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pmid:37051591

Screening ANLN and ASPM as bladder urothelial carcinoma-related biomarkers based on weighted gene co-expression network analysis.

Tenghao Yang · Zepai Chi · Guoyuan Liu · Xuwei Hong · Sizhe Cao · Kequan Cheng · Yonghai Zhang

Frontiers in genetics · 2023 doi:10.3389/fgene.2023.1107625

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title
Screening ANLN and ASPM as bladder urothelial carcinoma-related biomarkers based on weighted gene co-expression network analysis.
doi
10.3389/fgene.2023.1107625
pmid
37051591
authors array · 7 items
[0]
Tenghao Yang
[1]
Zepai Chi
[2]
Guoyuan Liu
[3]
Xuwei Hong
[4]
Sizhe Cao
[5]
Kequan Cheng
[6]
Yonghai Zhang
journal
Frontiers in genetics
year
2023
abstract
Introduction: Bladder cancer (BLCA) is one of the most common malignancies in the urinary system with a poor prognosis and high treatment costs. Identifying potential prognostic biomarkers is significant for exploring new therapeutic and predictive targets of BLCA. Methods: In this study, we screened differentially expressed genes using the GSE37815 dataset. We then performed a weighted gene co-expression network analysis (WGCNA) to identify the genes correlated with the histologic grade and T stage of BLCA using the GSE32548 dataset. Subsequently, Kaplan Meier survival analysis and Cox regression were used to further identify prognosis-related hub genes using the datasets GSE13507 and TCGA-BLCA. Moreover, we detected the expression of the hub genes in 35 paired samples, including BLCA and paracancerous tissue, from the Shantou Central Hospital by qRT-polymerase chain reaction. Results: This study showed that Anillin (ANLN) and Abnormal spindle-like microcephaly-associated gene (ASPM) were prognostic biomarkers for BLCA. High expression of ANLN and ASPM was associated with poor overall survival.The qRT-PCR results revealed that ANLN and ASPM genes were upregulated in BLCA, and there was a correlation between the expression of ANLN and ASPM in cancer tissues and paracancerous tissue. Additionally, the increasing multiples in the ANLN gene was obvious in high-grade BLCA. Discussion: In summary, this preliminary exploration indicated a correlation between ANLN and ASPM expression. These two genes, serving as the risk factors for BLCA progression, might be promising targets to improve the occurrence and progression of BLCA.
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We conducted the univariate and multivariate Cox regression analyses by R package “survival” to further search prognostic genes, using datasets GSE13507 and TCGA-BLCA as validation cohorts.
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sections[5] "2.3 Screening prognostic hub genes by Cox regression and K-M survival analyses" paragraph 2
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We conducted the univariate and multivariate Cox regression analyses by R package “survival” to further search prognostic genes, using datasets GSE13507 and TCGA-BLCA as validation cohorts.
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The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
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ANLN was identified as a prognosis-related hub gene for bladder cancer, with high expression associated with poor overall survival in the TCGA-BLCA and GSE13507 cohorts.
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Firstly, we conducted univariate Cox regression analysis and found that the ANLN gene (HR = 1.23, 95% CI = 1.07–1.42, p = 0.003) was the only risk factor in the TCGA-BLCA dataset.
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sections[12] "3.2 Identification of ANLN as a prognosisrelated hub gene" paragraph 2
quote
Firstly, we conducted univariate Cox regression analysis and found that the ANLN gene (HR = 1.23, 95% CI = 1.07–1.42, p = 0.003) was the only risk factor in the TCGA-BLCA dataset.
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sections[12] "3.2 Identification of ANLN as a prognosisrelated hub gene" paragraph 2
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In the GSE13507 dataset, univariate Cox regression analysis identified 43 genes related to BLCA prognosis, including ANLN (HR = 1.47, 95% CI = 1.18–1.83, p = 0.001).
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sections[12] "3.2 Identification of ANLN as a prognosisrelated hub gene" paragraph 2
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K-M survival curve suggested that the high-expression of ANLN had a poor OS in both datasets TCGA-BLCA and GSE13507 datasets (Figures 3A, B).
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[22]
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[23]
GSM340749
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24
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null
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null
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6102
taxon
Homo sapiens
title
DNA methylation and expression profiling study for bladder cancer [gene expression]
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2026-11-01T15:39:54Z
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identifier_resolution_only_no_download_no_licence_read
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[3]
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[4]
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[5]
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We conducted the univariate and multivariate Cox regression analyses by R package “survival” to further search prognostic genes, using datasets GSE13507 and TCGA-BLCA as validation cohorts.
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capability object · 3 fields
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: kaplan_meier.
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owned
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The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
