Hsa_circ_101280 promotes hepatocellular carcinoma by regulating miR-375/JAK2.
Animals
Apoptosis
/ genetics
Carcinogenesis
/ genetics
Carcinoma, Hepatocellular
/ genetics
Cell Line, Tumor
Cell Proliferation
/ genetics
Gene Expression Regulation, Neoplastic
Humans
Janus Kinase 2
/ metabolism
Liver Neoplasms
/ genetics
Mice, Nude
MicroRNAs
/ metabolism
RNA, Circular
/ biosynthesis
Transplantation, Heterologous
JAK2
Hepatocellular carcinoma
hsa_circ_101280
miR-375
Journal
Immunology and cell biology
ISSN: 1440-1711
Titre abrégé: Immunol Cell Biol
Pays: United States
ID NLM: 8706300
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
received:
19
04
2018
revised:
08
10
2018
accepted:
08
10
2018
pubmed:
12
10
2018
medline:
15
1
2020
entrez:
11
10
2018
Statut:
ppublish
Résumé
In this study, we sought to predict the effects of a certain circular RNA (circRNA), hsa_circ_101280 (also known as hsa_circ_0100929 and hsa_circ_SLAIN1), on hepatocellular carcinoma (HCC) cells and to determine the potential mechanism. After screening differentially expressed circRNAs in HCC tissues through Gene Expression Omnibus data analysis, hsa_circ_101280 was found to be highly expressed, and its high expression was verified in HCC cell lines with qRT-PCR along with the low expression of its downstream miRNA miR-375. Colony formation and flow cytometry assays showed that both hsa_circ_101280 silencing and miR-375 overexpression restrained proliferation and promoted apoptosis in HCC cells. JAK2 was identified as a downstream mRNA target of miR-375 by RNA pull-down and dual-luciferase reporter gene assays, its expression in HCC cell lines were positively regulated by hsa_circ_101280 and negatively by miR-375 expression. Furthermore, the silencing of hsa_circ_101280 significantly inhibited the growth of HCC xenografts in nude mice, with the downregulated expression of JAK2. Overall, both the in vitro and in vivo studies revealed that hsa_circ_101280 largely facilitated the tumorigenesis of HCC, characterized by the promoted proliferation and suppressed apoptosis of HCC cells, by sponging miR-375 and upregulating JAK2.
Substances chimiques
MIRN375 microRNA, human
0
MicroRNAs
0
RNA, Circular
0
Janus Kinase 2
EC 2.7.10.2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
218-228Informations de copyright
© 2018 Australasian Society for Immunology Inc.