Volume 11 Issue 1
Jan.  2020
Turn off MathJax
Article Contents
Chen-xi YU, Shui SUN. Roles of Long Noncoding RNAs in the Development and Progression of Osteoarthritis[J]. Medical Journal of Peking Union Medical College Hospital, 2020, 11(1): 85-90. doi: 10.3969/j.issn.1674-9081.20170138
Citation: Chen-xi YU, Shui SUN. Roles of Long Noncoding RNAs in the Development and Progression of Osteoarthritis[J]. Medical Journal of Peking Union Medical College Hospital, 2020, 11(1): 85-90. doi: 10.3969/j.issn.1674-9081.20170138

Roles of Long Noncoding RNAs in the Development and Progression of Osteoarthritis

doi: 10.3969/j.issn.1674-9081.20170138
More Information
  • Corresponding author: SUN Shui Tel: 86-531-68776351, E-mail: shunshui1965@foxmail.com
  • Received Date: 2017-07-17
  • Publish Date: 2020-01-30
  • Osteoarthritis (OA), the most common chronic joint disease in the elderly population, is mainly characterized by the degeneration of articular cartilage and its pathogenesis is not fully understood yet. Long non-coding RNAs(lncRNAs)are of a new class of regulatory non-coding RNAs with a length longer than 200 nucleotides. They lack open reading frames and have no potential capacity forprotein translation. Increasing evidence indicates that LncRNAs can be differentially expressed in the normal articular cartilage and OA cartilage. Moreover, some lncRNAs have been shown to be involved in multiple pathological processes of OA, including extracellular matrix degradation, inflammatory responses, apoptosis, angiogenesis, autophagy, the response of chondrocytes to mechanic stress, etc. In this review article, we will focus on the function of lnc-RNAs in the development and progression of OA and the potential new targets that might be used for the diagnosis and treatment of OA.
  • loading
  • [1] Hwang HS, Kim HA. Chondrocyte apoptosis in the pathogenesis of osteoarthritis[J]. Int J Mol Sci, 2015, 16:26035-26054. doi:  10.3390/ijms161125943
    [2] Chen D, Shen J, Zhao W, et al. Osteoarthritis:toward a comprehensive understanding of pathological mechanism[J].Bone Res, 2017, 5:16044. doi:  10.1038/boneres.2016.44
    [3] McAninch D, Roberts CT, Bianco-Miotto T. Mechanistic insight into long noncoding RNAs and the placenta[J]. Int J Mol Sci, 2017, 18:E1371. doi:  10.3390/ijms18071371
    [4] Harries LW. Long non-coding RNAs and human disease[J]. Biochem Soc Trans, 2012, 40:902-906. doi:  10.1042/BST20120020
    [5] Jiang SD, Lu J, Deng ZH, et al. Long noncoding RNAs in osteoarthritis[J]. Joint Bone Spine, 2016, 84:553-556.
    [6] Chen WK, Yu XH, Yang W, et al. lncRNAs:novel players in intervertebral disc degeneration and osteoarthritis[J]. Cell Prolif, 2017, 50. doi: 10.1111/cpr.12313.
