Identification of novel cell glycolysis related gene signature predicting survival in patients with breast cancer

One of the most frequently identified tumors and a contributing cause of death in women is breast cancer (BC). Many biomarkers associated with survival and prognosis were identified in previous studies through database mining. Nevertheless, the predictive capabilities of single-gene biomarkers are n...

Full description

Saved in:
Bibliographic Details
Published inScientific reports Vol. 11; no. 1; p. 3986
Main Authors Jiang, Feng, Wu, Chuyan, Wang, Ming, Wei, Ke, Wang, Jimei
Format Journal Article
LanguageEnglish
Published England Nature Publishing Group 17.02.2021
Nature Publishing Group UK
Nature Portfolio
Subjects
Online AccessGet full text

Cover

Loading…
Abstract One of the most frequently identified tumors and a contributing cause of death in women is breast cancer (BC). Many biomarkers associated with survival and prognosis were identified in previous studies through database mining. Nevertheless, the predictive capabilities of single-gene biomarkers are not accurate enough. Genetic signatures can be an enhanced prediction method. This research analyzed data from The Cancer Genome Atlas (TCGA) for the detection of a new genetic signature to predict BC prognosis. Profiling of mRNA expression was carried out in samples of patients with TCGA BC (n = 1222). Gene set enrichment research has been undertaken to classify gene sets that vary greatly between BC tissues and normal tissues. Cox models for additive hazards regression were used to classify genes that were strongly linked to overall survival. A subsequent Cox regression multivariate analysis was used to construct a predictive risk parameter model. Kaplan-Meier survival predictions and log-rank validation have been used to verify the value of risk prediction parameters. Seven genes (PGK1, CACNA1H, IL13RA1, SDC1, AK3, NUP43, SDC3) correlated with glycolysis were shown to be strongly linked to overall survival. Depending on the 7-gene-signature, 1222 BC patients were classified into subgroups of high/low-risk. Certain variables have not impaired the prognostic potential of the seven-gene signature. A seven-gene signature correlated with cellular glycolysis was developed to predict the survival of BC patients. The results include insight into cellular glycolysis mechanisms and the detection of patients with poor BC prognosis.
AbstractList One of the most frequently identified tumors and a contributing cause of death in women is breast cancer (BC). Many biomarkers associated with survival and prognosis were identified in previous studies through database mining. Nevertheless, the predictive capabilities of single-gene biomarkers are not accurate enough. Genetic signatures can be an enhanced prediction method. This research analyzed data from The Cancer Genome Atlas (TCGA) for the detection of a new genetic signature to predict BC prognosis. Profiling of mRNA expression was carried out in samples of patients with TCGA BC (n = 1222). Gene set enrichment research has been undertaken to classify gene sets that vary greatly between BC tissues and normal tissues. Cox models for additive hazards regression were used to classify genes that were strongly linked to overall survival. A subsequent Cox regression multivariate analysis was used to construct a predictive risk parameter model. Kaplan-Meier survival predictions and log-rank validation have been used to verify the value of risk prediction parameters. Seven genes (PGK1, CACNA1H, IL13RA1, SDC1, AK3, NUP43, SDC3) correlated with glycolysis were shown to be strongly linked to overall survival. Depending on the 7-gene-signature, 1222 BC patients were classified into subgroups of high/low-risk. Certain variables have not impaired the prognostic potential of the seven-gene signature. A seven-gene signature correlated with cellular glycolysis was developed to predict the survival of BC patients. The results include insight into cellular glycolysis mechanisms and the detection of patients with poor BC prognosis.
Abstract One of the most frequently identified tumors and a contributing cause of death in women is breast cancer (BC). Many biomarkers associated with survival and prognosis were identified in previous studies through database mining. Nevertheless, the predictive capabilities of single-gene biomarkers are not accurate enough. Genetic signatures can be an enhanced prediction method. This research analyzed data from The Cancer Genome Atlas (TCGA) for the detection of a new genetic signature to predict BC prognosis. Profiling of mRNA expression was carried out in samples of patients with TCGA BC (n = 1222). Gene set enrichment research has been undertaken to classify gene sets that vary greatly between BC tissues and normal tissues. Cox models for additive hazards regression were used to classify genes that were strongly linked to overall survival. A subsequent Cox regression multivariate analysis was used to construct a predictive risk parameter model. Kaplan–Meier survival predictions and log-rank validation have been used to verify the value of risk prediction parameters. Seven genes (PGK1, CACNA1H, IL13RA1, SDC1, AK3, NUP43, SDC3) correlated with glycolysis were shown to be strongly linked to overall survival. Depending on the 7-gene-signature, 1222 BC patients were classified into subgroups of high/low-risk. Certain variables have not impaired the prognostic potential of the seven-gene signature. A seven-gene signature correlated with cellular glycolysis was developed to predict the survival of BC patients. The results include insight into cellular glycolysis mechanisms and the detection of patients with poor BC prognosis.
