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lncRNA MT1JP Suppresses Biological Activities of Breast Cancer Cells in vitro and in vivo by Regulating the miRNA-214/RUNX3 Axis.
Ouyang, Qianwen; Cui, Yanru; Yang, Shixin; Wei, Wensong; Zhang, Mingyue; Zeng, Jie; Qu, Fei.
Afiliación
  • Ouyang Q; Department of Breast Surgery, The Third Hospital of Nanchang, Jiangxi, China Jiangxi Province Key Laboratory for Breast Diseases, Nanchang, Jiangxi 330009, People's Republic of China.
  • Cui Y; Department of Physiology, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, People's Republic of China.
  • Yang S; Department of Breast Surgery, The Third Hospital of Nanchang, Jiangxi, China Jiangxi Province Key Laboratory for Breast Diseases, Nanchang, Jiangxi 330009, People's Republic of China.
  • Wei W; Department of Breast Surgery, The Third Hospital of Nanchang, Jiangxi, China Jiangxi Province Key Laboratory for Breast Diseases, Nanchang, Jiangxi 330009, People's Republic of China.
  • Zhang M; Department of Pharmacology, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, People's Republic of China.
  • Zeng J; Department of Breast Surgery, The Third Hospital of Nanchang, Jiangxi, China Jiangxi Province Key Laboratory for Breast Diseases, Nanchang, Jiangxi 330009, People's Republic of China.
  • Qu F; Department of Pharmacology, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, People's Republic of China.
Onco Targets Ther ; 13: 5033-5046, 2020.
Article en En | MEDLINE | ID: mdl-32581560
ABSTRACT

INTRODUCTION:

The purpose of our research was to evaluate MT1JP in breast cancer. MATERIAL AND

METHODS:

For clinical purpose, tissues were collected, and a correlation analysis ofMT1JP and miRNA-214 gene expressions was conducted. Using an in vitro study, MDA-MB-231 and MCF-7 cell lines were used as research objects in our research. Colony, flow cytometry, TUNEL, transwell, adhesion and wound healing assay were used to discuss the biological activities of the cells. In an in vivo study, tumor weight and volume were measured, and cell apoptosis was measured by TUNEL assay. The relative mechanism's proteins were evaluated by Western blotting or immunohistochemistry assay.

RESULTS:

Compared with adjacent tissues, MT1JP and miRNA-214 gene expressions were significantly different (P<0.001, respectively). By in vitro and in vivo studies, the biological activities of the cells were significantly decreased in MDA-MB-231 and MCF-7 cell lines with MT1JP overexpression. The relative mechanism was correlated with miRNA-214/RUNX3 axis.

CONCLUSION:

The overexpression of MT1JP suppresses the biological activities of breast cancer cells by regulation miRNA-214/RUNX3 axis in vitro and vivo study.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Onco Targets Ther Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Onco Targets Ther Año: 2020 Tipo del documento: Article
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