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pmid:39085446

Machine learning-based screening and validation of liver metastasis-specific genes in colorectal cancer.

Shiyao Zheng · Hongxin He · Jianfeng Zheng · Xingshu Zhu · Nan Lin · Qing Wu · Enhao Wei · Caiming Weng · Shuqian Chen · Xinxiang Huang · Chenxing Jian · Shen Guan · Chunkang Yang

Scientific reports · 2024 doi:10.1038/s41598-024-68706-y

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Experiment

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Data

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Analysis

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pmid:39085446
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2026-11-01T20:29:09Z
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title
Machine learning-based screening and validation of liver metastasis-specific genes in colorectal cancer.
doi
10.1038/s41598-024-68706-y
pmid
39085446
authors array · 13 items
[0]
Shiyao Zheng
[1]
Hongxin He
[2]
Jianfeng Zheng
[3]
Xingshu Zhu
[4]
Nan Lin
[5]
Qing Wu
[6]
Enhao Wei
[7]
Caiming Weng
[8]
Shuqian Chen
[9]
Xinxiang Huang
[10]
Chenxing Jian
[11]
Shen Guan
[12]
Chunkang Yang
journal
Scientific reports
year
2024
abstract
Colorectal liver metastasis (CRLM) is challenging in the clinical treatment of colorectal cancer. Limited research has been conducted on how CRLM develops. RNA sequencing data were obtained from the Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA). Four machine learning algorithms were used to screen the hub CRLM-specific genes, including Least Absolute Shrinkage and Selection Operator (Lasso), Random forest, SVM-RFE, and XGboost. The model for identifying CRLM was developed using stepwise logistic regression and was validated using internal and independent datasets. The prognostic value of hub CRLM-specific genes was assessed using the Lasso-Cox method. The in vitro experiments were performed using SW620 cells. The CRLM identification model was developed based on four CRLM-specific genes (SPP1, ZG16, P2RY14, and PRKAR2B), and the model efficacy was validated using GSE41258 and three external cohorts. Five CRLM-specific prognostic hub genes, SPP1, ZG16, P2RY14, CYP2E1, and C5, were identified using the Lasso-Cox algorithm, and a risk score was constructed. The risk score was validated using the GSE39582 cohort. Three genes have both efficacy in identifying CRLM and prognostic value: ZG16, P2RY14, and SPP1. Immune infiltration and enrichment analyses demonstrated that SPP1 was associated with M2 macrophage polarization and extracellular matrix remodeling. In vitro experiments indicated that SPP1 may act as a cancer-promoting factor. The hub CRLM-specific gene SPP1 can help determine the diagnosis, prognosis, and immune infiltration of patients with CRLM.
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Four machine learning algorithms were used to screen the hub CRLM-specific genes, including Least Absolute Shrinkage and Selection Operator (Lasso), Random forest, SVM-RFE, and XGboost.
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Four machine learning algorithms were used to screen the hub CRLM-specific genes, including Least Absolute Shrinkage and Selection Operator (Lasso), Random forest, SVM-RFE, and XGboost.
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All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
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sections[29] "Data availability" paragraph 2
quote
All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
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The CRLM identification model was developed based on four CRLM-specific genes (SPP1, ZG16, P2RY14, and PRKAR2B), and the model efficacy was validated using GSE41258 and three external cohorts.
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sections[0] "Abstract" paragraph 1
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The CRLM identification model was developed based on four CRLM-specific genes (SPP1, ZG16, P2RY14, and PRKAR2B), and the model efficacy was validated using GSE41258 and three external cohorts.
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The CRLM identification model was developed based on four CRLM-specific genes (SPP1, ZG16, P2RY14, and PRKAR2B), and the model efficacy was validated using GSE41258 and three external cohorts.
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All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
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585
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null
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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
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All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
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All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
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sample_count
390
group_sizes
null
group_sizes_basis
null
platform
96
taxon
Homo sapiens
title
Expression data from colorectal cancer patients
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
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data:geo:GSE49355
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All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
structure object · 15 fields
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All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
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Homo sapiens
title
Specific extracellular matrix remodeling signature of colon hepatic metastases [HG-U133A]
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2026-11-01T15:39:54Z
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identifier_resolution_only_no_download_no_licence_read
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access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE68468
version
null
note
All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
access_statement_kind
data_availability_statement
sample_accessions array · 390 items
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[71]
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[76]
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[79]
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[90]
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[95]
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[99]
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[100]
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[114]
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[120]
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[121]
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[124]
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[127]
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[130]
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[131]
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[132]
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[133]
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[134]
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[135]
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[144]
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[145]
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[146]
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[147]
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[148]
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[149]
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[150]
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[152]
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[154]
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[155]
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[156]
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[157]
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[158]
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[159]
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[160]
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[161]
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[162]
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[163]
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[164]
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[165]
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[168]
