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

Authors :
Shibamoto, Jun
Arita, Tomohiro
Konishi, Hirotaka
Kataoka, Satoshi
Furuke, Hirotaka
Takaki, Wataru
Kiuchi, Jun
Shimizu, Hiroki
Yamamoto, Yusuke
Komatsu, Shuhei
Shiozaki, Atsushi
Kuriu, Yoshiaki
Otsuji, Eigo
Source :
Genes; Jul2023, Vol. 14 Issue 7, p1414, 18p
Publication Year :
2023

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20734425
Volume :
14
Issue :
7
Database :
Complementary Index
Journal :
Genes
Publication Type :
Academic Journal
Accession number :
169325967
Full Text :
https://doi.org/10.3390/genes14071414