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pmid:35468097

MicroRNA-181a-5p prevents the progression of esophageal squamous cell carcinoma in vivo and in vitro via the MEK1-mediated ERK-MMP signaling pathway.

Mingbo Wang · Chao Huang · Wenda Gao · Yonggang Zhu · Fan Zhang · Zhenhua Li · Ziqiang Tian

Aging · 2022 doi:10.18632/aging.204028

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:35468097
kind
science-record
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2026-11-01T18:14:20Z
updated_at
2026-11-01T22:48:56Z
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paper object · 10 fields
state
complete
title
MicroRNA-181a-5p prevents the progression of esophageal squamous cell carcinoma in vivo and in vitro via the MEK1-mediated ERK-MMP signaling pathway.
doi
10.18632/aging.204028
pmid
35468097
authors array · 7 items
[0]
Mingbo Wang
[1]
Chao Huang
[2]
Wenda Gao
[3]
Yonggang Zhu
[4]
Fan Zhang
[5]
Zhenhua Li
[6]
Ziqiang Tian
journal
Aging
year
2022
abstract
MicroRNAs (miRNAs) have been revealed to play a crucial role in oncogenesis of esophageal squamous cell carcinoma (ESCC). However, the biological role of miR-181a-5p in ESCC is currently less explored. The current study was designed to assess whether miR-181a-5p affects ESCC progression and further investigate relevant underlying mechanisms. Based on the data of GSE161533, GSE17351, GSE75241 and GSE67269 downloaded from GEO database, MAP2K1 (MEK1) was revealed to be one overlapping gene of the top 300 DGEs. Additionally, using the predicting software, miR-181a-5p was projected as the presumed target miRNA. Immunohistochemical staining and RT-qPCR research revealed that miR-181a-5p expression was decreased in human tumor tissues relative to surrounding peri-cancerous tissues. In an in vivo experiment, miR-181a-5p mimics could inhibit tumor growth and metastasis of ESCC. Gene expression profiles in combination with gene ontology (GO) and KEGG pathway analysis revealed that MAP2K1 (MEK1) gene and ERK-MMP pathway were implicated in ESCC progression. MiR-181a-5p mimics inhibited the activity of p-ERK1/2, MMP2 and MMP9 in vivo, as shown by Western blotting and immunohistochemistry labeling. There were no variations in the expression of p-P38 and p-JNK proteins. Additionally, miR-181a-5p mimics lowered p-ERK1/2, MMP2 and MMP9 levels in ECA109 cells, which were restored by MEK1-OE lentivirus. MEK1-OE Lentivirus significantly reversed the function induced by miR-181a-5p mimics in ECA109 cells. Moreover, further investigation indicated that the capability of migration, invasion and proliferation was repressed by miR-181a-5p mimics in ECA109 cells. In short, repressed ERK-MMP pathway mediated by miR-181a-5p can inhibit cell migration, invasion and proliferation by targeting MAP2K1 (MEK1) in ESCC.
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GSEA was used for pathway enrichment analysis to study the association of target genes. Fisher’s exact test was used to screen the significant pathways.
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sections[24] "Availability of data and materials" paragraph 2
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The data used to support the findings of this study are available from the corresponding author upon request.
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Repressed ERK-MMP pathway mediated by miR-181a-5p can inhibit cell migration, invasion and proliferation by targeting MAP2K1 (MEK1) in ESCC.
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In short, repressed ERK-MMP pathway mediated by miR-181a-5p can inhibit cell migration, invasion and proliferation by targeting MAP2K1 (MEK1) in ESCC.
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Repressed ERK-MMP pathway mediated by miR-181a-5p can inhibit cell migration, invasion and proliferation by targeting MAP2K1 (MEK1) in ESCC.
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MiRNA expression arrays from esophageal squamous cell carcinomas (ESCCs) and normal esophageal epithelia (Nes)
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Expression data from esophageal squamous cell carcinoma patients
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Homo sapiens
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Expression data from esophageal squamous cell carcinoma (ESCC)
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Expression data from esophageal squamous cell carcinomas and normal esophageal epithelia
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ession of esophageal squamous cell carcinoma in vivo and in vitro via the MEK1-mediated ERK-MMP s
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[2]
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was projected as the presumed target miRNA. Immunohistochemical staining and RT-qPCR research revealed that
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Complete file
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