Evidence map›Paper›PMID 30727821›Full record

ArticleCell cycle (Georgetown, Tex.)2019

Identification of a novel glycolysis-related gene signature that can predict the survival of patients with lung adenocarcinoma.

Chang Liu, Yinyan Li, Minjie Wei, Lin Zhao, Yangyang Yu, Guang Li

Abstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing 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

45 citing papers in PubMed.

  1. Article
  2. Article
  3. A Glycolysis and gluconeogenesis-related model for breast cancer prognosis.Cancer biomarkers : section A of Disease markers · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. The role of long non-coding RNA HCG18 in cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. A Novel Predictive Model Incorporating Ferroptosis-Related Gene Signatures for Overall Survival in Patients with Lung Adenocarcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Survival-associated NBMC cancer · 2021
    Article
  20. 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

6 authors.

Chang Liua Department of Radiation Oncology , The First Affiliated Hospital of China Medical University , Shenyang , China.
Yinyan Lib Department of Ultrasound , The First Affiliated Hospital of China Medical University , Shenyang , China.
Minjie Weic Department of Pharmacology, School of Pharmacy , China Medical University , Shenyang , China.
Lin Zhaoc Department of Pharmacology, School of Pharmacy , China Medical University , Shenyang , China.
Yangyang Yua Department of Radiation Oncology , The First Affiliated Hospital of China Medical University , Shenyang , China.
Guang Lia Department of Radiation Oncology , The First Affiliated Hospital of China Medical University , Shenyang , China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is one of the most malignant cancers worldwide, and lung adenocarcinoma (LUAD) is the most common histologic subtype. Thousands of biomarkers related to the survival and prognosis of patients with this cancer type have been investigated through database mining; however, the prediction effect of a single gene biomarker is not satisfactorily specific or sensitive. Thus, the present study aimed to develop a novel gene signature of prognostic values for patients with LUAD. Using a data-mining method, we performed expression profiling of 1145 mRNAs in large cohorts with LUAD (n = 511) from The Cancer Genome Atlas database. Using the Gene Set Enrichment Analysis, we selected 198 genes related to GLYCOLYSIS, which is the most important enrichment gene set. Moreover, these genes were identified using Cox proportional regression modeling. We established a risk score staging system to predict the outcome of patients with LUAD and subsequently identified four genes (AGRN, AKR1A1, DDIT4, and HMMR) that were closely related to the prognosis of patients with LUAD. The identified genes allowed us to classify patients into the high-risk group (with poor outcome) and low-risk group (with better outcome). Compared with other clinical factors, the risk score has a better performance in predicting the outcome of patients with LUAD, particularly in the early stage of LUAD. In conclusion, we developed a four-gene signature related to glycolysis by utilizing the Cox regression model and a risk staging model for LUAD, which might prove valuable for the clinical management of patients with LUAD.

Indexed as

AdenocarcinomaAgedAldehyde ReductaseDatabases, GeneticExtracellular Matrix ProteinsFemaleGlycolysisHumansHyaluronan ReceptorsKaplan-Meier EstimateLung NeoplasmsMaleMiddle AgedNeoplasm StagingPrognosisProportional Hazards ModelsAldehyde ReductaseDDIT4 protein, humanExtracellular Matrix Proteinshyaluronan-mediated motility receptorHyaluronan ReceptorsRNA, MessengerTranscription FactorsglycolysisLung cancermRNAsprognosticsurvival

Identifiers

PMID30727821
PMCPMC6464579

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.