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Circular RNA 100146 functions as an oncogene through direct binding to miR-361-3p and miR-615-5p in non-small cell lung cancer.
Chen, Lijian; Nan, Aruo; Zhang, Nan; Jia, Yangyang; Li, Xin; Ling, Yihui; Dai, Jiabin; Zhang, Shaozhu; Yang, Qiaoyuan; Yi, Yanni; Jiang, Yiguo.
Afiliación
  • Chen L; State Key Laboratory of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510120, People's Republic of China.
  • Nan A; Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Zhang N; Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Jia Y; Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Li X; Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Ling Y; Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Dai J; Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Zhang S; Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Yang Q; Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Yi Y; Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, People's Republic of China.
  • Jiang Y; Institute for Chemical Carcinogenesis, Guangzhou Medical University, Guangzhou, People's Republic of China.
Mol Cancer ; 18(1): 13, 2019 01 21.
Article en En | MEDLINE | ID: mdl-30665425
ABSTRACT
Circular RNAs are widely expressed in eukaryotic cells and associated with cancer. However, limited studies to date have focused on the potential role of circRNAs in progression of lung cancer. Data from the current investigation showed that circRNA 100146 is highly expressed in non-small cell lung cancer (NSCLC) cell lines and the chemically induced malignant transformed bronchial cell line, 16HBE-T, as well as 40 paired tissue samples of NSCLC. Suppression of circRNA 100146 inhibited the proliferation and invasion of cells and promoted apoptosis. Furthermore, circRNA 100146 could interact with splicing factors and bind miR-361-3p and miR-615-5p to regulate multiple downstream mRNAs. Our collective findings support a role of circRNA 100146 in the development of NSCLC and further demonstrate endogenous competition among circRNA 100146, SF3B3 and miRNAs, providing novel insights into the mechanisms underlying non-small cell lung cancer.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Oncogenes / ARN / Carcinoma de Pulmón de Células no Pequeñas / MicroARNs / Neoplasias Pulmonares Límite: Animals / Humans Idioma: En Revista: Mol Cancer Asunto de la revista: NEOPLASIAS Año: 2019 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Oncogenes / ARN / Carcinoma de Pulmón de Células no Pequeñas / MicroARNs / Neoplasias Pulmonares Límite: Animals / Humans Idioma: En Revista: Mol Cancer Asunto de la revista: NEOPLASIAS Año: 2019 Tipo del documento: Article