Evidence map›Paper›PMID 29891488›Full record

ArticleMolecular cancer therapeutics2018

The ATR Inhibitor AZD6738 Synergizes with Gemcitabine

Yann Wallez, Charles R Dunlop, Timothy Isaac Johnson, Siang-Boon Koh, Chiara Fornari, James W T Yates, Sandra Bernaldo de Quirós Fernández, Alan Lau, Frances M Richards, Duncan I Jodrell

Abstract read
In one paragraph

Article in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

77 citing papers in PubMed, 107 citations in OpenAlex.

  1. Trial
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  5. Targeted therapeutic strategies forTranslational lung cancer research · 2026
    Review
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  7. Article
  8. ATR kinase inhibitors induce mitochondrial fission in CD8bioRxiv : the preprint server for biology · 2026
    Article
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17 more citing papers are in PubMed but not listed here.

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

10 authors at 3 institutions in 3 countries.

Yann WallezCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom. Yann.Wallez@cruk.cam.ac.uk Fran.Richards@cruk.cam.ac.uk.ORCID 0000-0001-9654-6187
Charles R DunlopCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-8194-2598
Timothy Isaac JohnsonCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom.
Siang-Boon KohCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-5494-3800
Chiara FornariSafety and ADME Translational Sciences Department, Drug Safety and Metabolism, IMED Biotech Unit, AstraZeneca, Cambridge, United Kingdom.
James W T YatesOncology, IMED Biotech Unit, AstraZeneca, Cambridge, United Kingdom.
Sandra Bernaldo de Quirós FernándezCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom.
Alan LauOncology, IMED Biotech Unit, AstraZeneca, Cambridge, United Kingdom.
Frances M RichardsCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom. Yann.Wallez@cruk.cam.ac.uk Fran.Richards@cruk.cam.ac.uk.ORCID 0000-0001-7947-7853
Duncan I JodrellCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom.
University of Cambridge · GBAstraZeneca (United Kingdom) · GBHarvard University · US

Funding

Cancer Research UK 15678Cancer Research UK A15678
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is among the deadliest cancers, and overall survival rates have barely improved over the past five decades. The antimetabolite gemcitabine remains part of the standard of care but shows very limited antitumor efficacy. Ataxia telangiectasia and Rad3-related protein (ATR), the apical kinase of the intra-S-phase DNA damage response, plays a central role in safeguarding cells from replication stress and can therefore limit the efficacy of antimetabolite drug therapies. We investigated the ability of the ATR inhibitor, AZD6738, to prevent the gemcitabine-induced intra-S-phase checkpoint activation and evaluated the antitumor potential of this combination

Indexed as

AdenocarcinomaAnimalsAntimetabolites, AntineoplasticCarcinoma, Pancreatic DuctalDeoxycytidineGemcitabineHumansIndolesMiceMorpholinesPyrimidinesSulfonamidesSulfoxidesAntimetabolites, AntineoplasticceralasertibDeoxycytidineGemcitabineIndolesMorpholinesPyrimidinesSulfonamidesSulfoxides

Identifiers

PMID29891488
PMCPMC6076438
OpenAlexW2807942883

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.