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pmid:36465397

Development and validation of a prognostic 9-gene signature for colorectal cancer.

Junpeng Cui · Fangyu Guo · Yifan Yu · Zihuan Ma · Yuting Hong · Junyan Su · Yang Ge

Frontiers in oncology · 2022 doi:10.3389/fonc.2022.1009698

Paper

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Experiment

complete

Data

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Analysis

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Execution

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title
Development and validation of a prognostic 9-gene signature for colorectal cancer.
doi
10.3389/fonc.2022.1009698
pmid
36465397
authors array · 7 items
[0]
Junpeng Cui
[1]
Fangyu Guo
[2]
Yifan Yu
[3]
Zihuan Ma
[4]
Yuting Hong
[5]
Junyan Su
[6]
Yang Ge
journal
Frontiers in oncology
year
2022
abstract
Introduction: Colorectal cancer (CRC) is one of the most prevalent cancers globally with a high mortality rate. Predicting prognosis using disease progression and cancer pathologic stage is insufficient, and a prognostic factor that can accurately evaluate patient prognosis needs to be developed. In this study, we aimed to infer a prognostic gene signature to identify a functional signature associated with the prognosis of CRC patients. Methods: First, we used univariate Cox regression, least absolute shrinkage and selection operator (lasso) regression, and multivariate Cox regression analyses to screen genes significantly associated with CRC patient prognosis, from colorectal cancer RNA sequencing data in The Cancer Genome Atlas (TCGA) database. We then calculated the risk score (RS) for each patient based on the expression of the nine candidate genes and developed a prognostic signature. Results: Based on the optimal cut-off on the receiver operating characteristic (ROC) curve, patients were separated into high- and low-risk groups, and the difference in overall survival between the two groups was examined. Patients in the low-risk group had a better overall survival rate than those in the high-risk group. The results were validated using the GSE72970, GSE39582, and GSE17536 Gene Expression Omnibus (GEO) datasets, and the same conclusions were reached. ROC curve test of the RS signature also indicated that it had excellent accuracy. The RS signature was then compared with traditional clinical factors as a prognostic indicator, and we discovered that the RS signature had superior predictive ability. Conclusion: The RS signature developed in this study has excellent predictive power for the prognosis of patients with CRC and broad applicability as a prognostic indicator for patients.
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First, we used univariate Cox regression, least absolute shrinkage and selection operator (lasso) regression, and multivariate Cox regression analyses to screen genes significantly associated with CRC patient prognosis, from colorectal cancer RNA sequencing data in The Cancer Genome Atlas (TCGA) database.
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First, we used univariate Cox regression, least absolute shrinkage and selection operator (lasso) regression, and multivariate Cox regression analyses to screen genes significantly associated with CRC patient prognosis, from colorectal cancer RNA sequencing data in The Cancer Genome Atlas (TCGA) database.
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The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding author.
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The RS signature developed in this study has excellent predictive power for the prognosis of patients with CRC and broad applicability as a prognostic indicator for patients.
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The RS signature developed in this study has excellent predictive power for the prognosis of patients with CRC and broad applicability as a prognostic indicator for patients.
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The RS signature developed in this study has excellent predictive power for the prognosis of patients with CRC and broad applicability as a prognostic indicator for patients.
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[308]
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[309]
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[310]
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[311]
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[312]
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[313]
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[314]
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[315]
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[316]
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[317]
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[318]
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[319]
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[320]
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[321]
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[324]
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[325]
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[326]
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[327]
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[328]
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[329]
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[334]
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[336]
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[338]
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[341]
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[342]
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[343]
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[344]
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[346]
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[347]
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[348]
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[349]
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[350]
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[351]
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[352]
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[353]
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[354]
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[355]
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[356]
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[357]
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[358]
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[359]
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[360]
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[361]
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[362]
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[363]
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[364]
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[365]
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[366]
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[367]
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[368]
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[369]
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[370]
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[371]
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[372]
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[373]
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[374]
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[375]
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[376]
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[377]
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[378]
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[379]
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[380]
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[381]
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[382]
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[383]
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[384]
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[385]
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[386]
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[387]
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[388]
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[389]
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[390]
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[391]
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[392]
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[393]
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[394]
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[395]
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[396]
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[397]
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[398]
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[399]
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[400]
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[401]
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[402]
