Evidence map›Paper›PMID 32884288›Full record

ArticleOncoTargets and therapy2020

miR-133b Suppresses Invasion and Migration of Gastric Cancer Cells via the COL1A1/TGF-β Axis.

Yuan Guo, Guochun Lu, Huahui Mao, Shengkun Zhou, Xiangmei Tong, Junfei Wu, Qiang Sun, Hui Xu, Fu Fang

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  6. Deciphering Collagen Phenotype Dynamics Regulators: Insights from In-Silico Analysis.Journal of bioinformatics and systems biology : Open access · 2024
    Article
  7. Article
  8. Article
  9. A prognostic model based on the COL1A1-network in gastric cancer.American journal of translational research · 2023
    Article
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  13. Review
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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 at 1 institution in 1 country.

Yuan GuoDepartment of General Surgery, First People's Hospital of Tonglu, Hangzhou 311500, People's Republic of China.
Guochun LuDepartment of General Surgery, First People's Hospital of Tonglu, Hangzhou 311500, People's Republic of China.
Huahui MaoDepartment of General Surgery, First People's Hospital of Tonglu, Hangzhou 311500, People's Republic of China.
Shengkun ZhouDepartment of General Surgery, First People's Hospital of Tonglu, Hangzhou 311500, People's Republic of China.
Xiangmei TongDepartment of General Surgery, First People's Hospital of Tonglu, Hangzhou 311500, People's Republic of China.
Junfei WuDepartment of General Surgery, First People's Hospital of Tonglu, Hangzhou 311500, People's Republic of China.
Qiang SunDepartment of General Surgery, First People's Hospital of Tonglu, Hangzhou 311500, People's Republic of China.
Hui XuDepartment of General Surgery, First People's Hospital of Tonglu, Hangzhou 311500, People's Republic of China.
Fu FangDepartment of General Surgery, First People's Hospital of Tonglu, Hangzhou 311500, People's Republic of China.ORCID 0000-0001-7139-4711
Hangzhou First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe study aimed to explore the mechanism of miR-133b regulating the invasion and migration of gastric cancer (GC) cells via the COL1A1/TGF-β axis.

methodsThe miRNA expression profiles of GC downloaded from TCGA database were subjected to differential analysis to determine the target miRNA of interest, and the target genes of the miRNA were predicted by bioinformatics. GSEA was used for gene enrichment analysis. qRT-PCR was carried out to detect gene expression in GC cells. The effect of miR-133b on GC cells was examined by CCK-8, wound healing and Transwell assays. Western blot was conducted to assess the protein expression of EMT-related proteins. The binding relationship between genes was verified by dual-luciferase reporter gene assay.

resultsThe expression of miR-133b was markedly downregulated in GC tissue, while that of COL1A1 was upregulated. Overexpression of miR-133b decreased the migration and invasion of GC cells, and the EMT process was inhibited as well, while inverse results were observed when miR-133b was silenced. COL1A1 was a target gene of miR-133b and its overexpression had a significant impact on the prognosis of patients. GSEA pathway enrichment results showed that COL1A1 was markedly enriched in the TGF-β signaling pathway. In addition, COL1A1 overexpression induced the activation of the TGF-β signaling pathway to promote proliferation and migration of GC cells, whereas miR-133b overexpression suppressed the signaling pathway. Thus, overexpression of miR-133b and COL1A1 simultaneously would reverse the inhibitory effect of miR-133b on cell invasion and migration.

conclusionIn this study, miR-133b was found to inhibit the invasion and migration of GC cells via the COL1A1/TGF-β axis, which provides a new research direction for the diagnosis and targeted therapy of GC.

Indexed as

COL1A1gastric cancerinvasion and migrationmiR-133bTGF-β signaling pathway

Identifiers

PMID32884288
PMCPMC7434522
OpenAlexW3048791155

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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.