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tier
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The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
basis
The paper names GSE37815, GSE32548, GSE13507 in GEO and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
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single_reader
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paper
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PMID 37051591 full text
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We conducted the univariate and multivariate Cox regression analyses by R package “survival” to further search prognostic genes, using datasets GSE13507 and TCGA-BLCA as validation cohorts.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37051591", "kind": "science-record", "revision": 4, "content_hash": "sha256:2ee075babb70dfa2275d78ea649585d552692886fbfbf282d807730364240de4", "created_at": "2026-11-01T19:01:42Z", "updated_at": "2026-11-01T22:51:41Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Screening ANLN and ASPM as bladder urothelial carcinoma-related biomarkers based on weighted gene co-expression network analysis.", "doi": "10.3389/fgene.2023.1107625", "pmid": "37051591", "authors": ["Tenghao Yang", "Zepai Chi", "Guoyuan Liu", "Xuwei Hong", "Sizhe Cao", "Kequan Cheng", "Yonghai Zhang"], "journal": "Frontiers in genetics", "year": 2023, "abstract": "Introduction: Bladder cancer (BLCA) is one of the most common malignancies in the urinary system with a poor prognosis and high treatment costs. Identifying potential prognostic biomarkers is significant for exploring new therapeutic and predictive targets of BLCA. Methods: In this study, we screened differentially expressed genes using the GSE37815 dataset. We then performed a weighted gene co-expression network analysis (WGCNA) to identify the genes correlated with the histologic grade and T stage of BLCA using the GSE32548 dataset. Subsequently, Kaplan Meier survival analysis and Cox regression were used to further identify prognosis-related hub genes using the datasets GSE13507 and TCGA-BLCA. Moreover, we detected the expression of the hub genes in 35 paired samples, including BLCA and paracancerous tissue, from the Shantou Central Hospital by qRT-polymerase chain reaction. Results: This study showed that Anillin (ANLN) and Abnormal spindle-like microcephaly-associated gene (ASPM) were prognostic biomarkers for BLCA. High expression of ANLN and ASPM was associated with poor overall survival.The qRT-PCR results revealed that ANLN and ASPM genes were upregulated in BLCA, and there was a correlation between the expression of ANLN and ASPM in cancer tissues and paracancerous tissue. Additionally, the increasing multiples in the ANLN gene was obvious in high-grade BLCA. Discussion: In summary, this preliminary exploration indicated a correlation between ANLN and ASPM expression. These two genes, serving as the risk factors for BLCA progression, might be promising targets to improve the occurrence and progression of BLCA.", "claims": [{"id": "claim-method", "statement": "We conducted the univariate and multivariate Cox regression analyses by R package “survival” to further search prognostic genes, using datasets GSE13507 and TCGA-BLCA as validation cohorts.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37051591", "locator": "sections[5] \"2.3 Screening prognostic hub genes by Cox regression and K-M survival analyses\" paragraph 2", "quote": "We conducted the univariate and multivariate Cox regression analyses by R package “survival” to further search prognostic genes, using datasets GSE13507 and TCGA-BLCA as validation cohorts."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37051591", "locator": "sections[18] \"Data availability statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author."}], "state": "complete"}, {"id": "claim-target-result", "statement": "ANLN was identified as a prognosis-related hub gene for bladder cancer, with high expression associated with poor overall survival in the TCGA-BLCA and GSE13507 cohorts.", "kind": "quantitative", "target": {"value": 95.0, "unit": "per cent", "tolerance": null, "source": "Firstly, we conducted univariate Cox regression analysis and found that the ANLN gene (HR = 1.23, 95% CI = 1.07–1.42, p = 0.003) was the only risk factor in the TCGA-BLCA dataset."}, "evidence": [{"asset": "source:pmid:37051591", "locator": "sections[12] \"3.2 Identification of ANLN as a prognosisrelated hub gene\" paragraph 2", "quote": "Firstly, we conducted univariate Cox regression analysis and found that the ANLN gene (HR = 1.23, 95% CI = 1.07–1.42, p = 0.003) was the only risk factor in the TCGA-BLCA dataset."}, {"asset": "source:pmid:37051591", "locator": "sections[12] \"3.2 Identification of ANLN as a prognosisrelated hub gene\" paragraph 2", "quote": "In the GSE13507 dataset, univariate Cox regression analysis identified 43 genes related to BLCA prognosis, including ANLN (HR = 1.47, 95% CI = 1.18–1.83, p = 0.001)."}, {"asset": "source:pmid:37051591", "locator": "sections[12] \"3.2 Identification of ANLN as a prognosisrelated hub gene\" paragraph 2", "quote": "K-M survival curve suggested that the high-expression of ANLN had a poor OS in both datasets TCGA-BLCA and GSE13507 datasets (Figures 3A, B)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "ANLN was identified as a prognosis-related hub gene for bladder cancer, with high expression associated with poor overall survival in the TCGA-BLCA and GSE13507 cohorts.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:37051591"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE13507"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE13507"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37051591", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fgene.2023.1107625", "sha256": 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