Evidence map›Paper›PMID 34453119›Full record

ArticleCell death and differentiation2022

Stress-induced inflammation evoked by immunogenic cell death is blunted by the IRE1α kinase inhibitor KIRA6 through HSP60 targeting.

Nicole Rufo, Dimitris Korovesis, Sofie Van Eygen, Rita Derua, Abhishek D Garg, Francesca Finotello, Monica Vara-Perez, Jan Rožanc, Michael Dewaele, Peter A de Witte and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  10. Frontiers in genetics · 2026
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  19. Article
  20. Molecular Chaperonin HSP60: Current Understanding and Future Prospects.International journal of molecular sciences · 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

16 authors at 7 institutions in 5 countries.

Nicole RufoCell Death Research and Therapy Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
Dimitris KorovesisLaboratory of Chemical Biology, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
Sofie Van EygenCell Death Research and Therapy Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
Rita DeruaLaboratory of Protein Phosphorylation and Proteomics, Department of Cellular and Molecular Medicine and SyBioMa, KU Leuven, Leuven, Belgium.
Abhishek D GargCell Death Research and Therapy Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0002-9976-9922
Francesca FinotelloBiocenter, Institute of Bioinformatics, Medical University of Innsbruck, Innsbruck, Austria.
Monica Vara-PerezCell Death Research and Therapy Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
Jan RožancDepartment of Life Sciences and Medicine, University of Luxembourg, Belvaux, Luxembourg.
Michael DewaeleVIB Center for Cancer Biology Research, Leuven, Belgium.
Peter A de WitteLaboratory for Molecular Biodiscovery, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0002-9989-9567
Leonidas G AlexopoulosProtATonce Ltd, Science Park Demokritos, Athens, Greece.
Sophie JanssensLaboratory for ER stress and Inflammation, VIB Center for Inflammation Research and Department of Internal Medicine and Pediatrics, Ghent University, Ghent, Belgium.ORCID http://orcid.org/0000-0003-1702-1636
Lasse SinkkonenDepartment of Life Sciences and Medicine, University of Luxembourg, Belvaux, Luxembourg.ORCID http://orcid.org/0000-0002-4223-3027
Thomas SauterDepartment of Life Sciences and Medicine, University of Luxembourg, Belvaux, Luxembourg.
Steven H L VerhelstLaboratory of Chemical Biology, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0002-7400-1319
Patrizia AgostinisCell Death Research and Therapy Laboratory, Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium. Patrizia.agostinis@kuleuven.be.ORCID http://orcid.org/0000-0003-1314-2115
VIB-KU Leuven Center for Cancer Biology · BEKU Leuven · BEUniversity of Luxembourg · LUGhent University · BEInnsbruck Medical University · ATLeibniz Institute for Analytical Sciences - ISAS · DENational Technical University of Athens · GR

Funding

Austrian Science Fund FWF T 974
6 · The paper itself

Abstract

Mounting evidence indicates that immunogenic therapies engaging the unfolded protein response (UPR) following endoplasmic reticulum (ER) stress favor proficient cancer cell-immune interactions, by stimulating the release of immunomodulatory/proinflammatory factors by stressed or dying cancer cells. UPR-driven transcription of proinflammatory cytokines/chemokines exert beneficial or detrimental effects on tumor growth and antitumor immunity, but the cell-autonomous machinery governing the cancer cell inflammatory output in response to immunogenic therapies remains poorly defined. Here, we profiled the transcriptome of cancer cells responding to immunogenic or weakly immunogenic treatments. Bioinformatics-driven pathway analysis indicated that immunogenic treatments instigated a NF-κB/AP-1-inflammatory stress response, which dissociated from both cell death and UPR. This stress-induced inflammation was specifically abolished by the IRE1α-kinase inhibitor KIRA6. Supernatants from immunogenic chemotherapy and KIRA6 co-treated cancer cells were deprived of proinflammatory/chemoattractant factors and failed to mobilize neutrophils and induce dendritic cell maturation. Furthermore, KIRA6 significantly reduced the in vivo vaccination potential of dying cancer cells responding to immunogenic chemotherapy. Mechanistically, we found that the anti-inflammatory effect of KIRA6 was still effective in IRE1α-deficient cells, indicating a hitherto unknown off-target effector of this IRE1α-kinase inhibitor. Generation of a KIRA6-clickable photoaffinity probe, mass spectrometry, and co-immunoprecipitation analysis identified cytosolic HSP60 as a KIRA6 off-target in the IKK-driven NF-κB pathway. In sum, our study unravels that HSP60 is a KIRA6-inhibitable upstream regulator of the NF-κB/AP-1-inflammatory stress responses evoked by immunogenic treatments. It also urges caution when interpreting the anti-inflammatory action of IRE1α chemical inhibitors.

Indexed as

EndoribonucleasesProtein Serine-Threonine KinasesEndoplasmic ReticulumHumansImidazolesImmunogenic Cell DeathInflammationNaphthalenesPyrazinesEndoribonucleasesImidazolesKIRA6NaphthalenesProtein Serine-Threonine KinasesPyrazines

Identifiers

PMID34453119
PMCPMC8738768
OpenAlexW3193841498

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.