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pmid:35132379

Identification of MAD2L1 as a Potential Biomarker in Hepatocellular Carcinoma via Comprehensive Bioinformatics Analysis.

Qian Chen · Sibo Yang · Yewei Zhang · Bo Li · Huanming Xu · Shi Zuo

BioMed research international · 2022 doi:10.1155/2022/9868022

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:35132379
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science-record
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sha256:245ce96afb1330020b41eb4e55dcbf5bc31ecbe765a0ea86800794b3175ac684
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2026-11-01T17:36:53Z
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2026-11-01T22:48:26Z
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paper object · 10 fields
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title
Identification of MAD2L1 as a Potential Biomarker in Hepatocellular Carcinoma via Comprehensive Bioinformatics Analysis.
doi
10.1155/2022/9868022
pmid
35132379
authors array · 6 items
[0]
Qian Chen
[1]
Sibo Yang
[2]
Yewei Zhang
[3]
Bo Li
[4]
Huanming Xu
[5]
Shi Zuo
journal
BioMed research international
year
2022
abstract
BACKGROUND: Hepatocellular carcinoma (HCC) is widely acknowledged as a malignant tumor with rapid progression, high recurrence rate, and poor prognosis. At present, there is a paucity of reliable biomarkers at the clinical level to guide the management of HCC and improve patient outcomes. Our research is aimed at assessing the prognostic value of MAD2L1 in HCC. METHODS: Four datasets, GSE121248, GSE101685, GSE85598, and GSE62232, were selected from the GEO database to analyze differentially expressed genes (DEGs) between HCC and normal liver tissues. After functional analysis, we constructed a protein-protein interaction network (PPI) for DEGs and identified core genes in this network with high connectivity with other genes. We assessed the relationship between core genes and the pathogenesis and prognosis of HCC. Finally, we explored the gene regulatory signaling mechanisms involved in HCC pathogenesis. RESULTS: 145 DEGs were screened from the intersection of the four GEO datasets. MAD2L1 was associated with most genes according to the PPI network and was selected as a candidate gene for further study. Survival analysis suggested that high MAD2L1 expression in HCC correlated with a worse prognosis. In addition, real-time quantitative PCR (RT-qPCR), western blot (WB), and immunohistochemistry (IHC) findings suggested that the expression of MAD2L1 was abnormally increased in HCC tissues and cells compared to paraneoplastic tissues and normal hepatocytes. CONCLUSION: We found that high MAD2L1 expression in HCC was significantly associated with overall patient survival and clinical features. We also explored the potential biological properties of this gene.
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GEO2R is an online tool used to conduct differential gene expression analysis on GEO data.
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The data used to support the findings of this study are available from the corresponding author upon request.
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The analysis identified 145 differentially expressed genes from the intersection of four GEO datasets.
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sections[0] "Abstract" paragraph 3
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145 DEGs were screened from the intersection of the four GEO datasets.
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The analysis identified 145 differentially expressed genes from the intersection of four GEO datasets.
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network_analysis
specific
pathway_enrichment
label
Network / pathway analysis
dsl_operations array · 1 item
[0]
pathway_enrich
missing_operations array · 0 items
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data_shapes array · 1 item
[0]
edge_list
evidence object · 3 fields
score
0.8
band
high
quote
pathway enrichment
[7] object · 10 fields
id
method-8
family
contingency_analysis
specific
chi_square
label
Categorical (contingency table) analysis
dsl_operations array · 1 item
[0]
chi_square_test
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data_shapes array · 1 item
[0]
categorical_cross_tabulation
evidence object · 3 fields
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0.8
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high
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chi-square
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gaps array · 1 item
[0]
method.reader_differs_from_extractor
capability object · 3 fields
state
complete
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[0] object · 6 fields
capability_id
capability:computational_analysis
label
Computational analysis platform
assay_families array · 9 items
[0]
meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
complete
tier
R1
blocked_on
nothing:replicable_now
axes object · 3 fields
method object · 5 fields
tier
R1
expressible
true
required_operations array · 1 item
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survival_km
missing_operations array · 0 items
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: kaplan_meier.
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
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true
accessions array · 4 items
[0]
GSE121248
[1]
GSE101685
[2]
GSE62232
[3]
GSE84598
resolved_accessions array · 4 items
[0]
GSE121248
[1]
GSE101685
[2]
GSE62232
[3]
GSE84598
statements array · 1 item
[0]
The data used to support the findings of this study are available from the corresponding author upon request.
basis
The paper names GSE121248, GSE101685, GSE62232, GSE84598 in NCBI 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 · 1 item
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survival_km
assets array · 2 items
[0]
source:pmid:35132379
[1]
data:geo:GSE101685
steps array · 1 item
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run_analysis
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readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE101685
gaps array · 0 items
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
2026-11-01T17:33:25Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
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5
usage object · 3 fields
prompt_tokens
8074
completion_tokens
1860
cached_tokens
264
stages array · 1 item
[0] object · 4 fields
id
extraction
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complete
reader
MiniMax-M3.1-Flash
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minimax
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review.independent_reader
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[2]
review.human_critique
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absent
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not_run
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gaps array · 1 item
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provenance object · 7 fields
entities array · 3 items
[0] object · 3 fields
id
pmid:35132379
type
paper
label
pmid:35132379
[1] object · 3 fields
id
source:pmid:35132379
type
manuscript
label
PMID 35132379 full text
[2] object · 3 fields
id
data:geo:GSE101685
type
dataset
label
GEO GSE101685
activities array · 3 items
[0] object · 4 fields
id
activity-reading-sci-2026-11-01
type
