# Integrated Network Analysis Decipher ZNF384‐Related miR‐20b‐5p and miR‐424‐5p in Colon Adenocarcinoma

## TL;DR

This study identifies miR-20b-5p and miR-424-5p as important regulators in colon cancer through network analysis and machine learning.

## Contribution

The novel contribution is the identification of miR-20b-5p and miR-424-5p as key regulators of DNA repair and cell cycle genes in colon adenocarcinoma.

## Key findings

- miR-20b-5p and miR-424-5p are significantly associated with tumor progression in colon cancer.
- KIF14 and KIF18B are regulated by these miRNAs in DNA repair and cell cycle pathways.
- Expression patterns of miR-20b-5p and miR-424-5p were validated using an external GEO dataset.

## Abstract

ZNF384 is a C2H2‐type zinc finger protein (ZNF) which is implicated in DNA double‐strand break (DSB) repair through the classical non‐homologous end‐joining (cNHEJ) pathway.

To clarify the regulatory mechanisms involving ZNF384 in colon adenocarcinoma (COAD).

First, we conducted a differential expression gene (DEG) analysis of mRNA and lncRNA using TCGA‐COAD RNA‐Seq data. We also identified ZNF384‐related mRNAs through Pearson's correlation coefficient calculation and conducted weighted gene co‐expression network analysis (WGCNA) for these genes, leading to the identification of a cluster of 331 genes with strongly positive correlation to tumor, 84 of which overlapped with DEGs. Gene functional analysis showed enrichment of genes in DNA repair, replication fork, and cell cycle checkpoint signaling pathways. Protein–protein interaction (PPI) network analysis of these 84 genes led to the identification of the top 20 key mRNAs. Then we employed three machine learning methods to refine our selection of candidate genes from these intersecting mRNAs. We constructed a competitive endogenous RNA (ceRNA) network and identified two significant intersecting miRNAs, miR‐20b‐5p and miR‐424‐5p, which have been shown to act as a tumor suppressor gene and an oncogene, respectively. Additionally, we found that KIF14 and KIF18B are regulated by these two miRNAs in this ceRNA network, particularly in DNA damage repair and cell cycle. Finally, validation using an external dataset from the GEO database confirmed their expression patterns.

The current study clarifies the mechanisms of how miR‐20b‐5p and miR‐424‐5p work in colon cancer and underscores their predictive capabilities in colon cancer.