Evidence map›Paper›PMID 27667712›Full record

ReviewNature reviews. Immunology2016

Emerging roles of p53 and other tumour-suppressor genes in immune regulation.

César Muñoz-Fontela, Anna Mandinova, Stuart A Aaronson, Sam W Lee

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 224 papers.

0numbers the graph read from it
0cells of the map it votes in
224citing papers in PubMed
12.8field-weighted citation impact, top 1% 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

224 citing papers in PubMed, 337 citations in OpenAlex.

  1. Phase II Trial of IL-12 Plasmid Transfection and PD-1 Blockade in Immunologically Quiescent Melanoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
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  7. Oncology research · 2026
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164 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

4 authors at 3 institutions in 2 countries.

César Muñoz-FontelaHeinrich Pette Institute, Leibniz Institute for Experimental Virology, Martinistrasse 52, 20251 Hamburg, Germany.
Anna MandinovaCutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Building 149 13th Street, Charlestown, Massachusetts 02129, USA.
Stuart A AaronsonDepartment of Oncological Sciences, Mount Sinai School of Medicine, One Gustave L. Levy Place, New York, New York 10029, USA.
Sam W LeeCutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Building 149 13th Street, Charlestown, Massachusetts 02129, USA.
Massachusetts General Hospital · USIcahn School of Medicine at Mount Sinai · USLeibniz Institute of Virology (LIV) · DE

Funding

PW1--A mediator of cell survival by NFKB and cell death by p53P01CA080058 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI AARONSON, STUART A · 2000 to 2016
$20.2M
P53 survival target DDR1 kinase in DNA damage response and carcinogenesisR01CA195534 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, SAM W · 2015 to 2018
$1.6M
p53-mediated dead cell clearance in response to DNA damage and tumorigenesisR01CA203552 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, SAM W · 2016 to 2017
$736k
Tumor suppressor p53 and its targets in checkpoint regulationR01CA210560 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, SAM W · 2017 to 2018
$733k
NCI NIH HHS P01 CA080058NCI NIH HHS R01 CA195534NCI NIH HHS R01 CA203552NCI NIH HHS R01 CA210560
6 · The paper itself

Abstract

Tumour-suppressor genes are indispensable for the maintenance of genomic integrity. Recently, several of these genes, including those encoding p53, PTEN, RB1 and ARF, have been implicated in immune responses and inflammatory diseases. In particular, the p53 tumour- suppressor pathway is involved in crucial aspects of tumour immunology and in homeostatic regulation of immune responses. Other studies have identified roles for p53 in various cellular processes, including metabolism and stem cell maintenance. Here, we discuss the emerging roles of p53 and other tumour-suppressor genes in tumour immunology, as well as in additional immunological settings, such as virus infection. This relatively unexplored area could yield important insights into the homeostatic control of immune cells in health and disease and facilitate the development of more effective immunotherapies. Consequently, tumour-suppressor genes are emerging as potential guardians of immune integrity.

Indexed as

ImmunityImmunomodulationAdaptive ImmunityAnimalsAutoimmunityDisease SusceptibilityGene Expression RegulationHost-Pathogen InteractionsHumansImmune SystemImmunity, InnateSignal TransductionTumor Suppressor Protein p53Tumor Suppressor ProteinsTumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID27667712
PMCPMC5325695
OpenAlexW2527179423

What OpenQuestion holds

Textmetadata
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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.