Evidence map›Paper›PMID 34882936›Full record

ArticleEMBO reports2022

Licochalcone B specifically inhibits the NLRP3 inflammasome by disrupting NEK7-NLRP3 interaction.

Qiang Li, Hui Feng, Hongbo Wang, Yinghao Wang, Wenqing Mou, Guang Xu, Ping Zhang, Ruisheng Li, Wei Shi, Zhilei Wang and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 2% of its field
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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 100 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Ciclopirox Olamine Inhibits the NLRP3 Inflammasome to Alleviate Inflammatory Diseases.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  5. Review
  6. Article
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  19. Discovery of (Molecules (Basel, Switzerland) · 2025
    Article
  20. 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

26 authors at 2 institutions in 1 country.

Qiang Li *School of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, China.
Hui Feng *Department of Ultrasound, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Hongbo Wang *Department of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Yinghao Wang *School of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, China.
Wenqing MouChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Guang XuDepartment of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Ping ZhangDepartment of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Ruisheng LiResearch Center for Clinical and Translational Medicine, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Wei ShiChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Zhilei WangChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Zhie FangChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Lutong RenChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Yan WangChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Li LinChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Xiaorong HouChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Wenzhang DaiChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Zhiyong LiChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Ziying WeiChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Tingting LiuChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Jiabo WangChina Military Institute of Chinese Materia, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Yuming GuoDepartment of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Pengyan LiDepartment of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Xu ZhaoDepartment of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Xiaoyan ZhanDepartment of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.ORCID 0000-0002-2446-5967
Xiaohe XiaoSchool of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, China.ORCID 0000-0002-2836-2738
Zhaofang BaiDepartment of Hepatology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.ORCID 0000-0002-6208-150X
Chinese PLA General Hospital · CNFujian University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The activation of the nucleotide oligomerization domain (NOD)-like receptor (NLR) family, pyrin domain-containing protein 3 (NLRP3) inflammasome is related to the pathogenesis of a wide range of inflammatory diseases, but drugs targeting the NLRP3 inflammasome are still scarce. In the present study, we demonstrated that Licochalcone B (LicoB), a main component of the traditional medicinal herb licorice, is a specific inhibitor of the NLRP3 inflammasome. LicoB inhibits the activation of the NLRP3 inflammasome in macrophages but has no effect on the activation of AIM2 or NLRC4 inflammasome. Mechanistically, LicoB directly binds to NEK7 and inhibits the interaction between NLRP3 and NEK7, thus suppressing NLRP3 inflammasome activation. Furthermore, LicoB exhibits protective effects in mouse models of NLRP3 inflammasome-mediated diseases, including lipopolysaccharide (LPS)-induced septic shock, MSU-induced peritonitis and non-alcoholic steatohepatitis (NASH). Our findings indicate that LicoB is a specific NLRP3 inhibitor and a promising candidate for treating NLRP3 inflammasome-related diseases.

Indexed as

ChalconesInflammasomesAnimalsMiceMice, Inbred C57BLNIMA-Related KinasesNLR Family, Pyrin Domain-Containing 3 ProteinChalconesInflammasomeslicochalcone BNek7 protein, mouseNIMA-Related KinasesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseLicochalcone BLPS-induced septic shockMSU-induced peritonitisNASHNEK7NLRP3 inflammasome

Identifiers

PMID34882936
PMCPMC8811655
OpenAlexW4200591636

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.