Evidence map›Paper›PMID 34973923›Full record

ReviewTrends in immunology2022

Tumor microenvironment metabolites directing T cell differentiation and function.

Xia Liu, Daniel F Hoft, Guangyong Peng

Open access · greenAbstract readReview
In one paragraph

Review in Trends in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.6field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
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  7. Molecular therapy. Oncology · 2025
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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

3 authors at 1 institution in 1 country.

Xia LiuDivision of Infectious Diseases, Allergy and Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO 63104, USA.
Daniel F HoftDivision of Infectious Diseases, Allergy and Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO 63104, USA; Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, MO 63104, USA.
Guangyong PengDivision of Infectious Diseases, Allergy and Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO 63104, USA; Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, MO 63104, USA. Electronic address: guangyong.peng@health.slu.edu.
Saint Louis University · US

Funding

Gamma/Delta Treg Cells and Human Breast CancerR01CA184379 · NCI · SAINT LOUIS UNIVERSITY · PI PENG, GUANGYONG · 2015 to 2019
$1.7M
Targeting T Cell Senescence and Dysfunction for Anti-tumor ImmunityR01CA242188 · NCI · WASHINGTON UNIVERSITY · PI Guangyong Peng · 2020 to 2026
$1.7M
Metabolic Control of Innate and Adaptive Immunity in Breast CancerR01CA237149 · NCI · WASHINGTON UNIVERSITY · PI Guangyong Peng · 2020 to 2026
$1.7M
Role of Senescent T cells in Alzheimer's DiseaseR21AG067441 · NIA · WASHINGTON UNIVERSITY · PI PENG, GUANGYONG · 2020 to 2020
$417k
T Regulatory Cells and Neonatal Innate ImmunityR21AI094478 · NIAID · SAINT LOUIS UNIVERSITY · PI KOENIG, JOYCE MARIE, PENG, GUANGYONG · 2012 to 2013
$413k
NCI NIH HHS R01 CA184379NCI NIH HHS R01 CA237149NCI NIH HHS R01 CA242188NIAID NIH HHS R21 AI094478NIA NIH HHS R21 AG067441
6 · The paper itself

Abstract

Metabolic reprogramming of cancer cells creates a unique tumor microenvironment (TME) characterized by the limited availability of nutrients, which subsequently affects the metabolism, differentiation, and function of tumor-infiltrating T lymphocytes (TILs). TILs can also be inhibited by tumor-derived metabolic waste products and low oxygen. Therefore, a thorough understanding of how such unique metabolites influence mammalian T cell differentiation and function can inform novel anticancer therapeutic approaches. Here, we highlight the importance of these metabolites in modulating various T cell subsets within the TME, dissecting how these changes might alter clinical outcomes. We explore potential TME metabolic determinants that might constitute candidate targets for cancer immunotherapies, ideally leading to future strategies for reprogramming tumor metabolism to potentiate anticancer T cell functions.

Indexed as

NeoplasmsTumor MicroenvironmentAnimalsCell DifferentiationHumansImmunotherapyLymphocytes, Tumor-InfiltratingMammalsmetabolic reprogrammingmetabolitesT cellstumor immunotherapytumor microenvironment

Identifiers

PMID34973923
PMCPMC8810659
OpenAlexW4200087503

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.