Evidence map›Paper›PMID 32323922›Full record

ArticleEMBO molecular medicine2020

Inhibition of transcription by dactinomycin reveals a new characteristic of immunogenic cell stress.

Juliette Humeau, Allan Sauvat, Giulia Cerrato, Wei Xie, Friedemann Loos, Francesca Iannantuoni, Lucillia Bezu, Sarah Lévesque, Juliette Paillet, Jonathan Pol and 5 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
9.4field-weighted citation impact, top 1% 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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
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  14. The danger theory of immunity revisited.Nature reviews. Immunology · 2024
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  20. Progress of immunotherapies in gestational trophoblastic neoplasms.Journal of cancer research and clinical oncology · 2023
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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

15 authors at 4 institutions in 4 countries.

Juliette HumeauEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.
Allan SauvatEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.
Giulia CerratoEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.
Wei XieEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.
Friedemann LoosEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.ORCID 0000-0002-5976-5978
Francesca IannantuoniEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.
Lucillia BezuEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.
Sarah LévesqueEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.
Juliette PailletEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.
Jonathan PolEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.ORCID 0000-0002-8355-7562
Marion LeducEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.
Laurence ZitvogelFaculty of Medicine Kremlin Bicêtre, Université Paris Sud, Paris Saclay, Paris, France.
Hugues de ThéCollege de France, INSERM UMR 1050, CNRS UMR 7241, PSL University, Paris, France.
Oliver KeppEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.ORCID 0000-0002-6081-9558
Guido KroemerEquipe labellisée par la Ligue contre le Cancer, Sorbonne Université, INSERM UMR1138, Centre de Recherche des Cordeliers, Université de Paris, Paris, France.ORCID 0000-0002-9334-4405
Inserm · FRUniversité Paris-Sud · FRCentre National de la Recherche Scientifique · FRKarolinska University Hospital · SE

Funding

Agence National de la Recherche (ANR)Association pour la recherche sur le cancer (ARC)BMSCancéropôle Ile-de-FranceChancellerie des universités de Paris (Legs Poix)China Scholarship CouncilEliorEuropean Research Area Network on Cardiovascular Diseases (ERA-CVD, MINOTAUR)European Union Horizon 2020 Project OncobiomeFondation CarrefourFondation pour la recherche médicale FRM - FDT201805005722Fondation pour la Recherche Médicale (FRM)Foundation PhilanthropiaGustave Roussy OdysseaHigh-end Foreign Expert Program in China GDW20171100085High-end Foreign Expert Program in China GDW20181100051Inserm (HTE)Institut National du Cancer (INCa)Institut Universitaire de FranceLabEx Immuno-OncologyLeDucq FoundationLigue contre le Cancer (équipe labellisée)Regional Ministry for Education in Valencia GRISOLIAP/2016/015Regional Ministry for Education in Valencia-European Social Fund BEFPI/2018/030RHU Torino LumièreSeerave FoundationSIRIC Cancer Research and Personalized Medicine (CARPEM)SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE)
6 · The paper itself

Abstract

Chemotherapy still constitutes the standard of care for the treatment of most neoplastic diseases. Certain chemotherapeutics from the oncological armamentarium are able to trigger pre-mortem stress signals that lead to immunogenic cell death (ICD), thus inducing an antitumor immune response and mediating long-term tumor growth reduction. Here, we used an established model, built on artificial intelligence to identify, among a library of 50,000 compounds, anticancer agents that, based on their molecular descriptors, were predicted to induce ICD. This algorithm led us to the identification of dactinomycin (DACT, best known as actinomycin D), a highly potent cytotoxicant and ICD inducer that mediates immune-dependent anticancer effects in vivo. Since DACT is commonly used as an inhibitor of DNA to RNA transcription, we investigated whether other experimentally established or algorithm-selected, clinically employed ICD inducers would share this characteristic. As a common leitmotif, a panel of pharmacological ICD stimulators inhibited transcription and secondarily translation. These results establish the inhibition of RNA synthesis as an initial event for ICD induction.

Indexed as

Antineoplastic AgentsNeoplasmsArtificial IntelligenceDactinomycinHumansImmunogenic Cell DeathAntineoplastic AgentsDactinomycindactinomycineIF2α phosphorylationimmunogenic cell deathtranscriptiontranslation

Identifiers

PMID32323922
PMCPMC7207166
OpenAlexW2996902418

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.