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pmid:37025597

Identification of endothelial-related molecular subtypes for bladder cancer patients.

Deng-Xiong Li · De-Chao Feng · Xu Shi · Rui-Cheng Wu · Kai Chen · Ping Han

Frontiers in oncology · 2023 doi:10.3389/fonc.2023.1101055

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Experiment

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Data

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Analysis

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title
Identification of endothelial-related molecular subtypes for bladder cancer patients.
doi
10.3389/fonc.2023.1101055
pmid
37025597
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[0]
Deng-Xiong Li
[1]
De-Chao Feng
[2]
Xu Shi
[3]
Rui-Cheng Wu
[4]
Kai Chen
[5]
Ping Han
journal
Frontiers in oncology
year
2023
abstract
Background: Bladder cancer (BC) is a disease with significant heterogeneity and poor prognosis. The prognosis and therapeutic response of BC patients are significantly influenced by endothelial cells in the tumor microenvironment. In order to understand BC from the perspective of endothelial cells, we orchestrated molecular subtypes and identified key genes. Methods: Single-cell and bulk RNA sequencing data were extracted from online databases. R and its relative packages were used to analyze these data. Cluster analysis, prognostic value analysis, function analysis, immune checkpoints, tumor immune environment and immune prediction were conducted. Results: Five endothelial-related genes (CYTL1, FAM43A, HSPG2, RBP7, and TCF4) divided BC patients in the TCGA, GSE13507, and GSE32894 datasets into two clusters, respectively. In prognostic value analysis, patients in the cluster 2 were substantially associated with worse overall survival than those in the cluster 1 according to the results of TCGA, GSE13507 and GSE32894 datasets. In the results of functional analysis, the endothelial-related clusters was enriched in immune-related, endothelial-related and metabolism-related pathways. Samples in the cluster 1 had a statistically significant increase in CD4+ T cells and NK-cell infiltration. Cluster 1 was positively correlated with the cancer stem score and tumor mutational burden score. The results of immune prediction analysis indicated that 50.6% (119/235) of patients in the cluster 1 responded to immunotherapy, while the response rate in the cluster 2 decreased to 16.7% (26/155). Conclusion: In this study, we categorized and discovered distinctive prognosis-related molecular subtypes and key genes from the perspective of endothelial cells at the genetic level by integrating single-cell and bulk RNA sequencing data, primarily to provide a roadmap for precision medicine.
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After establishing the cluster, Kaplan−Meier curves were utilized to estimate the prognostic value of ERC.
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After establishing the cluster, Kaplan−Meier curves were utilized to estimate the prognostic value of ERC.
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Patients in cluster 1 had an immunotherapy response rate of 50.6% (119/235), whereas the response rate in cluster 2 was 16.7% (26/155).
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The results of immune prediction analysis indicated that 50.6% (119/235) of patients in the cluster 1 responded to immunotherapy, while the response rate in the cluster 2 decreased to 16.7% (26/155).
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title
Predective Value of Prognosis-Related Gene Expression Study in Primary Bladder Cancer
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sample_count
308
group_sizes
null
group_sizes_basis
null
platform
6947
taxon
Homo sapiens
title
A Molecular Taxonomy of Urothelial Carcinoma
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
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gaps array · 4 items
[0]
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[1]
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[2]
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[3]
asset:data:geo:GSE32894 licence not read
analysis object · 4 fields
state
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id
method-1
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survival_analysis
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cox_proportional_hazards
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[0]
cox_ph
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
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quote
After establishing the cluster, Kaplan−Meier curves were utilized to estimate the prognostic value of ERC.
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id
method-2
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label
Group comparison
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[0]
group_summary
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welch_t
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bootstrap_mean_difference
[3]
group_comparison_anova
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evidence object · 3 fields
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gaps array · 1 item
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method.reader_differs_from_extractor
capability object · 3 fields
state
complete
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[0] object · 6 fields
capability_id
capability:computational_analysis
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[0]
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[6]
network_analysis
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[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
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true
required_operations array · 1 item
[0]
cox_ph
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R1
reachable
true
accessions array · 2 items
[0]
GSE13507
[1]
GSE32894
resolved_accessions array · 2 items
[0]
GSE13507
[1]
GSE32894
statements array · 1 item
[0]
All data from this study were downloaded from an online database. Therefore, everyone can get the data online. Further inquiries can be directed to the corresponding author.
basis
The paper names GSE13507, GSE32894 in Gene Expression Omnibus and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 1 item
[0]
cox_ph
assets array · 2 items
[0]
source:pmid:37025597
[1]
data:geo:GSE13507
steps array · 1 item
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run_analysis
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capabilities array · 0 items
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data:geo:GSE13507
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review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T18:35:51Z
independence
single_reader
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method
verbatim
availability
verbatim
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5
usage object · 3 fields
prompt_tokens
9280
completion_tokens
2484
cached_tokens
128
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[0] object · 4 fields
id
extraction
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complete
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MiniMax-M3.1-Flash
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[2]
review.human_critique
execution object · 5 fields
state
absent
status
not_run
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null
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[0]
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provenance object · 7 fields
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id
