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pmid:39741650

Bioinformatics-Based Construction of Immune-Related microRNA and mRNA Prognostic Models for Hepatocellular Carcinoma.

Ying Chen · Dian Yin · Xiu Feng · Shennan He · Liang Zhang · Dongqin Chen

Cancer management and research · 2024 doi:10.2147/CMAR.S482688

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:39741650
kind
science-record
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sha256:ba084bbce3f19ace32d4d533150e108a571bbafc454bcb32435b9366bdab8f34
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2026-11-01T20:30:04Z
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2026-11-01T22:13:27Z
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paper object · 10 fields
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title
Bioinformatics-Based Construction of Immune-Related microRNA and mRNA Prognostic Models for Hepatocellular Carcinoma.
doi
10.2147/CMAR.S482688
pmid
39741650
authors array · 6 items
[0]
Ying Chen
[1]
Dian Yin
[2]
Xiu Feng
[3]
Shennan He
[4]
Liang Zhang
[5]
Dongqin Chen
journal
Cancer management and research
year
2024
abstract
Introduction: The development and progression of Hepatocellular Carcinoma (HCC) is more relevant to immune regulation. Therefore, there is an urgent need to find immune-related molecular markers that can predict the prognosis and immune status of HCC. Methods: RNA-seq and clinical HCC data from the Cancer Genome Atlas (TCGA) were analyzed for differential expression of microRNA (miRNAs), mRNAs, and lncRNAs. MiRNAs associated with immune scores were identified by Spearman analysis and Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment. MiRNAs and mRNAs were screened for prognosticity using COX regression. Kaplan-Meier survival analysis, risk scores, and correlation with clinical features were performed. Immune infiltration, Tumor Immune Dysfunction and Exclusion (TIDE), and chemotherapy prediction analyses were performed for high and low risk groups. Finally, prognostic mRNA expression was validated in cell lines. Results: Five prognostic miRNAs (hsa-miR-145-3p, hsa-miR-150-3p, hsa-miR-153-3p, hsa-miR-223-3p, hsa-miR-424-3p) were identified in the study. A risk score model based on these prognostic miRNAs accurately predicted overall survival and was validated in GSE31384. Six mRNAs (KCTD17, MAFG, RAB10, SFPQ, TRMT6, UBE2D2) were further identified as prognostic. A risk model including these mRNAs also accurately predicted overall survival, and higher risk scores were associated with lower survival. Univariate and multivariate Cox regression analyses confirmed that both miRNA and mRNA risk scores were independent prognostic factors. The TIDE results showed lower TIDE scores and T-cell exclusion scores in the low risk score group. Chemotherapeutic drug sensitivity analysis revealed that the high-risk group was more sensitive to multiple chemotherapeutic agents. In addition, real-time quantitative PCR (RT-qPCR) results of the cell lines supported the results of the public database analysis. Conclusion: This study validated immune-related prognostic miRNAs and mRNAs and identified risk signatures for HCC, potentially advancing HCC prognosis and treatment.
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Univariate and multivariate Cox regression analyses confirmed that both miRNA and mRNA risk scores were independent prognostic factors.
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Univariate and multivariate Cox regression analyses confirmed that both miRNA and mRNA risk scores were independent prognostic factors.
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The sequencing information and clinical data for the TCGA-HCC cohort were acquired from the TCGA database (https://xenabrowser.net) in the April of 2022.
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microRNA profile of human liver tissues: hepatocellular carcinoma vs. matched noncancerous liver tissue
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review.machine_critique
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review.human_critique
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gaps array · 1 item
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execution.not_run
provenance object · 7 fields
entities array · 3 items
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pmid:39741650
type
paper
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pmid:39741650
[1] object · 3 fields
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source:pmid:39741650
type
manuscript
label
PMID 39741650 full text
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id
data:geo:GSE31384
type
dataset
label
GEO GSE31384
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activity-reading-sci-2026-11-01
type
classification
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pmid:39741650
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pmid:39741650
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PMID 39741650 full text
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type
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GEO GSE31384
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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pmid:39741650
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sha256:3a37590c581fcad3ebcfe13b81434943c96e42fb367fac9bcc54f89c0061ef20
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null
gaps array · 9 items
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asset:data:geo:GSE31384 licence not read
[1]
asset:data:geo:GSE31384 not downloaded
[2]
asset:data:geo:GSE76427 licence not read
[3]
asset:data:geo:GSE76427 not downloaded
