Evidence map›Paper›PMID 34476408›Full record

ArticleNature cancer2020

Autophagy promotes growth of tumors with high mutational burden by inhibiting a T-cell immune response.

Laura Poillet-Perez, Daniel W Sharp, Yang Yang, Saurabh V Laddha, Maria Ibrahim, Praveen K Bommareddy, Zhixian Sherrie Hu, Joshua Vieth, Michael Haas, Marcus W Bosenberg and 8 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nature cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
9.0field-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

84 citing papers in PubMed, 110 citations in OpenAlex.

  1. Review
  2. AnGenes · 2026
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  7. Oxidative pentose phosphate pathway is required for T cell activation and antitumor immunity.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  19. Role of the USP family in autophagy regulation and cancer progression.Apoptosis : an international journal on programmed cell death · 2025
    Review
  20. Review

24 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 3 institutions in 1 country.

Laura Poillet-PerezRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Daniel W SharpRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Yang YangRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.ORCID http://orcid.org/0000-0001-8963-658X
Saurabh V LaddhaRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.ORCID http://orcid.org/0000-0002-8781-9478
Maria IbrahimRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Praveen K BommareddyRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.ORCID http://orcid.org/0000-0003-0089-8693
Zhixian Sherrie HuRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Joshua ViethRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Michael HaasDepartment of Cancer Biology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Marcus W BosenbergDepartment of Pathology, Yale University School of Medicine, New Haven, CT, USA.
Joshua D RabinowitzRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.ORCID http://orcid.org/0000-0002-1247-4727
Jian CaoRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.ORCID http://orcid.org/0000-0003-3424-6802
Jun-Lin GuanDepartment of Cancer Biology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.ORCID http://orcid.org/0000-0001-8720-8338
Shridar GanesanRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Chang S ChanRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Janice M MehnertRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.
Edmund C LattimeRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.ORCID http://orcid.org/0000-0003-4945-7741
Eileen WhiteRutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA. epwhite@cinj.rutgers.edu.ORCID http://orcid.org/0000-0003-2961-3065
Rutgers, The State University of New Jersey · USUniversity of Cincinnati Medical Center · USYale University · US

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
Tumor cell metabolism in actionR01CA163591 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI JOSHUA D RABINOWITZ, Eileen P. White · 2012 to 2026
$7.0M
Mechanisms of FIP200 regulation of breast cancer through its autophagy and non-autophagy functionsR01CA211066 · NCI · UNIVERSITY OF CINCINNATI · PI JUN-LIN GUAN · 2017 to 2026
$3.4M
Impact of mutation burden on cancer growth and the immune landscapeR01CA243547 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI WHITE, EILEEN P. · 2020 to 2024
$3.2M
Promoting Bim-driven apoptosis through MAPK inhibition: A therapeutic strategy in advanced melanomaR01CA193970 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI MEHNERT, JANICE M., SULLIVAN, RYAN J · 2016 to 2020
$2.3M
NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA163591NCI NIH HHS R01 CA193970NCI NIH HHS R01 CA211066NCI NIH HHS R01 CA243547
6 · The paper itself

Abstract

Macroautophagy (hereafter autophagy) degrades and recycles intracellular components to sustain metabolism and survival during starvation. Host autophagy promotes tumor growth by providing essential tumor nutrients. Autophagy also regulates immune cell homeostasis and function and suppresses inflammation. Although host autophagy does not promote a T-cell anti-tumor immune response in tumors with low tumor mutational burden (TMB), whether this was the case in tumors with high TMB was not known. Here we show that autophagy, especially in the liver, promotes tumor immune tolerance by enabling regulatory T-cell function and limiting stimulator of interferon genes, T-cell response and interferon-γ, which enables growth of high-TMB tumors. We have designated this as hepatic autophagy immune tolerance. Autophagy thereby promotes tumor growth through both metabolic and immune mechanisms depending on mutational load and autophagy inhibition is an effective means to promote an antitumor T-cell response in high-TMB tumors.

Indexed as

AutophagyNeoplasmsHomeostasisHumansImmunity, CellularMutation

Identifiers

PMID34476408
PMCPMC8409526
OpenAlexW3125329766

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.