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DGUOK-AS1 promotes cervical squamous cell carcinoma progression by suppressing miR-499a-5p that targets SPRR1B in vitro.

Authors :
Song, Yan
Pan, Hongjuan
Yang, Ling
Fan, Yan
Zhang, Hui
Pan, Meichen
Zhang, Yali
Source :
Biochemical & Biophysical Research Communications. Dec2021, Vol. 585, p177-184. 8p.
Publication Year :
2021

Abstract

Cervical squamous cell carcinoma (CESC) is the most common cancer type of cervical cancer, which threatens women's life seriously. LncRNA DGUOK-AS1has been reported to promote the biologic processes of CESC. We aim to figure out the role of DGUOK-AS1-miR-499a-5p-SPRR1B axis in modulating the CESC progression in vitro. The levels of DGUOK-AS1, miR-499a-5p, and SPRR1B in CESC tissues and cells were examined by RT-qPCR. The interaction of DGUOK-AS1-miR-499a-5p-SPRR1B was verified by luciferase assay. Inhibition of DGUOK-AS1, miR-499a-5p, and SPRR1B was applied for exploring the biological function based on detection of cell viability, proliferation, migration, and apoptosis in CESC SiHa and HeLa cells. DGUOK-AS1 and SPRR1B expressions were obviously elevated, whereas the expression of miR-499a-5p was reduced in both CESC tissues and cells. Silencing of DGUOK-AS1 attenuated cell growth and boosted apoptosis of CESC cells. Notably, DGUOK-AS1 inhibited miR-499a-5p to release SPRR1B, which significantly accelerated the development of CESC. DGUOK-AS1sponging miR-499a-5p facilitated CESC cells progression by releasing SPRR1B in vitro. It provides a new sight for the treatment of CESC patients involving DGUOK-AS1-miR-499a-5p-SPRR1B. • DGUOK-AS1/miR-499a-5p/SPRR1B is a potential regulator of CESC. • DGUOK-AS1- promoted cell growth and migration, but inhibited cell apoptosis of CESC cells. • DGUOK-AS1 interacted with miR-499a-5p in CESC cells. • DGUOK-AS1 sponging miR-499a-5p facilitated cell growth and repressed cell apoptosis of CESC cells. • MiR-499a-5p targeted to SPRR1B and inhibited the expression of SPRR1B in CESC cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0006291X
Volume :
585
Database :
Academic Search Index
Journal :
Biochemical & Biophysical Research Communications
Publication Type :
Academic Journal
Accession number :
153783587
Full Text :
https://doi.org/10.1016/j.bbrc.2021.11.003