Evidence map›Paper›PMID 33597614›Full record

ArticleScientific reports2021

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

Feng Jiang, Chuyan Wu, Ming Wang, Ke Wei, Jimei Wang

Abstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. SDC1 is a critical transmembrane proteoglycan in breast cancer.World journal of surgical oncology · 2025
    Review
  6. A Glycolysis and gluconeogenesis-related model for breast cancer prognosis.Cancer biomarkers : section A of Disease markers · 2024
    Article
  7. Review
  8. Advances in the understanding of nuclear pore complexes in human diseases.Journal of cancer research and clinical oncology · 2024
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Veterinary sciences · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Feng Jiang *Department of Neonatology, Obstetrics and Gynecology Hospital of Fudan University, No. 419, Fangxie Road, Shanghai, 200011, China.
Chuyan Wu *Department of Rehabilitation Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.
Ming WangPlastic Surgery Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.
Ke WeiMedical Department, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.
Jimei WangDepartment of Neonatology, Obstetrics and Gynecology Hospital of Fudan University, No. 419, Fangxie Road, Shanghai, 200011, China. wjm821920@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Adenylate KinaseBiomarkers, TumorBreast NeoplasmsCalcium Channels, T-TypeComputational BiologyData ManagementFemaleGene Expression Regulation, NeoplasticGlycolysisHumansInterleukin-13 Receptor alpha1 SubunitNuclear Pore Complex ProteinsPhosphoglycerate KinasePrognosisProportional Hazards ModelsRNA, MessengerAdenylate KinaseAK3 protein, humanBiomarkers, TumorCACNA1H protein, humanCalcium Channels, T-TypeIL13RA1 protein, humanInterleukin-13 Receptor alpha1 SubunitNuclear Pore Complex ProteinsNUP43 protein, humanPGK1 protein, humanPhosphoglycerate KinaseRNA, MessengerSDC1 protein, humanSDC3 protein, humanSyndecan-1Syndecan-3

Identifiers

PMID33597614
PMCPMC7889867

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.