Evidence map›Paper›PMID 40538537›Full record

ArticleFrontiers in pharmacology2025

Erdafitinib diminishes LPS-mediated neuroinflammatory responses through NLRP3 in wild-type mice.

Hyun-Ju Lee, Se Ha Kim, Tae-Mi Jung, Yu-Jin Kim, Chan-Hu Gu, Yoo Joo Jeong, Jeong-Heon Song, Hyang-Sook Hoe

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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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

8 authors.

Hyun-Ju LeeDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu, Republic of Korea.
Se Ha KimDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu, Republic of Korea.
Tae-Mi JungDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu, Republic of Korea.
Yu-Jin KimDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu, Republic of Korea.
Chan-Hu GuAI-based Neurodevelopmental Diseases Digital Therapeutics Group, Korea Brain Research Institute (KBRI), Daegu, Republic of Korea.
Yoo Joo JeongDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu, Republic of Korea.
Jeong-Heon SongAI-based Neurodevelopmental Diseases Digital Therapeutics Group, Korea Brain Research Institute (KBRI), Daegu, Republic of Korea.
Hyang-Sook HoeDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Erdafitinib is an FDA-approved inhibitor of fibroblast growth factor receptor (FGFR) that is used clinically to treat metastatic urothelial cancer. FGFR activation is involved in proinflammatory responses, but the potential effects of FGFR inhibitors like erdafitinib on neuroinflammatory responses in the brain have not been fully established. Methods: The effects of pretreatment with 1 μM or 5 μM erdafitinib on proinflammatory responses induced by 1 μg/mL or 200 ng/mL LPS Results and Discussion: In BV2 microglial cells, erdafitinib pretreatment significantly reduced the increases in proinflammatory cytokines, NLRP3 inflammasome activation and JNK/PLCγ signaling induced by LPS. In C57BL6/N mice, erdafitinib pretreatment significantly suppressed LPS-stimulated microglial/astroglial activation and proinflammatory cytokine expression. Importantly, erdafitinib pretreatment significantly downregulated LPS-induced NLRP3 inflammasome activation and astroglial neuroinflammation-associated molecules in C57BL6/N mice. Collectively, our experiments demonstrate that erdafitinib pretreatment diminishes LPS-induced neuroinflammation by suppressing NLRP3 inflammasome activation

Indexed as

erdafitinibFGFRJNKneuroinflammationNLRP3

Identifiers

PMID40538537
PMCPMC12177463

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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.