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circAGTPBP1 promotes the progression of papillary thyroid cancer through the notch pathway via the miR-34a-5p/notch1 axis.
Dai, Lei; Zhang, Weidong; Wang, Yinchun; Yu, Kejie; Le, Qi; Wu, Xianjiang.
Afiliação
  • Dai L; Department of Thyroid Surgery, Ningbo No.2 Hospital,No. 41 Xibei Street, Ningbo City 315000, Zhejiang Province, China.
  • Zhang W; Department of Thyroid Surgery, Ningbo No.2 Hospital,No. 41 Xibei Street, Ningbo City 315000, Zhejiang Province, China.
  • Wang Y; Department of Thyroid Surgery, Ningbo No.2 Hospital,No. 41 Xibei Street, Ningbo City 315000, Zhejiang Province, China.
  • Yu K; Department of Thyroid Surgery, Ningbo No.2 Hospital,No. 41 Xibei Street, Ningbo City 315000, Zhejiang Province, China.
  • Le Q; Department of Thyroid Surgery, Ningbo No.2 Hospital,No. 41 Xibei Street, Ningbo City 315000, Zhejiang Province, China.
  • Wu X; Department of Thyroid Surgery, Ningbo No.2 Hospital,No. 41 Xibei Street, Ningbo City 315000, Zhejiang Province, China.
iScience ; 26(9): 107564, 2023 Sep 15.
Article em En | MEDLINE | ID: mdl-37622004
ABSTRACT
The dysregulation of circular RNAs (circRNAs) has been implicated in the development and progression of papillary thyroid cancer (PTC). In this study, we analyzed the dysregulated circRNA profile using PTC tissues and matched adjacent normal tissues by RNA-seq. We conducted in vitro and in vivo experiments to investigate the biological functions of circAGTPBP1 in PTC progression. We found that circAGTPBP1 was upregulated in PTC tissues and cell lines, and its expression was positively correlated with tumor size, lymph node metastasis, and clinical stage. Using RNA-seq and bioinformatic analysis, we identified miR-34a-5p and NOTCH1 as downstream targets of circAGTPBP1. Functionally, circAGTPBP1 knockdown significantly inhibited the migration, invasion, and metastasis of PTC cell lines in vitro, while the miR-34a-5p inhibitor reversed these effects. Additionally, circAGTPBP1 knockdown inhibited tumor growth in vivo. Our findings suggest that circAGTPBP1 may act as a tumor promoter and could be a potential therapeutic target for PTC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article