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[169]
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[170]
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[172]
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[173]
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[175]
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[176]
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[178]
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[179]
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[180]
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[181]
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[182]
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[185]
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[186]
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[189]
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[190]
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[192]
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[193]
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[194]
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[195]
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[196]
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[197]
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[198]
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[199]
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[200]
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[201]
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[207]
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[208]
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[209]
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[210]
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[217]
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[223]
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[226]
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[227]
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[228]
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[229]
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[230]
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[233]
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[234]
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[236]
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[237]
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[238]
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[239]
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[240]
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[242]
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[243]
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[244]
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[245]
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[246]
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[247]
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[248]
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[249]
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[250]
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[251]
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[252]
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[253]
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[254]
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[255]
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[256]
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[257]
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[258]
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[259]
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[260]
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[261]
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[262]
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[263]
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[264]
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[265]
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[266]
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[267]
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[268]
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[269]
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[270]
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[271]
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[272]
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[273]
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[274]
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[275]
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[276]
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[277]
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[278]
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[279]
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[280]
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[281]
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[284]
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[285]
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[286]
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[287]
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[288]
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[289]
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[290]
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[291]
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[292]
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[293]
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[294]
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[295]
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[296]
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[297]
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[298]
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[299]
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[300]
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[301]
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[302]
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[303]
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[304]
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[305]
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[306]
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[307]
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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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[322]
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[323]
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[325]
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[326]
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[328]
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[329]
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[330]
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[331]
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[332]
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[333]
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[334]
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[335]
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[336]
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[337]
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[338]
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[339]
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[341]
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[342]
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[343]
GSM1673304
[344]
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[345]
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[346]
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[347]
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[348]
GSM1673309
[349]
GSM1673310
[350]
GSM1673311
[351]
GSM1673312
[352]
GSM1673313
[353]
GSM1673314
[354]
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[357]
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[358]
GSM1673319
[359]
GSM1673320
[360]
GSM1673321
[361]
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[362]
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[364]
GSM1673325
[365]
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[367]
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[368]
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[373]
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[374]
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[378]