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[403]
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[404]
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[405]
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[406]
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[407]
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[408]
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[409]
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[410]
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[411]
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[412]
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[413]
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[414]
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[415]
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[416]
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[417]
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[418]
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[419]
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[420]
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[421]
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[422]
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[423]
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[424]
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[425]
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[426]
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[427]
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[428]
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[429]
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[430]
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[431]
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[432]
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[433]
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[434]
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[435]
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[436]
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[437]
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[438]
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[439]
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[440]
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[441]
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[442]
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[443]
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[444]
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[445]
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[446]
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[447]
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[448]
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[449]
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[450]
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[451]
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[452]
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[453]
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[454]
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[455]
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[456]
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[457]
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[458]
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[459]
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[460]
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[461]
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[462]
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[463]
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[464]
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[465]
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[466]
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[467]
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[468]
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[469]
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[470]
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[471]
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[472]
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[473]
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[474]
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[475]
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[476]
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[477]
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[478]
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[479]
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[480]
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[481]
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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]
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[488]
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[489]
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[490]
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[491]
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[492]
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[493]
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[494]
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[495]
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[496]
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[497]
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[498]
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[499]
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[500]
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[501]
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[502]
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[503]
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[504]
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[505]
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[506]
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[507]
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[508]
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[509]
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[510]
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[511]
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[512]
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[513]
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[514]
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[515]
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[516]
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[517]
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[518]
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[519]
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[520]
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[521]
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[522]
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[523]
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[524]
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[525]
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[526]
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[528]
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[529]
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[531]
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[533]
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[534]
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[535]
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[536]
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[537]
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[538]
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[539]
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[541]
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[542]
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[543]
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[544]
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[545]
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[546]
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[547]
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[548]
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[549]
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[550]
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[551]
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[552]
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[553]
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[554]
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[555]
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[557]
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[560]
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[561]
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[562]
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[563]
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[564]
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[565]
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[566]
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[567]
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[568]
GSM972506
[569]
