The miR-218/GAB2 axis regulates proliferation, invasion and EMT via the PI3K/AKT/GSK-3β pathway in prostate cancer.
Adaptor Proteins, Signal Transducing
/ metabolism
Cell Line, Tumor
Cell Movement
/ genetics
Cell Proliferation
/ genetics
Epithelial-Mesenchymal Transition
Gene Expression Regulation, Neoplastic
/ genetics
Glycogen Synthase Kinase 3 beta
/ metabolism
Humans
Male
MicroRNAs
/ genetics
Neoplasm Invasiveness
Phosphatidylinositol 3-Kinases
/ metabolism
Prostatic Neoplasms
/ genetics
Proto-Oncogene Proteins c-akt
/ metabolism
Signal Transduction
Epithelial-mesenchymal transition
GAB2
Metastasis
Proliferation
Prostate cancer
miR-218
Journal
Experimental cell research
ISSN: 1090-2422
Titre abrégé: Exp Cell Res
Pays: United States
ID NLM: 0373226
Informations de publication
Date de publication:
01 09 2020
01 09 2020
Historique:
received:
09
02
2020
revised:
25
05
2020
accepted:
30
05
2020
pubmed:
12
6
2020
medline:
27
1
2021
entrez:
12
6
2020
Statut:
ppublish
Résumé
Altered expression of microRNA (miRNA) is associated with the occurrence and metastasis of various tumors. We previously found that miR-218 inhibits tumor angiogenesis through the RICTOR/VEGFA axis in prostate cancer (PCa). In this study, we determined that miR-218 also had a negative effect on cell growth, migration, and invasion ability in PCa. Our data showed that miR-218 bound to the Grb2-associated binding protein 2 (GAB2) 3'-UTR region and inhibited GAB2 expression. As a novel downstream target of miR-218, GAB2 has been reported to be involved in the occurrence and development of various human tumors, but its role in the progression and metastasis of PCa has not been addressed. We demonstrated for the first time that the expression of GAB2 in the PCa cell lines was increased, while knocking down GAB2 significantly inhibited cell growth, metastatic ability and EMT process in PCa. In addition, the recovery of GAB2 could reverse the changes in the biological function of PCa cells caused by the ectopic expression of miR-218. Mechanistically, miR-218-mediated GAB2 transcriptional suppression significantly inhibited the activity of the PI3K/AKT/GSK-3β pathway, whose abnormal activation was found to be related to the malignant progression of PCa. Taken together, our findings suggest that the miR-218/GAB2 axis may become a novel prognostic indicator and potential therapeutic target in PCa.
Identifiants
pubmed: 32522441
pii: S0014-4827(20)30375-X
doi: 10.1016/j.yexcr.2020.112128
pii:
doi:
Substances chimiques
Adaptor Proteins, Signal Transducing
0
GAB2 protein, human
0
MIRN218 microRNA, human
0
MicroRNAs
0
Glycogen Synthase Kinase 3 beta
EC 2.7.11.1
Proto-Oncogene Proteins c-akt
EC 2.7.11.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
112128Informations de copyright
Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.