Abstract One of the most frequently identified tumors and a contributing cause of death in women is breast cancer (BC). Many biomarkers associated with survival and prognosis were identified in previous studies through database mining. Nevertheless, the predictive capabilities of single-gene biomarkers are not accurate enough. Genetic signatures can be an enhanced prediction method. This research analyzed data from The Cancer Genome Atlas (TCGA) for the detection of a new genetic signature to predict BC prognosis. Profiling of mRNA expression was carried out in samples of patients with TCGA BC (n = 1222). Gene set enrichment research has been undertaken to classify gene sets that vary greatly between BC tissues and normal tissues. Cox models for additive hazards regression were used to classify genes that were strongly linked to overall survival. A subsequent Cox regression multivariate analysis was used to construct a predictive risk parameter model. Kaplan–Meier survival predictions and log-rank validation have been used to verify the value of risk prediction parameters. Seven genes (PGK1, CACNA1H, IL13RA1, SDC1, AK3, NUP43, SDC3) correlated with glycolysis were shown to be strongly linked to overall survival. Depending on the 7-gene-signature, 1222 BC patients were classified into subgroups of high/low-risk. Certain variables have not impaired the prognostic potential of the seven-gene signature. A seven-gene signature correlated with cellular glycolysis was developed to predict the survival of BC patients. The results include insight into cellular glycolysis mechanisms and the detection of patients with poor BC prognosis.
ArticleNumber 3986
Author Jiang, Feng
Wei, Ke
Wu, Chuyan
Wang, Jimei
Wang, Ming
Author_xml – sequence: 1
  givenname: Feng
  surname: Jiang
  fullname: Jiang, Feng
  organization: Department of Neonatology, Obstetrics and Gynecology Hospital of Fudan University, No. 419, Fangxie Road, Shanghai, 200011, China
– sequence: 2
  givenname: Chuyan
  surname: Wu
  fullname: Wu, Chuyan
  organization: Department of Rehabilitation Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China
– sequence: 3
  givenname: Ming
  surname: Wang
  fullname: Wang, Ming
  organization: Plastic Surgery Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China
– sequence: 4
  givenname: Ke
  surname: Wei
  fullname: Wei, Ke
  organization: Medical Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China
– sequence: 5
  givenname: Jimei
  surname: Wang
  fullname: Wang, Jimei
  email: wjm821920@163.com
  organization: Department of Neonatology, Obstetrics and Gynecology Hospital of Fudan University, No. 419, Fangxie Road, Shanghai, 200011, China. wjm821920@163.com
BackLink https://www.ncbi.nlm.nih.gov/pubmed/33597614$$D View this record in MEDLINE/PubMed
BookMark eNpdkstu1DAUhiNUREvpC7BAltiwCfia2BskVHEZqRIbWFuOfZJ65LGndjJo3h6nU6oWb2wd_-c7F_2vm7OYIjTNW4I_Eszkp8KJULLFlLSSdVS26kVzQTEXLWWUnj15nzdXpWxxPYIqTtSr5pwxofqO8IvmbuMgzn701sw-RZRGFNMBArIQAprC0aZwLL6gDMHM4NAEEVDxUzTzkgHtMzhvZx8nVJZ88AcTkI9oX2mVW9AfP9-iIYMpM7ImWshvmpejCQWuHu7L5ve3r7-uf7Q3P79vrr_ctJarbm4FoVwOkruBS2U6oDAOuFfMSonBmt4JRUTf9ZyJsU45KDCOCiZ7wKwfiGCXzebEdcls9T77nclHnYzX94GUJ23y7G0AjY3jY60zcqjFBymHYZRMOeOAYTN2lfX5xNovww6craNlE55Bn_9Ef6undNC9lEp2fQV8eADkdLdAmfXOl3XFJkJaiqZcEdxTTlbp-_-k27TkWFe1qjBTSuC1I3pS2ZxKyTA-NkOwXg2iTwbR1SD63iBa1aR3T8d4TPlnB_YXaSq6mA
CitedBy_id crossref_primary_10_3389_fimmu_2022_880959
crossref_primary_10_3389_fonc_2022_1061789
crossref_primary_10_12677_ACM_2023_1371653
crossref_primary_10_3389_fgene_2022_960567
crossref_primary_10_1038_s41598_022_25059_8
crossref_primary_10_3390_vetsci9050210
crossref_primary_10_3389_fgene_2022_834471
crossref_primary_10_3389_fphar_2022_895608
