Literature DB >> 20131229

Comparative analysis of gene expression profiles between primary knee osteoarthritis and an osteoarthritis endemic to Northwestern China, Kashin-Beck disease.

Chen Duan1, Xiong Guo, Xiao-Dong Zhang, Han-Jie Yu, Hua Yan, Ying Gao, Wei-Juan Ma, Zong-Qiang Gao, Peng Xu, Mikko Lammi.   

Abstract

OBJECTIVE: To investigate the differences in gene expression profiles of adult articular cartilage from patients with Kashin-Beck disease (KBD) versus those with primary knee osteoarthritis (OA).
METHODS: The messenger RNA expression profiles of articular cartilage from patients with KBD, diagnosed according to the clinical criteria for KBD in China, were compared with those of cartilage from patients with OA, diagnosed according to the Western Ontario and McMaster Universities OA Index. Total RNA was isolated separately from 4 pairs of the KBD and OA cartilage samples, and the expression profiles were evaluated by Agilent 4x44k Whole Human Genome density oligonucleotide microarray analysis. The microarray data for selected transcripts were confirmed by quantitative real-time reverse transcription-polymerase chain reaction (RT-PCR) amplification.
RESULTS: For 1.2 x 10(4) transcripts, corresponding to 58.4% of the expressed transcripts, 2-fold changes in differential expression were revealed. Expression levels higher in KBD than in OA samples were observed in a mean + or - SD 6,439 + or - 1,041 (14.6 + or - 2.4%) of the transcripts, and expression levels were lower in KBD than in OA samples in 6,147 + or - 1,222 (14.2 + or - 2.8%) of the transcripts. After application of the selection criteria, 1.85% of the differentially expressed genes (P < 0.001 between groups) were detected. These included 233 genes, of which 195 (0.4%) were expressed at higher levels and 38 (0.08%) were expressed at lower levels in KBD than in OA cartilage. Comparisons of the quantitative RT-PCR data supported the validity of our microarray data.
CONCLUSION: Differences between KBD and OA cartilage exhibited a similar pattern among all 4 of the pairs examined, indicating the presence of disease mechanisms, mainly chondrocyte matrix metabolism, cartilage degeneration, and apoptosis induction pathways, which contribute to cartilage destruction in KBD.

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Year:  2010        PMID: 20131229     DOI: 10.1002/art.27282

Source DB:  PubMed          Journal:  Arthritis Rheum        ISSN: 0004-3591


  34 in total

1.  Serum levels of TNF-α, IL-1β, COMP, and CTX-II in patients with Kashin-Beck disease in Sichuan, China.

Authors:  Xin Tang; Zongke Zhou; Bin Shen; Jing Yang; Pengde Kang; Jian Li; Nicolas Crook; Qi Li; Li Min; Fuxing Pei
Journal:  Rheumatol Int       Date:  2011-11-09       Impact factor: 2.631

2.  A preliminary analysis of microRNA profiles in the subchondral bone between Kashin-Beck disease and primary knee osteoarthritis.

Authors:  Guang-Hui Zhao; Lei Yang; Mikko J Lammi; Xiong Guo
Journal:  Clin Rheumatol       Date:  2019-05-06       Impact factor: 2.980

3.  Exome sequencing identified FGF12 as a novel candidate gene for Kashin-Beck disease.

Authors:  Feng Zhang; Lanlan Dai; Weimin Lin; Wenyu Wang; Xuanzhu Liu; Jianguo Zhang; Tielin Yang; Xiaogang Liu; Hui Shen; Xiangding Chen; Lijun Tan; Qing Tian; Hong-Wen Deng; Xun Xu; Xiong Guo
Journal:  Funct Integr Genomics       Date:  2015-08-20       Impact factor: 3.410

4.  Genome-wide copy number variation study and gene expression analysis identify ABI3BP as a susceptibility gene for Kashin-Beck disease.

Authors:  Feng Zhang; Xiong Guo; Yinping Zhang; Yan Wen; Weizhuo Wang; Sen Wang; Tielin Yang; Hui Shen; Xiangding Chen; Qing Tian; Lijun Tan; Hong-Wen Deng
Journal:  Hum Genet       Date:  2014-01-21       Impact factor: 4.132

5.  Association of TNF-α and Fas gene promoter polymorphism with the risk of Kashin-Beck disease in Northwest Chinese population.

Authors:  Quan-ming Zhao; Xiong Guo; Jiang-hua Lai; Wu-hong Tan; Wei-zhuo Wang; Xiao-qian Dang
Journal:  Clin Rheumatol       Date:  2012-03-20       Impact factor: 2.980

6.  Integrative analysis of genome-wide association studies and gene expression profiles identified candidate genes for osteoporosis in Kashin-Beck disease patients.

Authors:  Y Wen; X Guo; J Hao; X Xiao; W Wang; C Wu; S Wang; T Yang; H Shen; X Chen; L Tan; Q Tian; H-W Deng; F Zhang
Journal:  Osteoporos Int       Date:  2015-10-13       Impact factor: 4.507

7.  Comparative analysis of signaling pathways in peripheral blood from patients with Kashin-Beck disease and osteoarthritis.

Authors:  Yujie Ning; Xi Wang; Sen Wang; Xiong Guo
Journal:  Exp Ther Med       Date:  2016-11-07       Impact factor: 2.447

Review 8.  Role of inflammation in the process of clinical Kashin-Beck disease: latest findings and interpretations.

Authors:  Jing Han; Weizhuo Wang; Chengjuan Qu; Ruiyu Liu; Wenrong Li; Zongqiang Gao; Xiong Guo
Journal:  Inflamm Res       Date:  2015-08-11       Impact factor: 4.575

Review 9.  Human genome-wide expression analysis reorients the study of inflammatory mediators and biomechanics in osteoarthritis.

Authors:  J D Sandy; D D Chan; R L Trevino; M A Wimmer; A Plaas
Journal:  Osteoarthritis Cartilage       Date:  2015-11       Impact factor: 6.576

10.  T-2 Toxin Induces Epiphyseal Plate Lesions via Decreased SECISBP2-Mediated Selenoprotein Expression in DA Rats, Exacerbated by Selenium Deficiency.

Authors:  Jian Sun; Zixin Min; Wenxiang Zhao; Safdar Hussain; Yitong Zhao; Dongxian Guo; Fujun Zhang; Yuanxu Guo; Mengyao Sun; Huang Huang; Yan Han; Nannan Zhong; Peng Xu; Shemin Lu
Journal:  Cartilage       Date:  2018-12-29       Impact factor: 4.634

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