Evidence map›Paper›PMID 32509452›Full record

ArticlePeerJ2020

Identifying multiple collagen gene family members as potential gastric cancer biomarkers using integrated bioinformatics analysis.

Zhaoxing Li, Zhao Liu, Zhiting Shao, Chuang Li, Yong Li, Qingwei Liu, Yifei Zhang, Bibo Tan, Yu Liu

Abstract read
In one paragraph

Article in PeerJ, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Review
  2. Article
  3. Analysis of miRNAs inPharmaceuticals (Basel, Switzerland) · 2023
    Article
  4. Article
  5. ENTPD1-AS1-miR-144-3p-mediated high expression ofWorld journal of gastrointestinal oncology · 2023
    Article
  6. Up-regulation of collagen type V alpha 2 (Open medicine (Warsaw, Poland) · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. A tumour-resident Lgr5Nature cell biology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
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

9 authors.

Zhaoxing Li *Department of General Surgery, The Fourth Affiliated Hospital of Hebei Medical University, Shijiazhuang, China.
Zhao Liu *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Gastrointestinal Surgery, Peking University Cancer Hospital and Institute, Beijing, China.
Zhiting ShaoKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Renal Cancer and Melanoma, Peking University Cancer Hospital and Institute, Beijing, China.
Chuang LiThe Second Hospital of Shijiazhuang, Shijiazhuang, China.
Yong LiDepartment of General Surgery, The Fourth Affiliated Hospital of Hebei Medical University, Shijiazhuang, China.
Qingwei LiuDepartment of General Surgery, The Fourth Affiliated Hospital of Hebei Medical University, Shijiazhuang, China.
Yifei ZhangHebei General Hospital, Shijiazhuang, China.
Bibo TanDepartment of General Surgery, The Fourth Affiliated Hospital of Hebei Medical University, Shijiazhuang, China.
Yu LiuDepartment of General Surgery, The Fourth Affiliated Hospital of Hebei Medical University, Shijiazhuang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric cancer is one of the most common malignant cancers worldwide. Despite substantial developments in therapeutic strategies, the five-year survival rate remains low. Therefore, novel biomarkers and therapeutic targets involved in the progression of gastric tumors need to be identified.

methodsWe obtained the mRNA microarray datasets GSE65801, GSE54129 and GSE79973 from the Gene Expression Omnibus database to acquire differentially expressed genes (DEGs). We used the Database for Annotation, Visualization, and Integrated Discovery (DAVID) to analyze DEG pathways and functions, and the Search Tool for the Retrieval of Interacting Genes (STRING) and Cytoscape to obtain the protein-protein interaction (PPI) network. Next, we validated the hub gene expression levels using the Oncomine database and Gene Expression Profiling Interactive Analysis (GEPIA), and conducted stage expression and survival analysis.

resultsFrom the three microarray datasets, we identified nine major hub genes: COL1A1, COL1A2, COL3A1, COL5A2, COL4A1, FN1, COL5A1, COL4A2, and COL6A3.

conclusionOur study identified COL1A1 and COL1A2 as potential gastric cancer prognostic biomarkers.

Indexed as

BioinformaticsBiomarkerGastric cancerSurvival

Identifiers

PMID32509452
PMCPMC7255341

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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.