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pmid:38192979

Identification of the function of FOSB in cholangiocarcinoma using bioinformatics analysis.

Yihang Zhao · Hong Tang · Yaxian Kuai · Jianhua Xu · Bin Sun · Yang Li

Translational cancer research · 2023 doi:10.21037/tcr-23-829

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Experiment

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Data

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Identification of the function of FOSB in cholangiocarcinoma using bioinformatics analysis.
doi
10.21037/tcr-23-829
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38192979
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Yihang Zhao
[1]
Hong Tang
[2]
Yaxian Kuai
[3]
Jianhua Xu
[4]
Bin Sun
[5]
Yang Li
journal
Translational cancer research
year
2023
abstract
Background: Exploring the potential mechanism of cholangiocarcinoma (CCA) metabolic reprogramming is significant for guiding clinical treatment. However, related research and exploration are still lacking. Therefore, we aimed to identify a reliable metabolism-related gene or biomarker of CCA using bioinformatics analysis. Methods: The GSE26566, GSE45001, and GSE132305 datasets were obtained from the Gene Expression Omnibus (GEO) database. Differently expressed genes (DEGs) between CCA tissues and adjacent tissues were screened out. The key gene was identified through enrichment and functional analysis, and its immune and clinical correlation was investigated utilizing the Tumor Immune Evaluation Resource (TIMER2.0), the Tumor-Immune System Interactions Database (TISIDB), the Gene Expression Profiling Interactive Analysis (GEPIA2), and the Kaplan-Meier Plotter. Finally, immunohistochemistry (IHC) was performed to validate the results. Results: By analysis, the expression of FBJ murine osteosarcoma viral oncogene homolog B (FOSB) was significantly downregulated in CCA tissues when compared with adjacent tissues. Moreover, the expression levels of FOSB positively correlated with tumor-infiltrating immune cells in most tumors, and patients with high FOSB expression tended to have a better prognosis. The FOSB and SIRT3/HIF1A axes have similar expression trends and metabolic functions in CCA cells, and the correlation between of them was preliminarily explored by IHC experiments. Conclusions: The expression levels of FOSB are closely related to the prognosis of CCA patients, which may be a predictive indicator for prognosis and immunotherapy.
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The data were normalized using the limma package of RStudio (Posit; Boston, MA, USA) and differently expressed genes (DEGs) were obtained between CCA and adjacent tissues [|log fold change (FC)| >1, P value <0.05, and the base of |logFC| was 2]. Kaplan-Meier Plotter and Gene Expression Profiling Interactive Analysis (GEPIA2) website were used to plot the survival analysis map of tumors (28,29).
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The data were normalized using the limma package of RStudio (Posit; Boston, MA, USA) and differently expressed genes (DEGs) were obtained between CCA and adjacent tissues [|log fold change (FC)| >1, P value <0.05, and the base of |logFC| was 2].
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Kaplan-Meier Plotter and Gene Expression Profiling Interactive Analysis (GEPIA2) website were used to plot the survival analysis map of tumors (28,29).
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FOSB expression is closely related to prognosis in cholangiocarcinoma patients and may be a predictive indicator for prognosis and immunotherapy.
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The expression levels of FOSB are closely related to the prognosis of CCA patients, which may be a predictive indicator for prognosis and immunotherapy.
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FOSB expression is closely related to prognosis in cholangiocarcinoma patients and may be a predictive indicator for prognosis and immunotherapy.
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[19]
GSM1095652
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20
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null
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14550
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Homo sapiens
title
Gene expression profiling of tumor stroma in human intrahepatic cholangiocarcinoma
resolution_checked_at
2026-11-01T15:39:54Z
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identifier_resolution_only_no_download_no_licence_read
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quote