GSM972507
[570]
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[571]
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[572]
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[573]
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[574]
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[575]
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[576]
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[577]
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[578]
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[579]
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[580]
GSM972518
[581]
GSM972519
[582]
GSM972520
[583]
GSM972521
[584]
GSM972522
sample_count
585
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Gene expression Classification of Colon Cancer defines six molecular subtypes with distinct clinical, molecular and survival characteristics [Expression]
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[3] object · 15 fields
id
data:geo:GSE72970
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=GSE72970
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE72970
version
null
note
The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding author.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding author.
access_statement_kind
data_availability_statement
sample_accessions array · 124 items
[0]
GSM1875897
[1]
GSM1875898
[2]
GSM1875899
[3]
GSM1875900
[4]
GSM1875901
[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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[11]
GSM1875908
[12]
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[13]
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[14]
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[15]
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[16]
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[17]
GSM1875914
[18]
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[19]
GSM1875916
[20]
GSM1875917
[21]
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[22]
GSM1875919
[23]
GSM1875920
[24]
GSM1875921
[25]
GSM1875922
[26]
GSM1875923
[27]
GSM1875924
[28]
GSM1875925
[29]
GSM1875926
[30]
GSM1875927
[31]
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[32]
GSM1875929
[33]
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[34]
GSM1875931
[35]
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[36]
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[37]
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[38]
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[39]
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[40]
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[41]
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[42]
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[43]
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[44]
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[45]
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[46]
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[47]
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[48]
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[49]
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[50]
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[51]
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[52]
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[53]
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[54]
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[55]
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[56]
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[57]
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[58]
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[59]
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[60]
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[61]
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[62]
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[63]
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[64]
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[65]
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[66]
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[67]
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[68]
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[69]
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[70]
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[71]
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[72]
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[73]
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[74]
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[75]
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[76]
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[77]
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[78]
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[79]
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[80]
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[81]
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[82]
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[83]
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[84]
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[85]
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[86]
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[87]
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[88]
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[89]
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[90]
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[91]
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[92]
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[94]
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[98]
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[99]
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[100]
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[101]
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[102]
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[103]
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[104]
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[105]
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[106]
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[107]
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[108]
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[109]
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[110]
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[111]
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[112]
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[113]
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[114]
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[115]
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[116]
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[117]
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[118]
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[119]
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[120]
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[121]
GSM1876018
[122]
GSM1876019
[123]
GSM1876020
sample_count
124
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Molecular subtypes of metastatic colorectal cancer are predictive of patient response to chemo and targeted therapies
resolution_checked_at
2026-11-01T17:30:42Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 6 items
[0]
asset:data:geo:GSE17536 not downloaded
[1]
asset:data:geo:GSE17536 licence not read
[2]
asset:data:geo:GSE39582 not downloaded
[3]
asset:data:geo:GSE39582 licence not read
[4]
asset:data:geo:GSE72970 not downloaded
[5]
asset:data:geo:GSE72970 licence not read
analysis object · 4 fields
state
complete
methods array · 2 items
[0] object · 10 fields
id
method-1
family
survival_analysis
specific
cox_proportional_hazards
label
Survival analysis
dsl_operations array · 1 item
[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
score
1
band
verbatim
quote
First, we used univariate Cox regression, least absolute shrinkage and selection operator (lasso) regression, and multivariate Cox regression analyses to screen genes significantly associated with CRC patient prognosis, from colorectal cancer RNA sequencing data in The Cancer Genome Atlas (TCGA) database.
[1] object · 10 fields
id
method-2
family
diagnostic_evaluation
specific
roc
label
Diagnostic test evaluation
dsl_operations array · 6 items
[0]
confusion_counts
[1]
roc_curve
[2]
sensitivity_specificity
[3]
solve_confusion_matrix
[4]
classification_metrics
[5]
published_precision_envelope
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
reference_standard_and_test
evidence object · 3 fields
score
0.7
band
medium
quote
ROC curve
targets array · 0 items
gaps array · 0 items
capability object · 3 fields
state
complete
requirements array · 1 item
[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
[0]
cox_ph
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: cox_proportional_hazards.
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
reachable
true
accessions array · 3 items
[0]
GSE72970
[1]
GSE39582
[2]
GSE17536
resolved_accessions array · 3 items