crossref_primary_10_3390_cancers15061794
crossref_primary_10_1016_j_clbc_2023_10_011
crossref_primary_10_1007_s00432_023_04985_8
crossref_primary_10_3390_ijms24065561
Cites_doi 10.5858/arpa.2013-0435-OA
10.1016/j.ygeno.2004.08.010
10.3389/fgene.2019.00396
10.1677/erc.0.0100261
10.1007/s10549-013-2559-1
10.1038/nrg3722
10.1186/1471-2407-12-456
10.3322/caac.21590
10.1073/pnas.0506580102
10.1146/annurev.med.59.053006.104707
10.1080/15384047.2018.1564558
10.1186/s13058-015-0542-y
10.3322/caac.21349
10.1200/JCO.2009.23.1274
10.1158/1535-7163.MCT-13-0026
10.1007/s10555-019-09794-5
10.1186/bcr2607
10.1155/2015/453801
10.1016/j.biocel.2006.06.004
10.1002/gcc.21998
10.1038/nrc3038
10.3390/jcm5020013
10.1016/j.cmet.2006.01.012
10.1016/j.ajpath.2010.12.042
10.1093/jnci/djt282
10.1186/1471-2164-12-66
10.1002/mc.22014
10.1038/nature11017
ContentType Journal Article
Copyright The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
The Author(s) 2021
Copyright_xml – notice: The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: The Author(s) 2021
DBID NPM
AAYXX
CITATION
3V.
7X7
7XB
88A
88E
88I
8FE
8FH
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
HCIFZ
K9.
LK8
M0S
M1P
M2P
M7P
PIMPY
PQEST
PQQKQ
PQUKI
PRINS
Q9U
7X8
5PM
DOA
DOI 10.1038/s41598-021-83628-9
DatabaseName PubMed
CrossRef
ProQuest Central (Corporate)
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Biology Database (Alumni Edition)
Medical Database (Alumni Edition)
Science Database (Alumni Edition)
ProQuest SciTech Collection
ProQuest Natural Science Collection
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central
ProQuest Central Essentials
Biological Science Collection
ProQuest Central
ProQuest Natural Science Collection
ProQuest One Community College
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
SciTech Premium Collection
ProQuest Health & Medical Complete (Alumni)
ProQuest Biological Science Collection
Health & Medical Collection (Alumni Edition)
Medical Database
ProQuest Science Journals
Biological Science Database
Publicly Available Content Database
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
ProQuest Central Basic
MEDLINE - Academic
PubMed Central (Full Participant titles)
Directory of Open Access Journals
DatabaseTitle PubMed
CrossRef
Publicly Available Content Database
ProQuest Central Student
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest Natural Science Collection
ProQuest Central China
ProQuest Biology Journals (Alumni Edition)
ProQuest Central
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
Natural Science Collection
ProQuest Central Korea
Biological Science Collection
ProQuest Medical Library (Alumni)
ProQuest Science Journals (Alumni Edition)
ProQuest Biological Science Collection
ProQuest Central Basic
ProQuest Science Journals
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Biological Science Database
ProQuest SciTech Collection
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList PubMed
Publicly Available Content Database
CrossRef


Database_xml – sequence: 1
  dbid: DOA
  name: Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Biology
EISSN 2045-2322
EndPage 3986
ExternalDocumentID oai_doaj_org_article_0ad4fb48f4ec49b88bbf839dade30af6
10_1038_s41598_021_83628_9
33597614
Genre Journal Article
GroupedDBID 0R~
3V.
4.4
53G
5VS
7X7
88A
88E
88I
8FE
8FH
8FI
8FJ
AAFWJ
AAJSJ
AAKDD
ABDBF
ABUWG
ACGFS
ACSMW
ADBBV
ADRAZ
AENEX
AFKRA
AFPKN
AJTQC
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
AZQEC
BAWUL
BBNVY
BCNDV
BENPR
BHPHI
BPHCQ
BVXVI
C6C
CCPQU
DIK
DWQXO
EBD
EBLON
EBS
ESX
FYUFA
GNUQQ
GROUPED_DOAJ
GX1
HCIFZ
HH5
HMCUK
HYE
KQ8
LK8
M0L
M1P
M2P
M48
M7P
M~E
NAO
NPM
OK1
PIMPY
PQQKQ
PROAC
PSQYO
RIG
RNT
RNTTT
RPM
SNYQT
UKHRP
AAYXX
CITATION
7XB
8FK
K9.
