Evidence map›Paper›PMID 41372605›Full record

ArticleCell biology and toxicology2025

Gentisic acid ameliorates lumbar disc herniation by regulating M1/M2 Polarization via the MAPK14/S100A9/Rac1/2 pathway.

Shuoqi Li, Tiezhu Chen, Xiongjie Shen, Wanying Su, Xiaosheng Li

Abstract read
In one paragraph

Article in Cell biology and toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Shuoqi LiDepartment of Scientific Research, Hunan Provincial People's Hospital, Changsha, China.
Tiezhu ChenDepartment of Orthopedics, Hunan Provincial People's Hospital, Changsha, China.
Xiongjie ShenDepartment of Spine Surgery, Hunan Provincial People's Hospital, Changsha, China.
Wanying SuDepartment of Orthopedics, Hunan Provincial People's Hospital, Changsha, China.
Xiaosheng LiHunan Provincial People's Hospital, Changsha, China. lxsld2009@163.com.

Funding

Research and Development Program of Hunan Province of China 2022SK2024
6 · The paper itself

Abstract

Traditional Chinese medicine is gaining prominence in lumbar disc herniation (LDH) management, but the mechanisms of its active compounds and their molecular targets remain largely unclear. Herein, we aim to elucidate the therapeutic mechanism of Gentisic acid by investigating its role in regulating S100A9 in LDH. Clinical analysis reveals that S100A9 expression and inflammatory levels correlat positively with LDH severity. S100A9 is found to promote M1 macrophage polarization and impair dorsal root ganglion (DRG) neuronal activity. Mechanistically, Gentisic acid binds to MAPK14, downregulates S100A9 via MAPK14, and then suppresses M1 polarization, enhances neuronal autophagic flux, and improves neuronal viability through the S100A9/Rac1/2 pathway. In vivo experiments demonstrate that Gentisic acid ameliorates disc injury, improves neurological function, and alleviates pain in a rat LDH model, with efficacy comparable to celecoxib. These results suggest that Gentisic acid could alleviate LDH symptoms by modulating macrophage polarization and autophagy through the MAPK14/S100A9/Rac1/2 axis, offering a promising therapeutic strategy for LDH.

Indexed as

Intervertebral Disc DisplacementAnimalsAutophagyDisease Models, AnimalGanglia, SpinalHumansLumbar VertebraeMacrophagesMalerac1 GTP-Binding ProteinRatsRats, Sprague-DawleySignal Transductionrac1 GTP-Binding ProteinGentisic acidLumbar disc herniationM1/M2 polarizationMAPK14Rac1/2S100A9

Identifiers

PMID41372605
PMCPMC12696013

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.