Evidence map›Paper›PMID 32200350›Full record

ArticleCancer discovery2020

Repression of the Type I Interferon Pathway Underlies MYC- and KRAS-Dependent Evasion of NK and B Cells in Pancreatic Ductal Adenocarcinoma.

Nathiya Muthalagu, Tiziana Monteverde, Ximena Raffo-Iraolagoitia, Robert Wiesheu, Declan Whyte, Ann Hedley, Sarah Laing, Björn Kruspig, Rosanna Upstill-Goddard, Robin Shaw and 12 more

Open access · greenAbstract read
In one paragraph

Article in Cancer discovery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 2 pooled it
9.0field-weighted citation impact, top 2% 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

125 citing papers in PubMed, 2 syntheses or guidelines pooled it, 172 citations in OpenAlex.

  1. Hyperprogressive disease in carcinoma induced by immune checkpoint inhibitor therapy: a systematic review.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Pooled it
  2. Pooled it
  3. Article
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  7. Formic acid released by intratumoralActa pharmaceutica Sinica. B · 2026
    Article
  8. NAT10-Mediated ac4C Modification of circANKRD12 Reprograms the Tumor Microenvironment.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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65 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

22 authors at 3 institutions in 1 country.

Nathiya MuthalaguCRUK Beatson Institute, Glasgow, Scotland, United Kingdom.
Tiziana MonteverdeInstitute of Cancer Sciences, University of Glasgow, Glasgow, Scotland, United Kingdom.ORCID 0000-0002-4115-2188
Ximena Raffo-IraolagoitiaCRUK Beatson Institute, Glasgow, Scotland, United Kingdom.
Robert WiesheuInstitute of Cancer Sciences, University of Glasgow, Glasgow, Scotland, United Kingdom.ORCID 0000-0002-2079-4413
Declan WhyteInstitute of Cancer Sciences, University of Glasgow, Glasgow, Scotland, United Kingdom.
Ann HedleyCRUK Beatson Institute, Glasgow, Scotland, United Kingdom.
Sarah LaingInstitute of Cancer Sciences, University of Glasgow, Glasgow, Scotland, United Kingdom.ORCID 0000-0003-3761-5749
Björn KruspigInstitute of Cancer Sciences, University of Glasgow, Glasgow, Scotland, United Kingdom.
Rosanna Upstill-GoddardWolfson Wohl Translational Cancer Research Centre, University of Glasgow, Glasgow, Scotland, United Kingdom.ORCID 0000-0002-2666-0934
Robin ShawCRUK Beatson Institute, Glasgow, Scotland, United Kingdom.
Sarah NeidlerInstitute of Cancer Sciences, University of Glasgow, Glasgow, Scotland, United Kingdom.ORCID 0000-0003-1075-3535
Curtis RinkCRUK Beatson Institute, Glasgow, Scotland, United Kingdom.
Saadia A KarimCRUK Beatson Institute, Glasgow, Scotland, United Kingdom.ORCID 0000-0002-3727-0667
Katarina GyuraszovaInstitute of Cancer Sciences, University of Glasgow, Glasgow, Scotland, United Kingdom.
Colin NixonCRUK Beatson Institute, Glasgow, Scotland, United Kingdom.
William ClarkCRUK Beatson Institute, Glasgow, Scotland, United Kingdom.
Andrew V BiankinWolfson Wohl Translational Cancer Research Centre, University of Glasgow, Glasgow, Scotland, United Kingdom.ORCID 0000-0002-0362-5597
Leo M CarlinCRUK Beatson Institute, Glasgow, Scotland, United Kingdom.ORCID 0000-0001-7172-5234
Seth B CoffeltCRUK Beatson Institute, Glasgow, Scotland, United Kingdom.ORCID 0000-0003-2257-2862
Owen J SansomCRUK Beatson Institute, Glasgow, Scotland, United Kingdom.
Jennifer P MortonCRUK Beatson Institute, Glasgow, Scotland, United Kingdom. daniel.murphy@glasgow.ac.uk Jennifer.morton@glasgow.ac.uk.
Daniel J MurphyCRUK Beatson Institute, Glasgow, Scotland, United Kingdom. daniel.murphy@glasgow.ac.uk Jennifer.morton@glasgow.ac.uk.ORCID 0000-0002-5538-5468
Cancer Research UK Scotland Institute · GBUniversity of Glasgow · GBBeatson West of Scotland Cancer Centre · GB

Funding

Cancer Research UK 21139Cancer Research UK 23983Cancer Research UK 29996Cancer Research UK A17196Cancer Research UK A21139Cancer Research UK A23983Cancer Research UK A25142Wellcome Trust 105614Wellcome Trust 105614/Z/14/ZWorldwide Cancer Research 15-0279
6 · The paper itself

Abstract

MYC is implicated in the development and progression of pancreatic cancer, yet the precise level of MYC deregulation required to contribute to tumor development has been difficult to define. We used modestly elevated expression of human MYC, driven from the

Indexed as

B-LymphocytesCarcinoma, Pancreatic DuctalCell ProliferationHumansInterferon Type IKiller Cells, NaturalPancreatic NeoplasmsInterferon Type I

Identifiers

PMID32200350
PMCPMC7611248
OpenAlexW3011578554

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.