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pmid:25288503

A four-long non-coding RNA signature in predicting breast cancer survival.

Jin Meng · Ping Li · Qing Zhang · Zhangru Yang · Shen Fu

Journal of experimental & clinical cancer research : CR · 2014 doi:10.1186/s13046-014-0084-7

Paper

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Experiment

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Data

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title
A four-long non-coding RNA signature in predicting breast cancer survival.
doi
10.1186/s13046-014-0084-7
pmid
25288503
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Jin Meng
[1]
Ping Li
[2]
Qing Zhang
[3]
Zhangru Yang
[4]
Shen Fu
journal
Journal of experimental & clinical cancer research : CR
year
2014
abstract
BACKGROUND: Many long non-coding RNAs(lncRNAs) have been found to be a good marker for several tumors. Using lncRNA-mining approach, we aimed to identify lncRNA expression signature that can predict breast cancer patient survival. METHODS: We performed LncRNA expression profiling in 887 breast cancer patients from Gene Expression Omnibus (GEO) datasets. The association between lncRNA signature and clinical survival was analyzed using the training set(n = 327, from GSE 20685). The validation for the association was performed in another three independent testing sets(252 from GSE21653, 204 from GSE12276, and 104 from GSE42568). RESULTS: A set of four lncRNA genes (U79277, AK024118, BC040204, AK000974) have been identified by the random survival forest algorithm. Using a risk score based on the expression signature of these lncRNAs, we separated the patients into low-risk and high-risk groups with significantly different survival times in the training set. This signature was validated in the other three cohorts. Further study revealed that the four-lncRNA expression signature was independent of age and subtype. Gene Set Enrichment Analysis (GSEA) suggested that gene sets were involved in several cancer metastasis related pathways. CONCLUSIONS: These findings indicate that lncRNAs may be implicated in breast cancer pathogenesis. The four-lncRNA signature may have clinical implications in the selection of high-risk patients for adjuvant therapy.
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Considering that a smaller number of genes in the model would make the model more practical, we then performed the random survival forests-variable hunting (RSFVH) algorithm [39].
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Considering that a smaller number of genes in the model would make the model more practical, we then performed the random survival forests-variable hunting (RSFVH) algorithm [39].
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Breast cancer gene expression data and corresponding clinical data used in this study were obtained from the publicly available GEO databases. We followed the strategy of using the largest data set (GSE20685) as training set. After filtering out samples without clinical survival information, there were a total of 887 samples, including 327 from GSE20685, 252 from GSE21653, 204 from GSE12276, and 104 from GSE42568, respectively.
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Breast cancer gene expression data and corresponding clinical data used in this study were obtained from the publicly available GEO databases.
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We followed the strategy of using the largest data set (GSE20685) as training set.
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sections[3] "GEO breast cancer gene expression data" paragraph 2
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After filtering out samples without clinical survival information, there were a total of 887 samples, including 327 from GSE20685, 252 from GSE21653, 204 from GSE12276, and 104 from GSE42568, respectively.
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Using breast-cancer microarray data obtained from GEO and re-annotated for lncRNA expression, the study applied univariable Cox regression and random survival forests to identify and validate a four-lncRNA survival signature (U79277, AK024118, BC040204, and AK000974).
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sample_count
327
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null
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570
taxon
Homo sapiens
title
Microarray-based molecular subtyping of breast cancer
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
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data:geo:GSE21653
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Breast cancer gene expression data and corresponding clinical data used in this study were obtained from the publicly available GEO databases. We followed the strategy of using the largest data set (GSE20685) as training set. After filtering out samples without clinical survival information, there were a total of 887 samples, including 327 from GSE20685, 252 from GSE21653, 204 from GSE12276, and 104 from GSE42568, respectively.
structure object · 15 fields
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GEO accession URL
