Copyright (c) 2023 Wenbo Yang, Yuyou Chen
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
The undersigned hereby assign all rights, included but not limited to copyright, for this manuscript to CMB Association upon its submission for consideration to publication on Cellular and Molecular Biology. The rights assigned include, but are not limited to, the sole and exclusive rights to license, sell, subsequently assign, derive, distribute, display and reproduce this manuscript, in whole or in part, in any format, electronic or otherwise, including those in existence at the time this agreement was signed. The authors hereby warrant that they have not granted or assigned, and shall not grant or assign, the aforementioned rights to any other person, firm, organization, or other entity. All rights are automatically restored to authors if this manuscript is not accepted for publication.LncRNA TEX41 promotes the proliferation and migration of squamous cell carcinoma cells by upregulating Atg5 via sponging miR-153-3p
Corresponding Author(s) : Wenbo Yang
Cellular and Molecular Biology,
Vol. 69 No. 14: Cancer molecular biology: Diagnosis and treatment
Abstract
This study was conducted to investigate if lncRNA TEX41 could have effects on SCC. The aim was to confirm that TEX41 could promote SCC progression by up-regulating Atg5 via miR-153-3p. TEX41, miR-153-3p, and Atg5 mRNA expression were examined by qRT-PCR. Western blot was used to examine Atg5 protein expression. CCK-8 assay and transwell assay were used to examine SCC cell proliferation and migration. Dual-luciferase reporter assay was used to forecast the binding site of miR-153-3p with Atg5 or TEX41. TEX41 expression was enhanced in SCC tissues and cells. TEX41 knockdown could reduce the SCC cell proliferation and migration. There was a binding site between TEX41 and miR-153-3p, and TEX41 negatively adjusted miR-153-3p in SCC cells. Atg5 was bonded with miR-153-3p, which was adjusted by TEX41. Our study revealed that TEX41 expression was increased in SCC cell lines and tissues. TEX41 could aggravate SCC progression through adjusting the miR-153-3p/Atg5 axis, providing a key target for SCC.
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