Gene expression profile analysis of human intervertebral disc degeneration

被引:22
|
作者
Chen, Kai [1 ]
Wu, Dajiang [1 ]
Zhu, Xiaodong [1 ]
Ni, Haijian [1 ]
Wei, Xianzhao [1 ]
Mao, Ningfang [1 ]
Xie, Yang [1 ]
Niu, Yunfei [1 ]
Li, Ming [1 ]
机构
[1] Second Mil Med Univ, Changhai Hosp, Dept Orthoped, Shanghai 200433, Peoples R China
关键词
genes; intervertebral disc degeneration; molecular classification; protein-protein interaction; EXTRACELLULAR-MATRIX; II COLLAGEN; MUTATION; COL1A2; OSTEOARTHRITIS; SUSCEPTIBILITY; PATHOGENESIS; ASPORIN; COL3A1; PAIN;
D O I
10.1590/S1415-47572013000300021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we used microarray analysis to investigate the biogenesis and progression of intervertebral disc degeneration. The gene expression profiles of 37 disc tissue samples obtained from patients with herniated discs and degenerative disc disease collected by the National Cancer Institute Cooperative Tissue Network were analyzed. Differentially expressed genes between more and less degenerated discs were identified by significant analysis of microarray. A total of 555 genes were significantly overexpressed in more degenerated discs with a false discovery rate of < 3%. Functional annotation showed that these genes were significantly associated with membrane-bound vesicles, calcium ion binding and extracellular matrix. Protein-protein interaction analysis showed that these genes, including previously reported genes such as fibronectin, COL2A1 and beta-catenin, may play key roles in disc degeneration. Unsupervised clustering indicated that the widely used morphology-based Thompson grading system was only marginally associated with the molecular classification of intervertebral disc degeneration. These findings indicate that detailed, systematic gene analysis may be a useful way of studying the biology of intervertebral disc degeneration.
引用
收藏
页码:448 / 454
页数:7
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