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MiR-1260b promotes the migration and invasion in non-small cell lung cancer via targeting PTPRK.
Xu, Limin; Xu, Xuting; Huang, Huilian; Ma, Zhihong; Zhang, Shuangmei; Niu, Pingping; Chen, Yingrong; Ping, Jinliang; Lu, Ping; Yu, Caihua; Min, Lishan; Chen, Jing; Dai, Licheng; Dong, Shunli.
Afiliação
  • Xu L; Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Xu X; Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Huang H; Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Ma Z; Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Zhang S; Respiratory Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Niu P; Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Chen Y; Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Ping J; Department of Pathology, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Lu P; Department of Pathology, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Yu C; Department of Thoracic Surgery, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Min L; Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Chen J; Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.
  • Dai L; Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China. Electronic address: dlc171@hzhospital.com.
  • Dong S; Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China. Electronic address: dongshunli@hzhospital.com.
Pathol Res Pract ; 214(5): 776-783, 2018 May.
Article em En | MEDLINE | ID: mdl-29628123
OBJECTIVE: Non-small cell lung cancer (NSCLC) accounts for 80-85% of lung cancer cases which cause most of cancer-related deaths globally. As our previous study discovered miR-1260b can be regarded as a specific signature for metastasis in NSCLC patients. However, the molecular mechanisms of miR-1260b underlying NSCLC progression and metastasis remain dismal. METHODS: The expression of miR-1260b in NSCLC tissues and cell lines were examined by real-time PCR, the effects of miR-1260b on cell migration, invasion and proliferation were evaluated in vitro. Furthermore, luciferase reporter assay was performed to identify the targets of miR-1260b, and the association between miR-1260b and its target gene was determined by real-time PCR and western blot assay. RESULTS: The results showed that miR-1260b was significantly upregulated in NSCLC cell lines. The inhibition of miR-1260b expression decreased the migratory and invasive rates in A549 cells while miR-1260b overexpression had the opposite effect. Furthermore, PTPRK was identified as a direct target of miR-1260b, and PTPRK expression was inversely correlated with miR-1260b in NSCLC cell lines and clinical tissues. CONCLUSIONS: These results suggested that miR-1260b may play an important role in NSCLC metastasis progression and could serve as a putative target for diagnosis and treatment of NSCLC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação Neoplásica da Expressão Gênica / Carcinoma Pulmonar de Células não Pequenas / MicroRNAs / Proteínas Tirosina Fosfatases Classe 2 Semelhantes a Receptores / Neoplasias Pulmonares Limite: Humans Idioma: En Revista: Pathol Res Pract Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação Neoplásica da Expressão Gênica / Carcinoma Pulmonar de Células não Pequenas / MicroRNAs / Proteínas Tirosina Fosfatases Classe 2 Semelhantes a Receptores / Neoplasias Pulmonares Limite: Humans Idioma: En Revista: Pathol Res Pract Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China