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Authors Chen G, Shi Y, Zhang Y, Sun J
Received 2 September 2017
Accepted for publication 2 November 2017
Published 5 December 2017 Volume 2017:10 Pages 5783—5794
DOI https://doi.org/10.2147/OTT.S150678
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Akshita Wason
Peer reviewer comments 2
Editor who approved publication: Dr Carlos Vigil Gonzales
Abstract: Circular
RNAs (circRNAs) are a novel class of noncoding RNAs that play an important role
in cancer. However, the mechanisms by which circRNAs regulate gene expression
in pancreatic ductal adenocarcinoma (PDAC) remain unclear. This study seeks to elucidate
the role that circRNAs play in the proliferation of PDAC cells. On the basis of
previous studies of circRNA expression profiles in PDAC, we found that the
circRNA_100782 was markedly upregulated in PDAC tissue. Functional experiments
revealed that circRNA_100782 downregulation inhibited BxPC3 cell proliferation
and colony formation. Loss-of-function studies showed that knockdown of
circRNA_100782 inhibited cell proliferation by downregulating the microRNA-124
(miR-124) target genes interleukin-6 receptor (IL6R) and signal transducer and
activator of transcription 3 (STAT3). Overexpression of miR-124 also inhibited
BxPC3 cell proliferation by reducing the expression of IL6R and STAT3, which
was consistent with the result of silencing circRNA_100782. In addition,
luciferase assay revealed that miR-124 was a direct target of circRNA_100782.
Silencing STAT3 inhibited BxPC3 cell proliferation and colony formation. Cell
viability was reduced in BxPC3 cells treated with si-circRNA_100782 and miR-124
mimic, and this effect could be attenuated by activating STAT3. In vivo study
validated that circRNA_100782 knockdown suppressed BxPC3 xenografts in nude
mice. Taken together, these results suggest that circRNA_100782 regulates BxPC3
cell proliferation by acting as miR-124 sponge through the IL6–STAT3 pathway.
Keywords: circular RNA, pancreatic ductal adenocarcinoma, sponge, proliferation,
microRNA, IL6-STAT3 pathway