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Breast cancer gene expression data and corresponding clinical data used in this study were obtained from the publicly available GEO databases. We followed the strategy of using the largest data set (GSE20685) as training set. After filtering out samples without clinical survival information, there were a total of 887 samples, including 327 from GSE20685, 252 from GSE21653, 204 from GSE12276, and 104 from GSE42568, respectively.
access_statement_kind
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GSM540373
sample_count
266
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
A gene expression signature identifies two prognostic subgroups of basal breast cancer
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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[4] object · 15 fields
id
data:geo:GSE42568
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geo-series
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application/vnd.ncbi.geo-series+json
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE42568
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GSE42568
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Breast cancer gene expression data and corresponding clinical data used in this study were obtained from the publicly available GEO databases. We followed the strategy of using the largest data set (GSE20685) as training set. After filtering out samples without clinical survival information, there were a total of 887 samples, including 327 from GSE20685, 252 from GSE21653, 204 from GSE12276, and 104 from GSE42568, respectively.
structure object · 15 fields
repository
GEO
access_route
GEO accession URL
access_statement_verbatim
Breast cancer gene expression data and corresponding clinical data used in this study were obtained from the publicly available GEO databases. We followed the strategy of using the largest data set (GSE20685) as training set. After filtering out samples without clinical survival information, there were a total of 887 samples, including 327 from GSE20685, 252 from GSE21653, 204 from GSE12276, and 104 from GSE42568, respectively.
access_statement_kind
repository_route_statement
sample_accessions array · 121 items
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[44]
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[49]
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[119]
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[120]
GSM1045311
sample_count
121
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Breast Cancer Gene Expression Analysis
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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[5] object · 16 fields
id
asset:table:pmid:25288503:1
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table
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jats-table
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application/vnd.jats.table+json
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null
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sha256:b706d690919da1bfb51474e989622b0d8d9b0f2dbc45e3730d2280961f6e49dd
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read_table
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section[8]/table-wrap[1]#Tab1
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Four LncRNAs significantly associated with the overall survival in the training-set patients (n = 327)
structure object · 5 fields
pmcid
PMC4198622
section_index
8
section_title
Identification of lncRNA genes from the training set
row_count
5
column_count
7
table object · 8 fields
label
Table 1
caption
Four LncRNAs significantly associated with the overall survival in the training-set patients (n = 327)
rows array · 5 items
[0] array · 7 items
[0]
Gene symbol
[1]
Chromosomal position
[2]
Parametric P value
[3]
Hazard ratio
[4]
Coefficient
[5]
Variable importance
[6]
Relative importance
[1] array · 7 items
[0]
AK024118
[1]
chr18:59125236-59125296
[2]
7.00E-07
[3]
0.579
[4]
−0.35717
[5]
0.0369
[6]
1.0000
[2] array · 7 items
[0]
BC040204
[1]
chr6:72153349-72153409
[2]
1.93E-05
[3]
0.428
[4]
−0.48664
[5]
0.0198
[6]
0.5368
[3] array · 7 items
[0]
AK000974
[1]
chr10:97810995-97811055
[2]
2.85E-05
[3]
0.416
[4]
−0.48122
[5]
0.0173
[6]
0.4683
[4] array · 7 items
[0]
U79277
[1]
chr8:101998264-101998324
[2]
4.30E-06
[3]
2.17
[4]
0.518242
[5]
0.0200
[6]
0.5411
locator
section[8]/table-wrap[1]#Tab1
[6] object · 16 fields
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asset:table:pmid:25288503:2
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table
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jats-table
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application/vnd.jats.table+json
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null
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sha256:07b6e57b39e8c7396c3cc8bc5c0df13abaf9f67226de668a143566ebd3a5c8fb
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read_table
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section[11]/table-wrap[1]#Tab2
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null
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Univariable and multivariable Cox regression analyses in each data set
structure object · 5 fields
pmcid
PMC4198622
section_index
11
section_title
