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Updated: Jul 15, 2025

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
Biological functions and molecular subtypes regulated by miR-142-3p in colon cancer
Liang Dai1, Weiyan Guo2, Xingwei Xuan2
1General Surgery Department, North China University of Science and Technology Affiliated Hospital, Tangshan City, China.
Abstract:
MicroRNA-142-3p (miR-142-3p) has been reported to be implicated in colon cancer; however, the possible regulatory mechanisms and molecular subtypes regulated by miR-142-3p have not been fully elucidated. This study aimed to investigate the biological functions and regulatory mechanism of miR-142-3p in colon cancer. The expression level of miR-142-3p in colon cancer was analyzed based on the mRNA and miRNA expression datasets of colon cancer retrieved from The Cancer Genome Atlas. Target genes of miR-142-3p were also predicted. Based on these target genes, the functions and subtypes of miR-142-3p were investigated. The metabolic and tumor-related pathways, immune microenvironment, and target gene expression between the 2 subtypes were analyzed. MiR-142-3p was upregulated in tumor tissues, and its high expression indicated a poor prognosis. A total of 39 target genes were predicted, which were significantly involved in autophagy- and metabolism-related functions and pathways. Based on these target genes, the colon cancer samples were clustered into 2 subtypes. There were 35 metabolism-related pathways that were significantly different between the 2 clusters. The immune and stromal scores in cluster 2 were higher than those in cluster 1, whereas the tumor purity of cluster 2 was significantly lower than that of cluster 1. TP53INP2 expression in cluster 2 was higher than that in cluster 1. MiR-142-3p may promote colon cancer progression via autophagy- and metabolism-related pathways. MiR-142-3p may be served as a candidate target for the treatment of colon cancer.
Insights
MicroRNA-142-3p (miR-142-3p) is upregulated in colon cancer, correlating with poor prognosis. This microRNA promotes cancer progression through autophagy and metabolism pathways, suggesting it as a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA-142-3p (miR-142-3p) is linked to colon cancer, but its precise roles and regulated subtypes remain unclear.
- Understanding miR-142-3p's regulatory mechanisms is crucial for advancing colon cancer treatment strategies.
Purpose of the Study:
- To investigate the biological functions and regulatory mechanisms of miR-142-3p in colon cancer.
- To identify molecular subtypes of colon cancer associated with miR-142-3p expression.
Main Methods:
- Analysis of The Cancer Genome Atlas (TCGA) datasets for miR-142-3p and mRNA expression in colon cancer.
- Prediction of miR-142-3p target genes and functional enrichment analysis.
- Clustering of colon cancer samples into subtypes based on target gene expression and analysis of metabolic pathways and immune microenvironment.
Main Results:
- MiR-142-3p was found to be upregulated in colon cancer tissues, with high expression linked to a poor prognosis.
- 39 target genes of miR-142-3p were identified, significantly associated with autophagy and metabolism.
- Colon cancer samples were clustered into two subtypes with distinct metabolic pathway profiles, immune scores, and tumor purity. TP53INP2 expression was higher in cluster 2.
Conclusions:
- MiR-142-3p promotes colon cancer progression by influencing autophagy- and metabolism-related pathways.
- MiR-142-3p represents a potential therapeutic target for colon cancer treatment.
- The study identified distinct molecular subtypes of colon cancer based on miR-142-3p targets, offering insights into personalized medicine approaches.
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