Evidence map›Paper›PMID 33739392›Full record

ArticleBioscience reports2021

High expression of COL5A2, a member of COL5 family, indicates the poor survival and facilitates cell migration in gastric cancer.

Yuen Tan, Qingchuan Chen, Yao Xing, Chao Zhang, Siwei Pan, Wen An, Huimian Xu

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.6field-weighted citation impact, top 5% 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

29 citing papers in PubMed, 50 citations in OpenAlex.

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  19. Review
  20. Up-regulation of collagen type V alpha 2 (Open medicine (Warsaw, Poland) · 2023
    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

7 authors at 2 institutions in 1 country.

Yuen Tan *Department of Surgical Oncology, First Affiliated Hospital of China Medical University, Shenyang, China.
Qingchuan Chen *Department of Surgical Oncology, First Affiliated Hospital of China Medical University, Shenyang, China.
Yao Xing *Department of Cell Biology, Key Laboratory of Cell Biology of Ministry of Public Health, and Key Laboratory of Medical Cell Biology of Ministry of Education, China Medical University, No. 77, Puhe Road, Shenyang North New Area, 110122 Shenyang, Liaoning, China.
Chao ZhangDepartment of Surgical Oncology, First Affiliated Hospital of China Medical University, Shenyang, China.
Siwei PanDepartment of Surgical Oncology, First Affiliated Hospital of China Medical University, Shenyang, China.
Wen AnDepartment of Surgical Oncology, First Affiliated Hospital of China Medical University, Shenyang, China.
Huimian XuDepartment of Surgical Oncology, First Affiliated Hospital of China Medical University, Shenyang, China.
First Hospital of China Medical University · CNChina Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastric cancer (GC) metastasis determines the prognosis of patients, and exploring the molecular mechanism of GC metastasis is expected to provide a theoretical basis for clinical treatment. Recent studies have shown that extracellular matrix protein is closely related to GC metastasis. The present study aimed to explore the expression profile and role of COL5A2, as an extracellular matrix protein, in GC.

methodsThe expression, overall survival, and progression-free survival data of COL5 family members were extracted from The Cancer Genome Atlas (TCGA) database, respectively. Weighted gene co-expression network analysis of the GSE62229 database was performed out to identify modules and associated genes.

resultsCOL5A2 was selected as our research target in the TCGA database, and was also verified in the GSE62229 and GSE15459 datasets. COL5A2 was up-regulated in GC tissues by paraffin immunohistochemistry and RT-qPCR. The prognosis of patients with low COL5A2 expression was better than that of patients with high COL5A2 expression. Scratch and migration experiments showed that knockdown of COL5A2 decreased the migration ability of gastric cancer cells compared with the control group. In vivo, mice with tail vein injection COL5A2 knockdown had fewer and smaller metastatic nodules in liver. GSEA results showed that the TCGA and GSE62229 samples were significantly enriched in several well-known cancer-related pathways, such as the TGF-β, MAPK, and JAK2 signaling pathways.

conclusionCOL5A2 was most closely related to advanced GC among COL5 family members. High COL5A2 expression is associated with a poor prognosis, and may be a novel therapeutic target for GC.

Indexed as

AnimalsBiomarkers, TumorCell Line, TumorCell MovementCollagen Type VFemaleHumansJanus Kinase 2MaleMAP Kinase Signaling SystemMiceMiddle AgedNeoplasm MetastasisStomach NeoplasmsSurvival AnalysisTransforming Growth Factor betaBiomarkers, TumorCollagen Type VJAK2 protein, humanJanus Kinase 2Transforming Growth Factor betaadvanced gastric cancer (AGC)COL5A2COL5 familyTCGA and GEO databasesWGCNA

Identifiers

PMID33739392
PMCPMC8039095
OpenAlexW3137928145

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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.