Multivariate regression analysis shows that the four-lncRNA expression signature is independent of age and subtype
row_count
14
column_count
7
table object · 8 fields
label
Table 2
caption
Univariable and multivariable Cox regression analyses in each data set
rows array · 14 items
[0] array · 3 items
[0]
Variables
[1]
Univariable model
[2]
Multivariable model
[1] array · 6 items
[0]
HR
[1]
95% CI of HR
[2]
p value
[3]
HR
[4]
95% CI of HR
[5]
p value
[2] array · 2 items
[0]
Training set (GSE 20685) (N = 327)
[1]
[3] array · 7 items
[0]
Four-lncRNA risk score
[1]
3.89
[2]
2.33-6.51
[3]
2.10E-8
[4]
3.88
[5]
2.32-6.48
[6]
2.30E-7
[4] array · 7 items
[0]
Age
[1]
0.99
[2]
0.97-1.01
[3]
0.49
[4]
0.99
[5]
0.97-1.02
[6]
0.62
[5] array · 2 items
[0]
Testing set (GSE 21653) (N = 252)
[1]
[6] array · 7 items
[0]
Four-lncRNA risk score
[1]
2.12
[2]
1.35-3.34
[3]
0.001
[4]
2.28
[5]
1.44-3.63
[6]
4.84E-4
[7] array · 7 items
[0]
Age
[1]
1.00
[2]
0.98-1.02
[3]
0.95
[4]
1.00
[5]
0.98-1.02
[6]
0.88
[8] array · 7 items
[0]
Subtype
[1]
1.04
[2]
0.88-1.23
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0.64
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[2]
1.30-4.27
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2.34
[5]
1.29-4.24
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1.00
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0.97-1.02
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0.78
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section[11]/table-wrap[1]#Tab2
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[4]
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[5]
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[6]
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[7]
asset:data:geo:GSE42568 licence not read
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time_to_event_with_censoring
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specific
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random survival forests-variable hunting (RSFVH) algorithm
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missing_operations array · 0 items
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1
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Considering that a smaller number of genes in the model would make the model more practical, we then performed the random survival forests-variable hunting (RSFVH) algorithm [39].
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gaps array · 1 item
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candidate
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GSE20685
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Breast cancer gene expression data and corresponding clinical data used in this study were obtained from the publicly available GEO databases. We followed the strategy of using the largest data set (GSE20685) as training set. After filtering out samples without clinical survival information, there were a total of 887 samples, including 327 from GSE20685, 252 from GSE21653, 204 from GSE12276, and 104 from GSE42568, respectively.
basis
The paper names GSE20685, GSE21653, GSE12276, GSE42568 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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MiniMax-M3.1-Flash
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minimax
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minimax
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GEO GSE12276
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Materials and methods Microarray data processing and LncRNA profile mining Th
[1]
A customized R scripts was used to perform a microarray expression calculation according to the re-m
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paper_text_order:1540
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o a database for non-coding RNA of human and mouse (derived from RNAdb [34]). A customized R sc
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:25288503", "kind": "science-record", "revision": 7, "content_hash": "sha256:80bd84dc0a42ff01f1d205aae89130d5199ed52c1eed241a5bafac3654c00486", "created_at": "2026-11-01T15:40:06Z", "updated_at": "2026-11-01T21:19:52Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A four-long non-coding RNA signature in predicting breast cancer survival.", "doi": "10.1186/s13046-014-0084-7", "pmid": "25288503", "authors": ["Jin Meng", "Ping Li", "Qing Zhang", "Zhangru Yang", "Shen Fu"], "journal": "Journal of experimental & clinical cancer research : CR", "year": 2014, "abstract": "BACKGROUND: Many long non-coding RNAs(lncRNAs) have been found to be a good marker for several tumors. Using lncRNA-mining approach, we aimed to identify lncRNA expression signature that can predict breast cancer patient survival.\nMETHODS: We performed LncRNA expression profiling in 887 breast cancer patients from Gene Expression Omnibus (GEO) datasets. The association between lncRNA signature and clinical survival was analyzed using the training set(n = 327, from GSE 20685). The validation for the association was performed in another three independent testing sets(252 from GSE21653, 204 from GSE12276, and 104 from GSE42568).