Roles of miR-4442 in Colorectal Cancer: Predicting Early Recurrence and Regulating Epithelial-Mesenchymal Transition

Genes (Basel). 2023 Jul 8;14(7):1414. doi: 10.3390/genes14071414.

Abstract

Early recurrence in patients with colorectal cancer (CRC) is associated with a poor prognosis. We aimed to identify circulating microRNAs that are biomarkers of early CRC recurrence and elucidate their functions. We identified miR-4442 as a candidate biomarker by microRNA array analysis comparing preoperative and postoperative plasma levels in patients with CRC, with and without recurrence. The association between preoperative plasma miR-4442 levels, clinicopathological features, and recurrence-free survival was analyzed in 108 patients with CRC after curative surgery. Furthermore, cell-function analyses were performed, and the involvement of miR-4442 in regulating epithelial-mesenchymal transition (EMT) was examined. Preoperatively plasma miR-4442 levels were associated with CRC recurrence and exhibited an incremental increase with earlier recurrence dates. Moreover, miR-4442 demonstrated high sensitivity and specificity as a potential biomarker for early CRC recurrence. The expression of miR-4442 in cancer tissues of patients with metastatic liver cancer from CRC was higher than in normal liver, CRC, and normal colorectal tissues. The overexpression of miR-4442 promoted the proliferative, migratory, and invasive activities of CRC cells, decreased levels of RBMS1 and E-cadherin, and increased levels of N-cadherin and Snail1. Plasma miR-4442 is a clinically useful biomarker for predicting the early recurrence of CRC. Furthermore, miR-4442 regulates EMT in CRC by directly targeting the messenger RNA of RBMS1.

Keywords: biomarker; colorectal cancer; epithelial–mesenchymal transition; microRNA; recurrence.

MeSH terms

  • Circulating MicroRNA*
  • Colorectal Neoplasms* / pathology
  • DNA-Binding Proteins / metabolism
  • Epithelial-Mesenchymal Transition / genetics
  • Humans
  • MicroRNAs* / genetics
  • Neoplasm Recurrence, Local / genetics
  • RNA-Binding Proteins

Substances

  • Circulating MicroRNA
  • DNA-Binding Proteins
  • MicroRNAs
  • RBMS1 protein, human
  • RNA-Binding Proteins
  • MIRN4442 microRNA, human

Grants and funding

This research received no external funding.