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METTL9 derived circular RNA circ-METTL9 sponges miR-551b-5p to accelerate colorectal cancer progression by upregulating CDK6.
Li, Ming; Zhi, Zheng; Jiang, Xuan; Duan, Guo-Cai; Zhu, Wei-Na; Pang, Zheng; Wang, Lian; Ge, Rui; Dai, Xin; Liu, Jia-Meng; Chen, Ting-Yue; Jia, Jin-Jing; Li, Jian-Ming; Sun, Li-Na.
Afiliação
  • Li M; Department of Pathology and Pathophysiology, Suzhou Medical College, Soochow University, Suzhou 215123, People's Republic of China.
  • Zhi Z; Department of Pathology, Suzhou Municipal Hospital affiliated to Nanjing Medical University, Suzhou 215008, People's Republic of China.
  • Jiang X; Department of Pathology and Pathophysiology, Suzhou Medical College, Soochow University, Suzhou 215123, People's Republic of China.
  • Duan GC; Department of Pathology, Suzhou Municipal Hospital affiliated to Nanjing Medical University, Suzhou 215008, People's Republic of China.
  • Zhu WN; Department of Pathology and Pathophysiology, Suzhou Medical College, Soochow University, Suzhou 215123, People's Republic of China.
  • Pang Z; Department of Pathology and Pathophysiology, Suzhou Medical College, Soochow University, Suzhou 215123, People's Republic of China.
  • Wang L; Central Laboratory, Nanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine, Nanjing 210022, People's Republic of China.
  • Ge R; Department of Pathology and Pathophysiology, Suzhou Medical College, Soochow University, Suzhou 215123, People's Republic of China.
  • Dai X; Department of Pathology and Pathophysiology, Suzhou Medical College, Soochow University, Suzhou 215123, People's Republic of China.
  • Liu JM; Department of Pathology and Pathophysiology, Suzhou Medical College, Soochow University, Suzhou 215123, People's Republic of China.
  • Chen TY; Department of Pathology, Suzhou Science and Technology Town Hospital, Suzhou 215163, People's Republic of China.
  • Jia JJ; Department of Pathology, Suzhou Municipal Hospital affiliated to Nanjing Medical University, Suzhou 215008, People's Republic of China.
  • Li JM; Department of Pathology, Suzhou Municipal Hospital affiliated to Nanjing Medical University, Suzhou 215008, People's Republic of China.
  • Sun LN; Department of Pathology and Pathophysiology, Suzhou Medical College, Soochow University, Suzhou 215123, People's Republic of China.
Carcinogenesis ; 44(6): 463-475, 2023 08 18.
Article em En | MEDLINE | ID: mdl-37158456
ABSTRACT
Circular RNAs (circRNAs) have been accepted to play key roles in the development and progression of mutiple cancers including colorectal cancer (CRC). Here, we identified circ-METTL9, derived from 2 to 4 exons of METTL9 gene, may promote CRC progression by accelerating cell cycle progression. However, the role and mechanism of circ-METTL9 in CRC remains unclear. Based on our data, the expression of circ-METTL9 was significantly upregulated in CRC tissues and markedly increased in advanced tumors in CRC patients. Functional experiments demonstrated that circ-METTL9 overexpression promoted CRC cells proliferation and migration in vitro, and simultaneously enhanced CRC tumor growth and metastasis in vivo. Mechanistically, RNA immunoprecipitation (RIP) assays proved that circ-METTL9 might be a miRNA sponge, and RNA pulldown assays showed the interaction between circ-METTL9 and miR-551b-5p. Notably, cyclin-dependent kinase 6 (CDK6), a key regulator in cell cycle, is a conserved downstream target of miR-551b-5p. Taken together, our findings highlight a novel oncogenic function of circ-METTL9 in CRC progression via circ-METTL9/miR-551b-5p/CDK6 axis, which may serve as a prognostic biomarker and therapeutic target for CRC patients.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / MicroRNAs Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / MicroRNAs Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article