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[380]
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[381]
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[383]
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[386]
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GSM1673348
[388]
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[389]
GSM1673350
sample_count
390
group_sizes
null
group_sizes_basis
null
platform
96
taxon
Homo sapiens
title
caArray_notte-00422: Molecular Dissection of Colon Cancer
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
[5] object · 15 fields
id
data:geo:GSE81585
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=GSE81585
sha256
null
bytes
null
access
open
state
resolved
reader
null
reader_status
reader_required
identifier
GSE81585
version
null
note
All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
access_statement_kind
data_availability_statement
sample_accessions array · 118 items
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GSM2183952
[1]
GSM2183953
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GSM2183954
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GSM2183955
[4]
GSM2183956
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GSM2183957
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GSM2183958
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GSM2183959
[8]
GSM2183960
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GSM2183961
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GSM2183962
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GSM2183963
[12]
GSM2183964
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GSM2183965
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GSM2183966
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GSM2183967
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GSM2183968
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GSM2183970
[19]
GSM2183971
[20]
GSM2183972
[21]
GSM2183973
[22]
GSM2183974
[23]
GSM2183975
[24]
GSM2183976
[25]
GSM2183977
[26]
GSM2183978
[27]
GSM2183979
[28]
GSM2183980
[29]
GSM2183981
[30]
GSM2183982
[31]
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[32]
GSM2183984
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GSM2183985
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GSM2183986
[35]
GSM2183987
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GSM2183988
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GSM2183989
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GSM2183990
[39]
GSM2183991
[40]
GSM2183992
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GSM2183993
[42]
GSM2183994
[43]
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[44]
GSM2183996
[45]
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GSM2183998
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GSM2184001
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GSM2184002
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[52]
GSM2184004
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GSM2184005
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GSM2184006
[55]
GSM2184007
[56]
GSM2184008
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GSM2184011
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GSM2184012
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GSM2184019
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GSM2184020
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GSM2184021
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GSM2184022
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[96]
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[100]
GSM2430859
[101]
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[103]
GSM2430862
[104]
GSM2430863
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[106]
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[107]
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[110]
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[111]
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[112]
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[113]
GSM2430872
[114]
GSM2430873
[115]
GSM2430874
[116]
GSM2430875
[117]
GSM2430876
sample_count
118
group_sizes
null
group_sizes_basis
null
platform
20301;11154;17303
taxon
Homo sapiens
title
Transcriptome signatures of human induced pluripotent stem cell-derived cardiomyocytes classify cardiomyocyte subtype populations
resolution_checked_at
2026-11-01T20:16:08Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 10 items
[0]
asset:data:geo:GSE39582 not downloaded
[1]
asset:data:geo:GSE39582 licence not read
[2]
asset:data:geo:GSE41258 not downloaded
[3]
asset:data:geo:GSE41258 licence not read
[4]
asset:data:geo:GSE49355 not downloaded
[5]
asset:data:geo:GSE49355 licence not read
[6]
asset:data:geo:GSE68468 not downloaded
[7]
asset:data:geo:GSE68468 licence not read
[8]
asset:data:geo:GSE81585 not downloaded
[9]
asset:data:geo:GSE81585 licence not read
analysis object · 4 fields
state
partial
methods array · 5 items
[0] object · 10 fields
id
method-1
family
machine_learning
specific
random_forest
label
Machine learning
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
machine_learning_random_forest
expressible
false
parameters object · 0 fields
data_shapes array · 1 item
[0]
labelled_feature_matrix
evidence object · 3 fields
score
1
band
verbatim
quote
Four machine learning algorithms were used to screen the hub CRLM-specific genes, including Least Absolute Shrinkage and Selection Operator (Lasso), Random forest, SVM-RFE, and XGboost.
[1] object · 10 fields
id
method-2
family
group_comparison
specific
wilcoxon
label
Group comparison
dsl_operations array · 0 items
missing_operations array · 1 item
[0]
group_comparison_wilcoxon
expressible
false
parameters object · 0 fields
data_shapes array · 1 item
[0]
two_or_more_groups_continuous
evidence object · 3 fields
score
0.8
band
high
quote
Wilcoxon
[2] object · 10 fields
id
method-3
family
machine_learning
specific
support_vector_machine
label
Machine learning
dsl_operations array · 3 items
[0]
train_classifier
[1]
cross_validate
[2]
roc_auc
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
labelled_feature_matrix
evidence object · 3 fields
score
0.7
band
medium
quote
SVM
[3] object · 10 fields
id
method-4
family
machine_learning
specific
gradient_boosting
label
Machine learning
dsl_operations array · 3 items
[0]
train_classifier
[1]
cross_validate
[2]
roc_auc
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
labelled_feature_matrix
evidence object · 3 fields
score
0.7
band
medium
quote
XGboost
[4] object · 10 fields
id
method-5
family
regression_modelling
specific
logistic
label
Regression modelling
dsl_operations array · 1 item
[0]
glm_logit_fit
missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 1 item
[0]
predictors_and_outcome
evidence object · 3 fields
score
0.7
band
medium
quote
logistic regression
targets array · 0 items
gaps array · 2 items
[0]
method.reader_differs_from_extractor
[1]
method.machine_learning_random_forest
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
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machine_learning_random_forest
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: random_forest.
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R1
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capability:computational_analysis
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basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
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GSE41258
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GSE49355
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GSE68468
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GSE81585
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GSE39582
resolved_accessions array · 5 items
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GSE41258
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GSE49355
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GSE68468
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GSE81585
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GSE39582
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[0]
All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. GEO database under accession number GSE41258, GSE49355, GSE68468, and GSE81585.
basis
