Your browser doesn't support javascript.
loading
miR-27b inhibits gastric cancer metastasis by targeting NR2F2
Protein & Cell ; (12): 114-122, 2017.
Artículo en Inglés | WPRIM | ID: wpr-757355
ABSTRACT
Increasing attention is focused on the down-regulation of miRNAs in cancer process. Nuclear receptor subfamily 2 (NR2F2, also known as COUP-TFII) is involved in the development of many types of cancers, but its role in gastric cancer remains elusive. In this experiment, oncomine and Kaplan-meier database revealed that NR2F2 was up-regulated in gastric cancer and that the high NR2F2 expression contributed to poor survival. MicroRNA-27b was targeted and down-regulated by NR2F2 in human gastric cancer tissues and cells. The ectopic expression of miR-27b inhibited gastric cancer cell proliferation and tumor growth in vitro and in vivo. Assays suggested that the overexpression of miR-27b could promote MGC-803 cells' migration and invasion and retard their metastasis to the liver. In addition, down-regulation of miR-27b enhanced GES-1 cells' proliferation and metastasis in vitro. These findings reveal that miR-27b is a tumor suppressor in gastric cancer and a biomarker for improving patients' survival.
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Neoplasias Gástricas / ARN Neoplásico / Biomarcadores de Tumor / Genes Supresores de Tumor / MicroARNs / Línea Celular Tumoral / Factor de Transcripción COUP II / Xenoinjertos / Genética Límite: Animales / Femenino / Humanos / Masculino Idioma: Inglés Revista: Protein & Cell Año: 2017 Tipo del documento: Artículo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Neoplasias Gástricas / ARN Neoplásico / Biomarcadores de Tumor / Genes Supresores de Tumor / MicroARNs / Línea Celular Tumoral / Factor de Transcripción COUP II / Xenoinjertos / Genética Límite: Animales / Femenino / Humanos / Masculino Idioma: Inglés Revista: Protein & Cell Año: 2017 Tipo del documento: Artículo