    [7] Dykes IM, Emanueli C. Transcriptional and post-transcriptional gene regulation by long non-coding RNA[J]. Genomics Proteomics Bioinformatics, 2017, 15:177-186. doi:  10.1016/j.gpb.2016.12.005
    [8] Liu Q, Zhang X, Dai L, et al. Long noncoding RNA related to cartilage injury promotes chondrocyte extracellular matrix degradation in osteoarthritis[J]. Arthritis Rheumatol, 2014, 66:969-978. https://www.ncbi.nlm.nih.gov/pubmed/24757148
    [9] Fu M, Huang G, Zhang Z, et al. Expression profile of long noncoding RNAs in cartilage from knee osteoarthritis patients[J]. Osteoarthritis Cartilage, 2015, 23:423-432. doi:  10.1016/j.joca.2014.12.001
    [10] Xing D, Liang JQ, Li Y, et al. Identification of long noncoding RNA associated with osteoarthritis in humans[J]. Orthop Surg, 2014, 6:288-293. doi:  10.1111/os.12147
    [11] Zhang C, Wang P, Jiang P, et al. Upregulation of lncRNA HOTAIR contributes to IL-1β-induced MMP overexpression and chondrocytes apoptosis in temporomandibular joint osteoarthritis[J].Gene, 2016, 586:248-253. doi:  10.1016/j.gene.2016.04.016
    [12] Huang Z, Li J, Du S, et al. Effect of UCP4 on the proliferation and apoptosis of chondrocyte:its possible involvement and regulation in osteoarthritis[J]. PLoS One, 2016, 11:e0150684. doi:  10.1371/journal.pone.0150684
    [13] Hwang HS, Kim HA. Chondrocyte apoptosis in the pathogenesis of osteoarthritis[J]. Int J Mol Sci, 2015, 16:26035-26054. doi:  10.3390/ijms161125943
    [14] Li Y, Li S, Luo Y, et al. LncRNA PVT1 regulates chondrocyte apoptosis in osteoarthritis by acting as a sponge for miR-488-3p[J].DNA Cell Biol, 2017, 36:571-580. doi:  10.1089/dna.2017.3678
    [15] Zhang C, Wang P, Jiang P, et al. Upregulation of lncRNA HOTAIR contributes to IL-1β-induced MMP overexpression and chondrocytes apoptosis in temporomandibular joint osteoarthritis[J].Gene, 2016, 586:248-253. doi:  10.1016/j.gene.2016.04.016
    [16] Song J, Ahn C, Chun CH, et al. A long non-coding RNA, GAS5, plays a critical role in the regulation of miR-21 during osteoarthritis[J]. J Orthop Res, 2014, 32:1628-1635. doi:  10.1002/jor.22718
    [17] Zhang G, Wu Y, Xu D, et al. Long Noncoding RNA UFC1 Promotes Proliferation of Chondrocyte in Osteoarthritis by Acting as a Sponge for miR-34a[J]. DNA Cell Biol, 2016, 35:691-695. doi:  10.1089/dna.2016.3397
    [18] Nair A, Kanda V, Bush-Joseph C, et al. Synovial fluid from patients with early osteoarthritis modulates fibroblast-like synoviocyte responses to toll-like receptor 4 and toll-like receptor 2 ligands via soluble CD14[J]. Arthritis Rheum, 2012, 64:2268-2277. doi:  10.1002/art.34495
    [19] Kang Y, Song J, Kim D, et al. PCGEM1 stimulates proliferation of osteoarthritic synoviocytes by acting as a sponge for miR-770[J]. J Orthop Res, 2016, 34:412-418. doi:  10.1002/jor.23046
    [20] Man GS, Mologhianu G. Osteoarthritis pathogenesis- a complex process that involves the entire joint[J].J Med Life, 2014, 7:37-41.
    [21] Wang KC, Yang YW, Liu B, et al.A long noncoding RNA maintains active chromatin to coordinate homeoticgene expression[J]. Nature, 2011, 472:120-124. doi:  10.1038/nature09819
    [22] Kim D, Song J, Han J, et al. Two non-coding RNAs, MicroRNA-101 and HOTTIP contribute cartilage integrity by epigenetic and homeotic regulation of integrin-α1[J]. Cell Signal, 2013, 25:2878-2887. doi:  10.1016/j.cellsig.2013.08.034
    [23] Dudek KA, Lafont JE, Martinez-Sanchez A, etal.Type Ⅱ collagen expression is regulated by tissue-specific miR-675 in human articular chondrocytes[J]. J Biol Chem, 2010, 285:24381-24387. doi:  10.1074/jbc.M110.111328
