Evidence map›Paper›PMID 42432768›Full record

ReviewCell & bioscience2026

The diversity of STING in regulating immune cell function and its role in liver diseases: from bench to bedside.

Jing Lin, Yongle Liu, Yu Chen, Xiaohui Zhang

Abstract readReview
In one paragraph

Review in Cell & bioscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Jing LinFourth Department of Liver Disease, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Yongle LiuFourth Department of Liver Disease, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Yu ChenFourth Department of Liver Disease, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Xiaohui ZhangFourth Department of Liver Disease, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China. xiaohui.zhang@ccmu.edu.cn.

Funding

the Beijing Liver and Gallbladder Mutual Support Public Welfare Foundation LiGan Special Fund iGandanF-1082024-LG021the Beijing You'an Hospital Affiliated to Capital Medical University Talent Pool Cultivation Programme YARCKC2022004the High-level Public Health Technical Talent Development Project Discipline Backbone-02-24the National Natural Science Foundation of China 82470606
6 · The paper itself

Abstract

backgroundThe cyclic guanosine monophosphate-adenylate synthase (cGAS)-stimulator of interferon genes (STING) pathway is a critical innate immune signaling pathway that recognizes and transmits cytoplasmic DNA signals, triggering interferon and inflammatory responses. Immune cells enriched in the liver participate in the development of various liver diseases through the STING pathway; however, the precise regulatory mechanisms of this pathway within the immune cells remain poorly integrated. Elucidating these mechanisms holds promise for developing novel therapeutic strategies to address related clinical challenges. MAIN BODY: This review systematically elucidates the mechanisms by which immune cells from both innate and adaptive immune systems influence liver diseases via the STING pathway, viewed through the lens of immune cell classification. Considering the differential expression of STING across immune cell types and their cross-regulatory interactions, the review categorizes STING's impact on liver diseases into two patterns: direct regulation by endogenous STING (intracellular STING) and indirect regulation by exogenous STING (STING originating from other cells). The diseases discussed encompass common liver disorders, such as viral hepatitis, metabolic dysfunction-associated steatotic liver disease(MASLD), hepatocellular carcinoma(HCC), and autoimmune hepatitis (AIH),among others.Integrating the latest preclinical research findings, the review thoroughly explores the potential feasibility and research progress of targeting the STING pathway to modulate the progression of liver diseases, including traditional STING agonist/antagonist, and novel approaches such as targeted delivery systems and microbiotherapy in STING drug development, along with their therapeutic potential in liver diseases.

conclusionsThe cGAS-STING pathway serves as a pivotal signaling axis linking innate and adaptive immunity, playing a crucial role in the immune regulation of liver diseases. In-depth investigation of this pathway provides theoretical and translational foundations for elucidating the mechanisms underlying immune-metabolic dysregulation in the liver and developing precision immunotherapy strategies, thereby facilitating its transition from basic research to clinical treatment.

Indexed as

cGAS-STING pathwayImmune cellsLiver immunityLver diseases

Identifiers

PMID42432768
PMCPMC13644183

What OpenQuestion holds

Textmetadata
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.