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miR-340 and ZEB1 negative feedback loop regulates TGF-ß- mediated breast cancer progression.
Hou, Li-Kun; Yu, Yue; Xie, Ye-Gong; Wang, Jie; Mao, Jie-Fei; Zhang, Bin; Wang, Xin; Cao, Xu-Chen.
Afiliación
  • Hou LK; The First Department of Breast Cancer, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin 300060, China.
  • Yu Y; Key Laboratory of Cancer Prevention and Therapy, Tianjin 300060, China.
  • Xie YG; Key Laboratory of Breast Cancer Prevention and Therapy, Tianjin Medical University, Ministry of Education, Tianjin 300060, China.
  • Wang J; The First Department of Breast Cancer, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin 300060, China.
  • Mao JF; Key Laboratory of Cancer Prevention and Therapy, Tianjin 300060, China.
  • Zhang B; Key Laboratory of Breast Cancer Prevention and Therapy, Tianjin Medical University, Ministry of Education, Tianjin 300060, China.
  • Wang X; The First Department of Breast Cancer, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin 300060, China.
  • Cao XC; Key Laboratory of Cancer Prevention and Therapy, Tianjin 300060, China.
Oncotarget ; 7(18): 26016-26, 2016 May 03.
Article en En | MEDLINE | ID: mdl-27036021
ABSTRACT
MicroRNAs act as key regulators in carcinogenesis and progression in various cancers. In present study, we explored the role of miR-340 in the breast cancer progression. Our results showed that overexpression of miR-340 inhibits breast cancer cell proliferation and invasion, whereas depletion of miR-340 promotes breast cancer progression. Molecularly, ZEB1 was identified as a target gene of miR-340 and miR-340 suppressed the expression of ZEB1 by directly binding to the 3'-UTR of ZEB1. Furthermore, ZEB1 transcriptionally suppresses miR-340 expression. The negative feedback loop regulated TGF-ß-mediated breast cancer progression. In conclusion, our data suggested that miR-340 acted as a tumor suppressor in breast cancer progression.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Biomarcadores de Tumor / Regulación Neoplásica de la Expresión Génica / Factor de Crecimiento Transformador beta / Retroalimentación Fisiológica / MicroARNs / Homeobox 1 de Unión a la E-Box con Dedos de Zinc Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: Oncotarget Año: 2016 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Biomarcadores de Tumor / Regulación Neoplásica de la Expresión Génica / Factor de Crecimiento Transformador beta / Retroalimentación Fisiológica / MicroARNs / Homeobox 1 de Unión a la E-Box con Dedos de Zinc Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: Oncotarget Año: 2016 Tipo del documento: Article País de afiliación: China
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