classification
used array · 3 items
[0] object · 3 fields
id
pmid:35132379
type
paper
label
pmid:35132379
[1] object · 3 fields
id
source:pmid:35132379
type
manuscript
label
PMID 35132379 full text
[2] object · 3 fields
id
data:geo:GSE101685
type
dataset
label
GEO GSE101685
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-35132379
type
extraction
used array · 1 item
[0]
source:pmid:35132379
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE101685
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE101685
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
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agent:corpus-assay-engine
type
software
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Corpus assay engine
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id
agent:minimax-reader
type
software
label
MiniMax literature reader
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reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
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lineage object · 4 fields
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pmid:35132379
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sha256:2f7e2adb4e21348b0c7ef1c2136c641ec14178b44a46c1f7b0bf933bea549e9c
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gaps array · 13 items
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[1]
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[2]
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[3]
asset:data:geo:GSE121248 not downloaded
[4]
asset:data:geo:GSE62232 licence not read
[5]
asset:data:geo:GSE62232 not downloaded
[6]
asset:data:geo:GSE84598 licence not read
[7]
asset:data:geo:GSE84598 not downloaded
[8]
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[10]
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data_generation
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99e1195c7d6f
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partial
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99e1195c7d6f
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0.99
evidence array · 3 items
[0]
is. In addition, real-time quantitative PCR (RT-qPCR), western blot (WB), and immunohistochemistr
[1]
In addition, real-time quantitative PCR (RT-qPCR), western blot (WB), and immunohistochemistr
[2]
related with a worse prognosis. In addition, real-time quantitative PCR (RT-qPCR), western blot (WB), and immunohist
order_basis
paper_text_order:1308
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assay:1
[1] object · 11 fields
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data_generation
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99e1195c7d6f
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ition, real-time quantitative PCR (RT-qPCR), western blot (WB), and immunohistochemistry (IHC) finding
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[0]
tative PCR (RT-qPCR), western blot (WB), and immunohistochemistry (IHC) findings suggested that the expression
[1]
western blot (WB), and immunohistochemistry (IHC) findings suggested that the expression of M
order_basis
paper_text_order:1369
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assay:3
[3] object · 11 fields
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analysis
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f2132e96ae6c7a4e
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GEO2R is an online tool used to conduct differential gene expression analysis on GEO data.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35132379", "kind": "science-record", "revision": 5, "content_hash": "sha256:245ce96afb1330020b41eb4e55dcbf5bc31ecbe765a0ea86800794b3175ac684", "created_at": "2026-11-01T17:36:53Z", "updated_at": "2026-11-01T22:48:26Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of MAD2L1 as a Potential Biomarker in Hepatocellular Carcinoma via Comprehensive Bioinformatics Analysis.", "doi": "10.1155/2022/9868022", "pmid": "35132379", "authors": ["Qian Chen", "Sibo Yang", "Yewei Zhang", "Bo Li", "Huanming Xu", "Shi Zuo"], "journal": "BioMed research international", "year": 2022, "abstract": "BACKGROUND: Hepatocellular carcinoma (HCC) is widely acknowledged as a malignant tumor with rapid progression, high recurrence rate, and poor prognosis. At present, there is a paucity of reliable biomarkers at the clinical level to guide the management of HCC and improve patient outcomes. Our research is aimed at assessing the prognostic value of MAD2L1 in HCC.\nMETHODS: Four datasets, GSE121248, GSE101685, GSE85598, and GSE62232, were selected from the GEO database to analyze differentially expressed genes (DEGs) between HCC and normal liver tissues. After functional analysis, we constructed a protein-protein interaction network (PPI) for DEGs and identified core genes in this network with high connectivity with other genes. We assessed the relationship between core genes and the pathogenesis and prognosis of HCC. Finally, we explored the gene regulatory signaling mechanisms involved in HCC pathogenesis.\nRESULTS: 145 DEGs were screened from the intersection of the four GEO datasets. MAD2L1 was associated with most genes according to the PPI network and was selected as a candidate gene for further study. Survival analysis suggested that high MAD2L1 expression in HCC correlated with a worse prognosis. In addition, real-time quantitative PCR (RT-qPCR), western blot (WB), and immunohistochemistry (IHC) findings suggested that the expression of MAD2L1 was abnormally increased in HCC tissues and cells compared to paraneoplastic tissues and normal hepatocytes.\nCONCLUSION: We found that high MAD2L1 expression in HCC was significantly associated with overall patient survival and clinical features. We also explored the potential biological properties of this gene.", "claims": [{"id": "claim-method", "statement": "GEO2R is an online tool used to conduct differential gene expression analysis on GEO data.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35132379", "locator": "sections[4] \"2.2. Identification of DEGs\" paragraph 2", "quote": "GEO2R is an online tool used to conduct differential gene expression analysis on GEO data."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The data used to support the findings of this study are available from the corresponding author upon request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35132379", "locator": "sections[23] \"Data Availability\" paragraph 2", "quote": "The data used to support the findings of this study are available from the corresponding author upon request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The analysis identified 145 differentially expressed genes from the intersection of four GEO datasets.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35132379", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "145 DEGs were screened from the intersection of the four GEO datasets."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The analysis identified 145 differentially expressed genes from the intersection of four GEO datasets.", "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:35132379"], "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:GSE101685"], "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:GSE101685"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:35132379", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1155/2022/9868022", "sha256": 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