Circular RNA circ_HIPK3 is down-regulated and suppresses cell proliferation, migration and invasion in osteosarcoma

被引:124
|
作者
Ma Xiao-Long [1 ,2 ]
Zhu Kun-Peng [1 ,2 ]
Zhang Chun-Lin [1 ,2 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 10, Sch Med, Dept Orthopaed Surg, 301 Yan Chang Middle Rd, Shanghai 200072, Peoples R China
[2] Tongji Univ, Sch Med, Inst Bone Tumor, Shanghai 200072, Peoples R China
来源
JOURNAL OF CANCER | 2018年 / 9卷 / 10期
基金
中国国家自然科学基金;
关键词
circRNA; circ_HIPK3; osteosarcoma; biomarker; progression; CANCER; BIOMARKER; EXPRESSION; TUMORIGENESIS; BIOGENESIS; CIRCHIPK3; CIRS-7; MIR-7;
D O I
10.7150/jca.24619
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Circular RNA (circRNA) is associated with human cancers, however, few studies have reported its value in the diagnosis and prognosis prediction of osteosarcoma (OS). In this study, we investigated the expression level of eight selected cancer-related circRNAs including circ-Cdrlas, circ_HIPK3 and circ-ITCH in OS cell lines, tissues and plasmas by quantitative real-time polymerase chain reaction (qRT-PCR) and found that only circ_HIPK3 could stably down-regulate in the OS cell lines, tissues and plasmas than the corresponding controlled. One-way analysis of variance was further conducted to analyze the relationship between circ_HIPK3 expression level and clinic pathological factors of OS patients. Receiver operating characteristic (ROC) curve was built to evaluate the diagnostic values of circ_HIPK3. Circ_HIPK3 expression was significantly correlated with Enneking stage (P=0.042) and lung metastasis (P=0.036). The area under the ROC curve was 0.783 and the sensitivity and specificity were 0.56 and 0.84, respectively. Kaplan-Maier analysis also showed that lower expression of circ_HIPK3 correlated with shorter overall survival time and poor prognosis of OS patients. Besides, function analysis demonstrated that circHIPK3 overexpression significantly suppressed OS cell proliferation, migration and invasion in vitro. Overall, our data suggest that circ_HIPK3 may become a novel potential biomarker for diagnosis and treatment target of OS.
引用
收藏
页码:1856 / 1862
页数:7
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