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pmid:37684377

Adhesion-regulating molecule 1 (ADRM1) can be a potential biomarker and target for bladder cancer.

Qing-Xin Yu · Jiao-Chen Wang · Jun-Fei Liu · Lu-Xia Ye · Yi-Qing Guo · Hai-Hong Zheng

Scientific reports · 2023 doi:10.1038/s41598-023-41992-8

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Adhesion-regulating molecule 1 (ADRM1) can be a potential biomarker and target for bladder cancer.
doi
10.1038/s41598-023-41992-8
pmid
37684377
authors array · 6 items
[0]
Qing-Xin Yu
[1]
Jiao-Chen Wang
[2]
Jun-Fei Liu
[3]
Lu-Xia Ye
[4]
Yi-Qing Guo
[5]
Hai-Hong Zheng
journal
Scientific reports
year
2023
abstract
Adhesion-regulating molecule 1 (ADRM1) has been implicated in tumor development, yet its specific role in bladder cancer (BC) remains undefined. This study aimed to elucidate the function of ADRM1 in BC through a combination of bioinformatics analysis and immunohistochemical analysis (IHC). Utilizing R version 3.6.3 and relevant packages, we analyzed online database data. Validation was conducted through IHC data, approved by the Institutional Ethics Committee (Approval No. K20220830). In both paired and unpaired comparisons, ADRM1 expression was significantly elevated in BC tissues compared to adjacent tissues, as evidenced by the results of TCGA dataset and IHC data. Patients with high ADRM1 expression had statistically worse overall survival than those with low ADRM1 expression in TCGA dataset, GSE32548 dataset, GSE32894 dataset, and IHC data. Functional analysis unveiled enrichment in immune-related pathways, and a robust positive correlation emerged between ADRM1 expression and pivotal immune checkpoints, including CD274, PDCD1, and PDCD1LG2. In tumor microenvironment, samples with the high ADRM1 expression contained statistical higher proportion of CD8 + T cells and Macrophage infiltration. Meanwhile, these high ADRM1-expressing samples displayed elevated tumor mutation burden scores and stemness indices, implying potential benefits from immunotherapy. Patients with low ADRM1 expression were sensitive to cisplatin, docetaxel, vinblastine, mitomycin C, and methotrexate. According to the findings from bioinformatics and IHC analyses, ADRM1 demonstrates prognostic significance for BC patients and holds predictive potential for both immunotherapy and chemotherapy responses. This underscores its role as a biomarker and therapeutic target in BC.
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To evaluated the prognostic value of ADRM1, Kaplan‒Meier curves was use to compare the survival outcome among the high and low ADRM1 expression groups within the TCGA, GSE32548, and GSE32894 datasets.
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To evaluated the prognostic value of ADRM1, Kaplan‒Meier curves was use to compare the survival outcome among the high and low ADRM1 expression groups within the TCGA, GSE32548, and GSE32894 datasets.
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Since human data are involved, you should contact the corresponding authors to obtain relevant information.
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ADRM1 demonstrated prognostic significance for bladder cancer patients and potential for predicting responses to immunotherapy and chemotherapy.
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According to the findings from bioinformatics and IHC analyses, ADRM1 demonstrates prognostic significance for BC patients and holds predictive potential for both immunotherapy and chemotherapy responses.
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ADRM1 demonstrated prognostic significance for bladder cancer patients and potential for predicting responses to immunotherapy and chemotherapy.
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score
0.8
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quote
ANOVA
[1] object · 10 fields
id
method-2
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null
specific
null
label
Kaplan–Meier survival analysis
dsl_operations array · 0 items
missing_operations array · 0 items
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evidence object · 3 fields
score
1
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verbatim
quote
To evaluated the prognostic value of ADRM1, Kaplan‒Meier curves was use to compare the survival outcome among the high and low ADRM1 expression groups within the TCGA, GSE32548, and GSE32894 datasets.
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gaps array · 1 item
[0]
method.reader_named_unmapped
capability object · 3 fields
state
complete
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capability_id
capability:computational_analysis
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assay_families array · 9 items
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gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
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complete
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R1
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group_summary
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welch_t
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group_comparison_anova
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: anova.
capability object · 4 fields
tier
R1
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capability:computational_analysis
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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
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accessions array · 2 items
[0]
GSE32548
[1]
GSE32894
resolved_accessions array · 2 items
[0]
GSE32548
[1]
GSE32894
statements array · 1 item
[0]
Since human data are involved, you should contact the corresponding authors to obtain relevant information.
basis
The paper names GSE32548, GSE32894 in Gene Expression Omnibus (https://www.ncbi.nlm.nih.gov, GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 4 items
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group_summary
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welch_t
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group_comparison_anova
assets array · 2 items
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source:pmid:37684377
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data:geo:GSE32548
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run_analysis
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data:geo:GSE32548
gaps array · 0 items
review object · 5 fields
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partial
machine_critique object · 5 fields
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extraction_review
reader object · 5 fields
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MiniMax-M3.1-Flash
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minimax
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minimax
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2026-11-01T18:52:47Z
independence
single_reader
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method
verbatim
availability
verbatim
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[0] object · 4 fields
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extraction
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complete
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MiniMax-M3.1-Flash
