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pmid:33194424

Prognostic model of invasive ductal carcinoma of the breast based on differentially expressed glycolysis-related genes.

Xiaoping Li · Qihe Yu · Jishang Chen · Hui Huang · Zhuangsheng Liu · Chengxing Wang · Yaoming He · Xin Zhang · Weiwen Li · Chao Li · Jinglin Zhao · Wansheng Long

PeerJ · 2020 doi:10.7717/peerj.10249

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title
Prognostic model of invasive ductal carcinoma of the breast based on differentially expressed glycolysis-related genes.
doi
10.7717/peerj.10249
pmid
33194424
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[0]
Xiaoping Li
[1]
Qihe Yu
[2]
Jishang Chen
[3]
Hui Huang
[4]
Zhuangsheng Liu
[5]
Chengxing Wang
[6]
Yaoming He
[7]
Xin Zhang
[8]
Weiwen Li
[9]
Chao Li
[10]
Jinglin Zhao
[11]
Wansheng Long
journal
PeerJ
year
2020
abstract
BACKGROUND: Invasive ductal carcinoma (IDC) is a common pathological type of breast cancer that is characterized by high malignancy and rapid progression. Upregulation of glycolysis is a hallmark of tumor growth, and correlates with the progression of breast cancer. We aimed to establish a model to predict the prognosis of patients with breast IDC based on differentially expressed glycolysis-related genes (DEGRGs). METHODS: Transcriptome data and clinical data of patients with breast IDC were from The Cancer Genome Atlas (TCGA). Glycolysis-related gene sets and pathways were from the Molecular Signatures Database (MSigDB). DEGRGs were identified by comparison of tumor tissues and adjacent normal tissues. Univariate Cox regression and least absolute shrinkage and selection operator (LASSO) regression were used to screen for DEGRGs with prognostic value. A risk-scoring model based on DEGRGs related to prognosis was constructed. Receiver operating characteristic (ROC) analysis and calculation of the area under the curve (AUC) were used to evaluate the performance of the model. The model was verified in different clinical subgroups using an external dataset (GSE131769). A nomogram that included clinical indicators and risk scores was established. Gene function enrichment analysis was performed, and a protein-protein interaction network was developed. RESULTS: We analyzed data from 772 tumors and 88 adjacent normal tissues from the TCGA database and identified 286 glycolysis-related genes from the MSigDB. There were 185 DEGRGs. Univariate Cox regression and LASSO regression indicated that 13 of these genes were related to prognosis. A risk-scoring model based on these 13 DEGRGs allowed classification of patients as high-risk or low-risk according to median score. The duration of overall survival (OS) was longer in the low-risk group (P < 0.001), and the AUC was 0.755 for 3-year OS and 0.726 for 5-year OS. The results were similar when using the GEO data set for external validation (AUC for 3-year OS: 0.731, AUC for 5-year OS: 0.728). Subgroup analysis showed there were significant differences in OS among high-risk and low-risk patients in different subgroups (T1-2, T3-4, N0, N1-3, M0, TNBC, non-TNBC; all P < 0.01). The C-index was 0.824, and the AUC was 0.842 for 3-year OS and 0.808 for 5-year OS from the nomogram. Functional enrichment analysis demonstrated the DEGRGs were mainly involved in regulating biological functions. CONCLUSIONS: Our prognostic model, based on 13 DEGRGs, had excellent performance in predicting the survival of patients with IDC of the breast. These DEGRGs appear to have important biological functions in the progression of this cancer.
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Univariate Cox regression and least absolute shrinkage and selection operator (LASSO) regression were used to screen for DEGRGs with prognostic value.
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The RNA-seq transcriptome data and corresponding clinicopathological information of the data are available at the TCGA project: TCGA-BRCA.The raw measurements are available in the Supplemental Tables.
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The RNA-seq transcriptome data and corresponding clinicopathological information of the data are available at the TCGA project: TCGA-BRCA.The raw measurements are available in the Supplemental Tables.
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accession_resolution
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data:geo:GSE131769
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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review.machine_critique