\nRESULTS: A set of four lncRNA genes (U79277, AK024118, BC040204, AK000974) have been identified by the random survival forest algorithm. Using a risk score based on the expression signature of these lncRNAs, we separated the patients into low-risk and high-risk groups with significantly different survival times in the training set. This signature was validated in the other three cohorts. Further study revealed that the four-lncRNA expression signature was independent of age and subtype. Gene Set Enrichment Analysis (GSEA) suggested that gene sets were involved in several cancer metastasis related pathways.\nCONCLUSIONS: These findings indicate that lncRNAs may be implicated in breast cancer pathogenesis. The four-lncRNA signature may have clinical implications in the selection of high-risk patients for adjuvant therapy.", "claims": [{"id": "claim-method", "statement": "Considering that a smaller number of genes in the model would make the model more practical, we then performed the random survival forests-variable hunting (RSFVH) algorithm [39].", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:25288503", "locator": "sections[6] \"Statistical analysis\" paragraph 2", "quote": "Considering that a smaller number of genes in the model would make the model more practical, we then performed the random survival forests-variable hunting (RSFVH) algorithm [39]."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Breast cancer gene expression data and corresponding clinical data used in this study were obtained from the publicly available GEO databases. We followed the strategy of using the largest data set (GSE20685) as training set. 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121, "group_sizes": null, "group_sizes_basis": null, "platform": "570", "taxon": "Homo sapiens", "title": "Breast Cancer Gene Expression Analysis", "resolution_checked_at": "2026-11-01T15:39:54Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}, {"id": "asset:table:pmid:25288503:1", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:b706d690919da1bfb51474e989622b0d8d9b0f2dbc45e3730d2280961f6e49dd", "bytes": 735, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[8]/table-wrap[1]#Tab1", "version": null, "note": "Four LncRNAs significantly associated with the overall survival in the training-set patients (n = 327)", "structure": {"pmcid": "PMC4198622", "section_index": 8, "section_title": "Identification of lncRNA genes from the training set", "row_count": 5, "column_count": 7}, "table": {"label": "Table 1", "caption": "Four LncRNAs significantly associated with the overall survival in the training-set patients (n = 327)", "rows": [["Gene symbol", "Chromosomal position", "Parametric P value", "Hazard ratio", "Coefficient", "Variable importance", "Relative importance"], ["AK024118", "chr18:59125236-59125296", "7.00E-07", "0.579", "−0.35717", "0.0369", "1.0000"], ["BC040204", "chr6:72153349-72153409", "1.93E-05", "0.428", "−0.48664", "0.0198", "0.5368"], ["AK000974", "chr10:97810995-97811055", "2.85E-05", "0.416", "−0.48122", "0.0173", "0.4683"], ["U79277", "chr8:101998264-101998324", "4.30E-06", "2.17", "0.518242", "0.0200", "0.5411"]], "row_count": 5, "column_count": 7, "numeric_cells": 28, "header_rows": 1, "locator": "section[8]/table-wrap[1]#Tab1"}}, {"id": "asset:table:pmid:25288503:2", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": 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"0.97-1.02", "0.62"], ["Testing set (GSE 21653) (N = 252)", ""], ["Four-lncRNA risk score", "2.12", "1.35-3.34", "0.001", "2.28", "1.44-3.63", "4.84E-4"], ["Age", "1.00", "0.98-1.02", "0.95", "1.00", "0.98-1.02", "0.88"], ["Subtype", "1.04", "0.88-1.23", "0.64", "1.12", "0.95-1.33", "0.19"], ["Testing set (GSE 12276) (N = 204)a", ""], ["Four-lncRNA risk score", "1.893", "1.40-2.56", "2.33E-5", "", "", ""], ["Testing set (GSE 42568) (N = 104)", ""], ["Four-lncRNA risk score", "2.36", "1.30-4.27", "0.005", "2.34", "1.29-4.24", "0.005"], ["Age", "1.00", "0.97-1.02", "0.59", "1.00", "0.97-1.02", "0.78"]], "row_count": 14, "column_count": 7, "numeric_cells": 51, "header_rows": 2, "locator": "section[11]/table-wrap[1]#Tab2"}}], "gaps": ["asset:data:geo:GSE12276 not downloaded", "asset:data:geo:GSE12276 licence not read", "asset:data:geo:GSE20685 not downloaded", "asset:data:geo:GSE20685 licence not read", "asset:data:geo:GSE21653 not downloaded", "asset:data:geo:GSE21653 licence not read", "asset:data:geo:GSE42568 not downloaded", "asset:data:geo:GSE42568 licence not read"]}, "analysis": {"state": "partial", "methods": [{"id": "method-1", "family": "survival_analysis", "specific": "kaplan_meier", "label": "Survival analysis", "dsl_operations": ["survival_km"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["time_to_event_with_censoring"], "evidence": {"score": 0.8, "band": "high", "quote": "Kaplan-Meier"}}, {"id": "method-2", "family": "survival_analysis", "specific": "cox_proportional_hazards", "label": "Survival analysis", "dsl_operations": ["cox_ph"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["time_to_event_with_censoring"], "evidence": {"score": 0.8, "band": "high", "quote": "Cox regression"}}, {"id": "method-3", "family": "survival_analysis", "specific": "log_rank_test", "label": "Survival analysis", "dsl_operations": ["logrank_test"], "missing_operations": [], "expressible": true, 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