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pmid:34185683

Identification and validation of a robust autophagy-related molecular model for predicting the prognosis of breast cancer patients.

Jian-Ying Ma · Qin Liu · Gang Liu · Shasha Peng · Gaosong Wu

Aging · 2021 doi:10.18632/aging.203187

Paper

complete

Experiment

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Data

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Analysis

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Identification and validation of a robust autophagy-related molecular model for predicting the prognosis of breast cancer patients.
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10.18632/aging.203187
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34185683
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Jian-Ying Ma
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Qin Liu
[2]
Gang Liu
[3]
Shasha Peng
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Gaosong Wu
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Aging
year
2021
abstract
Despite a relatively low mortality rate, high recurrence rates represent a significant problem for breast cancer (BC) patients. Autophagy affects the development, progression, and prognosis of various cancers, including BC. The aim of the present study was to identify candidate autophagy-related genes (ARGs) and construct a molecular-clinicopathological signature to predict recurrence risk in BC. A 10-ARG-based signature was established in a training cohort (GEO-BC dataset GSE25066) with LASSO Cox regression and assessed in an independent validation cohort (GEO-BC GSE22219). Significant differences in recurrence-free survival were observed for high- and low-risk patients segregated based on their signature-based risk score. Time-dependent receiver operating characteristic (tdROC) analysis of signature performance demonstrated satisfactory accuracy and predictive power in both the training and validation cohorts. Moreover, we developed a nomogram to predict 3- and 5-year recurrence-free survival by combining the autophagy-related risk score and clinicopathological data. Both the tdROC and calibration curves indicated high discriminating ability for the nomogram. This study indicates that our ARG-based signature is an independent prognostic classifier for recurrence-free survival in BC. In addition, individualized survival risk assessment and treatment decisions might be effectively improved by implementing the proposed nomogram.
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Then, we performed LASSO Cox regression analysis and identified, among those, 10 recurrence-related genes (ATF4, BAK1, BCL2, BIRC5, CCL2, DDIT3, HIF1A, PRKAB1, RPS6KB1, and TM9SF1).
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sections[3] "Development and validation of an autophagy-related prognostic gene signature for breast cancer" paragraph 5
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Then, we performed LASSO Cox regression analysis and identified, among those, 10 recurrence-related genes (ATF4, BAK1, BCL2, BIRC5, CCL2, DDIT3, HIF1A, PRKAB1, RPS6KB1, and TM9SF1).
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The GSE25066 and GSE22219 datasets analyzed in the current study are available from the GEO database (https://www.ncbi.nlm.nih.gov/geo/). Additional information about results of this work is available from the corresponding author upon reasonable request.
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sections[14] "Availability of data and material" paragraph 2
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The GSE25066 and GSE22219 datasets analyzed in the current study are available from the GEO database (https://www.ncbi.nlm.nih.gov/geo/). Additional information about results of this work is available from the corresponding author upon reasonable request.
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title
Genomic predictor of response and survival following neoadjuvant taxane-anthracycline chemotherapy in breast cancer
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2026-11-01T15:39:54Z
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Baseline characteristics of study patients.
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Development and validation of an autophagy-related prognostic gene signature for breast cancer
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Table 1
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Baseline characteristics of study patients.
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[2]
Validation cohort
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[0]
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[2]
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[2]
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The AUC of ROC curve show the sensitivity and specificity of the known signatures in predicting the prognosis of BC patients.
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4
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Comparison with other prognostic signatures
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Table 2
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The AUC of ROC curve show the sensitivity and specificity of the known signatures in predicting the prognosis of BC patients.
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[0] array · 4 items
[0]
Author
[1]
Year
[2]
Gene signature
[3]
AUC for RFS
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[0]
Tang et al.
[1]
2019
[2]
13-miRNA signature
[3]
0.676 (5-year)
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[0]
Chen et al.
[1]
2020
[2]
9-TF signature
[3]
0.794 (1-year), 0.822 (3-year), 0.843 (5-year)
