BRAF-activated LncRNA functions as a tumor suppressor in papillary thyroid cancer

被引:83
作者
Liao, Tian [1 ]
Qu, Ning [1 ]
Shi, Rong-Liang [1 ,2 ]
Guo, Kai [1 ]
Ma, Ben [1 ]
Cao, Yi-Ming [1 ]
Xiang, Jun [1 ]
Lu, Zhong-Wu [1 ]
Zhu, Yong-Xue [1 ]
Li, Duan-Shu [1 ]
Ji, Qing-Hai [1 ]
机构
[1] Fudan Univ, Fudan Univ Shanghai Canc Ctr, Shanghai Med Coll, Dept Oncol,Dept Head & Neck Surg, Shanghai 200032, Peoples R China
[2] Fudan Univ, Minhang Hosp, Dept Gen Surg, Shanghai 201199, Peoples R China
基金
中国国家自然科学基金;
关键词
papillary thyroid cancer; BRAF; lncRNA; proliferation; migration; NONCODING RNA; PROLIFERATION; METASTASIS; MECHANISMS; CARCINOMA; BANCR;
D O I
10.18632/oncotarget.10825
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Long non-coding RNAs (lncRNAs) participate in cancer cell tumorigenesis, cell cycle control, migration, proliferation, apoptosis, metastasis and drug resistance. The BRAF-activated non-coding RNA (BANCR) functions as both an oncogene and a tumor suppressor. Here, we investigated BANCR's role in papillary thyroid carcinoma (PTC) by assessing BANCR levels in PTC and matched normal thyroid epithelial tissues from 92 patients using qRT-PCR. We also used lentiviral vectors to establish PTC cell lines to investigate the effects of BANCR overexpression on cancer cell proliferation, apoptosis, migration and invasion. Our results indicate BANCR levels are lower in PTC tumor tissues than control tissues. Decreased BANCR levels correlate with tumor size, the presence of multifocal lesions and advanced PTC stage. BANCR overexpression reduced PTC cell proliferation and promoted apoptosis, which inhibited metastasis. It also inactivated ERK1/2 and p38, and this effect was enhanced by treatment with the MEK inhibitor U0126. Finally, BANCR overexpression dramatically inhibited tumor growth from PTC cells in xenograft mouse models. These results suggest BANCR inhibits tumorigenesis in PTC and that BANCR levels may be used as a novel prognostic marker.
引用
收藏
页码:238 / 247
页数:10
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