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CircMAST1 inhibits cervical cancer progression by hindering the N4-acetylcytidine modification of YAP mRNA

Authors :
Chunyu Zhang
Li Yuan
Qiaojian Zou
Caixia Shao
Yan Jia
Jiaying Li
Yan Liao
Xueyuan Zhao
Weijia Wen
Xu Jing
Guofen Yang
Wei Wang
Hongye Jiang
Shuzhong Yao
Source :
Cellular & Molecular Biology Letters, Vol 29, Iss 1, Pp 1-20 (2024)
Publication Year :
2024
Publisher :
BMC, 2024.

Abstract

Abstract Background Cervical cancer (CCa) is the fourth most common cancer among females, with high incidence and mortality rates. Circular RNAs (circRNAs) are key regulators of various biological processes in cancer. However, the biological role of circRNAs in cervical cancer (CCa) remains largely unknown. This study aimed to elucidate the role of circMAST1 in CCa. Methods CircRNAs related to CCa progression were identified via a circRNA microarray. The relationship between circMAST1 levels and clinicopathological features of CCa was evaluated using the clinical specimens and data of 131 patients with CCa. In vivo and in vitro experiments, including xenograft animal models, cell proliferation assay, transwell assay, RNA pull-down assay, whole-transcriptome sequencing, RIP assay, and RNA-FISH, were performed to investigate the effects of circMAST1 on the malignant behavior of CCa. Results CircMAST1 was significantly downregulated in CCa tissues, and low expression of CircMAST1 was correlated with a poor prognosis. Moreover, our results demonstrated that circMAST1 inhibited tumor growth and lymph node metastasis of CCa. Mechanistically, circMAST1 competitively sequestered N-acetyltransferase 10 (NAT10) and hindered Yes-associated protein (YAP) mRNA ac4C modification to promote its degradation and inhibit tumor progression in CCa. Conclusions CircMAST1 plays a major suppressive role in the tumor growth and metastasis of CCa. In particular, circMAST1 can serve as a potential biomarker and novel target for CCa.

Details

Language :
English
ISSN :
16891392
Volume :
29
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Cellular & Molecular Biology Letters
Publication Type :
Academic Journal
Accession number :
edsdoj.04635db9ed2462a8ec0ee2941e3de75
Document Type :
article
Full Text :
https://doi.org/10.1186/s11658-024-00540-6