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miR-326的功能及其在自身免疫病中作用的研究进展 被引量:1

Research progress on function of miR-326 and its role in autoimmune diseases
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摘要 自身免疫病(AD)是由免疫系统对自身抗原失耐受引起,并进一步诱发组织损伤和炎症的一类疾病。miRNA通过与靶基因3’端非编码区特异性结合阻止蛋白质翻译或引起mRNA降解,从而在转录后水平调控基因表达,参与多种免疫细胞的生长发育和机体的免疫调节,因此miRNA可能成为AD的潜在治疗靶点。miR-326作为miRNA大家族中的研究热点之一,在AD中发挥重要作用,但其在AD中的研究尚存在许多不足之处,积极探索miR-326在AD中的作用对阐明AD的病理过程及开拓AD治疗新策略具有重要意义。 Autoimmune disease(AD)is a type of disease that caused by intolerance of autoantigens and further induces tissue damage and inflammation.miRNA specifically binds to 3’non-coding region of the target gene to prevent protein translation or cause mRNA degradation,thereby regulating gene expression at post-transcriptional level,participating in growth and development of a variety of immune cells and body’s immune regulation functions,so miRNA may become a potential therapeutic target for AD.As one of the research hotspots in miRNA family,miR-326 is considered to play an important role in AD,while has many shortcomings.Actively explore the role of miR-326 in AD to clarify pathological process of AD and open up new strategy of AD treatment is of great significance.
作者 徐璐 王丽华 卢晓宇 王健健 张荟雪(指导) XU Lu;WANG Lihua;LU Xiaoyu;WANG Jianjian;ZHANG Huixue(Department of Neurology,the Second Affiliated Hospital of Harbin Medical University,Harbin 150081,China)
出处 《中国免疫学杂志》 CAS CSCD 北大核心 2022年第19期2420-2424,2429,共6页 Chinese Journal of Immunology
基金 国家自然科学基金青年科学基金项目(81901277)。
关键词 miR-326 自身免疫病 T淋巴细胞 生物标志物 治疗靶点 miR-326 Autoimmune diseases T lymphocytes Biomarkers Therapeutic targets
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  • 1王迎雪,阎胜利.肿瘤坏死因子α基因多态性与甲状腺相关性眼病相关[J].中华内分泌代谢杂志,2006,22(1):57-58. 被引量:7
  • 2郑瑞芝,李蓉,张素华.PTPN22基因多态性与自身免疫性内分泌疾病[J].国际内分泌代谢杂志,2007,27(2):89-91. 被引量:6
  • 3Filipowicz Witold,Bhattacharyya Suvendra N,Sonenberg Nahum.Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight?. Nature Reviews Genetics . 2008
  • 4Manel Esteller.Non-coding RNAs in human disease. Nature Reviews Genetics . 2011
  • 5Wightman B,Ha I,Ruvkun G.Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans. Cell . 1993
  • 6Hang Thi Thu Nguyen,Guillaume Dalmasso,Stefan Müller,Jessica Carrière,Frank Seibold,Arlette Darfeuille–Michaud.Crohn’s Disease–Associated Adherent Invasive Escherichia coli Modulate Levels of microRNAs in Intestinal Epithelial Cells to Reduce Autophagy[J]. Gastroenterology . 2014 (2)
  • 7Rosalind C. Lee,Rhonda L. Feinbaum,Victor Ambros.The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell . 1993
  • 8Kathrin Ludwig,Matteo Fassan,Claudia Mescoli,Marco Pizzi,Mariangela Balistreri,Laura Albertoni,Salvatore Pucciarelli,Marco Scarpa,Giacomo Carlo Sturniolo,Imerio Angriman,Massimo Rugge.PDCD4/miR-21 dysregulation in inflammatory bowel disease-associated carcinogenesis[J].Virchows Archiv.2013(1)
  • 9M. Iborra,F. Bernuzzi,C. Correale,S. Vetrano,G. Fiorino,B. Beltrán,F. Marabita,M. Locati,A. Spinelli,P. Nos,P. Invernizzi,S. Danese.Identification of serum and tissue micro‐ RNA expression profiles in different stages of inflammatory bowel disease[J].Clin Exp Immunol.2013(2)
  • 10Xiuli Liu,John R. Goldblum,Zijin Zhao,Michael Landau,Brandie Heald,Rish Pai,Jingmei Lin.Distinct Clinicohistologic Features of Inflammatory Bowel Disease-associated Colorectal Adenocarcinoma: In Comparison With Sporadic Microsatellite-stable and Lynch Syndrome-related Colorectal Adenocarcinoma[J].The American Journal of Surgical Pathology.2012(8)

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