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pmid:39041652

A Novel Amino Acid-Related Gene Signature Predicts Overall Survival in Patients With Hepatocellular Carcinoma.

Shuyi Wang · Hong Huang · Xingwang Hu · Meifang Xiao · Kaili Yang · Haiyan Bu · Yupeng Jiang · Zebing Huang

Cancer reports (Hoboken, N.J.) · 2024 doi:10.1002/cnr2.2131

Paper

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Experiment

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Data

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Analysis

partial

Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:39041652
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science-record
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2026-11-01T20:29:07Z
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2026-11-01T22:12:17Z
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paper object · 10 fields
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complete
title
A Novel Amino Acid-Related Gene Signature Predicts Overall Survival in Patients With Hepatocellular Carcinoma.
doi
10.1002/cnr2.2131
pmid
39041652
authors array · 8 items
[0]
Shuyi Wang
[1]
Hong Huang
[2]
Xingwang Hu
[3]
Meifang Xiao
[4]
Kaili Yang
[5]
Haiyan Bu
[6]
Yupeng Jiang
[7]
Zebing Huang
journal
Cancer reports (Hoboken, N.J.)
year
2024
abstract
BACKGROUND AND AIMS: Hepatocellular carcinoma (HCC) is an extremely harmful malignant tumor in the world. Since the energy metabolism and biosynthesis of HCC cells are closely related to amino acids, it is necessary to further explore the relationship between amino acid-related genes and the prognosis of HCC to achieve individualized treatment. We herein aimed to develop a prognostic model for HCC based on amino acid genes. METHODS: In this study, RNA-sequencing data of HCC patients were downloaded from the TCGA-LIHC cohort as the training cohort and the GSE14520 cohort as the validation cohort. Amino acid-related genes were derived from the Molecular Signatures Database. Univariate Cox and Lasso regression analysis were used to construct an amino acid-related signature (AARS). The predictive value of this risk score was evaluated by Kaplan-Meier (K-M) curve, receiver operating characteristic (ROC) curve, univariate and multivariate Cox regression analysis. Gene set variation analysis (GSVA) and immune characteristics evaluation were used to explore the underlying mechanisms. Finally, a nomogram was established to help the personalized prognosis assessment of patients with HCC. RESULTS: The AARS comprises 14 amino acid-related genes to predict overall survival (OS) in HCC patients. HCC patients were divided into AARS-high group and AARS-low group according to the AARS scores. The K-M curve, ROC curve, and univariate and multivariate Cox regression analysis verified the good prediction efficiency of the risk score. Using GSVA, we found that AARS variants were concentrated in four pathways, including cholesterol metabolism, delayed estrogen response, fatty acid metabolism, and myogenesis metabolism. CONCLUSION: Our results suggest that the AARS as a prognostic model based on amino acid-related genes is of great value in the prediction of survival of HCC, and can help improve the individualized treatment of patients with HCC.
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Univariate Cox and Lasso regression analysis were used to construct an amino acid‐related signature (AARS).
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Univariate Cox and Lasso regression analysis were used to construct an amino acid‐related signature (AARS).
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The datasets generated and/or analyzed during the current study are available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/).
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sections[29] "Data Availability Statement" paragraph 2
quote
The datasets generated and/or analyzed during the current study are available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/).
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The AARS comprises 14 amino acid‐related genes to predict overall survival (OS) in HCC patients.
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sections[0] "Abstract" paragraph 3
quote
The AARS comprises 14 amino acid‐related genes to predict overall survival (OS) in HCC patients.
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The AARS comprises 14 amino acid‐related genes to predict overall survival (OS) in HCC patients.
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https://doi.org/10.1002/cnr2.2131
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The datasets generated and/or analyzed during the current study are available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/).
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The datasets generated and/or analyzed during the current study are available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/).
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[483]
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[484]
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[485]
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[486]
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[487]
GSM712542
sample_count
488
group_sizes
null
group_sizes_basis
null
platform
3921;571
taxon
Homo sapiens
title
Gene expression data of human hepatocellular carcinoma (HCC)
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 2 items
[0]
asset:data:geo:GSE14520 not downloaded
[1]
asset:data:geo:GSE14520 licence not read
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method-1
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group_comparison
specific
wilcoxon
label
Group comparison
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
group_comparison_wilcoxon
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false
parameters object · 0 fields
data_shapes array · 1 item
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two_or_more_groups_continuous
evidence object · 3 fields
score
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high
quote
Wilcoxon
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id
method-2
family
survival_analysis
specific
kaplan_meier
label
Survival analysis
dsl_operations array · 1 item
