TY - JOUR T1 - The Role of Inflammation-associated microRNA-4257 as a Promoter of Malignancy in Colorectal Cancer JF - Anticancer Research JO - Anticancer Res SP - 3349 LP - 3360 DO - 10.21873/anticanres.15822 VL - 42 IS - 7 AU - SATOSHI KATAOKA AU - TOMOHIRO ARITA AU - HIROTAKA KONISHI AU - YUSUKE YAMAMOTO AU - RIE SHIBATA AU - TAIGA YAMAMOTO AU - JUN SHIBAMOTO AU - HIROTAKA FURUKE AU - KAZUYA TAKABATAKE AU - WATARU TAKAKI AU - JUN KIUCHI AU - HIROKI SHIMIZU AU - SHUHEI KOMATSU AU - ATSUSHI SHIOZAKI AU - YOSHIAKI KURIU AU - EIGO OTSUJI Y1 - 2022/07/01 UR - http://ar.iiarjournals.org/content/42/7/3349.abstract N2 - Background/Aim: The clinical significance ofmiR-4257 in patients with colorectal cancer (CRC) remains unclear. Here, we investigated the usefulness of measuring miR-4257 levels in the plasma and cancer tissues of patients with CRC, and the function of miR-4257 in CRC cell lines. Materials and Methods: miR-4257 levels were measured in the plasma and cancer tissues of patients with CRC using quantitative polymerase chain reaction. The relationships between miR-4257 level and clinicopathological features were examined. Proliferation, transwell, wound healing, and adhesion assays were performed using a miR-4257 mimic and inflammatory cytokines. Results: Relapse-free survival was significantly lower in patients with high miR-4257 levels in the plasma and cancer tissue (p<0.001 andp=0.016, respectively). High miR-4257 expression was an independent predictive factor for recurrence (p=0.017 and p=0.028). Addition of inflammatory cytokines to CRC and normal cell lines increased the expression of miR-4257 in the cell lines and cell culture medium. Over-expression of miR-4257 in CRC cells increased malignancy, while over-expression in normal cells increased adhesion to CRC cells. The addition of inflammatory cytokines to normal cell lines enhanced adhesion to CRC cell lines. Conclusion: miR-4257 level in plasma and cancer tissues is a biomarker of disease recurrence in patients with CRC. Moreover, miR-4257 promoted tumour growth and was associated with cancer-induced inflammation. ER -