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pmid:32953265
Identification of a prognostic signature of nine metabolism-related genes for hepatocellular carcinoma.
Chaozhi Tang · Jiakang Ma · Xiuli Liu · Zhengchun Liu
PeerJ · 2020 doi:10.7717/peerj.9774
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Experiment
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Complete file
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Since changes in liver metabolism contribute to liver disease development, it is necessary to build a metabolism-related prognostic model for HCC.\nMETHODS: We constructed a metabolism-related-gene (MRG) signature comprising nine genes, which segregated HCC patients into high- and low-risk groups.\nRESULTS: The survival rate (overall survival: OS; relapse-free survival; and progression-free survival) of patients in the low-risk group of The Cancer Genome Atlas (TCGA) cohort was significantly higher than that of patients in the high-risk group. The OS prognostic signature was validated in the International Cancer Genome Consortium independent cohort. The corresponding receiver operating characteristic curves of the model indicated that the signature had good diagnostic efficiency, in terms of improving OS over 1, 3, and 5 years. Hierarchical analysis demonstrated that the MRG signature was significantly associated with better prognosis in male patients, patients aged ≤ 65 years, and patients carrying the wild-type TP53 or CTNNB1 genes. A nomogram was established, and good performance and clinical practicability were confirmed. Additionally, using the GSE109211 dataset from the Gene Expression Omnibus database, we were able to verify that the nine genes in this MRG signature had different responses to sorafenib, suggesting that some of these MRGs may act as therapeutic targets for HCC.\nCONCLUSIONS: We believe that these findings will add value in terms of the diagnosis, treatment, and prognosis of HCC.", "claims": [{"id": "claim-method", "statement": "Next, the “glmnet” package was used to implement the LASSO Cox regression model. 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For the discovery cohort (n = 374 patients), fragments per kilobase of exon per million mapped reads (FPKM) data and the corresponding clinical information related to gene expression were downloaded from The Cancer Genome Atlas (TCGA). 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The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R1", "reachable": true, "accessions": ["GSE109211"], "resolved_accessions": ["GSE109211"], "statements": ["The following information was supplied regarding data availability:\nThe data is available at the Cancer Genome Altas (TCGA, https://cancergenome.nih.gov).\nunder TCGA search term: TCGA-LIHC and from the International cancer genomics consortium (ICGC, https://icgc.org) using ICGC search term: LIRI-JP (https://dcc.icgc.org/releases/current/Projects/LIRI-JP), and NCBI GEO: GSE109211."], "basis": "The paper names GSE109211 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read."}}, "can_run": {"dsl_operations": ["cox_ph"], "assets": ["source:pmid:32953265", "data:geo:GSE109211", "asset:table:pmid:32953265:1", "asset:table:pmid:32953265:2"], "steps": ["run_analysis"]}, "must_build": {"dsl_operations": [], "converters": [], "readers": [], "capabilities": [], "data_gaps": ["data:geo:GSE109211"]}, "gaps": []}, "review": {"state": "partial", "machine_critique": {"kind": "extraction_review", "reader": {"model": "MiniMax-M3.1-Flash", "provider": "minimax", "provider_family": "minimax", "read_at": "2026-10-31T18:22:40Z", "independence": "single_reader"}, "evidence_check": {"method": "reordered", "availability": "verbatim"}, "calls": 3, "usage": {"prompt_tokens": 38704, "completion_tokens": 1993, "cached_tokens": 648}}, "human_critique": null, "stages": [{"id": "extraction", "state": "complete", "reader": "MiniMax-M3.1-Flash", "provider": "minimax"}], "gaps": ["review.independent_reader", "review.machine_critique", "review.human_critique"]}, "execution": {"state": "absent", "status": "not_run", "mode": null, "runs": [], "gaps": ["execution.not_run"]}, "provenance": {"entities": [{"id": "pmid:32953265", "type": "paper", "label": "pmid:32953265"}, {"id": "source:pmid:32953265", "type": "manuscript", "label": "PMID 32953265 full text"}, {"id": "data:geo:GSE109211", "type": "dataset", "label": "GEO GSE109211"}], "activities": [{"id": "activity-reading-sci-2026-11-01", "type": "classification", "used": [{"id": "pmid:32953265", "type": "paper", "label": "pmid:32953265"}, {"id": "source:pmid:32953265", "type": "manuscript", "label": "PMID 32953265 full text"}, {"id": "data:geo:GSE109211", "type": "dataset", "label": "GEO GSE109211"}], "agent": "agent:corpus-assay-engine"}, {"id": "activity-read-32953265", "type": "extraction", "used": ["source:pmid:32953265"], "agent": "agent:minimax-reader"}, {"id": "activity-resolve-GSE109211", "type": "accession_resolution", "used": ["data:geo:GSE109211"], "agent": "agent:corpus-assay-engine"}], "agents": [{"id": "agent:corpus-assay-engine", "type": "software", "label": "Corpus assay engine"}, {"id": "agent:minimax-reader", "type": "software", "label": "MiniMax literature reader"}], "source_run_id": "reading-sci-2026-11-01", "dsl_catalogue_fingerprint": "343fb30756ba6ec3", "capability_table_fingerprint": "2cb3e42f047d2ecf", "snapshot_id": "ba34b49490d9bfaf"}, "lineage": {"parent_id": "pmid:32953265", "parent_hash": "sha256:dad7e099570d35e6e23f8b87ca7bb33546b4519ef1dd8cd221f5d83a119fef47", "fork_of": null, "generation": 6}, "gaps": ["asset:data:geo:GSE109211 licence not read", "asset:data:geo:GSE109211 not downloaded", "execution.not_run", "review.human_critique", "review.independent_reader", "review.machine_critique"], "assays": [{"role": "analysis", "definition_id": "survival_analysis", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["cox_ph"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["Next, the “glmnet” package was used to implement the LASSO Cox regression model. For the discovery cohort (n = 374 patients), fragments per kilobase of exon per million mapped reads (FPKM) data and the corresponding clinical information related to gene expression were downloaded from The Cancer Genome Atlas (TCGA). For the validation cohort (n = 243 patients), the original data and corresponding clinical data related to gene expression were downloaded from the Liver Cancer-RIKEN, Japan (LIRI-JP) project of the International Cancer Genome Consortium (ICGC)."], "order_basis": "analysis_only", "id": "assay:1"}]}