PQEST
PQUKI
PRINS
Q9U
7X8
5PM
ID FETCH-LOGICAL-c496t-51248b84db489a6e2efb0793c880eca7d5915767435f232b9ead25387e037b153
IEDL.DBID RPM
ISSN 2045-2322
IngestDate Fri Oct 04 13:12:30 EDT 2024
Tue Sep 17 21:06:20 EDT 2024
Tue Aug 27 04:45:11 EDT 2024
Fri Sep 13 10:35:08 EDT 2024
Fri Aug 23 01:03:32 EDT 2024
Sat Sep 28 08:30:18 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
License Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c496t-51248b84db489a6e2efb0793c880eca7d5915767435f232b9ead25387e037b153
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889867/
PMID 33597614
PQID 2490399506
PQPubID 2041939
PageCount 1
ParticipantIDs doaj_primary_oai_doaj_org_article_0ad4fb48f4ec49b88bbf839dade30af6
pubmedcentral_primary_oai_pubmedcentral_nih_gov_7889867
proquest_miscellaneous_2491072417
proquest_journals_2490399506
crossref_primary_10_1038_s41598_021_83628_9
pubmed_primary_33597614
PublicationCentury 2000
PublicationDate 2021-02-17
PublicationDateYYYYMMDD 2021-02-17
PublicationDate_xml – month: 02
  year: 2021
  text: 2021-02-17
  day: 17
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
– name: London
PublicationTitle Scientific reports
PublicationTitleAlternate Sci Rep
PublicationYear 2021
Publisher Nature Publishing Group
Nature Publishing Group UK
Nature Portfolio
Publisher_xml – name: Nature Publishing Group
– name: Nature Publishing Group UK
– name: Nature Portfolio
References R Rouzier (83628_CR9) 2013; 139
KV Morris (83628_CR17) 2014; 15
TP Das (83628_CR26) 2014; 53
KM Parnell (83628_CR30) 2013; 12
I Papandreou (83628_CR31) 2006; 3
A Manni (83628_CR7) 1980; 46
MY Polley (83628_CR15) 2013; 105
H Rochefort (83628_CR5) 2003; 10
YC Shao (83628_CR18) 2018; 53
A Romero (83628_CR10) 2011; 178
KD Miller (83628_CR2) 2016; 66
WH Koppenol (83628_CR22) 2011; 11
IO Farah (83628_CR24) 2013; 49
EA Rakha (83628_CR3) 2010; 12
R Kronenwett (83628_CR11) 2012; 12
N Ilan (83628_CR21) 2006; 38
C Wu (83628_CR28) 2019; 10
M Dowsett (83628_CR8) 2010; 28
B Altenberg (83628_CR23) 2004; 84
Y Wu (83628_CR20) 2016; 5
J Lu (83628_CR25) 2019; 38
R Garzon (83628_CR16) 2009; 60
A Subramanian (83628_CR14) 2005; 102
G Ye (83628_CR27) 2019; 20
AM Schwartz (83628_CR4) 2014; 138
ML Poeta (83628_CR29) 2012; 51
RL Siegel (83628_CR1) 2020; 70
PJ Stephens (83628_CR12) 2012; 486
EL Hayes (83628_CR6) 2015; 17
MA Thomas (83628_CR13) 2011; 12
MA Soares (83628_CR19) 2015; 2015
References_xml – volume: 138
  start-page: 1048
  year: 2014
  ident: 83628_CR4
  publication-title: Arch. Pathol. Lab. Med.
  doi: 10.5858/arpa.2013-0435-OA
  contributor:
    fullname: AM Schwartz
– volume: 84
  start-page: 1014
  year: 2004
  ident: 83628_CR23
  publication-title: Genomics
  doi: 10.1016/j.ygeno.2004.08.010
  contributor:
    fullname: B Altenberg
– volume: 10
  start-page: 396
  year: 2019
  ident: 83628_CR28
  publication-title: Front. Genet.
  doi: 10.3389/fgene.2019.00396
  contributor:
    fullname: C Wu
– volume: 10
  start-page: 261
  year: 2003
  ident: 83628_CR5
  publication-title: Endocr. Relat. Cancer
  doi: 10.1677/erc.0.0100261
  contributor:
    fullname: H Rochefort
– volume: 53
  start-page: 2555
  year: 2018
  ident: 83628_CR18
  publication-title: Int. J. Oncol.
