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MiR-221 Exacerbate Cell Proliferation and Invasion by Targeting TIMP3 in Papillary Thyroid Carcinoma
被引:23
作者:
Diao, Yingbin
[1
]
Fu, Hongyu
[1
]
Wang, Qian
[2
]
机构:
[1] Daqing Oilfield Gen Hosp, Dept Endocrinol, Daqing, Heilongjiang, Peoples R China
[2] Daqing Oilfield Gen Hosp, Dept Rheumatol, Daqing, Heilongjiang, Peoples R China
关键词:
papillary thyroid cancer;
miR-221;
TIMP3;
cell proliferation and invasion;
EXPRESSION AFFECTS;
TUMOR PROGRESSION;
DOWN-REGULATION;
CANCER;
GROWTH;
OVEREXPRESSION;
TUMORIGENICITY;
APOPTOSIS;
MIGRATION;
PTEN;
D O I:
10.1097/MJT.0000000000000420
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
MiR-221 is frequently upregulated in papillary thyroid cancer (PTC) tissues and cell lines, and this study was designed to validate the association of miR-221 with PTC proliferation, apoptosis, and migration. We observed that miR-221 suppressed TIMP3 expression by binding to 39 untranslated region of TIMP3 mRNA, and TIMP3 expression was increased with the presence of miR-221 inhibitors; TIMP3 siRNA could reverse the effects of miR-221 inhibitors on PTC cells. The results indicated that miR-221 exacerbated PTC by downregulating the expression of TIMP3. The effects of miR-221 and TIMP3 in vivo were also confirmed by human PTC-bearing mice models which suggest consistent results with those in vitro studies. In summary, miR-221 could aggravate cell proliferation and invasion of PTC by targeting TIMP3.
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页码:E317 / E328
页数:12
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