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assays array · 3 items
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evidence array · 1 item
[0]
prognosis and immune status of HCC. Methods: RNA-seq and clinical HCC data from the Cancer Genome
order_basis
paper_text_order:334
id
assay:1
[1] object · 11 fields
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data_generation
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99e1195c7d6f
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assay_lexicon
99e1195c7d6f
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evidence array · 4 items
[0]
ts. In addition, real-time quantitative PCR (RT-qPCR) results of the cell lines supported the res
[1]
In addition, real-time quantitative PCR (RT-qPCR) results of the cell lines supported the res
[2]
ltiple chemotherapeutic agents. In addition, real-time quantitative PCR (RT-qPCR) results of the cell lines supporte
[3]
s by using Wilcoxon test. The discrepancy in RT-qPCR results were compared by employing the Stude
order_basis
paper_text_order:1906
id
assay:2
[2] object · 11 fields
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survival_analysis
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f2132e96ae6c7a4e
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cox_ph
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dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
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Univariate and multivariate Cox regression analyses confirmed that both miRNA and mRNA risk scores were independent prognostic factors.
order_basis
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39741650", "kind": "science-record", "revision": 3, "content_hash": "sha256:ba084bbce3f19ace32d4d533150e108a571bbafc454bcb32435b9366bdab8f34", "created_at": "2026-11-01T20:30:04Z", "updated_at": "2026-11-01T22:13:27Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Bioinformatics-Based Construction of Immune-Related microRNA and mRNA Prognostic Models for Hepatocellular Carcinoma.", "doi": "10.2147/CMAR.S482688", "pmid": "39741650", "authors": ["Ying Chen", "Dian Yin", "Xiu Feng", "Shennan He", "Liang Zhang", "Dongqin Chen"], "journal": "Cancer management and research", "year": 2024, "abstract": "Introduction: The development and progression of Hepatocellular Carcinoma (HCC) is more relevant to immune regulation. Therefore, there is an urgent need to find immune-related molecular markers that can predict the prognosis and immune status of HCC.\nMethods: RNA-seq and clinical HCC data from the Cancer Genome Atlas (TCGA) were analyzed for differential expression of microRNA (miRNAs), mRNAs, and lncRNAs. MiRNAs associated with immune scores were identified by Spearman analysis and Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment. MiRNAs and mRNAs were screened for prognosticity using COX regression. Kaplan-Meier survival analysis, risk scores, and correlation with clinical features were performed. Immune infiltration, Tumor Immune Dysfunction and Exclusion (TIDE), and chemotherapy prediction analyses were performed for high and low risk groups. Finally, prognostic mRNA expression was validated in cell lines.\nResults: Five prognostic miRNAs (hsa-miR-145-3p, hsa-miR-150-3p, hsa-miR-153-3p, hsa-miR-223-3p, hsa-miR-424-3p) were identified in the study. A risk score model based on these prognostic miRNAs accurately predicted overall survival and was validated in GSE31384. Six mRNAs (KCTD17, MAFG, RAB10, SFPQ, TRMT6, UBE2D2) were further identified as prognostic. A risk model including these mRNAs also accurately predicted overall survival, and higher risk scores were associated with lower survival. Univariate and multivariate Cox regression analyses confirmed that both miRNA and mRNA risk scores were independent prognostic factors. The TIDE results showed lower TIDE scores and T-cell exclusion scores in the low risk score group. Chemotherapeutic drug sensitivity analysis revealed that the high-risk group was more sensitive to multiple chemotherapeutic agents. In addition, real-time quantitative PCR (RT-qPCR) results of the cell lines supported the results of the public database analysis.\nConclusion: This study validated immune-related prognostic miRNAs and mRNAs and identified risk signatures for HCC, potentially advancing HCC prognosis and treatment.", "claims": [{"id": "claim-method", "statement": "Univariate and multivariate Cox regression analyses confirmed that both miRNA and mRNA risk scores were independent prognostic factors.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39741650", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "Univariate and multivariate Cox regression analyses confirmed that both miRNA and mRNA risk scores were independent prognostic factors."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The sequencing information and clinical data for the TCGA-HCC cohort were acquired from the TCGA database (https://xenabrowser.net) in the April of 2022.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39741650", "locator": "sections[3] \"Data Source\" paragraph 2", "quote": "The sequencing information and clinical data for the TCGA-HCC cohort were acquired from the TCGA database (https://xenabrowser.net) in the April of 2022."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "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:39741650"], "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:GSE31384"], "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:GSE31384"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:39741650", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.2147/CMAR.S482688", "sha256": 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