ER stress genes (COL1A1, LOXL2, VWF) predicts IKK-16 as a Candidate therapeutic target for colitis-related inflammation and fibrosis suppression

These results suggest that ERS-related genes, particularly COL1A1, LOXL2, and VWF, may regulate UC fibrosis through interactions with immune cells. IKK-16 shows promise as a therapeutic agent. These findings provide new insights into UC pathogenesis and potential clinical treatment strategies.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-06-18
DOI
https://doi.org/10.3389/fimmu.2025.1587860
Citations
3
Primary Topic
Macrophage Migration Inhibitory Factor
Type
article
Field-Weighted Citation Impact
2.39

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article

ER stress genes (COL1A1, LOXL2, VWF) predicts IKK-16 as a Candidate therapeutic target for colitis-related inflammation and fibrosis suppression

Qingqing Yang, Jun‐Meng Wang, Yuemei Wang, Qianhui Huang et al.
3 citations
Frontiers in Immunology
Macrophage Migration Inhibitory Factor
2.39
article

ER stress genes (COL1A1, LOXL2, VWF) predicts IKK-16 as a Candidate therapeutic target for colitis-related inflammation and fibrosis suppression

Qingqing Yang, Jun‐Meng Wang, Yuemei Wang, Qianhui Huang, Jianping Guo, Yang Jiao, Chengshuai Cui, Ke Zhang, Qiao‐Feng Wu
article en
3 citations

Abstract

These results suggest that ERS-related genes, particularly COL1A1, LOXL2, and VWF, may regulate UC fibrosis through interactions with immune cells. IKK-16 shows promise as a therapeutic agent. These findings provide new insights into UC pathogenesis and potential clinical treatment strategies.

Frontiers in ImmunologyVol. 16
Chengdu University of Traditional Chinese Medicine (CN)
National Natural Science Foundation of China
Good health and well-being
Openalex Percentile: Top 11%
Macrophage Migration Inhibitory Factor
2.39
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ER stress genes (COL1A1, LOXL2, VWF) predicts IKK-16 as a Candidate therapeutic target for colitis-related inflammation and fibrosis suppression — Qingqing Yang, Jun‐Meng Wang, et al. · Frontiers in Immunology (2025) | TGRS Research Map | TGRS