[0]
GSE72970
[1]
GSE39582
[2]
GSE17536
statements array · 1 item
[0]
The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding author.
basis
The paper names GSE72970, GSE39582, GSE17536 in Gene Expression Omnibus (GEO) database 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
[0]
cox_ph
assets array · 2 items
[0]
source:pmid:36465397
[1]
data:geo:GSE17536
steps array · 1 item
[0]
run_analysis
must_build object · 5 fields
dsl_operations array · 0 items
converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
[0]
data:geo:GSE17536
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
2026-11-01T18:17:55Z
independence
single_reader
evidence_check object · 2 fields
method
verbatim
availability
verbatim
calls
5
usage object · 3 fields
prompt_tokens
10563
completion_tokens
1975
cached_tokens
128
stages array · 1 item
[0] object · 4 fields
id
extraction
state
complete
reader
MiniMax-M3.1-Flash
provider
minimax
gaps array · 3 items
[0]
review.independent_reader
[1]
review.machine_critique
[2]
review.human_critique
execution object · 5 fields
state
absent
status
not_run
mode
null
runs array · 0 items
gaps array · 1 item
[0]
execution.not_run
provenance object · 7 fields
entities array · 3 items
[0] object · 3 fields
id
pmid:36465397
type
paper
label
pmid:36465397
[1] object · 3 fields
id
source:pmid:36465397
type
manuscript
label
PMID 36465397 full text
[2] object · 3 fields
id
data:geo:GSE17536
type
dataset
label
GEO GSE17536
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:36465397
type
paper
label
pmid:36465397
[1] object · 3 fields
id
source:pmid:36465397
type
manuscript
label
PMID 36465397 full text
[2] object · 3 fields
id
data:geo:GSE17536
type
dataset
label
GEO GSE17536
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-36465397
type
extraction
used array · 1 item
[0]
source:pmid:36465397
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE17536
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE17536
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
label
Corpus assay engine
[1] object · 3 fields
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 object · 4 fields
parent_id
pmid:36465397
parent_hash
sha256:808606f927f5aa1c78f0c8250708131096ca732fe93474cb48db97a46b7deba5
fork_of
null
gaps array · 10 items
[0]
asset:data:geo:GSE17536 licence not read
[1]
asset:data:geo:GSE17536 not downloaded
[2]
asset:data:geo:GSE39582 licence not read
[3]
asset:data:geo:GSE39582 not downloaded
[4]
asset:data:geo:GSE72970 licence not read
[5]
asset:data:geo:GSE72970 not downloaded
[6]
execution.not_run
[7]
review.human_critique
[8]
review.independent_reader
[9]
review.machine_critique
assays array · 3 items
[0] object · 11 fields
role
data_generation
definition_id
rna_seq
definition_version
99e1195c7d6f
required_operations array · 0 items
support_state
partial
source_hashes object · 1 field
assay_lexicon
99e1195c7d6f
confidence
0.93
evidence array · 1 item
[0]
RC patient prognosis, from colorectal cancer RNA sequencing data in The Cancer Genome Atlas (TCGA) datab
order_basis
paper_text_order:731
id
assay:1
[1] object · 11 fields
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e Human Protein Atlas (HPA) is a database of immunohistochemistry (IHC)-based protein expression profiles of d
[1]
and normal tissues. Based on an analysis of immunohistochemically staining data from the Human Protein Atlas d
[2]
(HPA) is a database of immunohistochemistry (IHC)-based protein expression profiles of differ
[3]
n expression of candidate genes, we obtained IHC staining images of candidate genes in tumor
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First, we used univariate Cox regression, least absolute shrinkage and selection operator (lasso) regression, and multivariate Cox regression analyses to screen genes significantly associated with CRC patient prognosis, from colorectal cancer RNA sequencing data in The Cancer Genome Atlas (TCGA) database.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36465397", "kind": "science-record", "revision": 3, "content_hash": "sha256:441a8432b6d33470595fd9bfb460f93cf3fd993b4a398603e6056bfa90190c5c", "created_at": "2026-11-01T19:00:56Z", "updated_at": "2026-11-01T22:08:13Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Development and validation of a prognostic 9-gene signature for colorectal cancer.", "doi": "10.3389/fonc.2022.1009698", "pmid": "36465397", "authors": ["Junpeng Cui", "Fangyu Guo", "Yifan Yu", "Zihuan Ma", "Yuting Hong", "Junyan Su", "Yang Ge"], "journal": "Frontiers in oncology", "year": 2022, "abstract": "Introduction: Colorectal cancer (CRC) is one of the most prevalent cancers globally with a high mortality rate. Predicting prognosis using disease progression and cancer pathologic stage is insufficient, and a prognostic factor that can accurately evaluate patient prognosis needs to be developed. In this study, we aimed to infer a prognostic gene signature to identify a functional signature associated with the prognosis of CRC patients.\nMethods: First, we used univariate Cox regression, least absolute shrinkage and selection operator (lasso) regression, and multivariate Cox regression analyses to screen genes significantly associated with CRC patient prognosis, from colorectal cancer RNA sequencing data in The Cancer Genome Atlas (TCGA) database. We then calculated the risk score (RS) for each patient based on the expression of the nine candidate genes and developed a prognostic signature.\nResults: Based on the optimal cut-off on the receiver operating characteristic (ROC) curve, patients were separated into high- and low-risk groups, and the difference in overall survival between the two groups was examined. Patients in the low-risk group had a better overall survival rate than those in the high-risk group. The results were validated using the GSE72970, GSE39582, and GSE17536 Gene Expression Omnibus (GEO) datasets, and the same conclusions were reached. ROC curve test of the RS signature also indicated that it had excellent accuracy. The RS signature was then compared with traditional clinical factors as a prognostic indicator, and we discovered that the RS signature had superior predictive ability.\nConclusion: The RS signature developed in this study has excellent predictive power for the prognosis of patients with CRC and broad applicability as a prognostic indicator for patients.", "claims": [{"id": "claim-method", "statement": "First, we used univariate Cox regression, least absolute shrinkage and selection operator (lasso) regression, and multivariate Cox regression analyses to screen genes significantly associated with CRC patient prognosis, from colorectal cancer RNA sequencing data in The Cancer Genome Atlas (TCGA) database.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36465397", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "First, we used univariate Cox regression, least absolute shrinkage and selection operator (lasso) regression, and multivariate Cox regression analyses to screen genes significantly associated with CRC patient prognosis, from colorectal cancer RNA sequencing data in The Cancer Genome Atlas (TCGA) database."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding author.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36465397", "locator": "sections[19] \"Data availability statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/ Supplementary Material . Further inquiries can be directed to the corresponding author."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The RS signature developed in this study has excellent predictive power for the prognosis of patients with CRC and broad applicability as a prognostic indicator for patients.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:36465397", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "The RS signature developed in this study has excellent predictive power for the prognosis of patients with CRC and broad applicability as a prognostic indicator for patients."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The RS signature developed in this study has excellent predictive power for the prognosis of patients with CRC and broad applicability as a prognostic indicator for 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:36465397"], "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:GSE17536"], "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:GSE17536"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:36465397", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fonc.2022.1009698", "sha256": "sha256:366d28cd9e208379b57e4fb8d862e30e4a8857cd59840e8556ecb43cd72c6087", "bytes": 40171, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fonc.2022.1009698", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC9714635", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE17536", "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=GSE17536", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE17536", "version": null, "note": "The original contributions presented in the study are included in the article/ Supplementary Material . 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