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pmid:32071556

Prognostic values of a novel multi-mRNA signature for predicting relapse of cholangiocarcinoma.

Han Guo · Jie Cai · Xuan Wang · Bingrui Wang · Fang Wang · Xiang Li · Xiaoye Qu · Xianming Kong · Yueqiu Gao · Hailong Wu · Xuehua Sun · Qiang Xia · Xiaoni Kong

International journal of biological sciences · 2020 doi:10.7150/ijbs.38846

Paper

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Experiment

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Data

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title
Prognostic values of a novel multi-mRNA signature for predicting relapse of cholangiocarcinoma.
doi
10.7150/ijbs.38846
pmid
32071556
authors array · 13 items
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Han Guo
[1]
Jie Cai
[2]
Xuan Wang
[3]
Bingrui Wang
[4]
Fang Wang
[5]
Xiang Li
[6]
Xiaoye Qu
[7]
Xianming Kong
[8]
Yueqiu Gao
[9]
Hailong Wu
[10]
Xuehua Sun
[11]
Qiang Xia
[12]
Xiaoni Kong
journal
International journal of biological sciences
year
2020
abstract
Cholangiocarcinoma (CCA) is an epithelial cancer and has high death and recurrence rates, current methods cannot satisfy the need for predicting cancer relapse effectively. So, we aimed at conducting a multi-mRNA signature to improve the relapse prediction of CCA. We analyzed mRNA expression profiling in large CCA cohorts from the Gene Expression Omnibus (GEO) database (GSE76297, GSE32879, GSE26566, GSE31370, and GSE45001) and The Cancer Genome Atlas (TCGA) database. The Least absolute shrinkage and selection operator (LASSO) regression model was used to establish a 7-mRNA-based signature that was significantly related to the recurrence-free survival (RFS) in two test series. Based on the 7-mRNA signature, the cohort TCGA patients could be divided into high-risk or low-risk subgroups with significantly different RFS [p < 0.001, hazard ratio (HR): 48.886, 95% confidence interval (CI): 6.226-3.837E+02]. Simultaneously, the prognostic value of the 7-mRNA signature was confirmed in clinical samples of Ren Ji hospital (p < 0.001, HR: 4.558, 95% CI: 1.829-11.357). Further analysis including multivariable and sub-group analyses revealed that the 7-mRNA signature was an independent prognostic value for recurrence of patients with CCA. In conclusion, our results might provide an efficient tool for relapse prediction and were beneficial to individualized management for CCA patients.
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title
Gene expression data of human hepatocellular carcinoma (HCC) and Cholangiocarcinoma (CCA) from Thailand Initiative in Genomics and Expression Research for Liver Cancer (TIGER-LC)
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2026-11-01T15:39:55Z
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GEO datasets enrolled in the study.
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Preparation of CCA datasets
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Table 1
caption
GEO datasets enrolled in the study.
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GSE26566
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE26566
[2]
106
[3]
59
[4]
6
[5]
Illumina v2.0
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GSE32879
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE32879
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16
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-
[4]
7
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Affymetrix 1.0 ST
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GSE76297
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE76297
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91
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92
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-
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE45001
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10
[4]
-
[5]
Agilent-028004
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GSE31370
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE31370
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section[3]/table-wrap[1]#T1
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asset:data:geo:GSE32879 licence not read
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“The gene expression data of CCAs were downloaded from Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) database.” “Based on the expression status data of these 127 DEGs, we constructed LASSO COX regression models with the R package “glmnet”.” “Ten-time cross validations were used to determine the optimal values of λ and a value λ = 0.20770 with log (λ) = -0.68256 was chosen by 10-fold cross-validation via minimum criteria”
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The gene expression data of CCAs were downloaded from Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) database. There were five appropriate CCA datasets from the GEO database (GSE76297, GSE32879, GSE26566, GSE31370, and GSE45001) met the following criteria: a). a total of more than 10 samples, including both tumor and non-tumor samples; b) annotated genes accounting for more than 90% of the total transcriptomes (n > 17000); and c) the number of differentially expressed genes (DEGs) more than 100.
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“The gene expression data of CCAs were downloaded from Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) database.” “Based on the expression status data of these 127 DEGs, we constructed LASSO COX regression models with the R package “glmnet”.” “Ten-time cross validations were used to determine the optimal values of λ and a value λ = 0.20770 with log (λ) = -0.68256 was chosen by 10-fold cross-validation via minimum criteria”