  contributor:
    fullname: YC Shao
– volume: 139
  start-page: 621
  year: 2013
  ident: 83628_CR9
  publication-title: Breast Cancer Res. Treat.
  doi: 10.1007/s10549-013-2559-1
  contributor:
    fullname: R Rouzier
– volume: 15
  start-page: 423
  year: 2014
  ident: 83628_CR17
  publication-title: Nat. Rev. Genet.
  doi: 10.1038/nrg3722
  contributor:
    fullname: KV Morris
– volume: 12
  start-page: 456
  year: 2012
  ident: 83628_CR11
  publication-title: BMC Cancer
  doi: 10.1186/1471-2407-12-456
  contributor:
    fullname: R Kronenwett
– volume: 70
  start-page: 7
  year: 2020
  ident: 83628_CR1
  publication-title: CA Cancer J. Clin.
  doi: 10.3322/caac.21590
  contributor:
    fullname: RL Siegel
– volume: 102
  start-page: 15545
  year: 2005
  ident: 83628_CR14
  publication-title: Proc. Natl. Acad. Sci. U S A
  doi: 10.1073/pnas.0506580102
  contributor:
    fullname: A Subramanian
– volume: 60
  start-page: 167
  year: 2009
  ident: 83628_CR16
  publication-title: Annu. Rev. Med.
  doi: 10.1146/annurev.med.59.053006.104707
  contributor:
    fullname: R Garzon
– volume: 20
  start-page: 711
  year: 2019
  ident: 83628_CR27
  publication-title: Cancer Biol. Ther.
  doi: 10.1080/15384047.2018.1564558
  contributor:
    fullname: G Ye
– volume: 17
  start-page: 40
  year: 2015
  ident: 83628_CR6
  publication-title: Breast Cancer Res.
  doi: 10.1186/s13058-015-0542-y
  contributor:
    fullname: EL Hayes
– volume: 66
  start-page: 271
  year: 2016
  ident: 83628_CR2
  publication-title: CA Cancer J. Clin.
  doi: 10.3322/caac.21349
  contributor:
    fullname: KD Miller
– volume: 49
  start-page: 101
  year: 2013
  ident: 83628_CR24
  publication-title: Biomed. Sci. Instrum.
  contributor:
    fullname: IO Farah
– volume: 28
  start-page: 509
  year: 2010
  ident: 83628_CR8
  publication-title: J. Clin. Oncol.
  doi: 10.1200/JCO.2009.23.1274
  contributor:
    fullname: M Dowsett
– volume: 12
  start-page: 1453
  year: 2013
  ident: 83628_CR30
  publication-title: Mol. Cancer Ther.
  doi: 10.1158/1535-7163.MCT-13-0026
  contributor:
    fullname: KM Parnell
– volume: 38
  start-page: 157
  year: 2019
  ident: 83628_CR25
  publication-title: Cancer Metastasis Rev.
  doi: 10.1007/s10555-019-09794-5
  contributor:
    fullname: J Lu
– volume: 12
  start-page: 207
  year: 2010
  ident: 83628_CR3
  publication-title: Breast Cancer Res.
  doi: 10.1186/bcr2607
  contributor:
    fullname: EA Rakha
– volume: 2015
  start-page: 453801
  year: 2015
  ident: 83628_CR19
  publication-title: Biomed. Res. Int.
  doi: 10.1155/2015/453801
  contributor:
    fullname: MA Soares
– volume: 38
  start-page: 2018
  year: 2006
  ident: 83628_CR21
  publication-title: Int. J. Biochem. Cell. Biol.
  doi: 10.1016/j.biocel.2006.06.004
  contributor:
    fullname: N Ilan
– volume: 46
  start-page: 2838
  year: 1980
  ident: 83628_CR7
  publication-title: Cancer Am. Cancer Soc.
  contributor:
    fullname: A Manni
– volume: 51
  start-page: 1133
  year: 2012
  ident: 83628_CR29
  publication-title: Genes Chromosomes Cancer
  doi: 10.1002/gcc.21998
  contributor:
    fullname: ML Poeta
– volume: 11
  start-page: 325
  year: 2011
  ident: 83628_CR22
  publication-title: Nat. Rev. Cancer
  doi: 10.1038/nrc3038
  contributor:
    fullname: WH Koppenol
– volume: 5
  start-page: 2
  year: 2016
  ident: 83628_CR20
  publication-title: J. Clin. Med.
  doi: 10.3390/jcm5020013
  contributor:
    fullname: Y Wu
– volume: 3
  start-page: 187
  year: 2006
  ident: 83628_CR31
  publication-title: Cell. Metab.
