Evidence map›Paper›PMID 41706744›Full record

ArticlePloS one2026

Prognostic value of cGAS-STING-IRF3 signaling in cholangiocarcinoma patients.

Parawee Artbua, Naruemon Kentachalee, Sirinya Sitthirak, Prakasit Sa-Ngiamwibool, Phongsathorn Wichian, Raksawan Deenonpoe

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Article in PloS one, 2026. 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 it

What it found

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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Parawee ArtbuaDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Naruemon KentachaleeDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Sirinya SitthirakSchool of Allied Health Sciences, Walailak University, Nakorn Si Thamarat, Thailand.
Prakasit Sa-NgiamwiboolDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Phongsathorn WichianDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.ORCID https://orcid.org/0000-0003-3941-9370
Raksawan DeenonpoeDepartment of Pathology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.ORCID https://orcid.org/0000-0002-8387-6061

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholangiocarcinoma (CCA) is an aggressive malignancy with a poor prognosis, often diagnosed at an advanced stage. Chromosomal instability (CIN), a hallmark of cancer, leads to the release of cytosolic double-stranded DNA (dsDNA), which activates the cGAS-STING pathway and its downstream immune signaling. However, the prognostic implications of this pathway in CCA remain poorly understood. This study aims to examine the cGAS-STING pathway-related proteins in CCA and their correlation with clinicopathological parameters. A total of 164 formalin-fixed paraffin-embedded (FFPE) CCA tissue samples were analyzed using tissue microarray (TMA) and immunohistochemistry (IHC). Statistical analysis assessed correlations between proteins expression and clinicopathological features were assessed using Chi-square tests, logistic regression, Kaplan-Meier survival analysis, Cox proportional hazards models, and Spearman's rank correlation coefficient. Moderate-to-high STING expression was significantly associated with reduced tumor size and lymphovascular invasion but paradoxically correlated with short overall survival (p < 0.05). In contrast, moderate-to-high γH2AX expression predicted improved survival. IRF3 expression was significantly higher in the tubular histological subtype of CCA compared to the papillary subtype (p = 0.012), indicating a possible morphological correlation. Multivariate analysis confirmed STING as an independent prognostic marker for CCA. Our findings suggest that STING appears to function as a double-edged sword in CCA, limiting local invasion while paradoxically contributing to poor survival outcomes. IRF3 expression appears linked to histological subtypes, supporting its role in tumor biology. These markers may provide valuable insights into tumor behavior and may guide treatment strategies in CCA patients.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaInterferon Regulatory Factor-3Membrane ProteinsNucleotidyltransferasesSignal TransductionAgedBiomarkers, TumorcGAS-STING Signaling PathwayCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseFemaleHumansKaplan-Meier EstimateMaleMiddle AgedPrognosisBiomarkers, TumorcGAS protein, humanCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseInterferon Regulatory Factor-3IRF3 protein, humanMembrane ProteinsNucleotidyltransferasesSTING1 protein, humanSTING Protein

Identifiers

PMID41706744
PMCPMC12915935

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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.