Evidence map›Paper›PMID 36821379›Full record

ArticleThe Journal of clinical investigation2023

Glycolysis drives STING signaling to facilitate dendritic cell antitumor function.

Zhilin Hu, Xiaoyan Yu, Rui Ding, Ben Liu, Chuanjia Gu, Xiu-Wu Pan, Qiaoqiao Han, Yuerong Zhang, Jie Wan, Xin-Gang Cui and 2 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
13.2field-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

64 citing papers in PubMed, 80 citations in OpenAlex.

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4 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

12 authors at 6 institutions in 2 countries.

Zhilin HuDepartment of Immunology, Key Laboratory of Immune Microenvironment and Disease, The School of Basic Medicine, Nanjing Medical University, Nanjing, China.
Xiaoyan YuShanghai Institute of Immunology, Department of Immunology and Microbiology, National Key Laboratory of Cancer Systems Medicine.
Rui DingShanghai Institute of Immunology, Department of Immunology and Microbiology, National Key Laboratory of Cancer Systems Medicine.
Ben LiuDepartment of Immunology, Key Laboratory of Immune Microenvironment and Disease, The School of Basic Medicine, Nanjing Medical University, Nanjing, China.
Chuanjia GuDepartment of Respiratory Endoscopy, Department of Respiratory and Critical Care Medicine, Shanghai Chest Hospital, and.
Xiu-Wu PanDepartment of Urology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Qiaoqiao HanShanghai Institute of Immunology, Department of Immunology and Microbiology, National Key Laboratory of Cancer Systems Medicine.
Yuerong ZhangShanghai Institute of Immunology, Department of Immunology and Microbiology, National Key Laboratory of Cancer Systems Medicine.
Jie WanShanghai Institute of Immunology, Department of Immunology and Microbiology, National Key Laboratory of Cancer Systems Medicine.
Xin-Gang CuiDepartment of Urology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Jiayuan SunDepartment of Respiratory Endoscopy, Department of Respiratory and Critical Care Medicine, Shanghai Chest Hospital, and.
Qiang ZouShanghai Institute of Immunology, Department of Immunology and Microbiology, National Key Laboratory of Cancer Systems Medicine.
Institute of Immunology · HRShanghai Cancer Institute · CNShanghai Chest Hospital · CNNanjing Medical University · CNShanghai Jiao Tong University · CNXinHua Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activation of STING signaling in DCs promotes antitumor immunity. Aerobic glycolysis is a metabolic hallmark of activated DCs, but how the glycolytic pathway intersects with STING signaling in tumor-infiltrating DCs remains elusive. Here, we show that glycolysis drives STING signaling to facilitate DC-mediated antitumor immune responses. Tumor-infiltrating DCs exhibited elevated glycolysis, and blockade of glycolysis by DC-specific Ldha/Ldhb double deletion resulted in defective antitumor immunity. Mechanistically, glycolysis augmented ATP production to boost STING activation and STING-dependent DC antitumor functions. Moreover, DC-intrinsic STING activation accelerated HIF-1α-mediated glycolysis and established a positive feedback loop. Importantly, glycolysis facilitated STING-dependent DC activity in tissue samples from patients with non-small cell lung cancer. Our results provide mechanistic insight into how the crosstalk of glycolytic metabolism and STING signaling enhances DC antitumor activity and can be harnessed to improve cancer therapies.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsDendritic CellsGlycolysisHumansSignal TransductionCancer immunotherapyGlucose metabolismImmunologyInnate immunityMetabolism

Identifiers

PMID36821379
PMCPMC10065062
OpenAlexW4321612870

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.