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.2018.04.020Additional 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.