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MicroRNA-139-5p inhibits bladder cancer proliferation and self-renewal by targeting the Bmi1 oncogene.
- Source :
-
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine [Tumour Biol] 2017 Jul; Vol. 39 (7), pp. 1010428317718414. - Publication Year :
- 2017
-
Abstract
- MiR-139-5p has been reported to be overexpressed in many types of cancers, but its role in bladder cancer has not been elucidated yet. Here, we report that miR-139-5p functions as a tumor suppressor in bladder cancer and inhibits the cancer stem cell self-renewal by targeting Bmi1 directly. We found that miR-139-5p expression was significantly downregulated in the bladder cancer specimens compared with that in adjacent normal tissues. In vitro, restoration of miR-139-5p expression significantly inhibited the proliferation of bladder cancer cells. Mechanism analysis revealed that miR-139-5p could decrease Bmi1 protein levels by binding to the 3' untranslated region of Bmi1 messenger RNA. Stem cell-related proteins such as c-MYC, NANOG, OCT4, and KLF4 and signaling pathways such as Wnt signaling were suppressed by restoration of miR-139-5p in bladder cancer cells. In addition, miR-139-5p expression also blocked self-renewal of bladder cancer stem cells by inhibiting Bmi1. In summary, our study supports that miR-139-5p acts as a tumor suppressor in bladder cancer development and suppresses cancer stem cell property of bladder cancer. Our study also suggests that miR-139-5p has the potential to be used as a therapeutic molecule for bladder cancer treatment.
- Subjects :
- Apoptosis genetics
Cell Line, Tumor
Cell Movement genetics
Cell Self Renewal genetics
Female
Gene Expression Regulation, Neoplastic
Humans
Kruppel-Like Factor 4
Male
Neoplastic Stem Cells pathology
Polycomb Repressive Complex 1 genetics
Urinary Bladder Neoplasms pathology
Wnt Signaling Pathway genetics
Cell Proliferation genetics
MicroRNAs genetics
Polycomb Repressive Complex 1 biosynthesis
Urinary Bladder Neoplasms genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1423-0380
- Volume :
- 39
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine
- Publication Type :
- Academic Journal
- Accession number :
- 28720065
- Full Text :
- https://doi.org/10.1177/1010428317718414