Evidence map›Paper›PMID 40948397›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

GSK461364 Inhibits NLRP3 Inflammasome by Targeting NEK7 Phosphorylation.

Ruiheng Luo, Mingliang Ma, Dan Wang, Ling Luo, Xueming Xu, Lingmin Huang, Fupeng Wang, Guangyan Kuang, Huiqi Liu, Rui Ni and 4 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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.

  1. Article
  2. Review
  3. GSK461364 Inhibits NLRP3 Inflammasome by Targeting NEK7 Phosphorylation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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

14 authors.

Ruiheng LuoDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410000, P. R. China.
Mingliang MaDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410000, P. R. China.
Dan WangDepartment of Dermatology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410000, P. R. China.
Ling LuoDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410000, P. R. China.
Xueming XuDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410000, P. R. China.
Lingmin HuangHealthcare Security Department, The Affiliated Changsha Central Hospital, Hengyang Medical School, University of South China, Changsha, Hunan, 410000, P. R. China.
Fupeng WangDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410000, P. R. China.
Guangyan KuangDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410000, P. R. China.
Huiqi LiuDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410000, P. R. China.
Rui NiDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410000, P. R. China.
Xin LiDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410000, P. R. China.
Qinghua ZhangKey Laboratory of Exploration and Utilization of Aquatic Genetic Resources, Ministry of Education, Shanghai Ocean University, Shanghai, 201306, P. R. China.
Shengfeng WangDepartment of Pharmacy, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, P. R. China.
Kai ZhaoDepartment of Hematology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410000, P. R. China.ORCID https://orcid.org/0000-0002-3889-2118

Funding

National Natural Science Foundation of China 82202391National Natural Science Foundation of China 82202398National Natural Science Foundation of China 82272207National Natural Science Foundation of China 82502634Provincial Natural Science Foundation of Hunan in China 2022JJ20093Provincial Natural Science Foundation of Hunan in China 2025JJ30033Shanghai Municipal Commission of Science and Technology 22YF1416600Third xiangya hospital of Central South University JC202201Third xiangya hospital of Central South University YX202201
6 · The paper itself

Abstract

NLRP3 inflammasome is a multiple protein complex sensing exogenous or endogenous stimuli, and aberrant activation of the NLRP3 inflammasome is implicated in various inflammatory disorders. While numerous small-molecule compounds targeting NLRP3 inflammasome activity have been developed, most have encountered limited success in clinical translation. Through screening of a kinase compound library, GSK461364 is identified as a potent and selective NLRP3 inflammasome inhibitor. Notably, GSK461364 confers significant protective effects in murine models of LPS-induced endotoxemia and DSS-induced colitis. Mechanistic study reveals that GSK461364 exerts its inhibitory effects via targeting Polo-like Kinase 1(PLK1). Specifically, that PLK1-mediated phosphorylation of NEK7, likely occurring at evolutionarily conserved serine residues (Ser221 and Ser260), is shown to enhance NEK7-NLRP3 binding, a critical step for NLRP3 inflammasome assembly. These findings not only establish GSK461364 as a novel therapeutic candidate for NLRP3-driven inflammatory diseases but also provide new insights into the regulatory mechanisms governing inflammasome activation through post-translational modification.

Indexed as

InflammasomesNIMA-Related KinasesNLR Family, Pyrin Domain-Containing 3 ProteinAnimalsColitisDisease Models, AnimalHumansMiceMice, Inbred C57BLPhosphorylationProtein Serine-Threonine KinasesInflammasomesNEK7 protein, humanNek7 protein, mouseNIMA-Related KinasesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseProtein Serine-Threonine KinasesGSK461364NEK7NLRP3 inflammasomePLK1

Identifiers

PMID40948397
PMCPMC12667451

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Registered trials

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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.