Evidence map›Paper›PMID 34120141›Full record

ArticleOncogene2021

NK and NKT cells have distinct properties and functions in cancer.

Xia Liu, Lingyun Li, Fusheng Si, Lan Huang, Yangjing Zhao, Chenchen Zhang, Daniel F Hoft, Guangyong Peng

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

54 citing papers in PubMed, 74 citations in OpenAlex.

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  15. The Effects of Released Exosomes from NK-92 Cells with IL15 on the Apoptosis of HL-60 Cell Line.International journal of hematology-oncology and stem cell research · 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

8 authors at 2 institutions in 2 countries.

Xia Liu *Division of Infectious Diseases, Allergy & Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO, USA.ORCID http://orcid.org/0000-0002-5372-1245
Lingyun Li *Division of Infectious Diseases, Allergy & Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO, USA.
Fusheng SiDivision of Infectious Diseases, Allergy & Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO, USA.
Lan HuangDivision of Infectious Diseases, Allergy & Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO, USA.
Yangjing ZhaoDivision of Infectious Diseases, Allergy & Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO, USA.
Chenchen ZhangDivision of Infectious Diseases, Allergy & Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO, USA.
Daniel F HoftDivision of Infectious Diseases, Allergy & Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO, USA.
Guangyong PengDivision of Infectious Diseases, Allergy & Immunology and Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO, USA. guangyong.peng@health.slu.edu.ORCID http://orcid.org/0000-0001-7268-0234
Saint Louis University · USSaint Louis University · ES

Funding

Metabolic Control of T Cell Senescence in Pathogenesis and Immunotherapy of Alzheimer's DiseaseR01AG078822 · NIA · WASHINGTON UNIVERSITY · PI Guangyong Peng · 2022 to 2026
$1.9M
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
Excessive lipid metabolism in T cell senescence and immunosuppressionR01AI173260 · NIAID · WASHINGTON UNIVERSITY · PI Guangyong Peng · 2023 to 2026
$1.6M
Role of Senescent T cells in Alzheimer's DiseaseR21AG067441 · NIA · WASHINGTON UNIVERSITY · PI PENG, GUANGYONG · 2020 to 2020
$417k
NCI NIH HHS R01 CA184379NCI NIH HHS R01 CA237149NCI NIH HHS R01 CA242188NIAID NIH HHS R01 AI173260NIA NIH HHS R01 AG078822NIA NIH HHS R21 AG067441
6 · The paper itself

Abstract

Natural killer (NK) and natural killer T (NKT) cells are two important cell subsets of the innate immune system. NK and NKT cells share many phenotypes and functions for anti-tumor immunity; however, the dynamic changes in phenotypes and functional interactions within the tumor microenvironment during tumor development and progression are unknown. Here we report that NK and NKT cells have distinct properties, metabolic profiles, and functions during tumor development. Using the mouse E0771 breast cancer and B16 melanoma models, we found that both NK and NKT cells are dynamically involved in the immune responses to cancer but have distinct distributions and phenotypic profiles in tumor sites and other peripheral organs during the course of tumor development and progression. In the early stages of tumor development, both NK and NKT cells exhibit effector properties. In the later cancer stages, NK and NKT cells have impaired cytotoxic capacities and dysfunctional states. NK cells become senescent cells, while NKT cells, other than invariant NKT (iNKT) cells, are exhausted in the advanced cancers. In contrast, iNKT cells develop increases in activation and effector function within the breast tumor microenvironment. In addition, senescent NK cells have heightened glucose and lipid metabolism, but exhausted NKT cells display unbalanced metabolism in tumor microenvironments of both breast cancer and melanoma tumor models. These studies provide a better understanding of the dynamic and distinct functional roles of NK and NKT cells in anti-tumor immunity, which may facilitate the development of novel immunotherapies targeting NK and NKT cells for cancer treatment.

Indexed as

Killer Cells, NaturalMelanoma, ExperimentalNatural Killer T-CellsTumor MicroenvironmentAnimalsCell Line, TumorFemaleHumansMiceMice, Inbred C57BL

Identifiers

PMID34120141
PMCPMC12416827
OpenAlexW3169600697

What OpenQuestion holds

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LicenceTDM
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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.