pmid:37025597
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paper
label
pmid:37025597
[1] object · 3 fields
id
source:pmid:37025597
type
manuscript
label
PMID 37025597 full text
[2] object · 3 fields
id
data:geo:GSE13507
type
dataset
label
GEO GSE13507
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[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
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type
paper
label
pmid:37025597
[1] object · 3 fields
id
source:pmid:37025597
type
manuscript
label
PMID 37025597 full text
[2] object · 3 fields
id
data:geo:GSE13507
type
dataset
label
GEO GSE13507
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-37025597
type
extraction
used array · 1 item
[0]
source:pmid:37025597
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE13507
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accession_resolution
used array · 1 item
[0]
data:geo:GSE13507
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agent:corpus-assay-engine
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[0] object · 3 fields
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agent:corpus-assay-engine
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software
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Corpus assay engine
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agent:minimax-reader
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dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
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snapshot_id
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lineage object · 4 fields
parent_id
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[0] object · 11 fields
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data_generation
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evidence array · 2 items
[0]
ied key genes. Methods: Single-cell and bulk RNA sequencing data were extracted from online databases. R
[1]
ic level by integrating single-cell and bulk RNA sequencing data, primarily to provide a roadmap for pre
order_basis
paper_text_order:432
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assay:1
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cox_ph
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dsl_catalogue
f2132e96ae6c7a4e
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After establishing the cluster, Kaplan−Meier curves were utilized to estimate the prognostic value of ERC.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37025597", "kind": "science-record", "revision": 3, "content_hash": "sha256:db4f47a99fc42287965250a44344f3e10121cab9c25b47fe472037b071543237", "created_at": "2026-11-01T19:01:40Z", "updated_at": "2026-11-01T22:09:12Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of endothelial-related molecular subtypes for bladder cancer patients.", "doi": "10.3389/fonc.2023.1101055", "pmid": "37025597", "authors": ["Deng-Xiong Li", "De-Chao Feng", "Xu Shi", "Rui-Cheng Wu", "Kai Chen", "Ping Han"], "journal": "Frontiers in oncology", "year": 2023, "abstract": "Background: Bladder cancer (BC) is a disease with significant heterogeneity and poor prognosis. The prognosis and therapeutic response of BC patients are significantly influenced by endothelial cells in the tumor microenvironment. In order to understand BC from the perspective of endothelial cells, we orchestrated molecular subtypes and identified key genes.\nMethods: Single-cell and bulk RNA sequencing data were extracted from online databases. R and its relative packages were used to analyze these data. Cluster analysis, prognostic value analysis, function analysis, immune checkpoints, tumor immune environment and immune prediction were conducted.\nResults: Five endothelial-related genes (CYTL1, FAM43A, HSPG2, RBP7, and TCF4) divided BC patients in the TCGA, GSE13507, and GSE32894 datasets into two clusters, respectively. In prognostic value analysis, patients in the cluster 2 were substantially associated with worse overall survival than those in the cluster 1 according to the results of TCGA, GSE13507 and GSE32894 datasets. In the results of functional analysis, the endothelial-related clusters was enriched in immune-related, endothelial-related and metabolism-related pathways. Samples in the cluster 1 had a statistically significant increase in CD4+ T cells and NK-cell infiltration. Cluster 1 was positively correlated with the cancer stem score and tumor mutational burden score. The results of immune prediction analysis indicated that 50.6% (119/235) of patients in the cluster 1 responded to immunotherapy, while the response rate in the cluster 2 decreased to 16.7% (26/155).\nConclusion: In this study, we categorized and discovered distinctive prognosis-related molecular subtypes and key genes from the perspective of endothelial cells at the genetic level by integrating single-cell and bulk RNA sequencing data, primarily to provide a roadmap for precision medicine.", "claims": [{"id": "claim-method", "statement": "After establishing the cluster, Kaplan−Meier curves were utilized to estimate the prognostic value of ERC.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37025597", "locator": "sections[5] \"Evaluation of the cluster and function analysis\" paragraph 2", "quote": "After establishing the cluster, Kaplan−Meier curves were utilized to estimate the prognostic value of ERC."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All data from this study were downloaded from an online database. Therefore, everyone can get the data online. Further inquiries can be directed to the corresponding author.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37025597", "locator": "sections[15] \"Data availability statement\" paragraph 2", "quote": "All data from this study were downloaded from an online database. Therefore, everyone can get the data online. Further inquiries can be directed to the corresponding author."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Patients in cluster 1 had an immunotherapy response rate of 50.6% (119/235), whereas the response rate in cluster 2 was 16.7% (26/155).", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37025597", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The results of immune prediction analysis indicated that 50.6% (119/235) of patients in the cluster 1 responded to immunotherapy, while the response rate in the cluster 2 decreased to 16.7% (26/155)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Patients in cluster 1 had an immunotherapy response rate of 50.6% (119/235), whereas the response rate in cluster 2 was 16.7% (26/155).", "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:37025597"], "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:37025597", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fonc.2023.1101055", "sha256": "sha256:5c9c5a345b79c99cf26135a2a46cc7f0419c2718ee9c65bab6b6c57889f1077a", "bytes": 34166, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fonc.2023.1101055", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC10070733", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE13507", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE13507", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE13507", "version": null, "note": "All data from this study were downloaded from an online database. Therefore, everyone can get the data online. Further inquiries can be directed to the corresponding author.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "All data from this study were downloaded from an online database. Therefore, everyone can get the data online. 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