Evidence map›Paper›PMID 41063281›Full record

ReviewJournal of experimental & clinical cancer research : CR2025

The cGAS‒STING pathway in colorectal cancer: bridging innate immunity and therapeutic strategies.

Wen-Jing Li, Guang-Hui Dong, Yao Bi, You-Yan Han, Long-Long Sun, Tong Wang, Zhen-Hua Lin, Xiang-Shan Ren

Abstract readReview
In one paragraph

Review in Journal of experimental & clinical cancer research : CR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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.

Wen-Jing Li *Central Laboratory, Yanbian University Hospital & Key Laboratory of Pathobiology, State Ethnic Affairs Commission, Yanbian University, Yanji, China.
Guang-Hui Dong *Department of Neurology, Affiliated Hospital of Yanbian University, Yanji, China.
Yao BiDepartment of Pathology & Key Laboratory of Pathobiology, Cancer Research Center, Yanbian University Medical College, State Ethnic Affairs, No. 977, Gongyuan Road, Yanji, 133002, China.
You-Yan HanDepartment of Pathology & Key Laboratory of Pathobiology, Cancer Research Center, Yanbian University Medical College, State Ethnic Affairs, No. 977, Gongyuan Road, Yanji, 133002, China.
Long-Long SunDepartment of Pathology & Key Laboratory of Pathobiology, Cancer Research Center, Yanbian University Medical College, State Ethnic Affairs, No. 977, Gongyuan Road, Yanji, 133002, China.
Tong WangDepartment of Pathology & Key Laboratory of Pathobiology, Cancer Research Center, Yanbian University Medical College, State Ethnic Affairs, No. 977, Gongyuan Road, Yanji, 133002, China.
Zhen-Hua LinCentral Laboratory, Yanbian University Hospital & Key Laboratory of Pathobiology, State Ethnic Affairs Commission, Yanbian University, Yanji, China. zhlin720@ybu.edu.cn.
Xiang-Shan RenCentral Laboratory, Yanbian University Hospital & Key Laboratory of Pathobiology, State Ethnic Affairs Commission, Yanbian University, Yanji, China. renxsh@ybu.edu.cn.

Funding

Jilin Province Department of Education Doctoral Research Student Scientific Research Innovation Capacity Enhancement Project JJKH20250421BSJilin Province Science and Technology Department Project YDZJ202301ZYTS133
6 · The paper itself

Abstract

Colorectal cancer (CRC) continues to be a predominant cause of cancer-related mortality worldwide, with existing therapies constrained by systemic toxicity, resistance, and inadequate tumor targeting. While immunotherapy has potential in specific CRC subtypes, its overall effectiveness is still limited. The cyclic GMP‒AMP synthase-stimulator of interferon genes (cGAS‒STING) pathway, an essential cytosolic DNA sensor that facilitates innate immune responses, has surfaced as a prospective target for cancer immunotherapy. Recent studies have demonstrated that it plays dual roles in CRC: on the one hand, it triggers antitumor immune responses, while on the other hand, it promotes intestinal inflammation. Accurate delivery of STING agonists made feasible by developments in nanotechnology offers novel ways to modify the TME and overcome resistance. The current understanding of the activation and function of the cGAS-STING pathway in CRC, its impact on the TME, and recent developments in STING-targeted therapeutic approaches, comprising monotherapy and combination strategies with chemotherapy, radiotherapy, and immune checkpoint inhibitors, is summarized in this review. We also review new nanomedicine approaches designed to increase STING activation. Understanding the complex roles of cGAS-STING in CRC could help guide the development of next-generation immunotherapies with improved selectivity and efficacy.

Indexed as

Colorectal NeoplasmsImmunity, InnateMembrane ProteinsNucleotidyltransferasesAnimalsCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseHumansImmunotherapySignal TransductionSTING ProteincGAS protein, humanCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseMembrane ProteinsNucleotidyltransferasesSTING1 protein, humanSTING ProteincGAS-STING pathwayColorectal cancerImmunotherapyInnate immunityNanocarrierTumor microenvironment

Identifiers

PMID41063281
PMCPMC12506337

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.