Serum microRNA-17 functions as a prognostic biomarker in osteosarcoma

被引:25
作者
Li, Shuai [1 ]
Gao, Yong [1 ]
Wang, Yan [2 ]
Wang, Kun [1 ]
Dai, Zhi-Peng [1 ]
Xu, Dong [1 ]
Liu, Wei [1 ]
Li, Zhi-Liang [1 ]
Zhang, Zheng-Dong [1 ]
Yang, Shu-Hua [1 ]
Yang, Cao [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Dept Orthoped, Tongji Med Coll, 1277 Jiefang Rd, Wuhan 430022, Hubei, Peoples R China
[2] China Univ Geosci, Sect Phys Educ, Wuhan 430074, Hubei, Peoples R China
关键词
osteosarcoma; microRNA-17; phosphatase and tensin homolog; serum; biomarkers; prognosis; PROSTATE-CANCER; OSTEOGENIC-SARCOMA; DRUG-RESISTANCE; PTEN EXPRESSION; BREAST-CANCER; TUMOR-GROWTH; METASTASIS; INHIBITOR; CELLS; GENE;
D O I
10.3892/ol.2016.5362
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
MicroRNAs (miRNAs/miRs) are a class of small noncoding RNA molecules that have important roles in regulating the expression of target genes associated with the development and progression of cancer. The majority of miRNAs are expressed in a highly tissue- and region-specific manner, and released into the bloodstream as a consequences of different diseases. Furthermore, altered levels of miRNAs have been observed in several diseases, including cancer. In the present study, reverse transcription-quantitative polymerase chain reaction (RT-qPCR) demonstrated that circulating miR-17 levels were significantly upregulated in patients with osteosarcoma (OS) compared with healthy subjects. RT-qPCR also revealed that high levels of circulating miR-17 expression were inversely correlated with phosphatase and tensin homolog expression, which was identified as a target gene of miR-17 in OS tissues. Furthermore, the overall survival of patients with OS was shorter in those with high miR-17 expression compared with moderate and low expression. Taken together, these findings indicate that miR-17 may function as a useful diagnostic and prognosis biomarker or therapeutic target of OS.
引用
收藏
页码:4905 / 4910
页数:6
相关论文
共 36 条
[1]
Amankwah Ernest K, 2013, Clin Epidemiol, V5, P147, DOI 10.2147/CLEP.S28390
[2]
The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[3]
Long-term results (>25 years) of a randomized, prospective clinical trial evaluating chemotherapy in patients with high-grade, operable osteosarcoma [J].
Bernthal, Nicholas M. ;
Federman, Noah ;
Eilber, Frederick R. ;
Nelson, Scott D. ;
Eckardt, Jeffrey J. ;
Eilber, Fritz C. ;
Tap, William D. .
CANCER, 2012, 118 (23) :5888-5893
[4]
Serum miR-122 as a Biomarker of Necroinflammation in Patients With Chronic Hepatitis C Virus Infection [J].
Bihrer, Verena ;
Friedrich-Rust, Mireen ;
Kronenberger, Bernd ;
Forestier, Nicole ;
Haupenthal, Joerg ;
Shi, Ying ;
Peveling-Oberhag, Jan ;
Radeke, Heinfried H. ;
Sarrazin, Christoph ;
Herrmann, Eva ;
Zeuzem, Stefan ;
Waidmann, Oliver ;
Piiper, Albrecht .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2011, 106 (09) :1663-1669
[5]
MicroRNAs in the control of metastatic bone disease [J].
Browne, Gillian ;
Taipaleenmaeki, Hanna ;
Stein, Gary S. ;
Stein, Janet L. ;
Lian, Jane B. .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2014, 25 (06) :320-327
[6]
On the current management of osteosarcoma. A critical evaluation and a proposal for a modified treatment strategy [J].
Bruland, OS ;
Pihl, A .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (11) :1725-1731
[7]
Changes in circulating microRNA levels associated with prostate cancer [J].
Bryant, R. J. ;
Pawlowski, T. ;
Catto, J. W. F. ;
Marsden, G. ;
Vessella, R. L. ;
Rhees, B. ;
Kuslich, C. ;
Visakorpi, T. ;
Hamdy, F. C. .
BRITISH JOURNAL OF CANCER, 2012, 106 (04) :768-774
[8]
Nasopharyngeal carcinoma: molecular biomarker discovery and progress [J].
Cho, William Chi-shing .
MOLECULAR CANCER, 2007, 6 (1)
[9]
Role of Epigenetic Modulation for the Treatment of Sarcoma [J].
Cote, Gregory M. ;
Choy, Edwin .
CURRENT TREATMENT OPTIONS IN ONCOLOGY, 2013, 14 (03) :454-464
[10]
The multiple roles of PTEN in tumor suppression [J].
Di Cristofano, A ;
Pandolfi, PP .
CELL, 2000, 100 (04) :387-390