|
|
Research progress of miR-223 and pregnancy-related diseases |
YAO Yanjiao1 DU Nan1 XIE Yanyan1 LU Dan2 |
1.Graduate School, Dalian Medical University, Liaoning Province, Dalian 116044, China;
2.Department of Obstetrics and Gynecology, Clinical Medical School of Yangzhou University Subei People′s Hospital, Jiangsu Province, Yangzhou 225001, China |
|
|
Abstract MicroRNAs (miRNAs) are a class of endogenous non-coding single-stranded RNA molecules of approximately 21-25 bases that have been found in different species and are involved in a variety of biological processes, such as embryonic development, apoptosis, cell division, hematopoiesis, carcinogenesis and viral infection, etc. MicroRNA 223 (miR-223) is a type of miRNA targeting the q12 chromosome of X chromosome. The study found that miR-223 can affect early embryo transfer by inhibiting the expression of leukemia inhibitory factor, insulin-like growth factor. It is abnormally low expressed in peripheral blood and placenta of preeclampsia, involved in the development of preeclampsia. It is low expressed in cardiomyocytes and overexpression in subcutaneous fat of pregnant women with gestational diabetes, regulating the glucose metabolism in the body through different mechanisms. It is highly expressed in pregnant women with premature rupture of membranes. The biological process of the target gene involved in the negative regulation of immune response and anti-inflammatory response, is considered to be closely related to chorioamnionitis. In addition, miR-223 has high expression in children with Down′s syndrome the amount. This article will summarize the research progress of miR-223 expression level and pathological pregnancy such as embryo implantation, pre-eclampsia and gestational diabetes.
|
|
|
|
|
[1] Lee RC,Feinbaum RL,Ambros V. The C.elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14 [J]. Cell,1993,75(5):843-854.
[2] Wheeler BM,Heimberg AM,Moy VN,et al. The deep evolution of metazoan microRNAs [J]. Evol Dev,2010,11(1):50-68.
[3] Musavi Shenas MH,Eghbal-Fard S,Mehrisofiani V,et al. MicroRNAs and signaling networks involved in epithelial-mesenchymal transition [J]. J Cell Physiol,2019,234(5):5775-5785.
[4] Suh N. MicroRNA controls of cellular senescence [J]. BMB Rep,2018,51(10):493-499.
[5] 朱光辉,刘海军,张学利.MicroRNA在缺氧诱导肿瘤生物学行为改变中的研究进展[J].肿瘤预防与治疗,2017, 30(1):57-61.
[6] Rupal O,Raj N,Kumar PR,et al. Emerging role of circulating microRNA in the diagnosis of human infectious diseases [J]. J Cell Physiol,2018,234(2):1030-1043.
[7] Ta?觙bi F,Meuth ML,Massy ZA,et al. miR-223:An inflammatory oncomiR enters the cardiovascular field [J]. Biochim Biophys Acta,2014,1842(7):1001-1009.
[8] Chen CZ,Li L,Lodish HF,et al. MicroRNAs modulate hem-atopoietic lineage differentiation [J]. Science,2004,303(5654):83-86.
[9] Jia W,Wu Y,Zhang Q,et al. Identification of four serum microRNAs from a genome-wide serum microRNA expression profile as potential non-invasive biomarkers for endometrioid endometrial cancer [J]. Oncol Lett,2013,6(1):261-267.
[10] McGirt LY,Adams CM,Baerenwald DA,et al. miR-223 regulates cell growth and targets proto-oncogenes in mycosis fungoides/cutaneous T-cell lymphoma [J]. J Invest Dermatol,2014,134(4):1101-1107.
[11] 姜芳,许敏.miR-223和HLA-B27在强直性脊柱炎患者外周血中的表达分析[J].中国民康医学,2017(4):61-62.
[12] 苏显都,贺美,邹纯,等.miR-326及miR-223在类风湿关节炎患者中的表达及其临床意义[J].解放军医学院学报,2017(11):1009-1013.
[13] Wang X,Ye L,Hou W,et al. Cellular microRNA expression correlates with susceptibility of monocytes/macro-phages to HIV-1 infection [J]. Blood,2009,113(3):671-674.
[14] Galliano D,Pellicer A. MicroRNA and implantation [J]. Fertil Steril,2014,101(6):1531-1544.
[15] Macklon NS,Stouffer RL,Giudice LC,et al. The science behind 25 years of ovarian stimulation for in vitro fertilization [J]. Endocr Rev,2006,27(2):170-207.
