Evidence map›Paper›PMID 34322027›Full record

ArticleFrontiers in pharmacology2021

C646 Protects Against DSS-Induced Colitis Model by Targeting NLRP3 Inflammasome.

Xueming Xu, Jing Li, Xiuyan Long, Sifan Tao, Xiaoyu Yu, Xixian Ruan, Kai Zhao, Li Tian

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

8 authors at 2 institutions in 1 country.

Xueming XuDepartment of Hematology and Key Laboratory of Non-Resolving Inflammation and Cancer of Hunan Province, the Third Xiangya Hospital, Central South University, Changsha, China.
Jing LiDepartment of Hematology and Key Laboratory of Non-Resolving Inflammation and Cancer of Hunan Province, the Third Xiangya Hospital, Central South University, Changsha, China.
Xiuyan LongDepartment of Gastroenterology, the Third Xiangya Hospital, Central South University, Changsha, China.
Sifan TaoDepartment of Gastroenterology, the Third Xiangya Hospital, Central South University, Changsha, China.
Xiaoyu YuDepartment of Gastroenterology, the Third Xiangya Hospital, Central South University, Changsha, China.
Xixian RuanDepartment of Gastroenterology, the Third Xiangya Hospital, Central South University, Changsha, China.
Kai ZhaoDepartment of Hematology and Key Laboratory of Non-Resolving Inflammation and Cancer of Hunan Province, the Third Xiangya Hospital, Central South University, Changsha, China.
Li TianDepartment of Gastroenterology, the Third Xiangya Hospital, Central South University, Changsha, China.
Central South University · CNThird Xiangya Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Numerous pieces of evidence have identified that the NLRP3 inflammasome plays a pivotal role in the development and pathogenesis of colitis. Targeting the NLRP3 inflammasome represents a potential therapeutic treatment. Our previous studies have suggested that acetylation of NLRP3 is indispensable to NLRP3 inflammasome activation, and some acetyltransferase inhibitors could suppress the NLRP3 inflammasome activation. Here, we identified that C646, an inhibitor of histone acetyltransferase p300, exerts anti-inflammatory effects in DSS-induced colitis mice by targeting the NLRP3 inflammasome. Mechanistically, C646 not only inhibits NF-κB activation, leading to the decreased expression of pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α) and NLRP3, but also suppresses the NLRP3 inflammasome assembly by disrupting the interaction between NLRP3 and ASC. In addition, C646 attenuated the LPS-induced acute systemic inflammation model. Thus, our results demonstrate the ability of C646 to suppress the NLRP3 inflammasome activity and its potential application in the treatment of inflammatory bowel disease.

Indexed as

ASC speckC646DSS-inducedNF-κBNLRP3 inflammsome

Identifiers

PMID34322027
PMCPMC8313226
OpenAlexW3177659905

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.