Evidence map›Paper›PMID 34359633›Full record

ArticleCancers2021

Targeting Replication Stress Using CHK1 Inhibitor Promotes Innate and NKT Cell Immune Responses and Tumour Regression.

Martina Proctor, Jazmina L Gonzalez Cruz, Sheena M Daignault-Mill, Margaret Veitch, Bijun Zeng, Anna Ehmann, Muhammed Sabdia, Cameron Snell, Colm Keane, Riccardo Dolcetti and 3 more

Abstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. 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

13 authors.

Martina ProctorMater Research Institute, The University of Queensland, Brisbane, QLD 4102, Australia.
Jazmina L Gonzalez CruzThe University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD 4102, Australia.ORCID 0000-0003-2671-7408
Sheena M Daignault-MillThe University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD 4102, Australia.ORCID 0000-0002-8791-853X
Margaret VeitchThe University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD 4102, Australia.
Bijun ZengThe University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD 4102, Australia.ORCID 0000-0002-6199-0584
Anna EhmannMater Research Institute, The University of Queensland, Brisbane, QLD 4102, Australia.
Muhammed SabdiaMater Research Institute, The University of Queensland, Brisbane, QLD 4102, Australia.
Cameron SnellMater Pathology, Mater Research, Mater Hospital, Raymond Terrace, South Brisbane, QLD 4101, Australia.ORCID 0000-0001-7847-3041
Colm KeaneMater Research Institute, The University of Queensland, Brisbane, QLD 4102, Australia.ORCID 0000-0002-9009-9934
Riccardo DolcettiThe University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD 4102, Australia.ORCID 0000-0003-1625-9853
Nikolas K HaassThe University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD 4102, Australia.ORCID 0000-0002-3928-5360
James W WellsThe University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD 4102, Australia.ORCID 0000-0002-9618-6940
Brian GabrielliMater Research Institute, The University of Queensland, Brisbane, QLD 4102, Australia.ORCID 0000-0003-3933-1651

Funding

CSRD VA 1
6 · The paper itself

Abstract

Drugs selectively targeting replication stress have demonstrated significant preclinical activity, but this has not yet translated into an effective clinical treatment. Here we report that targeting increased replication stress with a combination of Checkpoint kinase 1 inhibitor (CHK1i) with a subclinical dose of hydroxyurea targets also promotes pro-inflammatory cytokine/chemokine expression that is independent of cGAS-STING pathway activation and immunogenic cell death in human and murine melanoma cells. In vivo, this drug combination induces tumour regression which is dependent on an adaptive immune response. It increases cytotoxic CD8

Indexed as

adaptive immune responseCHK1 inhibitorimmunogenic cell deathinnate immune responsemelanomaNKT cellsreplication stress

Identifiers

PMID34359633
PMCPMC8345057

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.