[16] Enders AC,Schlafke S. A morphological analysis of the early implantation stages in the rat [J]. Dev Dyn,1967, 120(2):185-225.
[17] 徐慧颖,李娜,张云山.胚胎植入—子宫内膜容受性是关键[J].生殖医学杂志,2014,23(3):198-202.
[18] Lessey BA. Assessment of endometrial receptivity [J]. Fertil Steril,2011,96(3):522-529.
[19] Paria BC,Reese J,Das SK,et al. Deciphering the cross-talk of implantation:advances and challenges [J]. Science,2002,296(5576):2185-2188.
[20] Hilton DJ. LIF:lots of interesting functions [J]. Trends Biochem Sci,1992,17(2):72-76.
[21] 董熙远.microRNA-223-3p通过抑制LIF的表达和胞饮突的形成调控胚胎植入的机制研究[D].武汉:华中科技大学,2016.
[22] 黄凯.MicroRNA-223调控胚胎着床的机制研究[D].武汉:华中科技大学,2015.
[23] 宋梅,唐卉,张丽,卢丹.miRNA与子痫前期相关性的研究进展[J].中国医刊,2017,52(10):13-16.
[24] Lv Y,Lu C,Ji X,et al. Roles of microRNAs in preeclampsia [J]. J Cell Physiol,2018,234(2):1052-1061.
[25] Yang Q,Lu J,Wang S,et al. Application of next-generation sequencing technology to profile the circulating microRNAs in the serum of preeclampsia versus normal pregnant women [J]. Clin Chim Acta,2011,412(23-24):2167-2173.
[26] Xu P,Zhao Y,Liu M,et al. Variations of microRNAs in human placentas and plasma from preeclamptic pregnancy [J]. Hypertension,2014,63(6):1276-1284.
[27] Choi SY,Yun J,Lee OJ,et al. MicroRNA expression profiles in placenta with severe preeclampsia using a PNA-based microarray [J]. Placenta,2013,34(9):799-804.
[28] Bui FQ,Johnson L,Roberts J,et al. Fusobacterium nucleatum infection of gingival epithelial cells leads to NLRP3 inflammasome-dependent secretion of IL-1β and the danger signals ASC and HMGB1 [J]. Cell Microbiol,2016,18(7):970-981.
[29] Rabadi MM,Kuo MC,Ghaly T,et al. Interaction between uric acid and HMGB1 translocation and release from endothelial cells [J]. Am J Physiol Renal Physiol,2012,302(6):F730-F741.
[30] 吴秀燕,胡继芬.高迁移率族蛋白及其受体在子痫前期中的研究[J].中国妇产科临床杂志,2013,14(3):277-279.
[31] Wu JH,Gao Y,Ren AJ,et al. Altered microRNA expression profiles in retinas with diabetic retinopathy [J]. Ophthalmic Res,2012,47(4):195-201.
[32] Beltrami C,Angelini TG,Emanueli C. Noncoding RNAs in diabetes vascular complications [J]. J Mol Cell Cardiol,2015,89(Pt A):42-50.
[33] Zampetaki A,Kiechl S,Drozdov I,et al. Plasma MicroRNA Profiling Reveals Loss of Endothelial MiR-126 and Other MicroRNAs in Type 2 Diabetes [J]. Circ Res,2010,107(6):810-817.
[34] 徐菁,陈颖.miR-223和miR-155在妊娠糖尿病患者中的表达及诊断意义[J].中国临床医生杂志,2017,45(12):89-90.
[35] Lu H,Buchan RJ,Cook SA. MicroRNA-223 regulates Glut4 expression and cardiomyocyte glucose metabolism [J]. Cardiovasc Res,2010,86(3):410-420.
[36] Chuang TY,Wu HL,Chen CC,et al. MicroRNA-223 Expression Is Upregulated in Insulin Resistant Human Adipose Tissue [J]. J Diabetes Res,2015(2015):943659.
[37] 邱晓媛.HMGB1及其受体在绒毛膜羊膜炎相关早产中的意义[D].天津:天津医科大学,2017.
[38] Montenegro D,Romero R,Pineles BL,et al. Differential expression of microRNAs with progression of gestation and inflammation in the human chorioamniotic membranes [J]. Am J Obstet Gynecol,2007,197(3):289.e1-e6.
[39] 史向荣,马威,姜怡邓.产前筛查与产前诊断的临床应用价值探讨[J].人人健康,2018(4):28.
[40] 林颖,胡平,马定远,等.21-三体综合征胎儿中孕期母体血清microRNA的表达谱[J].临床检验杂志,2012,30(1):41-42. |
|
|
|