ArticleResearch square2024
HIF1α-glycolysis engages activation-induced cell death to drive IFN-γ induction in hypoxic T cells.
Hongxing Shen, Logan Mullen, Oluwagbemiga A Ojo, Chuan Xing, Abdelrahman Yassin, Zach Lewis, James A Bonner, Lewis Zhichang Shi
Open access · greenAbstract readPreprint
In one paragraphArticle in Research square, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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1 · What the graph read from itWhat it found
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2 · The registryThe trial behind it
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3 · Its place in the literatureWho cites it
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4 · The recordCorrections and comments
5 · Who and what moneyAuthors and funding
8 authors at 3 institutions in 1 country.
Hongxing ShenDepartment of Radiation Oncology, Heersink School of Medicine, University of Alabama at Birmingham (UAB-SOM), Birmingham, AL 35233, USA.ORCID 0000-0001-7400-6809 Logan MullenGenomics Core Laboratory, Institute of Arctic Biology, University of Alaska Fairbanks, Fairbanks, Alaska, 99775, USA.
Oluwagbemiga A OjoDepartment of Radiation Oncology, Heersink School of Medicine, University of Alabama at Birmingham (UAB-SOM), Birmingham, AL 35233, USA.
Chuan XingDepartment of Radiation Oncology, Heersink School of Medicine, University of Alabama at Birmingham (UAB-SOM), Birmingham, AL 35233, USA.
Abdelrahman YassinDepartment of Radiation Oncology, Heersink School of Medicine, University of Alabama at Birmingham (UAB-SOM), Birmingham, AL 35233, USA.
Zach LewisDepartment of Radiation Oncology, Heersink School of Medicine, University of Alabama at Birmingham (UAB-SOM), Birmingham, AL 35233, USA.
James A BonnerDepartment of Radiation Oncology, Heersink School of Medicine, University of Alabama at Birmingham (UAB-SOM), Birmingham, AL 35233, USA.
Lewis Zhichang ShiDepartment of Radiation Oncology, Heersink School of Medicine, University of Alabama at Birmingham (UAB-SOM), Birmingham, AL 35233, USA.ORCID 0000-0002-5351-8730 University of Alabama at Birmingham · USUniversity of Alabama · USUniversity of Alaska Fairbanks · US
Funding
T cell-intrinsic metabolic control of radiotherapyR01CA279849 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Lewis Z. Shi · 2024 to 2026
$1.2MOvercoming Tumor-Intrinsic Therapeutic Resistance to ImmunotherapiesR21CA259721 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SHI, LEWIS ZHICHANG · 2022 to 2023
$378kTargeting metabolic checkpoints in the tumor microenvironment to boost efficacy of anti-CTLA-4R21CA230475 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SHI, LEWIS ZHICHANG · 2019 to 2020
$355kNCI NIH HHS R01 CA279849NCI NIH HHS R21 CA230475NCI NIH HHS R21 CA259721
6 · The paper itselfAbstract
The role of HIF1α-glycolysis in regulating IFN-γ induction in hypoxic T cells is unknown. Given that hypoxia is a common feature in a wide array of pathophysiological contexts such as tumor and that IFN-γ is instrumental for protective immunity, it is of great significance to gain a clear idea on this. Combining pharmacological and genetic gain-of-function and loss-of-function approaches, we find that HIF1α-glycolysis controls IFN-γ induction in both human and mouse T cells activated under hypoxia. Specific deletion of HIF1α in T cells (HIF1α
Indexed as
acetate supplementationanaerobic glycolysisHIF1αhypoxiaICBIFN-γT cell
Identifiers
PMID38260594
PMCPMC10802708
OpenAlexW4390822763
What OpenQuestion holds
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LicenceCC BY
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