Publication: Circular RNA circFADS2 inhibits the progression of cutaneous squamous cell carcinoma by regulating miR-766-3p/HOXA9 axis
Authors
Zhang, Zhang ; Sun, Huijun ; Hou, Junzhi ; Lili Li, Lili Li ; Wu, Lijuan
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Publisher
Universidad de Murcia, Departamento de Biologia Celular e Histiologia
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DOI
https://doi.org/10.14670/HH-18-409
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info:eu-repo/semantics/article
Description
Abstract
Background. Mounting evidence indicates
that circular RNAs (circRNAs) play vital roles in human
diseases, especially in cancers. However, the biological
functions and underlying mechanism of circRNA fatty
acid desaturase 2 (circFADS2) in cutaneous squamous
cell carcinoma (CSCC) have not been reported.
Methods. The expression levels of circFADS2,
microRNA-766-3p (miR-766-3p) and homeobox A9
(HOXA9) were determined by quantitative real-time
PCR (qRT-PCR). Flow cytometry analysis was used to
determine cell cycle distribution. Cell proliferation was
evaluated by Cell Counting Kit-8 (CCK-8) and colony
formation assays. Wound healing and transwell assays
were used to assess cell migration and invasion abilities.
Glycolysis was examined via the measurement of
extracellular acidification rate (ECAR). All protein
levels were detected by western blot assay. The
interaction between miR-766-3p and circFADS2 or
HOXA9 was predicted by bioinformatics software and
confirmed by dual-luciferase reporter, RNA pull-down,
and RNA Immunoprecipitation (RIP) assays. The mouse
xenograft model was established to investigate the role
of circFADS2 in vivo.
Results. CircFADS2 was downregulated in CSCC
tissues and cells. CircFADS2 overexpression inhibited
CSCC cell proliferation, metastasis and glycolysis.
Moreover, miR-766-3p was able to directly bind to
circFADS2, and circFADS2 played an anti-cancer role in
CSCC by downregulating miR-766-3p. In addition,
HOXA9 was a direct target of miR-766-3p, and miR766-3p inhibition suppressed CSCC cell proliferation,
metastasis and glycolysis by upregulating HOXA9.
Furthermore, circFADS2 acted as a sponge of miR-766-
3p to regulate HOXA9 expression. Besides, circFADS2
suppressed tumor growth in vivo.
Conclusion. CircFADS2 suppressed CSCC
progression by regulating miR-766-3p/HOXA9 axis,
which might provide a promising therapeutic target for
CSCC
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Citation
Histology and Histopathology Vol. 37, nº4 (2022)
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