Evidence map›Paper›PMID 35666636›Full record

ArticleJournal of clinical laboratory analysis2022

miR-548d-3p inhibits the invasion and migration of gastric cancer cells by targeting GKN1.

Senlong Yu, Hongjie Meng, Shengguang Shi, Shenghui Cao, Tianhua Bian, Haifeng Zhao

Abstract read
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Article in Journal of clinical laboratory analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Senlong YuDepartment of Gastrointestinal Surgery, Zhuji People's Hospital of Zhejiang Province, Zhuji Affiliated Hospital of Shaoxing University, Zhuji, China.
Hongjie MengDepartment of Gastrointestinal Surgery, Zhuji People's Hospital of Zhejiang Province, Zhuji Affiliated Hospital of Shaoxing University, Zhuji, China.
Shengguang ShiDepartment of Gastrointestinal Surgery, Zhuji People's Hospital of Zhejiang Province, Zhuji Affiliated Hospital of Shaoxing University, Zhuji, China.
Shenghui CaoDepartment of General Surgery, Zhuji Chinese Traditional Medicine Hospital, Zhuji, China.
Tianhua BianDepartment of General Surgery, Zhuji Chinese Traditional Medicine Hospital, Zhuji, China.
Haifeng ZhaoDepartment of General Surgery, Zhuji Chinese Traditional Medicine Hospital, Zhuji, China.ORCID https://orcid.org/0000-0003-3221-0355

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of this study was to explore the function and mechanism of GKN1 in gastric cancer (GC) progression.

methodsFirstly, we used GEO2R to perform differential gene analysis on GSE26942 and GSE79973 and constructed the protein-protein interaction network of differential genes by STRING. Next, the cytoHubba, Mcode plugins, and GEPIA were used to obtain our follow-up research object GKN1. Then, the function of GKN1 in GC was verified by scratch and transwell assay in GC cells. We further analyzed the genes related to GKN1 through LinkedOmics, and exported top 100 genes positively or negatively correlated with GKN1. Meanwhile, Metascape was performed on these genes. Finally, we analyzed the miRNAs that bind to GKN1 through the miRDB and verified the correlation between miR-548d-3p and GKN1 using dual-fluorescence and quantitative PCR experiments.

resultsBioinformatics analysis showed that there were 52 differential genes on GSE26942 and GSE79973. In addition, the results of functional assays indicated that overexpressed GKN1 can inhibit GC cell migration and invasion, while GKN1 knockdown demonstrated the opposite effect. Additionally, Metascape analysis results showed that the 3'-UTR region of mRNA is rich in AU sequences, based on which we infer that mRNA may be regulated by miRNA. Dual-fluorescence and quantitative PCR assays clarified that miR-548d-3p may be one of the target miRNAs of GKN1, which was up-regulated in GC tissues.

conclusionsIn summary, we clarified that miR-548d-3p regulates GKN1 to participate in GC cell migration and invasion, and provides a possible target for the prognostic diagnosis and treatment of GC.

Indexed as

MicroRNAsPeptide HormonesStomach Neoplasms3' Untranslated RegionsCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansRNA, Messenger3' Untranslated RegionsGKN1 protein, humanMicroRNAsMIRN548 microRNA, humanPeptide HormonesRNA, Messengergastric cancerGKN1invasionmigrationmiR-548d-3p

Identifiers

PMID35666636
PMCPMC9279950

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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.