Expression Signatures of Long Noncoding RNAs in Adolescent Idiopathic Scoliosis.

Purpose. Adolescent idiopathic scoliosis (AIS), the most common pediatric spinal deformity, is considered a complex genetic disease. Causing genes and pathogenesis of AIS are still unclear. This study was designed to identify differentially expressed long noncoding RNAs (lncRNAs) involving the patho...

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Publicado en:BioMed Research International Vol. 2015; pp. 1 - 10
Autores principales: Liu, Xiao-Yang, Wang, Liang, Yu, Bin, Zhuang, Qian-yu, Wang, Yi-Peng
Formato: Journal Article
Publicado: Wiley-Blackwell 9/1/2015
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 9/1/2015
      vid: 2015
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2015/839590
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        atl: Expression Signatures of Long Noncoding RNAs in Adolescent Idiopathic Scoliosis.
      aug:
        au:
          Liu, Xiao-Yang
          Wang, Liang
          Yu, Bin
          Zhuang, Qian-yu
          Wang, Yi-Peng
        affil: Department of Orthopedic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, No. 1 Shuaifuyuan, Wangfujing, Dongcheng District, Beijing 100730, China
      sug:
      ab: Purpose. Adolescent idiopathic scoliosis (AIS), the most common pediatric spinal deformity, is considered a complex genetic disease. Causing genes and pathogenesis of AIS are still unclear. This study was designed to identify differentially expressed long noncoding RNAs (lncRNAs) involving the pathogenesis of AIS. Methods. We first performed comprehensive screening of lncRNA and mRNA in AIS patients and healthy children using Agilent human lncRNA + mRNA Array V3.0 microarray. LncRNAs expression in different AIS patients was further evaluated using quantitative PCR. Results. A total of 139 lncRNAs and 546 mRNAs were differentially expressed between AIS patients and healthy control. GO and Pathway analysis showed that these mRNAs might be involved in bone mineralization, neuromuscular junction, skeletal system morphogenesis, nucleotide and nucleic acid metabolism, and regulation of signal pathway. Four lncRNAs (ENST00000440778.1, ENST00000602322.1, ENST00000414894.1, and TCONS_00028768) were differentially expressed between different patients when grouped according to age, height, classification, severity of scoliosis, and Risser grade. Conclusions. This study demonstrates the abnormal expression of lncRNAs and mRNAs in AIS, and the expression of some lncRNAs was related to clinical features. This study is helpful for further understanding of lncRNAs in pathogenesis, treatment, and prognosis of AIS.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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