The expression and function of long noncoding RNA lncRNA-ATB in papillary thyroid cancer

被引:4
作者
Fu, X. -M. [1 ]
Guo, W. [2 ]
Li, N. [1 ]
Liu, H. -Z. [3 ]
Liu, J. [4 ]
Qiu, S. -Q. [5 ]
Zhang, Q. [6 ]
Wang, L. -C. [7 ]
Li, F. [8 ]
Li, C. -L. [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Geriatr Endocrinol, Beijing, Peoples R China
[2] Fuzhou Gen Hosp Nanjing Mil Command, Dept Endocrinol, Fuzhou, Fujian, Peoples R China
[3] Cent Hosp Handan City, Dept Med Record Management, Handan, Hebei, Peoples R China
[4] Chinese Peoples Liberat Army Gen Hosp, Dept Hematol, Beijing, Peoples R China
[5] Johns Hopkins Univ, Dept Pediat, Div Endocrinol & Metab, Baltimore, MD 21218 USA
[6] Chinese Peoples Liberat Army Gen Hosp, Dept Endocrinol, Beijing, Peoples R China
[7] Air Force Gen Hosp PLA, Dept Endocrinol, Beijing, Peoples R China
[8] Army Gen Hosp PLA, Dept Hlth Care, Beijing, Peoples R China
关键词
Long noncoding RNA; lncRNA-ATB; Papillary thyroid cancer; Proliferation; Migration; INVASION-METASTASIS CASCADE; SERUM THYROGLOBULIN; POOR-PROGNOSIS; TGF-BETA; PROMOTES; CARCINOMA; PROLIFERATION; PROGRESSION; PREDICTS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: This study aimed to investigate the expression and clinical significances of long noncoding RNA-ATB (lncRNA-ATB) in papillary thyroid cancer (PTC), and to explore the roles of lncRNA-ATB in PTC cell proliferation and migration. PATIENTS AND METHODS: The expression of lncRNA-ATB in 64 PTC tissues and paired adjacent noncancerous thyroid tissues was measured. The association between lncRNA-ATB expression and clinicopathological characteristics was analyzed by Pearson X2. The diagnostic value of lncRNA-ATB was evaluated by receiver operating characteristic curve (ROC) analyses. The effects of lncRNA-ATB on PTC cell proliferation were evaluated by Cell Counting Kit-8 assays and Ethynyl deoxyuridine incorporation assays. The effects of lncRNA-ATB on PTC cell migration were evaluated by transwell assays. RESULTS: LncRNA-ATB is upregulated in PTC tissues compared with noncancerous tissues. LncRNA-ATB is also increased in PTC cell lines compared with normal thyroid follicular epithelial cell line. High-expression of lncRNA-ATB is associated with large tumor size and lymph node metastasis. ROC analyses revealed that lncRNA-ATB could sensitively discriminate PTCs from noncancerous tissues, as well as discriminating PTCs with lymph node metastasis from those without lymph node metastasis. Functional experiments showed that depletion of lncRNA-ATB significantly inhibits PTC cell proliferation and migration. CONCLUSIONS: LncRNA-ATB is upregulated and functions as an oncogene in PTC. Furthermore, lncRNA-ATB may serve as a diagnostic biomarker and therapeutic target for PTC.
引用
收藏
页码:3239 / 3246
页数:8
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