    [24] Lo Dico A, Costa V, Martelli C, et al. MiR675-5p acts on HIF-1α to sustain hypoxic responses:a new therapeutic strategy for glioma[J].Theranostics, 2016, 6:1105-1118. doi:  10.7150/thno.14700
    [25] Bouaziz W, Sigaux J, Modrowski D, et al. Interaction of HIF1α and β-catenin inhibits matrix metalloproteinase 13 expression and prevents cartilage damage in mice[J]. Proc Natl Acad Sci U S A, 2016, 113:5453-5458. doi:  10.1073/pnas.1514854113
    [26] Steck E, Boeuf S, Gabler J, et al. Regulation of H19 and its encoded microRNA-675 in osteoarthritis and under anabolic and catabolic in vitro conditions[J]. J Mol Med(Berl), 2012, 90:1185-1195. doi:  10.1007%2Fs00109-012-0895-y
    [27] Liu-Bryan R. Inflammation and intracellular metabolism:new targets in OA[J]. Osteoarthritis Cartilage, 2015, 23:1835-1842. doi:  10.1016/j.joca.2014.12.016
    [28] Mathy NW, Chen XM.Long non-coding RNAs (lncRNAs) and their transcriptional control of inflammatory responses[J]. J Biol Chem, 2017, 292:12375-12382. doi:  10.1074/jbc.R116.760884
    [29] Pearson MJ, Philp AM, Heward JA, et al. Long intergenic noncoding RNAs mediate the human chondrocyte inflammatory response and are differentially Eexpressed in osteoarthritis cartilage[J].Arthritis Rheumatol, 2016, 68:845-856. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950001/
    [30] Zhou Y, Zhang X, Klibanski A. MEG3 noncoding RNA:a tumor suppressor[J]. J Mol Endocrinol, 2012, 48:R45-R53. doi:  10.1530/JME-12-0008
    [31] Su W, Xie W, Shang Q, et al. The Long noncoding RNA MEG3 is downregulated and inverselyassociated with VEGF levels in osteoarthritis[J]. Biomed Res Int, 2015, 2015:356893. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4454735/
    [32] Zhu X, Yang S, Lin W, et al. Roles of cell cycle regulators cyclin D1, CDK4, and p53 in knee osteoarthritis[J]. Genet Test Mol Biomarkers, 2016, 20、:529-534. doi:  10.1089/gtmb.2016.0020
    [33] Li YS, Zhang FJ, Zeng C, et al. Autophagy in osteoarthritis[J]. Joint Bone Spine, 2016, 83:143-148. doi:  10.1016/j.jbspin.2015.06.009
    [34] Xu Z, Yan Y, Qian L, et al. Long non-coding RNAs act as regulators of cell autophagy in diseases (Review)[J]. Oncol Rep, 2017, 37:1359-1366. doi:  10.3892/or.2017.5416
    [35] Guilak F. Biomechanical factors in osteoarthritis[J].Best Pract Res Clin Rheumatol, 2011, 25:815-823. doi:  10.1016/j.berh.2011.11.013
    [36] Liu Q, Hu X, Zhang X, et al. The psendogene LncRNA function as a competing endogenous RNA to promote cartilage degradation in human osteoarthritis[J]. Mol Ther, 2016, 24:1726-1733. doi:  10.1038/mt.2016.151
    [37] Dana H, Chalbatani GM, Mahmoodzadeh H, et al. Molecular mechanisms and biological functions of siRNA[J]. Int J Biomed Sci, 2017, 13:48-57.
    [38] Lam JK, Chow MY, Zhang Y, et al. siRNA versus miRNA as therapeutic for gene silencing[J]. Mol Ther Nucleic Acids, 2015, 4:e252. doi:  10.1038/mtna.2015.23
    [39] Barata P, Sood AK, Hong DS. RNA-targeted therapeutics in cancer clinical trials:Current status and future direction[J].Cancer Treat Rev, 2016, 50:35-47. doi:  10.1016/j.ctrv.2016.08.004
    [40] Pastori C, Kapranov P, Penas C, et al. The Bromodomain protein BRD4 controls HOTAIR, a long noncoding RNA essential forglioblastoma proliferation[J]. Proc Natl Acad Sci U S A, 2015, 112:8326-8331. doi:  10.1073/pnas.1424220112
    [41] Zhou T, Kim Y, MacLeod AR.Targeting long noncoding RNA with antisense oligonucleotide technology as cancer therapeutics[J]. Methods Mol Biol, 2016, 1402:199-213.
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Article Metrics

    Article views (369) PDF downloads(221) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return