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32071556", "kind": "science-record", "revision": 8, "content_hash": "sha256:54005c953686bb96c92498ab740de2758178a09a174eaa2891357accea7cb2a1", "created_at": "2026-11-01T15:40:56Z", "updated_at": "2026-11-01T22:01:18Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Prognostic values of a novel multi-mRNA signature for predicting relapse of cholangiocarcinoma.", "doi": "10.7150/ijbs.38846", "pmid": "32071556", "authors": ["Han Guo", "Jie Cai", "Xuan Wang", "Bingrui Wang", "Fang Wang", "Xiang Li", "Xiaoye Qu", "Xianming Kong", "Yueqiu Gao", "Hailong Wu", "Xuehua Sun", "Qiang Xia", "Xiaoni Kong"], "journal": "International journal of biological sciences", "year": 2020, "abstract": "Cholangiocarcinoma (CCA) is an epithelial cancer and has high death and recurrence rates, current methods cannot satisfy the need for predicting cancer relapse effectively. So, we aimed at conducting a multi-mRNA signature to improve the relapse prediction of CCA. We analyzed mRNA expression profiling in large CCA cohorts from the Gene Expression Omnibus (GEO) database (GSE76297, GSE32879, GSE26566, GSE31370, and GSE45001) and The Cancer Genome Atlas (TCGA) database. The Least absolute shrinkage and selection operator (LASSO) regression model was used to establish a 7-mRNA-based signature that was significantly related to the recurrence-free survival (RFS) in two test series. Based on the 7-mRNA signature, the cohort TCGA patients could be divided into high-risk or low-risk subgroups with significantly different RFS [p < 0.001, hazard ratio (HR): 48.886, 95% confidence interval (CI): 6.226-3.837E+02]. Simultaneously, the prognostic value of the 7-mRNA signature was confirmed in clinical samples of Ren Ji hospital (p < 0.001, HR: 4.558, 95% CI: 1.829-11.357). Further analysis including multivariable and sub-group analyses revealed that the 7-mRNA signature was an independent prognostic value for recurrence of patients with CCA. In conclusion, our results might provide an efficient tool for relapse prediction and were beneficial to individualized management for CCA patients.", "claims": [{"id": "claim-data-access", "statement": "The gene expression data of CCAs were downloaded from Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) database. 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"family": "contingency_analysis", "specific": "fisher_exact", "label": "Categorical (contingency table) analysis", "dsl_operations": ["contingency_table", "chi_square_test"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["categorical_cross_tabulation"], "evidence": {"score": 0.8, "band": "high", "quote": "Fisher's exact"}}], "targets": [], "gaps": []}, "capability": {"state": "complete", "requirements": [{"capability_id": "capability:computational_analysis", "label": "Computational analysis platform", "assay_families": ["meta_analysis", "machine_learning", "survival_analysis", "statistical_regression", "pca", "molecular_docking", "network_analysis", "differential_expression", "gwas"], "availability_state": "owned", "tier_unlocked": "R1", "candidate": "Automated Assays Laravel application and simulated adapters"}], "gaps": []}, "readiness": {"state": "complete", "tier": "R1", "blocking_axis": "none", "blocked_on": "nothing:replicable_now", "axes": {"method": {"tier": "R1", "expressible": true, "required_operations": ["cox_ph"], "missing_operations": [], "basis": "The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards."}, "capability": {"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": {"tier": "R1", "reachable": true, "accessions": ["GSE76297", "GSE32879", "GSE26566", "GSE31370", "and GSE45001"], "resolved_accessions": ["GSE76297", "GSE32879", "GSE26566", "GSE31370"], "statements": ["The gene expression data of CCAs were downloaded from Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) database. There were five appropriate CCA datasets from the GEO database (GSE76297, GSE32879, GSE26566, GSE31370, and GSE45001) met the following criteria: a). a total of more than 10 samples, including both tumor and non-tumor samples; b) annotated genes accounting for more than 90% of the total transcriptomes (n > 17000); and c) the number of differentially expressed genes (DEGs) more than 100."], "basis": "The paper names GSE76297, GSE32879, GSE26566, GSE31370 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:32071556", "data:geo:GSE26566", "asset:table:pmid:32071556:1"], "steps": ["run_analysis"]}, "must_build": {"dsl_operations": [], "converters": [], "readers": [], "capabilities": [], "data_gaps": ["data:geo:GSE26566"]}, "gaps": []}, "review": {"state": "partial", "machine_critique": {"kind": "extraction_review", "reader": {"model": "MiniMax-M3.1-Flash", "provider": "minimax", "provider_family": "minimax", "read_at": "2026-10-31T18:18:19Z", "independence": "single_reader"}, "evidence_check": {"method": "reordered", "availability": null}, "calls": 3, "usage": {"prompt_tokens": 33612, "completion_tokens": 2188, "cached_tokens": 792}}, "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:32071556", "type": "paper", "label": "pmid:32071556"}, {"id": "source:pmid:32071556", "type": "manuscript", "label": "PMID 32071556 full text"}, {"id": "data:geo:GSE26566", "type": "dataset", "label": "GEO GSE26566"}], "activities": [{"id": "activity-reading-sci-2026-11-01", "type": "classification", "used": [{"id": "pmid:32071556", "type": "paper", "label": "pmid:32071556"}, {"id": "source:pmid:32071556", "type": "manuscript", "label": "PMID 32071556 full text"}, {"id": "data:geo:GSE26566", "type": "dataset", "label": "GEO GSE26566"}], "agent": "agent:corpus-assay-engine"}, {"id": "activity-read-32071556", "type": "extraction", "used": ["source:pmid:32071556"], "agent": "agent:minimax-reader"}, {"id": "activity-resolve-GSE26566", "type": "accession_resolution", "used": ["data:geo:GSE26566"], "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:32071556", "parent_hash": "sha256:df96a381aa70ce03f785e7d1fd1959af8e5192d4d42a51abf31538e32871f9a2", "fork_of": null, "generation": 7}, "gaps": ["asset:data:geo:GSE26566 licence not read", "asset:data:geo:GSE26566 not downloaded", "asset:data:geo:GSE31370 licence not read", "asset:data:geo:GSE31370 not downloaded", "asset:data:geo:GSE32879 licence not read", "asset:data:geo:GSE32879 not downloaded", "asset:data:geo:GSE76297 licence not read", "asset:data:geo:GSE76297 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": ["“The gene expression data of CCAs were downloaded from Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA) database.” “Based on the expression status data of these 127 DEGs, we constructed LASSO COX regression models with the R package “glmnet”.” “Ten-time cross validations were used to determine the optimal values of λ and a value λ = 0.20770 with log (λ) = -0.68256 was chosen by 10-fold cross-validation via minimum criteria”"], "order_basis": "analysis_only", "id": "assay:1"}]}