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LncRNA PCAT6 mediates UBFD1 expression via sponging miR-545-3p in breast cancer cells.

Authors :
Wu JD
Xu L
Chen W
Zhou Y
Zheng G
Gu W
Source :
Non-coding RNA research [Noncoding RNA Res] 2024 Feb 08; Vol. 9 (2), pp. 421-428. Date of Electronic Publication: 2024 Feb 08 (Print Publication: 2024).
Publication Year :
2024

Abstract

Background: LncRNA PCAT6 has been shown to involve in carcinogenesis of different tumors. In this study, we investigated underline mechanism by which PCAT6 promoted breast cancer cell progression.<br />Methods: RIP was used to identify lncRNAs associated with IMP1. Bioinformatics assays were used to predict potential miRNAs that interact with PCAT6 and mRNAs that are targeted by miR-545-3p. RNA-seq and RT-qPCR were used to analyze differential expression of lncRNAs and miRNA-targeted genes. Luciferase reporter and RNA pull-down assays were performed to identify the molecular interactions between PCAT6 and individual miRNAs. The role of PCAT6-mediated cell proliferation and invasion were tested by CCK-8 and transwell assays following loss-of-function and gain-of-function effects.<br />Results: We identified that PCAT6 is one of the lncRNAs that associated with IMP1. PCAT6 not only binds to IMP1, but also acts as a ceRNA to interact with multiple miRNAs, including miR-545-3p. Binding of IMP1 destabilized PCAT6, while competitive interaction with miR-545-3p allowed PCAT6 to positively regulate UBFD1 expression. Silencing UBFD1 mRNA could effectively rescue PCAT6-induced cell proliferation and invasive abilities.<br />Conclusions: Our study provided evidence that PCAT6 activates UBFD1 expression via sponging miR-545-3p to increase carcinogenesis of breast cancer cells. Based on the nature of UBFD1 as a polyubiquitin binding protein, our study suggested that ubiquitin pathway might contribute to breast cancer progression.<br />Competing Interests: The authors declare that they have no competing interests.<br /> (© 2024 The Authors.)

Details

Language :
English
ISSN :
2468-0540
Volume :
9
Issue :
2
Database :
MEDLINE
Journal :
Non-coding RNA research
Publication Type :
Academic Journal
Accession number :
38511057
Full Text :
https://doi.org/10.1016/j.ncrna.2024.01.019