Biomarker significance of plasma and tumor miR-21, miR-221, and miR-106a in osteosarcoma

被引:47
|
作者
Nakka, Manjula [1 ,2 ,3 ,4 ]
Allen-Rhoades, Wendy [1 ,2 ,3 ,4 ,6 ]
Li, Yiting [1 ,2 ,3 ,4 ]
Kelly, Aaron J. [3 ,4 ,5 ]
Shen, Jianhe [1 ,2 ,3 ,4 ]
Taylor, Aaron M. [3 ,4 ,5 ]
Barkauskas, Donald A. [7 ,8 ]
Yustein, Jason T. [1 ,2 ,3 ,4 ,6 ]
Andrulis, Irene L. [9 ,10 ]
Wunder, Jay S. [11 ]
Gorlick, Richard [8 ]
Meltzer, Paul S. [12 ]
Lau, Ching C. [1 ,2 ,3 ,4 ,5 ,6 ]
Man, Tsz-Kwong [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Texas Childrens Hosp, Texas Childrens Canc Ctr, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Texas Childrens Hematol Ctr, Houston, TX 77030 USA
[3] Dept Pediat, Houston, TX 77030 USA
[4] Baylor Coll Med, Houston, TX 77030 USA
[5] Baylor Coll Med, Program Struct & Computat Biol & Mol Biophys, Houston, TX 77030 USA
[6] Baylor Coll Med, Dan L Duncan Canc Ctr, Houston, TX 77030 USA
[7] Univ Southern Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA USA
[8] Childrens Oncol Grp, Monrovia, CA USA
[9] Sinai Hlth Syst, Lunenfeld Tanenbaum Res Inst, Toronto, ON, Canada
[10] Univ Toronto, Dept Mol Genet, Toronto, ON, Canada
[11] Univ Toronto, Dept Surg, Toronto, ON, Canada
[12] NCI, Genet Branch, NIH, Bethesda, MD 20892 USA
关键词
miRNA; osteosarcoma; biomarker; plasma; prognosis; B-CELL LYMPHOMA; BREAST-CANCER CELLS; PROGNOSTIC BIOMARKER; GASTRIC-CANCER; CIRCULATING MICRORNAS; COLORECTAL-CANCER; PROSTATE-CANCER; POOR-PROGNOSIS; ADJUVANT CHEMOTHERAPY; TAMOXIFEN RESISTANCE;
D O I
10.18632/oncotarget.18236
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteosarcoma is the most common malignant bone tumor in children and young adults. Despite the use of surgery and multi-agent chemotherapy, osteosarcoma patients who have a poor response to chemotherapy or develop relapses have a dismal outcome. Identification of biomarkers for active disease may help to monitor tumor burden, detect early relapses, and predict prognosis in these patients. In this study, we examined whether circulating miRNAs can be used as biomarkers in osteosarcoma patients. We performed genome-wide miRNA profiling on a discovery cohort of osteosarcoma and control plasma samples. A total of 56 miRNAs were upregulated and 164 miRNAs were downregulated in osteosarcoma samples when compared to control plasma samples. miR-21, miR-221 and miR-106a were selected for further validation based on their known biological importance. We showed that all three circulating miRNAs were expressed significantly higher in osteosarcoma samples than normal samples in an independent cohort obtained from the Children's Oncology Group. Furthermore, we demonstrated that miR-21 was expressed significantly higher in osteosarcoma tumors compared with normal bone controls. More importantly, lower expressions of miR21 and miR-221, but not miR-106a, significantly correlated with a poor outcome. In conclusion, our results indicate that miR-21, miR-221 and miR-106a were elevated in the circulation of osteosarcoma patients, whereas tumor expressions of miR-21 and miR-221 are prognostically significant. Further investigation of these miRNAs may lead to a better prognostic method and potential miRNA therapeutics for osteosarcoma.
引用
收藏
页码:96738 / 96752
页数:15
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