Published July 2018 | Version v1
Journal article

MicroRNA-485-5p reduces O-GlcNAcylation of Bmi-1 and inhibits colorectal cancer proliferation

  • 1. Department of Ophthalmology, Jiangxi Children's Hospital, Nanchang, Jiangxi Province 330006 (China)
  • 2. Department of Otorhinolaryngology, Jiangxi Provincial People's Hospital, Nanchang, Jiangxi Province 330006 (China)
  • 3. Department of Ultrasound, Jiangxi Provincial Maternal and Child Health Hospital, Nanchang, Jiangxi Province 330006 (China)
  • 4. Department of Gastrointestinal Surgery, Jiangxi Provincial Cancer Hospital, Nanchang 330029 (China)

Description

Highlights: • Down-regulation of miR-485-5p expression was significantly associated with the poor survival in CRC patients. • Overexpression of miR-485-5p can suppress CRC cells growth of CRC cells in vitro and in vitro study. • OGT is the direct target of miR-485-5p in CRC cells. • miR-485-5p could regulate the stability of Bmi-1 by modulating O-GlcNAcylation, and this would affect the proliferation in CRC cells. Emerging evidences showed that miRNAs are involved in the oncogenesis of many cancers. Here, miRNA microarray analysis was performed to screen the significant miRNAs involved in the progression of colorectal cancer (CRC), miR-485-5p was chosen for further study. We found that the expression of miR-485-5p was significantly lower in CRC specimens and cell lines. In addition, low expression level of miR-485-5p is correlated with tumor progression and poor survival in CRC patients. Based on in vitro and in vivo assays, we found that miR-485-5p significantly inhibits CRC proliferation. Moreover, our results showed that miR-485-5p inhibits cell proliferation by reducing Bmi-1 protein expression, which has been reported to control the proliferation of many cancers. Mechanistically, OGT is a direct target of miR-485-5p, and miR-485-5p could inhibit the O-GlcNAcylation level of Bmi-1 by OGT. Overall, these results suggested that as a tumor suppressor, miR-485-5p may regulate CRC cells proliferation, which could regulate the O-GlcNAcylation and the stability of Bmi-1 through targeting OGT. This may give insight into a novel mechanism and therapy of CRC growth.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.yexcr.2018.04.020

Additional details

Identifiers

DOI
10.1016/j.yexcr.2018.04.020;
PII
S0014482718302301;

Publishing Information

Journal Title
Experimental Cell Research
Journal Volume
368
Journal Issue
1
Journal Page Range
p. 111-118
ISSN
0014-4827
CODEN
ECREAL

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
52123483
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
CELL PROLIFERATION; NEOPLASMS; PLANT GROWTH; PROTEINS
Descriptors DEC
DISEASES; GROWTH; ORGANIC COMPOUNDS

Optional Information

Copyright
Copyright (c) 2018 Elsevier Inc. All rights reserved.