Evidence map›Paper›PMID 34180140›Full record

ArticleJournal of cellular and molecular medicine2021

HDAC6 inhibitor ACY1215 inhibits the activation of NLRP3 inflammasome in acute liver failure by regulating the ATM/F-actin signalling pathway.

Qian Chen, Yao Wang, Fangzhou Jiao, Pan Cao, Chunxia Shi, Maohua Pei, Luwen Wang, Zuojiong Gong

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Histone Deacetylase 6 (HDAC6) in Ciliopathies: Emerging Insights and Therapeutic Implications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Nafamostat mesilate prevented caerulein-induced pancreatic injury by targeting HDAC6-mediated NLRP3 inflammasome activation.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. 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

8 authors at 1 institution in 1 country.

Qian ChenDepartment of Infectious Diseases, Renmin Hospital of Wuhan University, China.
Yao WangDepartment of Infectious Diseases, Renmin Hospital of Wuhan University, China.
Fangzhou JiaoDepartment of Infectious Diseases, Renmin Hospital of Wuhan University, China.
Pan CaoDepartment of Infectious Diseases, Renmin Hospital of Wuhan University, China.
Chunxia ShiDepartment of Infectious Diseases, Renmin Hospital of Wuhan University, China.
Maohua PeiDepartment of Infectious Diseases, Renmin Hospital of Wuhan University, China.
Luwen WangDepartment of Infectious Diseases, Renmin Hospital of Wuhan University, China.
Zuojiong GongDepartment of Infectious Diseases, Renmin Hospital of Wuhan University, China.ORCID 0000-0002-4676-5856
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute liver failure (ALF) is a rare and critical medical condition. This study was designed to investigate the protective effects and underlying mechanism of ACY1215 in ALF mice. Our findings suggested that ACY1215 treatment ameliorates the pathological hepatic damage of ALF and decreases the serum levels of ALT and AST. Furthermore, ACY1215 pretreatment increased the level of ATM, γ-H2AX, Chk2, p53, p21, F-actin and vinculin in ALF. Moreover, ACY1215 inhibited the level of NLRP3, ASC, caspase-1, IL-1β and IL-18 in ALF. The ATM inhibitor KU55933 could decrease the level of ATM, γ-H2AX, Chk2, p53, p21, F-actin and vinculin in ALF with ACY1215 pretreatment. The F-actin inhibitor cytochalasin B decreased the level of F-actin and vinculin in ALF with ACY1215 pretreatment. However, cytochalasin B had no effect on protein levels of ATM, Chk2, p53 and p21 in ALF with ACY1215 pretreatment. Cytochalasin B could dramatically increase the level of NLRP3, ASC, caspase-1, IL-1β and IL-18 in ALF with ACY1215 pretreatment. These results indicated that ACY1215 exhibited hepatoprotective properties, which was associated with the inhibition of NLRP3 inflammasome, and this effect of ACY1215 was connected with upregulation of the ATM/F-actin mediated signalling pathways.

Indexed as

ActinsAnimalsAtaxia Telangiectasia Mutated ProteinsCell LineCheckpoint Kinase 2Histone Deacetylase 6Histone Deacetylase InhibitorsHumansHydroxamic AcidsInflammasomesInterleukin-18Interleukin-1betaLiver FailureMaleMiceMice, Inbred C57BLActinsAtaxia Telangiectasia Mutated ProteinsAtm protein, mouseCheckpoint Kinase 2Chek2 protein, mouseHdac6 protein, mouseHistone Deacetylase 6Histone Deacetylase InhibitorsHydroxamic AcidsInflammasomesInterleukin-18Interleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mousePyrimidinesricolinostatTumor Suppressor Protein p53acute liver failureACY1215ATMF-actinNLRP3

Identifiers

PMID34180140
PMCPMC8335684
OpenAlexW3176131984

What OpenQuestion holds

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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.