[3] array · 4 items
[0]
Zhang et al.
[1]
2020
[2]
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0.741 (1-year), 0.752 (3-year), 0.781 (5-year)
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[0]
Feng et al.
[1]
2021
[2]
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0.769 (3-year)
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[0]
Zhou et al.
[1]
2016
[2]
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0.847 (5-year)
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[0]
Lai et al.
[1]
2019
[2]
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0.710 (5-year)
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section[4]/table-wrap[1]#t2
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Then, we performed LASSO Cox regression analysis and identified, among those, 10 recurrence-related genes (ATF4, BAK1, BCL2, BIRC5, CCL2, DDIT3, HIF1A, PRKAB1, RPS6KB1, and TM9SF1).
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
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The GSE25066 and GSE22219 datasets analyzed in the current study are available from the GEO database (https://www.ncbi.nlm.nih.gov/geo/). Additional information about results of this work is available from the corresponding author upon reasonable request.
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The paper names GSE25066, GSE22219 in GEO database and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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Then, we performed LASSO Cox regression analysis and identified, among those, 10 recurrence-related genes (ATF4, BAK1, BCL2, BIRC5, CCL2, DDIT3, HIF1A, PRKAB1, RPS6KB1, and TM9SF1).
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34185683", "kind": "science-record", "revision": 6, "content_hash": "sha256:f64ee5cf9a6ab755f1a3e2f8db99dd64a4ab0990de0cf5cd80e1b0a0374368fc", "created_at": "2026-11-01T15:41:40Z", "updated_at": "2026-11-01T21:25:37Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification and validation of a robust autophagy-related molecular model for predicting the prognosis of breast cancer patients.", "doi": "10.18632/aging.203187", "pmid": "34185683", "authors": ["Jian-Ying Ma", "Qin Liu", "Gang Liu", "Shasha Peng", "Gaosong Wu"], "journal": "Aging", "year": 2021, "abstract": "Despite a relatively low mortality rate, high recurrence rates represent a significant problem for breast cancer (BC) patients. Autophagy affects the development, progression, and prognosis of various cancers, including BC. The aim of the present study was to identify candidate autophagy-related genes (ARGs) and construct a molecular-clinicopathological signature to predict recurrence risk in BC. A 10-ARG-based signature was established in a training cohort (GEO-BC dataset GSE25066) with LASSO Cox regression and assessed in an independent validation cohort (GEO-BC GSE22219). Significant differences in recurrence-free survival were observed for high- and low-risk patients segregated based on their signature-based risk score. Time-dependent receiver operating characteristic (tdROC) analysis of signature performance demonstrated satisfactory accuracy and predictive power in both the training and validation cohorts. Moreover, we developed a nomogram to predict 3- and 5-year recurrence-free survival by combining the autophagy-related risk score and clinicopathological data. Both the tdROC and calibration curves indicated high discriminating ability for the nomogram. This study indicates that our ARG-based signature is an independent prognostic classifier for recurrence-free survival in BC. In addition, individualized survival risk assessment and treatment decisions might be effectively improved by implementing the proposed nomogram.", "claims": [{"id": "claim-method", "statement": "Then, we performed LASSO Cox regression analysis and identified, among those, 10 recurrence-related genes (ATF4, BAK1, BCL2, BIRC5, CCL2, DDIT3, HIF1A, PRKAB1, RPS6KB1, and TM9SF1).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:34185683", "locator": "sections[3] \"Development and validation of an autophagy-related prognostic gene signature for breast cancer\" paragraph 5", "quote": "Then, we performed LASSO Cox regression analysis and identified, among those, 10 recurrence-related genes (ATF4, BAK1, BCL2, BIRC5, CCL2, DDIT3, HIF1A, PRKAB1, RPS6KB1, and TM9SF1)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The GSE25066 and GSE22219 datasets analyzed in the current study are available from the GEO database (https://www.ncbi.nlm.nih.gov/geo/). 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Additional information about results of this work is available from the corresponding author upon reasonable request."}], "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:34185683"], "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:GSE22219"], "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:GSE22219"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:34185683", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.18632/aging.203187", "sha256": "sha256:1ae830a49d3e6e823b4295fd61e646a804d0efc3f4e7eb0f6da44900c3536fc4", "bytes": 29667, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.18632/aging.203187", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC8266368", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE22219", "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=GSE22219", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE22219", "version": null, "note": "The GSE25066 and GSE22219 datasets analyzed in the current study are available from the GEO database (https://www.ncbi.nlm.nih.gov/geo/). 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