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Circular RNA Circ-0002570 Accelerates Cancer Progression by Regulating VCAN via MiR-587 in Gastric Cancer.
Yang, Lei; Zhou, Yong-Ning; Zeng, Miao-Miao; Zhou, Nan; Wang, Bin-Sheng; Li, Bo; Zhu, Xiao-Liang; Guan, Quan-Lin; Chai, Chen.
Afiliação
  • Yang L; Department of General Surgery, The First Hospital of Lanzhou University, Lanzhou, China.
  • Zhou YN; Department of Gastroenterology, The First hospital of Lanzhou University, Lanzhou, China.
  • Zeng MM; Department of General Surgery, The First Hospital of Lanzhou University, Lanzhou, China.
  • Zhou N; Department of Oncology, The First Hospital of Lanzhou University, Lanzhou, China.
  • Wang BS; Department of General Surgery, The First Hospital of Lanzhou University, Lanzhou, China.
  • Li B; Department of General Surgery, The First Hospital of Lanzhou University, Lanzhou, China.
  • Zhu XL; Department of General Surgery, The First Hospital of Lanzhou University, Lanzhou, China.
  • Guan QL; Department of Surgical Oncology, The First hospital of Lanzhou University, Lanzhou, China.
  • Chai C; Department of General Surgery, The People's Hospital of Suzhou New District (SND), Suzhou, China.
Front Oncol ; 11: 733745, 2021.
Article em En | MEDLINE | ID: mdl-34692507
ABSTRACT

BACKGROUND:

Circular RNAs (circRNAs) are closely associated with the occurrences and progress of gastric cancer (GC). We aimed to delve into the function and pathological mechanism of Circular RNA-0002570 (circ-0002570) in GC progression.

METHODS:

CircRNAs differentially expressed in GC were screened using bioinformatics technology. The expression of circ-0002570 was detected in GC specimens and cells via qRT-PCR, and the prognostic values of circ-0002570 were determined. The functional roles of circ-0002570 on proliferation, migration, and invasion in GC cells were explored in vitro and in vivo. Interaction of circ-0002570, miR-587, and VCAN was confirmed by dual-luciferase reporter assays, Western blotting, and rescue experiments.

RESULTS:

Circ-0002570 expression was distinctly increased in GC tissues compared to adjacent normal specimens, and GC patients with higher circ-0002570 expressions displayed a short survival. Functionally, knockdown of circ-0002570 resulted in the inhibition of cell proliferation, migration, and invasion, and suppressed tumor growth in vivo. Mechanistically, miR-587 was sponged by circ-0002570. VCAN expression in NSCLC was directly inhibited by miR-587. Overexpression of circ-0002570 prevented VCAN from miR-587-mediated degradation and thus facilitated GC progression.

CONCLUSION:

The circ-0002570-miR-587-VCAN regulatory pathway promoted the progression of GC. Our findings provided potential new targets for the diagnosis and therapy of GC.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article