  doi: 10.1016/j.cmet.2006.01.012
  contributor:
    fullname: I Papandreou
– volume: 178
  start-page: 1453
  year: 2011
  ident: 83628_CR10
  publication-title: Am. J. Pathol.
  doi: 10.1016/j.ajpath.2010.12.042
  contributor:
    fullname: A Romero
– volume: 105
  start-page: 1677
  year: 2013
  ident: 83628_CR15
  publication-title: J. Natl. Cancer Inst.
  doi: 10.1093/jnci/djt282
  contributor:
    fullname: MY Polley
– volume: 12
  start-page: 66
  year: 2011
  ident: 83628_CR13
  publication-title: BMC Genom.
  doi: 10.1186/1471-2164-12-66
  contributor:
    fullname: MA Thomas
– volume: 53
  start-page: 537
  year: 2014
  ident: 83628_CR26
  publication-title: Mol. Carcinog.
  doi: 10.1002/mc.22014
  contributor:
    fullname: TP Das
– volume: 486
  start-page: 400
  year: 2012
  ident: 83628_CR12
  publication-title: Nature
  doi: 10.1038/nature11017
  contributor:
    fullname: PJ Stephens
SSID ssj0000529419
Score 2.4355655
Snippet One of the most frequently identified tumors and a contributing cause of death in women is breast cancer (BC). Many biomarkers associated with survival and...
Abstract One of the most frequently identified tumors and a contributing cause of death in women is breast cancer (BC). Many biomarkers associated with...
Abstract One of the most frequently identified tumors and a contributing cause of death in women is breast cancer (BC). Many biomarkers associated with...
SourceID doaj
pubmedcentral
proquest
crossref
pubmed
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
StartPage 3986
SubjectTerms Biomarkers
Breast cancer
Gene expression
Genes
Genomes
Glycolysis
Interleukin 1
Medical prognosis
Multivariate analysis
Predictions
Prognosis
Regression analysis
Survival
Tumors
SummonAdditionalLinks – databaseName: Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1La9wwEBYhEMil9JXWTVpU6C2YyJZsSce2JIRCe2ogNyFZoyQQvOk-Cvn3mZGcZTcEeunVMkae-TQPaeYTY19MFEFG5cn6dZigWFP7TvW1iQGi9J1PmcT156_-_EL9uOwuN676opqwQg9cBHcifFQpKJMUDMoGY0JI6NSjjyAFfilb36bbSKYKq3drVWOnLhkhzckCPRV1k7VNbdBo4yrf8kSZsP-5KPNpseSG9zl7yV5MYSP_Wqb7iu3A-JrtlYsk79-wP6XfNk0bcHyW-Dj7C7ec9uX51e09qpuoR3huXYHIETbAqXYj83ryuzmd11AFNF-s0Hgg_PjNyCfS1QWn3VoeqH59yQfCyfwtuzg7_f39vJ4uU6hRbP2yRseuTDAqoiyt76GFFIgcb8AFDIPXsbNNR8w-sksYZQWLEGvRGmoQUge0iwdsd5yN8J5xNHLQo2HwqE6lkwhB2JBgAEy0dWpMxY4fBevuCmeGy2fd0riiBodqcFkNzlbsG8l-_SbxXecHiAI3ocD9CwUVO3rUnJsW4cJhZimoc1fg8Of1MC4fkr0fYbbK72ACjGGMrti7ouj1TKTEbAvDl4rpLQhsTXV7ZLy5zhTd2hhrev3hf_zbIdtvCbZ0C40-YrvL-Qo-YiS0DJ8y6B8Aa8QK0A
