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Osteoarthritis Year in Review 2014: genetics and genomics

机译:2014年骨关节炎年度回顾:遗传学和基因组学

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Recent developments in genetics/genomics of osteoarthritis (OA) are discussed to improve our understanding of OA pathophysiology. The discovery of a novel variant near the NCOA3 (nuclear receptor coactivator 3) gene associated with hip OA and the regulation of GDF5 gene by four transcription factors via the OA susceptibility locus rs143383 are among important findings in OA genetics. Several microarray-based gene expression studies were published for different tissues of the joint. In OA synovium elevation of collagens and cross-linking enzymes (COL1A1, COL5A1, PLOD2, LOX and TIMP1) responsive to TGF-beta was found as well as differential expression pattern between different areas of the osteoarthritic synovial membrane. In OA peripheral blood the role of apoptotic genes was highlighted, while whole genome expression profiling in OA subchondral bone and cartilage revealed common genes in cartilage and bone to be involved in OA development. In epigenetics, several microRNAs (miRNAs) were found to regulate genes' expression in chondrocytes, among which miR-125, miR-127b miR-21, miR-148a and their use as potential drug targets was highlighted. Future studies must focus on the integration of genetics, genomics and epigenetics for the identification of signaling pathways and regulatory networks responsible for OA development. (C) 2014 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
机译:讨论了骨关节炎(OA)的遗传学/基因组学的最新进展,以增进我们对OA病理生理学的理解。 OA遗传学中重要的发现之一是在与髋骨OA相关的NCOA3(核受体共激活因子3)基因附近发现了一个新的变体,并通过OA易感基因座rs143383通过四个转录因子调节了GDF5基因。针对关节的不同组织发表了几项基于微阵列的基因表达研究。在OA滑膜中,发现了对TGF-β敏感的胶原蛋白和交联酶(COL1A1,COL5A1,PLOD2,LOX和TIMP1)以及骨关节炎滑膜不同区域之间的差异表达模式。在OA外周血中,凋亡基因的作用得到了强调,而OA软骨下骨和软骨中的全基因组表达谱揭示了软骨和骨中的常见基因与OA的发育有关。在表观遗传学中,发现了几种微小RNA(miRNA)调节软骨细胞中基因的表达,其中突出了miR-125,miR-127b,miR-21,miR-148a及其作为潜在药物靶标的用途。未来的研究必须集中于遗传学,基因组学和表观遗传学的整合,以鉴定负责OA发展的信号传导途径和调控网络。 (C)2014国际骨关节炎研究学会。由Elsevier Ltd.出版。保留所有权利。

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