[0]
survival_km
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
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0.7
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quote
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[2] object · 10 fields
id
method-3
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survival_analysis
specific
cox_proportional_hazards
label
Survival analysis
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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
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0.7
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Cox regression
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differential_expression
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limma_voom
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normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
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parameters object · 0 fields
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[0]
count_matrix_with_condition
evidence object · 3 fields
score
0.8
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id
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label
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[0]
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[1]
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[2]
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[3]
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[4]
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[5]
published_precision_envelope
missing_operations array · 0 items
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data_shapes array · 1 item
[0]
reference_standard_and_test
evidence object · 3 fields
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0.7
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method-6
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null
specific
null
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Univariate Cox and Lasso regression analysis
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missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 0 items
evidence object · 3 fields
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1
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Univariate Cox and Lasso regression analysis were used to construct an amino acid‐related signature (AARS).
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gaps array · 2 items
[0]
method.reader_named_unmapped
[1]
method.group_comparison_wilcoxon
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capability_id
capability:computational_analysis
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assay_families array · 9 items
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meta_analysis
[1]
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[3]
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[4]
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[5]
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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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nothing:replicable_now
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tier
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group_comparison_wilcoxon
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: wilcoxon.
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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
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[0]
GSE14520
resolved_accessions array · 1 item
[0]
GSE14520
statements array · 1 item
[0]
The datasets generated and/or analyzed during the current study are available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/).
basis
The paper names GSE14520 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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assets array · 2 items
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[1]
data:geo:GSE14520
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group_comparison_wilcoxon
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null
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data:geo:GSE14520
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review object · 5 fields
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partial
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extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T19:24:38Z
independence
single_reader
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method
verbatim
availability
verbatim
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5
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extraction
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minimax
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[2]
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pmid:39041652
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paper
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pmid:39041652
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id
source:pmid:39041652
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manuscript
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PMID 39041652 full text
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data:geo:GSE14520
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dataset
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GEO GSE14520
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[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:39041652
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source:pmid:39041652
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manuscript
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PMID 39041652 full text
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data:geo:GSE14520
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dataset
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GEO GSE14520
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agent:corpus-assay-engine
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extraction
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[0]
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agent:minimax-reader
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activity-resolve-GSE14520
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used array · 1 item