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review.human_critique
execution object · 5 fields
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provenance object · 7 fields
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pmid:37684377
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paper
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pmid:37684377
[1] object · 3 fields
id
source:pmid:37684377
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manuscript
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PMID 37684377 full text
[2] object · 3 fields
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data:geo:GSE32548
type
dataset
label
GEO GSE32548
activities array · 3 items
[0] object · 4 fields
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activity-reading-sci-2026-11-01
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classification
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paper
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pmid:37684377
[1] object · 3 fields
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source:pmid:37684377
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manuscript
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PMID 37684377 full text
[2] object · 3 fields
id
data:geo:GSE32548
type
dataset
label
GEO GSE32548
agent
agent:corpus-assay-engine
[1] object · 4 fields
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activity-read-37684377
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extraction
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source:pmid:37684377
agent
agent:minimax-reader
[2] object · 4 fields
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activity-resolve-GSE32548
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accession_resolution
used array · 1 item
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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agent:minimax-reader
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MiniMax literature reader
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dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
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lineage object · 4 fields
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gaps array · 9 items
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[3]
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assays array · 2 items
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assay_lexicon
99e1195c7d6f
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evidence array · 4 items
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a combination of bioinformatics analysis and immunohistochemical analysis (IHC). Utilizing R version 3.6.3 an
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s analysis and immunohistochemical analysis (IHC). Utilizing R version 3.6.3 and relevant pac
[2]
abase data. Validation was conducted through IHC data, approved by the Institutional Ethics C
[3]
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order_basis
paper_text_order:310
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37684377", "kind": "science-record", "revision": 3, "content_hash": "sha256:44f5538d812054b75d74c89d7b4e38aab1703e10298ff7e74f1067d7b3507782", "created_at": "2026-11-01T19:02:29Z", "updated_at": "2026-11-01T22:10:14Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Adhesion-regulating molecule 1 (ADRM1) can be a potential biomarker and target for bladder cancer.", "doi": "10.1038/s41598-023-41992-8", "pmid": "37684377", "authors": ["Qing-Xin Yu", "Jiao-Chen Wang", "Jun-Fei Liu", "Lu-Xia Ye", "Yi-Qing Guo", "Hai-Hong Zheng"], "journal": "Scientific reports", "year": 2023, "abstract": "Adhesion-regulating molecule 1 (ADRM1) has been implicated in tumor development, yet its specific role in bladder cancer (BC) remains undefined. This study aimed to elucidate the function of ADRM1 in BC through a combination of bioinformatics analysis and immunohistochemical analysis (IHC). Utilizing R version 3.6.3 and relevant packages, we analyzed online database data. Validation was conducted through IHC data, approved by the Institutional Ethics Committee (Approval No. K20220830). In both paired and unpaired comparisons, ADRM1 expression was significantly elevated in BC tissues compared to adjacent tissues, as evidenced by the results of TCGA dataset and IHC data. Patients with high ADRM1 expression had statistically worse overall survival than those with low ADRM1 expression in TCGA dataset, GSE32548 dataset, GSE32894 dataset, and IHC data. Functional analysis unveiled enrichment in immune-related pathways, and a robust positive correlation emerged between ADRM1 expression and pivotal immune checkpoints, including CD274, PDCD1, and PDCD1LG2. In tumor microenvironment, samples with the high ADRM1 expression contained statistical higher proportion of CD8 + T cells and Macrophage infiltration. Meanwhile, these high ADRM1-expressing samples displayed elevated tumor mutation burden scores and stemness indices, implying potential benefits from immunotherapy. Patients with low ADRM1 expression were sensitive to cisplatin, docetaxel, vinblastine, mitomycin C, and methotrexate. According to the findings from bioinformatics and IHC analyses, ADRM1 demonstrates prognostic significance for BC patients and holds predictive potential for both immunotherapy and chemotherapy responses. This underscores its role as a biomarker and therapeutic target in BC.", "claims": [{"id": "claim-method", "statement": "To evaluated the prognostic value of ADRM1, Kaplan‒Meier curves was use to compare the survival outcome among the high and low ADRM1 expression groups within the TCGA, GSE32548, and GSE32894 datasets.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37684377", "locator": "sections[3] \"Online data acquisition\" paragraph 2", "quote": "To evaluated the prognostic value of ADRM1, Kaplan‒Meier curves was use to compare the survival outcome among the high and low ADRM1 expression groups within the TCGA, GSE32548, and GSE32894 datasets."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Since human data are involved, you should contact the corresponding authors to obtain relevant information.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37684377", "locator": "sections[20] \"Data availability\" paragraph 2", "quote": "Since human data are involved, you should contact the corresponding authors to obtain relevant information."}], "state": "complete"}, {"id": "claim-target-result", "statement": "ADRM1 demonstrated prognostic significance for bladder cancer patients and potential for predicting responses to immunotherapy and chemotherapy.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37684377", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "According to the findings from bioinformatics and IHC analyses, ADRM1 demonstrates prognostic significance for BC patients and holds predictive potential for both immunotherapy and chemotherapy responses."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "ADRM1 demonstrated prognostic significance for bladder cancer patients and potential for predicting responses to immunotherapy and chemotherapy.", "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:37684377"], "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. 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