PROM2 exacerbates CCl4-Induced liver fibrosis via NLRP3 inflammasome activation and hepatocyte pyroptosis

PROM2 contributes to liver fibrosis by promoting EMT and activating NLRP3-dependent inflammatory pathways, suggesting it as a potential therapeutic target for liver fibrosis.

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Publication Details

Journal
Cellular and Molecular Life Sciences
Published
2025-11-14
DOI
https://doi.org/10.1007/s00018-025-05920-5
Citations
1
Primary Topic
Inflammasome and immune disorders
Type
article
Field-Weighted Citation Impact
0.81

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article

PROM2 exacerbates CCl4-Induced liver fibrosis via NLRP3 inflammasome activation and hepatocyte pyroptosis

Jun Hu, Jingyuan Wan, Yan Lin, Ge Kuang et al.
1 citations
Cellular and Molecular Life Sciences
Inflammasome and immune disorders
0.81
article

PROM2 exacerbates CCl4-Induced liver fibrosis via NLRP3 inflammasome activation and hepatocyte pyroptosis

Jun Hu, Jingyuan Wan, Yan Lin, Ge Kuang, Xia Gong, Li Zhang, Hao Liu, Jiao Zhang, Hui Du, Ting Wang, Jiashi Guo
article en
1 citations

Abstract

PROM2 contributes to liver fibrosis by promoting EMT and activating NLRP3-dependent inflammatory pathways, suggesting it as a potential therapeutic target for liver fibrosis.

Cellular and Molecular Life SciencesVol. 82(1)
Dalian Medical University (CN), Second Affiliated Hospital of Chongqing Medical University (CN), Chongqing Medical University (CN)
China Postdoctoral Science Foundation, Chongqing Medical University
Openalex Percentile: Top 22%
Inflammasome and immune disorders
0.81
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PROM2 exacerbates CCl4-Induced liver fibrosis via NLRP3 inflammasome activation and hepatocyte pyroptosis — Jun Hu, Jingyuan Wan, et al. · Cellular and Molecular Life Sciences (2025) | TGRS Research Map | TGRS