The data were normalized using the limma package of RStudio (Posit; Boston, MA, USA) and differently expressed genes (DEGs) were obtained between CCA and adjacent tissues [|log fold change (FC)| >1, P value <0.05, and the base of |logFC| was 2]. Kaplan-Meier Plotter and Gene Expression Profiling Interactive Analysis (GEPIA2) website were used to plot the survival analysis map of tumors (28,29).
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Automated Assays Laravel application and simulated adapters
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[0]
Data Sharing Statement: Available at https://tcr.amegroups.com/article/view/10.21037/tcr-23-829/dss
basis
The paper names GSE26566, GSE45001, GSE132305 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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minimax
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minimax
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independence
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IA2), and the Kaplan-Meier Plotter. Finally, immunohistochemistry (IHC) was performed to validate the results.
[1]
eier Plotter. Finally, immunohistochemistry (IHC) was performed to validate the results. Resu
[2]
etween of them was preliminarily explored by IHC experiments. Conclusions: The expression lev
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paper_text_order:929
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Results: By analysis, the expression of FBJ murine osteosarcoma viral oncogene homolog B (FOSB)
[1]
represents negative correlation). FOSB, FBJ murine osteosarcoma viral oncogene homolog B.
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The data were normalized using the limma package of RStudio (Posit; Boston, MA, USA) and differently expressed genes (DEGs) were obtained between CCA and adjacent tissues [|log fold change (FC)| >1, P value <0.05, and the base of |logFC| was 2]. Kaplan-Meier Plotter and Gene Expression Profiling Interactive Analysis (GEPIA2) website were used to plot the survival analysis map of tumors (28,29).
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38192979", "kind": "science-record", "revision": 4, "content_hash": "sha256:11cf060afed7a99de6a73fb21dcdff3bcbcb329cb1035c3ac6da38ae1317ba6f", "created_at": "2026-11-01T19:20:06Z", "updated_at": "2026-11-01T22:53:24Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of the function of FOSB in cholangiocarcinoma using bioinformatics analysis.", "doi": "10.21037/tcr-23-829", "pmid": "38192979", "authors": ["Yihang Zhao", "Hong Tang", "Yaxian Kuai", "Jianhua Xu", "Bin Sun", "Yang Li"], "journal": "Translational cancer research", "year": 2023, "abstract": "Background: Exploring the potential mechanism of cholangiocarcinoma (CCA) metabolic reprogramming is significant for guiding clinical treatment. However, related research and exploration are still lacking. Therefore, we aimed to identify a reliable metabolism-related gene or biomarker of CCA using bioinformatics analysis.\nMethods: The GSE26566, GSE45001, and GSE132305 datasets were obtained from the Gene Expression Omnibus (GEO) database. Differently expressed genes (DEGs) between CCA tissues and adjacent tissues were screened out. The key gene was identified through enrichment and functional analysis, and its immune and clinical correlation was investigated utilizing the Tumor Immune Evaluation Resource (TIMER2.0), the Tumor-Immune System Interactions Database (TISIDB), the Gene Expression Profiling Interactive Analysis (GEPIA2), and the Kaplan-Meier Plotter. Finally, immunohistochemistry (IHC) was performed to validate the results.\nResults: By analysis, the expression of FBJ murine osteosarcoma viral oncogene homolog B (FOSB) was significantly downregulated in CCA tissues when compared with adjacent tissues. Moreover, the expression levels of FOSB positively correlated with tumor-infiltrating immune cells in most tumors, and patients with high FOSB expression tended to have a better prognosis. The FOSB and SIRT3/HIF1A axes have similar expression trends and metabolic functions in CCA cells, and the correlation between of them was preliminarily explored by IHC experiments.\nConclusions: The expression levels of FOSB are closely related to the prognosis of CCA patients, which may be a predictive indicator for prognosis and immunotherapy.", "claims": [{"id": "claim-method", "statement": "The data were normalized using the limma package of RStudio (Posit; Boston, MA, USA) and differently expressed genes (DEGs) were obtained between CCA and adjacent tissues [|log fold change (FC)| >1, P value <0.05, and the base of |logFC| was 2]. 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