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3fb9QwDLbGEBIviPFrHRsKEm-ourRJm_QJMcR0QoInJt1blDTJmDS1t7se0v772Wnv2CHEa9uHNP7s2I79GeCD9twJLy1ZvwoDlEbntpJ1rr0LXtjKxkTi-v1HPb-U3xbV4gDm214YKqvc2sRkqH3fUo58hmECpzZMXs-soyxAO8w-LW9zmh9F96zTMI1H8Lgo0a1AZKuF2mVb6D5LFs3UNcOFnq3x5KLusrLINRpx1Pq9kykR-P_L6_y7ePLBaXTxHJ5NbiT7PMr9CA5C9wKejIMl717C7dh_G6eEHOsj6_rf4YZRnp5d3dyh-ImKhKVWluAZwigwquVIPJ9suaL7G6qIZusNGhOEI7vu2ETCumaUvWWO6tkH1hJuVq_g8uLrzy_zfBqukLeyqYccD3qpnZbeSd3YOpQhOiLLa1GhQ2uVr5qiIqYfUUX0ulyDkCvROqrAhXJoJ1_DYdd34RgYGr1Qo6GwKF6pIneONy6GNmDgrWKhM_i43VizHDk0TLr7FtqMYjAoBpPEYJoMzmnvd18S_3V60K-uzKROhlsvI648yoC_47R2LqKr560PgiO-MjjdSs5MSrk2fyCUwfvda1Qn2nvbhX6TvsGAGN0alcGbUdC7lQiB0Re6MxmoPQjsLXX_TXf9K1F2K60bXauT_y_rLTwtCZA0b0adwuGw2oQz9HkG9y7B-R4AZwQK
  priority: 102
  providerName: ProQuest
– databaseName: Scholars Portal Open Access Journals
  dbid: M48
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Na9wwEB3ShEIvpW364TYtKvQW3Hot2ZIOpSQhIQTSUxdyE5IlpYHFTry7pfvvOyN7l27ZS6-WMfLMm9GMpHkD8En5wnEvLHm_ChMUrXJbiTpX3gXPbWVjInG9_l5fTsXVTXWzB-t2R6MA5ztTO-onNe1nn38_rL6hwX8dSsbVlzkuQlQoVk5yhf4YDfgRHJSCC0L89RjuD1zfpRap1weRsOcYTJRjHc3uz2ytVYnSf1cc-u91yr_Wp4tn8HQMLNnJgITnsBfaF_B4aDW5OoSHoSI3jlt0rIus7X6FGaOde3Y7WyEgiJyEpeKW4BkCKzC63ZGYP9l9Tyc6dEeazZfoXhCg7K5lIy3rnNF-LnN0w33BGkJS_xKmF-c_zi7zsd1C3ghdL3Jc-oVySngnlLZ1KEN0RJ_XoImHxkpf6UlF3D-8iig6pxGEJfpLGQouHXrOV7Dfdm14AwzdYKjRdVhUuJCxcK7QLoYmYCou40RlcLwWrLkfWDVMOg3nygxqMKgGk9RgdAanJPvNm8SInR50_a0ZDcwU1ouIM48i4O84pZyLGPx56wMvEHEZHK01Z9YoM5h7FlTbW-Dwx80wGhjJ3rahW6Z3MEXGQEdm8HpQ9GYmnGM-hgFOBnILAltT3R5p734mEm-plFa1fPtfkngHT0rCJzWkkUewv-iX4T0GRQv3ISH9D2ttCTY
  priority: 102
  providerName: Scholars Portal
Title Identification of novel cell glycolysis related gene signature predicting survival in patients with breast cancer
URI https://www.ncbi.nlm.nih.gov/pubmed/33597614
https://www.proquest.com/docview/2490399506/abstract/
https://search.proquest.com/docview/2491072417
https://pubmed.ncbi.nlm.nih.gov/PMC7889867
https://doaj.org/article/0ad4fb48f4ec49b88bbf839dade30af6
Volume 11
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1La9wwEB6SlJZcQp-p03RRobfirG3JlnRsQkIobAilgb0JyZLShY293Uch_74j2V6ypadefLBkkDXfjGakmU8An4XNDLVMB-tXYoAiRapLVqXCGmepLrWPJK6Tm-r6jn2bltM9KIdamJi0X5vZWTN_OGtmP2Nu5eKhHg95YuPbyQWGbVJUfLwP-5zSJyF6R-hdSJbLvkAmo2K8wkUqFJIVeSrQXqOCH8ILStGVrnK2sx5F2v5_-Zp_p0w-WYOuXsJR7zySr90gX8Gea17D8-46ycc38KuruvX9NhxpPWna325Owu48uZ8_otADAQmJBSzOEgSPIyGDI7J7ksUynNqEPGiy2qAJQRCSWUN66tUVCXu2xIQs9jWpA1qWb-Hu6vLHxXXaX6mQ1kxW6xSXdyaMYNYwIXXlCudNoMirUY1drbktZV4Gfh9aevS1jESgFWgTucsoN2gd38FB0zbuPRA0da5C86BRqIz7zJhMGu9qh-E297lI4MswsWrRMWeoeOJNheokolAiKkpEyQTOw9xvewbW6_iiXd6rXvYq05Z5HLlnDn_HCGGMRwfPautohqhK4HSQnOpVcaUwvsxC_W6GzZ-2zahEYe5149pN7INhMDozPIHjTtDbkQxASYDvQGBnqLstiNtI1N3j9OS_v_wAh0WAbbiAhp_CwXq5cR_RCVqbEUJ_ykfw7Pzy5vb7KG4l4HPCxCiqwx-fPQ2_
