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miR-29b inhibits non-small cell lung cancer progression by targeting STRN4
被引:20
作者:
Xie, Yuping
[1
]
Zhao, Fen
[1
]
Zhang, Ping
[1
]
Duan, Ping
[1
]
Shen, Yangmei
[1
,2
]
机构:
[1] Chengdu City First People's Hosp, Dept Oncology, Chengdu, Peoples R China
[2] w China Second Univ Hosp, Sichuan Univ, Dept Pathology, Chengdu, Peoples R China
来源:
关键词:
miR-29b;
STRN4;
Non-small cell lung cancer;
Progression;
Overexpression;
CALMODULIN-BINDING PROTEIN;
STRIATIN;
FAMILY;
EXPRESSION;
MICRORNAS;
APOPTOSIS;
MIGRATION;
INVASION;
STRIPAK;
KINASE;
D O I:
10.1007/s13577-019-00305-w
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Non-small cell lung cancer (NSCLC) is a malignant tumor with a high fatality, low overall cure, and survival rates worldwide. When only palliative therapy is available, the disease leads to malignant proliferation. Previous studies showed miR-29b serves as an NSCLC suppressor by inhibiting cells proliferation, migration, and invasion. However, the mechanism underlying NSCLC progression remains elusive. In this study, we identified Striatin 4 (STRN4), a target of miR-29b, which serves as a pro-oncogenic protein by promoting cells proliferation, migration, and invasion in NSCLC. Besides, the STRN4 was highly expressed in NSCLC and negatively regulated by miR-29b. Down-regulation of STRN4 inhibits NSCLC cells proliferation, migration, invasion, and promotes apoptosis in vitro, whereas overexpression-induced enhanced cell migration and invasion could be reverved by miR-29b. Notably, overexpression of miR-29b and down-regulation of STRN4 by shRNA suppressed cellular proliferation and delayed tumor progression in vivo. Together, these findings identify a miR-29b/STRN4 regulatory pathway in NSCLC progression, which may provide a new sight for the treatment of NSCLC.
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页码:220 / 231
页数:12
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