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Univariate Cox regression and least absolute shrinkage and selection operator (LASSO) regression were used to screen for DEGRGs with prognostic value.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33194424", "kind": "science-record", "revision": 7, "content_hash": "sha256:aa2a8a1952960df8b5a93ac9297d51d738b403306dd7abb052a4360c85d83b12", "created_at": "2026-11-01T15:41:16Z", "updated_at": "2026-11-01T22:02:32Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Prognostic model of invasive ductal carcinoma of the breast based on differentially expressed glycolysis-related genes.", "doi": "10.7717/peerj.10249", "pmid": "33194424", "authors": ["Xiaoping Li", "Qihe Yu", "Jishang Chen", "Hui Huang", "Zhuangsheng Liu", "Chengxing Wang", "Yaoming He", "Xin Zhang", "Weiwen Li", "Chao Li", "Jinglin Zhao", "Wansheng Long"], "journal": "PeerJ", "year": 2020, "abstract": "BACKGROUND: Invasive ductal carcinoma (IDC) is a common pathological type of breast cancer that is characterized by high malignancy and rapid progression. Upregulation of glycolysis is a hallmark of tumor growth, and correlates with the progression of breast cancer. We aimed to establish a model to predict the prognosis of patients with breast IDC based on differentially expressed glycolysis-related genes (DEGRGs).\nMETHODS: Transcriptome data and clinical data of patients with breast IDC were from The Cancer Genome Atlas (TCGA). Glycolysis-related gene sets and pathways were from the Molecular Signatures Database (MSigDB). DEGRGs were identified by comparison of tumor tissues and adjacent normal tissues. Univariate Cox regression and least absolute shrinkage and selection operator (LASSO) regression were used to screen for DEGRGs with prognostic value. A risk-scoring model based on DEGRGs related to prognosis was constructed. Receiver operating characteristic (ROC) analysis and calculation of the area under the curve (AUC) were used to evaluate the performance of the model. The model was verified in different clinical subgroups using an external dataset (GSE131769). A nomogram that included clinical indicators and risk scores was established. Gene function enrichment analysis was performed, and a protein-protein interaction network was developed.\nRESULTS: We analyzed data from 772 tumors and 88 adjacent normal tissues from the TCGA database and identified 286 glycolysis-related genes from the MSigDB. There were 185 DEGRGs. Univariate Cox regression and LASSO regression indicated that 13 of these genes were related to prognosis. A risk-scoring model based on these 13 DEGRGs allowed classification of patients as high-risk or low-risk according to median score. The duration of overall survival (OS) was longer in the low-risk group (P < 0.001), and the AUC was 0.755 for 3-year OS and 0.726 for 5-year OS. The results were similar when using the GEO data set for external validation (AUC for 3-year OS: 0.731, AUC for 5-year OS: 0.728). Subgroup analysis showed there were significant differences in OS among high-risk and low-risk patients in different subgroups (T1-2, T3-4, N0, N1-3, M0, TNBC, non-TNBC; all P < 0.01). The C-index was 0.824, and the AUC was 0.842 for 3-year OS and 0.808 for 5-year OS from the nomogram. Functional enrichment analysis demonstrated the DEGRGs were mainly involved in regulating biological functions.\nCONCLUSIONS: Our prognostic model, based on 13 DEGRGs, had excellent performance in predicting the survival of patients with IDC of the breast. These DEGRGs appear to have important biological functions in the progression of this cancer.", "claims": [{"id": "claim-method", "statement": "Univariate Cox regression and least absolute shrinkage and selection operator (LASSO) regression were used to screen for DEGRGs with prognostic value.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33194424", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "Univariate Cox regression and least absolute shrinkage and selection operator (LASSO) regression were used to screen for DEGRGs with prognostic value."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The RNA-seq transcriptome data and corresponding clinicopathological information of the data are available at the TCGA project: TCGA-BRCA.The raw measurements are available in the Supplemental Tables.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33194424", "locator": "sections[19] \"Additional Information and Declarations\" paragraph 4", "quote": "The RNA-seq transcriptome data and corresponding clinicopathological information of the data are available at the TCGA project: TCGA-BRCA.The raw measurements are available in the Supplemental Tables."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:33194424"], "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:GSE131769"], "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:GSE131769"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:33194424", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.7717/peerj.10249", "sha256": 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