[0]
data:geo:GSE14520
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agent:corpus-assay-engine
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null
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[0]
on amino acid genes. METHODS: In this study, RNA-sequencing data of HCC patients were downloaded from th
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paper_text_order:518
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39041652", "kind": "science-record", "revision": 3, "content_hash": "sha256:a8ac3e3ac58edae52f5e4223b4069635d2dec1109327617a3e3db9d9025e398d", "created_at": "2026-11-01T20:29:07Z", "updated_at": "2026-11-01T22:12:17Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A Novel Amino Acid-Related Gene Signature Predicts Overall Survival in Patients With Hepatocellular Carcinoma.", "doi": "10.1002/cnr2.2131", "pmid": "39041652", "authors": ["Shuyi Wang", "Hong Huang", "Xingwang Hu", "Meifang Xiao", "Kaili Yang", "Haiyan Bu", "Yupeng Jiang", "Zebing Huang"], "journal": "Cancer reports (Hoboken, N.J.)", "year": 2024, "abstract": "BACKGROUND AND AIMS: Hepatocellular carcinoma (HCC) is an extremely harmful malignant tumor in the world. Since the energy metabolism and biosynthesis of HCC cells are closely related to amino acids, it is necessary to further explore the relationship between amino acid-related genes and the prognosis of HCC to achieve individualized treatment. We herein aimed to develop a prognostic model for HCC based on amino acid genes.\nMETHODS: In this study, RNA-sequencing data of HCC patients were downloaded from the TCGA-LIHC cohort as the training cohort and the GSE14520 cohort as the validation cohort. Amino acid-related genes were derived from the Molecular Signatures Database. Univariate Cox and Lasso regression analysis were used to construct an amino acid-related signature (AARS). The predictive value of this risk score was evaluated by Kaplan-Meier (K-M) curve, receiver operating characteristic (ROC) curve, univariate and multivariate Cox regression analysis. Gene set variation analysis (GSVA) and immune characteristics evaluation were used to explore the underlying mechanisms. Finally, a nomogram was established to help the personalized prognosis assessment of patients with HCC.\nRESULTS: The AARS comprises 14 amino acid-related genes to predict overall survival (OS) in HCC patients. HCC patients were divided into AARS-high group and AARS-low group according to the AARS scores. The K-M curve, ROC curve, and univariate and multivariate Cox regression analysis verified the good prediction efficiency of the risk score. Using GSVA, we found that AARS variants were concentrated in four pathways, including cholesterol metabolism, delayed estrogen response, fatty acid metabolism, and myogenesis metabolism.\nCONCLUSION: Our results suggest that the AARS as a prognostic model based on amino acid-related genes is of great value in the prediction of survival of HCC, and can help improve the individualized treatment of patients with HCC.", "claims": [{"id": "claim-method", "statement": "Univariate Cox and Lasso regression analysis were used to construct an amino acid‐related signature (AARS).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39041652", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Univariate Cox and Lasso regression analysis were used to construct an amino acid‐related signature (AARS)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets generated and/or analyzed during the current study are available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39041652", "locator": "sections[29] \"Data Availability Statement\" paragraph 2", "quote": "The datasets generated and/or analyzed during the current study are available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The AARS comprises 14 amino acid‐related genes to predict overall survival (OS) in HCC patients.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:39041652", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The AARS comprises 14 amino acid‐related genes to predict overall survival (OS) in HCC patients."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": "The AARS comprises 14 amino acid‐related genes to predict overall survival (OS) in HCC patients.", "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:39041652"], "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:GSE14520"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "blocked", "blocked_on": "method:group_comparison_wilcoxon", "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:GSE14520"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": ["step:run_analysis blocked on method:group_comparison_wilcoxon"]}, "data": {"state": "partial", "assets": [{"id": "source:pmid:39041652", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1002/cnr2.2131", "sha256": "sha256:8dbdd8f4a2285d2c2d895616744f0e82ccb4ab0df83391825a2f1faf7a8393fa", "bytes": 38721, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1002/cnr2.2131", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC11264112", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE14520", "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=GSE14520", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE14520", "version": null, "note": "The datasets generated and/or analyzed during the current study are available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/).", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The datasets generated and/or analyzed during the current study are available in The Cancer Genome Atlas (TCGA, https://portal.gdc.cancer.gov/) and the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/geo/).", "access_statement_kind": "data_availability_statement", "sample_accessions": ["GSM362947", "GSM362948", "GSM362949", "GSM362950", "GSM362951", "GSM362952", "GSM362953", "GSM362954", "GSM362955", "GSM362956", "GSM362957", "GSM362958", "GSM362959", "GSM362960", "GSM362961", "GSM362962", "GSM362963", "GSM362964", "GSM362965", "GSM362966", "GSM362967", "GSM362968", "GSM362969", "GSM362970", "GSM362971", "GSM362972", "GSM362973", "GSM362974", "GSM362975", "GSM362976", "GSM362977", "GSM362978", "GSM362979", "GSM362980", "GSM362981", "GSM362982", 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