Evidence map›Paper›PMID 36117525›Full record

ArticleOncoimmunology2022

Targeting DNA damage response components induces enhanced STING-dependent type-I IFN response in ATM deficient cancer cells and drives dendritic cell activation.

Marta Lopez-Pelaez, Lucy Young, Mercedes Vazquez-Chantada, Nadine Nelson, Steve Durant, Robert W Wilkinson, Edmund Poon, Miguel Gaspar, Viia Valge-Archer, Paul Smith and 1 more

Abstract read
In one paragraph

Article in Oncoimmunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Article
  2. Review
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  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. When DNA-damage responses meet innate and adaptive immunity.Cellular and molecular life sciences : CMLS · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Review
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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

11 authors.

Marta Lopez-PelaezOncology R&D, AstraZeneca, UK.
Lucy YoungOncology R&D, AstraZeneca, UK.
Mercedes Vazquez-ChantadaDiscovery Sciences, R&D, AstraZeneca, UK.
Nadine NelsonOncology R&D, AstraZeneca, UK.
Steve DurantOncology R&D, AstraZeneca, UK.
Robert W WilkinsonOncology R&D, AstraZeneca, UK.
Edmund PoonOncology R&D, AstraZeneca, UK.
Miguel GasparOncology R&D, AstraZeneca, UK.
Viia Valge-ArcherOncology R&D, AstraZeneca, UK.
Paul SmithOncology R&D, AstraZeneca, UK.
Simon J DovediOncology R&D, AstraZeneca, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The concept of exploiting tumor intrinsic deficiencies in DNA damage repair mechanisms by inhibiting compensatory DNA repair pathways is well established. For example, ATM-deficient cells show increased sensitivity to the ATR inhibitor ceralasertib. DNA damage response (DDR)-deficient cells are also more sensitive to DNA damaging agents like the DNA crosslinker pyrrolobenzodiazepine (PBD) SG-3199. However, additional antitumor benefits from targeting the DDR pathways, which could operate through the activation of the innate immune system are less well studied. DNA accumulation in the cytosol acts as an immunogenic danger signal, inducing the expression of type-I interferon (IFN) stimulated genes (ISGs) by the activation of the cGAS-STING pathway. Here, we demonstrate that ATM

Indexed as

Interferon Type INeoplasmsDendritic CellsDNADNA DamageExodeoxyribonucleasesIndolesMembrane ProteinsMorpholinesNucleotidyltransferasesPyrimidinesSulfonamidesceralasertibDNAExodeoxyribonucleasesIndolesInterferon Type IMembrane ProteinsMorpholinesNucleotidyltransferasesPyrimidinesSulfonamidesATMATRceralasertibDCDDRDNA damage repairInterferonPBD SG-3199STINGTREX1

Identifiers

PMID36117525
PMCPMC9481087

What OpenQuestion holds

Textmetadata
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.