link.rule.ids 230,315,733,786,790,870,891,2115,12083,21416,24346,27957,27958,31754,31755,33779,33780,43345,43840,53827,53829,74102,74659
linkProvider National Library of Medicine
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3fb9MwED5BJwQviN9kDDASbyhaWjux84QY2lRgqxDapL1ZdmyPSVPSNe2k_ffcOW6hCPGa5MHxfXe-O999B_BeucJyJwxZvxIDlFrlphRVrpz1jpvShEjiejKrpmfi63l5nhJufSqrXNvEaKhd11COfB_DhILaMIvq4_w6p6lRdLuaRmjchR3BMVQZwc7B4ez7j02Whe6xxLhO3TIFV_s9nljUVTYZ5wqNN2r71okUifv_5W3-XTT5xyl09AgeJveRfRrk_Rju-PYJ3BsGSt4-heuh7zakRBzrAmu7G3_FKD_PLq5uUexEQcJiC4t3DOHjGdVwRH5PNl_QvQ1VQrN-hUYEYcguW5bIV3tGWVtmqY59yRrCy-IZnB0dnn6e5mmoQt6IulrmeMALZZVwVqjaVH7igyWSvAYV2TdGurIel8Tww8uA3patEWoTtIrSF1xatI_PYdR2rX8JDI2dr9BAGBSrkKGwtqht8I3HgFuGscrgw3pj9XzgztDxzpsrPYhBoxh0FIOuMzigvd98SbzX8UG3uNBJjXRhnAi48iA8_o5VytqALp4zzvMCcZXB3lpyOiljr39DJ4N3m9eoRrT3pvXdKn6DgTC6MzKDF4OgNyvhHKMudGMykFsQ2Frq9pv28mek6pZK1aqSu_9f1lu4Pz09OdbHX2bfXsGDCYGTZs7IPRgtFyv_Gv2epX2TwP0LZqEEow
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lj9MwEB7BIhAXxJvAAkbihqK6tRM7J8SrWl4rDqzUm2XH9rLSKuk2LdL-e2Yct1CEuCY5OJ5vXvbMNwAvtedOeGnJ-lWYoDS6tJWsS-1d8MJWNiYS16_H9dGJ_LSoFrn-achllVubmAy171s6I59gmsCpDZPXk5jLIr69n79eXpQ0QYpuWvM4jatwDb0kp2kGaqF25y10oyWnTe6b4UJPBvRd1F82m5YazTjq_Z5vShT-_4o7_y6f_MMfzW_DrRxIsjej5O_AldDdhevjaMnLe3AxduDGfCTH-si6_mc4Z3RSz07PLxEAREbCUjNL8AyBFBhVcySmT7Zc0Q0O1USzYYPmBAHJzjqWaVgHRue3zFFF-5q1hJzVfTiZf_j-7qjM4xXKVjb1ukRXL7XT0jupG1uHWYiO6PJaVOnQWuWrZloR14-oIsZdrkHQzdA-qsCFcmgpH8BB13fhETA0e6FGU2FRwFJF7hxvXAxtwNRbxaku4NV2Y81yZNEw6fZbaDOKwaAYTBKDaQp4S3u_-5IYsNODfnVqskIZbr2MuPIoA_6O09q5iMGetz4Ijggr4HArOZPVcjC_QVTAi91rVCjae9uFfpO-wZQYAxtVwMNR0LuVCIH5FwY0Bag9COwtdf9Nd_YjkXYrrRtdq8f_X9ZzuIGoNl8-Hn9-AjdnhE0aPqMO4WC92oSnGACt3bOE7F_2OAdp
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Identification+of+novel+cell+glycolysis+related+gene+signature+predicting+survival+in+patients+with+breast+cancer&rft.jtitle=Scientific+reports&rft.au=Jiang%2C+Feng&rft.au=Wu%2C+Chuyan&rft.au=Wang%2C+Ming&rft.au=Wei%2C+Ke&rft.date=2021-02-17&rft.issn=2045-2322&rft.eissn=2045-2322&rft.volume=11&rft.issue=1&rft_id=info:doi/10.1038%2Fs41598-021-83628-9&rft.externalDBID=n%2Fa&rft.externalDocID=10_1038_s41598_021_83628_9
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2045-2322&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2045-2322&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2045-2322&client=summon