Evidence map›Paper›PMID 38881895›Full record

ArticleFrontiers in immunology2024

Expression and clinical significance of interleukin-6 pathway in cholangiocarcinoma.

Dongqing Gu, Xin Zhao, Jing Song, Jianmei Xiao, Leida Zhang, Guohong Deng, Dajiang Li

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Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Dongqing Gu *Department of Infectious Diseases, First Affiliated Hospital, Army Medical University, Chongqing, China.
Xin Zhao *Department of Hepatobiliary Surgery, First Affiliated Hospital, Army Medical University, Chongqing, China.
Jing Song *Ministry of Education Key Laboratory of Child Development and Disorders, Children's Hospital of Chongqing Medical University (CHCMU), Chongqing, China.
Jianmei XiaoDepartment of Infectious Diseases, First Affiliated Hospital, Army Medical University, Chongqing, China.
Leida ZhangDepartment of Hepatobiliary Surgery, First Affiliated Hospital, Army Medical University, Chongqing, China.
Guohong DengDepartment of Infectious Diseases, First Affiliated Hospital, Army Medical University, Chongqing, China.
Dajiang LiDepartment of Hepatobiliary Surgery, First Affiliated Hospital, Army Medical University, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cholangiocarcinoma (CCA) is a typical inflammation-induced malignancy, and elevated serum interleukin-6 (IL-6) levels have been reported to be linked to the onset and progression of CCA. We aim to investigate the potential prognostic value of the IL-6 pathway for CCA. Methods: We detected the expressions of IL-6, IL-6R, glycoprotein (gp130), C-reactive protein (CRP), Janus kinase 2 (JAK2), and signal transducer and activator of transcription 3 (STAT3) in CCA tissue microarray using multiplex immunofluorescence. Furthermore, the clinical associations and prognostic values were assessed. Finally, single-cell transcriptome analysis was performed to evaluate the expression level of IL-6 pathway genes in CCA. Results: The results revealed that the expression of IL-6 was lower, while the expression of STAT3 was higher in tumor tissues compared to normal tissues. Especially in tumor microenvironment, the expression of IL-6 pathway genes was generally downregulated. Importantly, gp130 was strongly correlated with JAK2 in tumor tissues, while it was moderately correlated with JAK2 in normal tissue. Although none of the gene expressions were directly associated with overall survival and disease-free survival, our study found that IL-6, IL-6R, CRP, gp130, and JAK2 were inversely correlated with vascular invasion, which is a risk factor for poor prognosis in patients with CCA. Conclusion: The findings from this study suggest that the IL-6 signaling pathway may have a potential prognostic value for CCA. Further investigation is needed to understand the underlying molecular mechanisms of the IL-6 pathway in CCA.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaCytokine Receptor gp130Interleukin-6Janus Kinase 2Signal TransductionSTAT3 Transcription FactorAgedBiomarkers, TumorClinical RelevanceFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleMiddle AgedBiomarkers, TumorCytokine Receptor gp130IL6 protein, humanInterleukin-6JAK2 protein, humanJanus Kinase 2Receptors, Interleukin-6STAT3 protein, humanSTAT3 Transcription FactorcarcinogenesischolangiocarcinomaIL-6/STAT3 pathwaymultiplex immunofluorescenceprognosistissue microarray

Identifiers

PMID38881895
PMCPMC11176422

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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.