Evidence map›Paper›PMID 36332009›Full record

ArticleScience immunology2022

Oxidized thioredoxin-1 restrains the NLRP1 inflammasome.

Daniel P Ball, Lydia P Tsamouri, Alvin E Wang, Hsin-Che Huang, Charles D Warren, Qinghui Wang, Isabelle H Edmondson, Andrew R Griswold, Sahana D Rao, Darren C Johnson and 1 more

Open access · greenAbstract read
In one paragraph

Article in Science immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 48 citations in OpenAlex.

  1. The gasdermin family: from pyroptosis mechanisms to therapeutic targets.Signal transduction and targeted therapy · 2026
    Review
  2. Review
  3. Review
  4. Article
  5. An overview of human inflammasomes: Activation and regulation.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Review
  6. Reductive stress in cancer immunology and targeted therapy.Acta biochimica et biophysica Sinica · 2026
    Review
  7. Article
  8. Review
  9. Nanomedicine-Driven Modulation of Reductive Stress for Cancer Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Targeting ROS in cancer: rationale and strategies.Nature reviews. Drug discovery · 2024
    Review
  20. Mechanistic insights from inflammasome structures.Nature reviews. Immunology · 2024
    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

11 authors at 2 institutions in 1 country.

Daniel P BallChemical Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0003-0693-7614
Lydia P TsamouriPharmacology Program of the Weill Cornell Graduate School of Medical Sciences, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Alvin E WangChemical Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Hsin-Che HuangTri-Institutional PhD Program in Chemical Biology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0001-8677-7803
Charles D WarrenTri-Institutional PhD Program in Chemical Biology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Qinghui WangChemical Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0002-1223-8193
Isabelle H EdmondsonChemical Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0001-6014-0425
Andrew R GriswoldPharmacology Program of the Weill Cornell Graduate School of Medical Sciences, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0003-2957-2355
Sahana D RaoTri-Institutional PhD Program in Chemical Biology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0003-4592-8921
Darren C JohnsonTri-Institutional PhD Program in Chemical Biology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0002-0858-6152
Daniel A BachovchinChemical Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0001-8210-1662
Memorial Sloan Kettering Cancer Center · USTri-Institutional PhD Program in Chemical Biology · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Weill Cornell/Rockefeller/Sloan-Kettering MST ProgramT32GM007739 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI HSU, KATHARINE C · 1985 to 2023
$51.1M
Characterizing the Mechanism of DPP8/9 Inhibitor-Induced PyroptosisR01AI137168 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI Daniel Bachovchin · 2018 to 2026
$4.3M
Prolidase Inhibitors as Therapeutic Agents for Acute Myeloid LeukemiaR01CA266478 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Daniel Bachovchin · 2022 to 2026
$3.1M
Redox control of the NLRP1 inflammasomeR01AI163170 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI BACHOVCHIN, DANIEL · 2021 to 2025
$2.6M
Tri-Institutional PhD Program in Chemical BiologyT32GM136640 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI DEREK S TAN · 2020 to 2026
$2.4M
Characterizing the DPP8/9 Pyroptotic Checkpoint with Chemoproteomic Protease Substrate ProfilingF30CA243444 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI GRISWOLD, ANDREW · 2019 to 2022
$193k
NCI NIH HHS F30 CA243444NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA266478NIAID NIH HHS R01 AI137168NIAID NIH HHS R01 AI163170NIGMS NIH HHS T32 GM007739NIGMS NIH HHS T32 GM136640
6 · The paper itself

Abstract

The danger signals that activate the NLRP1 inflammasome have not been established. Here, we report that the oxidized, but not the reduced, form of thioredoxin-1 (TRX1) binds to NLRP1. We found that oxidized TRX1 associates with the NACHT-LRR region of NLRP1 in an ATP-dependent process, forming a stable complex that restrains inflammasome activation. Consistent with these findings, patient-derived and ATPase-inactivating mutations in the NACHT-LRR region that cause hyperactive inflammasome formation interfere with TRX1 binding. Overall, this work strongly suggests that reductive stress, the cellular perturbation that will eliminate oxidized TRX1 and abrogate the TRX1-NLRP1 interaction, is a danger signal that activates the NLRP1 inflammasome.

Indexed as

InflammasomesThioredoxinsAdaptor Proteins, Signal TransducingHumansNLR ProteinsAdaptor Proteins, Signal TransducingInflammasomesNLRP1 protein, humanNLR ProteinsThioredoxins

Identifiers

PMID36332009
PMCPMC9850498
OpenAlexW4308338215

What OpenQuestion holds

Textmetadata
LicenceTDM
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.