Upregulation of 15 Antisense Long Non-Coding RNAs in Osteosarcoma

被引:33
|
作者
Rothzerg, Emel [1 ,2 ]
Ho, Xuan Dung [3 ]
Xu, Jiake [1 ]
Wood, David [1 ]
Maertson, Aare [4 ]
Koks, Sulev [2 ,5 ]
机构
[1] Univ Western Australia, Sch Biomed Sci, Perth, WA 6009, Australia
[2] QEII Med Ctr, Perron Inst Neurol & Translat Sci, Nedlands, WA 6009, Australia
[3] Hue Univ, Coll Med & Pharm, Dept Oncol, Hue 53000, Vietnam
[4] Univ Tartu, Tartu Univ Hosp, Dept Traumatol & Orthopaed, EE-50411 Tartu, Estonia
[5] Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Murdoch, WA 6150, Australia
关键词
osteosarcoma; sarcoma; non-coding RNA; antisense RNA; alternative splicing; SQUAMOUS-CELL CARCINOMA; RUSC1-AS1; PROMOTES; LNCRNA SLC16A1-AS1; PROGNOSTIC MARKER; COCKAYNE-SYNDROME; PASSAGE NUMBER; CANCER CELLS; PROLIFERATION; EXPRESSION; IDENTIFICATION;
D O I
10.3390/genes12081132
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The human genome encodes thousands of natural antisense long noncoding RNAs (lncRNAs); they play the essential role in regulation of gene expression at multiple levels, including replication, transcription and translation. Dysregulation of antisense lncRNAs plays indispensable roles in numerous biological progress, such as tumour progression, metastasis and resistance to therapeutic agents. To date, there have been several studies analysing antisense lncRNAs expression profiles in cancer, but not enough to highlight the complexity of the disease. In this study, we investigated the expression patterns of antisense lncRNAs from osteosarcoma and healthy bone samples (24 tumour-16 bone samples) using RNA sequencing. We identified 15 antisense lncRNAs (RUSC1-AS1, TBX2-AS1, PTOV1-AS1, UBE2D3-AS1, ERCC8-AS1, ZMIZ1-AS1, RNF144A-AS1, RDH10-AS1, TRG-AS1, GSN-AS1, HMGA2-AS1, ZNF528-AS1, OTUD6B-AS1, COX10-AS1 and SLC16A1-AS1) that were upregulated in tumour samples compared to bone sample controls. Further, we performed real-time polymerase chain reaction (RT-qPCR) to validate the expressions of the antisense lncRNAs in 8 different osteosarcoma cell lines (SaOS-2, G-292, HOS, U2-OS, 143B, SJSA-1, MG-63, and MNNG/HOS) compared to hFOB (human osteoblast cell line). These differentially expressed IncRNAs can be considered biomarkers and potential therapeutic targets for osteosarcoma.
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页数:17
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