Evidence map›Paper›PMID 29038298›Full record

ArticleCancer immunology research2017

Subversion of NK-cell and TNFα Immune Surveillance Drives Tumor Recurrence.

Tim Kottke, Laura Evgin, Kevin G Shim, Diana Rommelfanger, Nicolas Boisgerault, Shane Zaidi, Rosa Maria Diaz, Jill Thompson, Elizabeth Ilett, Matt Coffey and 5 more

Abstract read
In one paragraph

Article in Cancer immunology research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  4. Article
  5. Tetrahedral DNA nanostructures synergize with MnOActa pharmaceutica Sinica. B · 2022
    Article
  6. APOBEC and Cancer Viroimmunotherapy: Thinking the Unthinkable.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Review
  7. Article
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  9. Article
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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 2 institutions in 2 countries.

Tim KottkeDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota.
Laura EvginDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota.
Kevin G ShimDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota.
Diana RommelfangerDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota.
Nicolas BoisgeraultDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota.
Shane ZaidiDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota.
Rosa Maria DiazDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota.
Jill ThompsonDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota.
Elizabeth IlettLeeds Institute of Cancer and Pathology, St. James' University Hospital, Leeds, United Kingdom.
Matt CoffeyOncolytics Biotech Incorporated, Calgary, Canada.
Peter SelbyLeeds Institute of Cancer and Pathology, St. James' University Hospital, Leeds, United Kingdom.
Hardev PandhaUniversity of Surrey, Guildford, United Kingdom.
Kevin HarringtonThe Institute of Cancer Research, London, United Kingdom.
Alan MelcherThe Institute of Cancer Research, London, United Kingdom.
Richard VileDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota. vile.richard@mayo.edu.
Institute of Cancer Research · GBMayo Clinic · US

Funding

Targeted MV-CEA as a Potent Antitumor Agent against GBMP50CA108961 · NCI · MAYO CLINIC ROCHESTER · PI O'NEILL, BRIAN PATRICK · 2004 to 2015
$22.5M
Enhancing Therapy of Primary and Recurrent Tumors With Systemic Oncolytic VirusR01CA175386 · NCI · MAYO CLINIC ROCHESTER · PI VILE, RICHARD G. · 2014 to 2018
$1.3M
Cancer Research UK 21855Department of Health RP-PG-0707-10101NCI NIH HHS P50 CA108961NCI NIH HHS R01 CA175386
6 · The paper itself

Abstract

Understanding how incompletely cleared primary tumors transition from minimal residual disease (MRD) into treatment-resistant, immune-invisible recurrences has major clinical significance. We show here that this transition is mediated through the subversion of two key elements of innate immunosurveillance. In the first, the role of TNFα changes from an antitumor effector against primary tumors into a growth promoter for MRD. Second, whereas primary tumors induced a natural killer (NK)-mediated cytokine response characterized by low IL6 and elevated IFNγ, PD-L1

Indexed as

AnimalsAntibodiesCell Line, TumorCytokinesFemaleGanciclovirImmunologic SurveillanceKiller Cells, NaturalMelanoma, ExperimentalMice, Inbred C57BLMice, TransgenicNeoplasm Recurrence, LocalOncolytic VirotherapyPaclitaxelReoviridaeSkin NeoplasmsAntibodiesCytokinesGanciclovirPaclitaxelTumor Necrosis Factor-alpha

Identifiers

PMID29038298
PMCPMC5858196
OpenAlexW2765326687

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.