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MicroRNA-488-3p inhibits proliferation and induces apoptosis by targeting ZBTB2 in esophageal squamous cell carcinoma.
Yang, Yi; Li, He; He, Zhifeng; Xie, Deyao; Ni, Jiangwei; Lin, Xiaoming.
Afiliación
  • Yang Y; Department of Clinical Skills Center, Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Li H; Department of Otolaryngoloy-Head and Neck Surgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • He Z; Department of Thoracic Surgery, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Xie D; Department of Thoracic Surgery, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Ni J; Department of Thoracic Surgery, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
  • Lin X; Department of Thoracic Surgery, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
J Cell Biochem ; 120(11): 18702-18713, 2019 11.
Article en En | MEDLINE | ID: mdl-31243806
ABSTRACT
Esophageal squamous cell carcinoma (ESCC) is the eighth most prevalent cancer and the sixth leading cause for cancer-associated mortality. MicroRNAs (miRNAs) are increasingly reported to exert important regulatory functions in human cancers by regulating certain gene expression. miR-488-3p has been identified to be a tumor suppressor in multiple cancers, but its role in ESCC is yet to be investigated. The present study aimed to uncover the biological role and modulatory mechanism of miR-488-3p in ESCC. We first revealed the downregulation of miR-488-3p in ESCC tissues and cell lines. Gain-of-function assays confirmed that miR-488-3p overexpression abrogated proliferation and accelerated apoptosis. Mechanistically, we identified via bioinformatics tool and confirmed that zinc finger and BTB domain containing 2 (ZBTB2) was a target for miR-488-3p. Moreover, miR-488-3p activated the p53 pathway through suppressing ZBTB2. Finally, rescue assays proved that ZBTB2 was involved in the regulation of miR-488-3p on proliferation and apoptosis in ESCC. Additionally, we verified that miR-488-3p had alternate targets in ESCC by confirming the involvement of protein kinase, DNA-activated, catalytic subunit (PRKDC), a known target for miR-488-3p, in miR-488-3p-mediated regulation on ESCC. In sum, this study revealed that miR-488-3p inhibited proliferation and induced apoptosis by targeting ZBTB2 and activating p53 pathway in esophageal squamous cell carcinoma, providing a novel biological target for ESCC.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Represoras / Neoplasias Esofágicas / Carcinoma de Células Escamosas / Regulación Neoplásica de la Expresión Génica / Apoptosis / MicroARNs / Proliferación Celular Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Cell Biochem Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Represoras / Neoplasias Esofágicas / Carcinoma de Células Escamosas / Regulación Neoplásica de la Expresión Génica / Apoptosis / MicroARNs / Proliferación Celular Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: J Cell Biochem Año: 2019 Tipo del documento: Article País de afiliación: China