex Percentile: Top 100%
Epigenetics and DNA Methylation
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