Evidence map›Paper›PMID 36426411›Full record

ArticleCancer medicine2023

Glucose metabolism and lncRNAs in breast cancer: Sworn friend.

Jia-Lin Xu, Qi Xu, Ya-Lin Wang, Di Xu, Wen-Xiu Xu, He-Da Zhang, Dan-Dan Wang, Jin-Hai Tang

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 32% of its field
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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Molecular Effects of Glucose onBritish journal of biomedical science · 2025
    Article
  4. A Glycolysis and gluconeogenesis-related model for breast cancer prognosis.Cancer biomarkers : section A of Disease markers · 2024
    Article
  5. Article
  6. Article
  7. Review
  8. 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

8 authors at 2 institutions in 1 country.

Jia-Lin XuDepartment of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, P.R. China.
Qi XuDepartment of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, P.R. China.
Ya-Lin WangSchool of Clinical Medicine, Xuzhou Medical University, Xuzhou, P.R. China.
Di XuDepartment of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, P.R. China.
Wen-Xiu XuDepartment of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, P.R. China.
He-Da ZhangDepartment of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, P.R. China.
Dan-Dan WangDepartment of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, P.R. China.
Jin-Hai TangDepartment of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, P.R. China.ORCID 0000-0003-2016-4216
Jiangsu Province Hospital · CNXuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlucose metabolism disorder is a common feature in cancer. Cancer cells generate much energy through anaerobic glycolysis, which promote the development of tumors. However, long non-coding RNA may play an important role in this process. Our aim is to explore a prognostic risk model based on the glucose metabolism-related lncRNAs which provides clues that lncRNAs predict a clinical outcome through glucose metabolism in breast cancer.

methods1222 RNA-seq were extracted from the TCGA database, and 74 glucose metabolism-related genes were loaded from the GSEA website. Then, 7 glucose metabolism-related lncRNAs risk score model was developed by univariate, Lasso, and multivariate regression analysis. The lncRNA risk model showed that high-risk patients predict a poor clinical outcome with high reliability (P=2.838×10-6). Univariate and multivariate independent prognostic analysis and ROC curve analysis proved that the risk score was an independent prognostic factor in breast cancer with an AUC value of 0.652. Finally, Gene set enrichment analysis showed that cell cycle-related pathways were significantly enriched in a high-risk group.

resultsOur results showed that glucose metabolism-related lncRNAs can affect breast cancer progression. 7 glucose metabolism-related lncRNAs prognostic signature was established to evaluate the OS of patients with breast cancer. PICSAR, LINC00839, AP001505.1, LINC00393 were risk factors and expressed highly in the high-risk group. A Nomogram was made based on this signature to judge patients' living conditions and prognosis.

conclusion7 glucose metabolism-related lncRNAs risk score model had a high prognostic value in breast cancer. PICSAR, LINC00839, AP001505.1, LINC00393 were risk factors. AP001505.1 expression was increased in most triple-negative breast cancer cells treated with high glucose, which may also take part in breast cancer progression and potential therapeutic targets.

Indexed as

RNA, Long NoncodingTriple Negative Breast NeoplasmsFriendsGlucoseHumansReproducibility of ResultsGlucoseRNA, Long Noncodingbreast cancerglucose metabolismlncRNAlncRNA risk model

Identifiers

PMID36426411
PMCPMC9972110
OpenAlexW4309936141

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.