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Authors Zheng H, Chen T, Li C, Xu C, Ding C, Chen J, Ju S, Zhang Z, Liang Z, Cui Z, Zhao J
Received 1 October 2018
Accepted for publication 7 November 2018
Published 3 January 2019 Volume 2019:11 Pages 443—454
DOI https://doi.org/10.2147/CMAR.S189338
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Colin Mak
Peer reviewer comments 2
Editor who approved publication: Dr Rituraj Purohit
Purpose: Most
recently, circular RNAs (circRNAs) were considered playing regulatory roles in
tumor initiation and development. The specific function of circRNAs in hepatocellular
carcinoma (HCC) remains unknown. This study was designed to detect specific
roles of a circRNA hsa_circ_0079299 in HCC.
Methods: The
expression of hsa_circ_0079299 in HCC and tumor cell lines was detected using
quantitative PCR (qPCR). Cell proliferation, migration, cell cycle and
apoptosis after overexpression of the circRNA were measured using cell counting
kit-8 (CCK8) assay, colony formation, 5-ethynyl-2′-deoxyuridine (EdU) assay,
wound healing assay, transwell culture system and flow cytometry. Western
blotting assay detected the protein expression of PI3K/AKT/mTOR signaling
pathway and cyclin B1 (CCNB1). Overexpression of the circRNA in vivo was
measured by nude mice tumorigenesis.
Results: The
expression of hsa_circ_0079299 was lower in HCC tissues. Overexpression of
hsa_circ_0079299 suppressed tumor growth in vitro and in vivo, retarded cell
cycle progression while had no effect on cell migration and apoptosis. The
inhibitory effect of hsa_circ_0079299 was partly mediated by PI3K/AKT/mTOR
signaling pathway.
Conclusion: Our study
shows that tumor suppressive role of hsa_circ_0079299 in HCC provides new
recognition of circRNAs in cancers.
Keywords: cell
proliferation, cell cycle, cyclin B1, liver cancer