The paper names GSE41258, GSE49355, GSE68468, GSE81585, GSE39582 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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data:geo:GSE39582
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machine_learning_random_forest
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review object · 5 fields
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MiniMax-M3.1-Flash
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minimax
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2026-11-01T19:25:59Z
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pmid:39085446
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PMID 39085446 full text
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data:geo:GSE39582
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dataset
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GEO GSE39582
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classification
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pmid:39085446
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PMID 39085446 full text
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data:geo:GSE39582
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GEO GSE39582
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agent:corpus-assay-engine
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agent:minimax-reader
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lineage object · 4 fields
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[9]
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step:run_analysis blocked on method:machine_learning_random_forest
assays array · 7 items
[0] object · 11 fields
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data_generation
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rna_seq
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99e1195c7d6f
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99e1195c7d6f
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evidence array · 1 item
[0]
rch has been conducted on how CRLM develops. RNA sequencing data were obtained from the Gene Expression
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paper_text_order:216
id
assay:1
[1] object · 11 fields
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data_generation
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transfection
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99e1195c7d6f
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[0]
iler’ R package16,22. Cell culture and siRNA transfection The human colon cancer cell line SW620, prov
[1]
ls were maintained at 37 °C in a 5% CO2. For knockdown studies of SPP1, siRNA and GP-transfect-mate
[2]
anghai, China). The siRNA sequences used for knockdown are detailed in Supplementary Table 1. Quant
[3]
me PCR (qRT-PCR) was performed to detect the knockdown efficiency using SYBR Green Supermix (TIANGE
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paper_text_order:2329
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assay:2
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data_generation
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99e1195c7d6f
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hejiang Meisen Cell Technology Co., LTD, was cultured in DMEM with 10% FBS (Cegrogen) and 1% penicill
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paper_text_order:2440
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assay:3
[3] object · 11 fields
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ailed in Supplementary Table 1. Quantitative real-time PCR (qRT-PCR) was performed to detect the knockd
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paper_text_order:2773
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assay:4
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data_generation
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99e1195c7d6f
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0.99
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vidence that SPP1 knockdown led to increased apoptosis. Cytologic experimental validation of hub co
[1]
and colony formation assay (F). The cellular apoptosis assay of SW620 cells treated with si-NC and
[2]
of the EdU (Fig. 7D, Supplementary Fig. 2), CCK-8 (Fig. 7E), and colony formation assays (Fig.
[3]
ted with si-NC and si-SPP1 by EdU assay (D), CCK-8 assay (E) and colony formation assay (F). Th
order_basis
paper_text_order:4476
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assay:5
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99e1195c7d6f
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99e1195c7d6f
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0.99
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omoted the proliferation of SW620 cells. The flow cytometry results (Fig. 7G) provided evidence that SPP
[1]
W620 cells treated with si-NC and si-SPP1 by flow cytometry (G). Supplementary Materials Supplementary L
order_basis
paper_text_order:4615
id
assay:6
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f2132e96ae6c7a4e
evidence array · 1 item
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Four machine learning algorithms were used to screen the hub CRLM-specific genes, including Least Absolute Shrinkage and Selection Operator (Lasso), Random forest, SVM-RFE, and XGboost.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39085446", "kind": "science-record", "revision": 4, "content_hash": "sha256:3b4d99a19e73f10625695363ca1b35c85eb4f1044859a8faad098e18c6121d17", "created_at": "2026-11-01T20:29:09Z", "updated_at": "2026-11-01T22:54:48Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Machine learning-based screening and validation of liver metastasis-specific genes in colorectal cancer.", "doi": "10.1038/s41598-024-68706-y", "pmid": "39085446", "authors": ["Shiyao Zheng", "Hongxin He", "Jianfeng Zheng", "Xingshu Zhu", "Nan Lin", "Qing Wu", "Enhao Wei", "Caiming Weng", "Shuqian Chen", "Xinxiang Huang", "Chenxing Jian", "Shen Guan", "Chunkang Yang"], "journal": "Scientific reports", "year": 2024, "abstract": "Colorectal liver metastasis (CRLM) is challenging in the clinical treatment of colorectal cancer. Limited research has been conducted on how CRLM develops. RNA sequencing data were obtained from the Gene Expression Omnibus (GEO) and The Cancer Genome Atlas (TCGA). Four machine learning algorithms were used to screen the hub CRLM-specific genes, including Least Absolute Shrinkage and Selection Operator (Lasso), Random forest, SVM-RFE, and XGboost. The model for identifying CRLM was developed using stepwise logistic regression and was validated using internal and independent datasets. The prognostic value of hub CRLM-specific genes was assessed using the Lasso-Cox method. The in vitro experiments were performed using SW620 cells. The CRLM identification model was developed based on four CRLM-specific genes (SPP1, ZG16, P2RY14, and PRKAR2B), and the model efficacy was validated using GSE41258 and three external cohorts. Five CRLM-specific prognostic hub genes, SPP1, ZG16, P2RY14, CYP2E1, and C5, were identified using the Lasso-Cox algorithm, and a risk score was constructed. The risk score was validated using the GSE39582 cohort. Three genes have both efficacy in identifying CRLM and prognostic value: ZG16, P2RY14, and SPP1. Immune infiltration and enrichment analyses demonstrated that SPP1 was associated with M2 macrophage polarization and extracellular matrix remodeling. In vitro experiments indicated that SPP1 may act as a cancer-promoting factor. The hub CRLM-specific gene SPP1 can help determine the diagnosis, prognosis, and immune infiltration of patients with CRLM.", "claims": [{"id": "claim-method", "statement": "Four machine learning algorithms were used to screen the hub CRLM-specific genes, including Least Absolute Shrinkage and Selection Operator (Lasso), Random forest, SVM-RFE, and XGboost.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39085446", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "Four machine learning algorithms were used to screen the hub CRLM-specific genes, including Least Absolute Shrinkage and Selection Operator (Lasso), Random forest, SVM-RFE, and XGboost."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All data presented in this paper are openly available in the TCGA (https://portal.gdc.cancer.gov) and GEO (https://www.ncbi.nlm.nih.gov/geo/) databases. 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