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pmid:33739392

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

Bioscience reports · 2021 doi:10.1042/BSR20204293

Paper

complete

Experiment

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Data

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Analysis

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pmid:33739392
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title
High expression of COL5A2, a member of COL5 family, indicates the poor survival and facilitates cell migration in gastric cancer.
doi
10.1042/BSR20204293
pmid
33739392
authors array · 7 items
[0]
Yuen Tan
[1]
Qingchuan Chen
[2]
Yao Xing
[3]
Chao Zhang
[4]
Siwei Pan
[5]
Wen An
[6]
Huimian Xu
journal
Bioscience reports
year
2021
abstract
BACKGROUND: Gastric 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. METHODS: The 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. RESULTS: COL5A2 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. CONCLUSION: COL5A2 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.
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High COL5A2 expression indicates a poor prognosis in GC tissues
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Correlation between COL5A2 expression and clinicopathologic features in GC patients
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2 was up-regulated in GC tissues by paraffin immunohistochemistry and RT-qPCR. The prognosis of patients with
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tissues by paraffin immunohistochemistry and RT-qPCR. The prognosis of patients with low COL5A2 e
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cratch and migration experiments showed that knockdown of COL5A2 decreased the migration ability of
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ancer cells compared with the control group. In vivo, mice with tail vein injection COL5A2 knockd
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33739392", "kind": "science-record", "revision": 6, "content_hash": "sha256:1a3a570ffb8c88800ed291f7a98343918410d0b366944a10a047188b7abfd9ee", "created_at": "2026-11-01T15:41:29Z", "updated_at": "2026-11-01T21:24:55Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "High expression of COL5A2, a member of COL5 family, indicates the poor survival and facilitates cell migration in gastric cancer.", "doi": "10.1042/BSR20204293", "pmid": "33739392", "authors": ["Yuen Tan", "Qingchuan Chen", "Yao Xing", "Chao Zhang", "Siwei Pan", "Wen An", "Huimian Xu"], "journal": "Bioscience reports", "year": 2021, "abstract": "BACKGROUND: Gastric 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.\nMETHODS: The 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.\nRESULTS: COL5A2 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.\nCONCLUSION: COL5A2 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.", "claims": [{"id": "claim-method", "statement": "The Kaplan–Meier method was used to calculate OS.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33739392", "locator": "sections[16] \"Statistical analysis\" paragraph 2", "quote": "The Kaplan–Meier method was used to calculate OS."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All data in this article were available, and could find and use in the websites. K-M plotter (http://kmplot.com/), GEPIA (http://gepia.cancer-pku.cn/), and GSE62229 and GSE15459 (https://www.ncbi.nlm.nih.gov/gds).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33739392", "locator": "sections[26] \"Data Availability\" paragraph 2", "quote": "All data in this article were available, and could find and use in the websites. 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