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miR-99a suppresses the metastasis of human non-small cell lung cancer cells by targeting AKT1 signaling pathway.
Yu, Shi-huan; Zhang, Chun-ling; Dong, Fu-shi; Zhang, Yi-mei.
  • Yu SH; Department of Pulmonary Disease, First Affiliated Hospital of Harbin Medical University, Harbin, Helongjiang, 150001, P.R. China.
J Cell Biochem ; 116(2): 268-76, 2015 Feb.
Article en En | MEDLINE | ID: mdl-25187230
ABSTRACT
MicroRNAs (miRNAs) play an important role in the development and progression of non-small cell lung cancer (NSCLC). Recently, several studies have shown that miR-99a is downregulated in various cancers, which can affect tumor initiation and maintenance. Herein, we found that miR-99a was downregulated in NSCLC tissues and suppressed tumor metastasis of NSCLC cells. Down-regulation of miR-99a is significantly associated with last-stage and tumor metastasis in NSCLC patients. Further functional experiments found that overexpression of miR-99a inhibit cell proliferation, migration, and invasion of NSCLC cells in vitro and tumor metastasis of NSCLC in vivo. In addition, we also found that AKT1 is directly involved in miR-99a-mediated tumor suppression. Restored the expression of AKT1 partially abolished the suppressive effects miR-99a on proliferation and invasion of NSCLC cells. Collectively, our data suggest that miR-99a plays an important role in the tumorigenesis and metastasis of NSCLC and may serve as a therapeutic target to avoid dissemination of NSCLC cells.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Carcinoma de Pulmón de Células no Pequeñas / MicroARNs / Proteínas Proto-Oncogénicas c-akt / Neoplasias Pulmonares Límite: Animals / Female / Humans / Male / Middle aged Idioma: En Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Carcinoma de Pulmón de Células no Pequeñas / MicroARNs / Proteínas Proto-Oncogénicas c-akt / Neoplasias Pulmonares Límite: Animals / Female / Humans / Male / Middle aged Idioma: En Año: 2015 Tipo del documento: Article