DNA甲基转移酶1和GJB2基因多态性与突发性聋易感性研究
Correlation between DNMT1 and GJB2 Gene Polymorphisms and Susceptibility to Sudden Sensorineural Hearing Loss
张岩岩;刘华;宋扬;郭海艳;
1:河北省唐山市工人医院耳鼻喉科
1 Becatti M,Marcucci R,Mannucci A,et al.Erythrocyte membrane fluidity alterations in sudden sensorineural hearing loss patients:the role of oxidative stress[J].Thromb Haemostasis,2017,117:2334.
2 Chen HC,Chung CH,Wang CH,et al.Increased risk of sudden sensorineural hearing loss in patients with hepatitis virus infection[J].PLoS One,2017,12:e0175266.
3 Lee JW,Park YA,Sang MP,et al.Clinical features and prognosis of sudden sensorineural hearing loss secondary to intralabyrinthine hemorrhage[J].J Audiol Otol,2016,20:31.
4 Leo ED,Coppola F,Nettis E,et al.Late recovery with cyclosporine-A of an auto-immunesudden sensorineural hearing loss[J].Acta Otorhinolaryngol Ital,2011,31:399.
5 Turekplewa J,Jagodziński PP.The role of mammalian DNA methyltransferases in the regulation of gene expression[J].Cell Mol Biol Lett,2005,10:631.
6 Hermann A,Goyal R,Jeltsch A.The Dnmt1 DNA-(cytosine-C5)-methyltransferase methylates DNA processively with high preference for hemimethylated target sites[J].J Biol Chem,2004,279:48350.
7 Klein CJ,Botuyan MV,Wu Y,et al.Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss[J].Nat Genet,2011,43:595.
8 Kikuchi T,Kimura RS,Paul DL,et al.Gap junctions in the rat cochlea:immunohistochemical and ultrastructural analysis[J].Anat Embryol,1995,191:101.
9 ?eker Y?ld?z K,Durmu? K,D?nmez G,et al.Studying the association between sudden hearing loss and DNA N-Methyltransferase 1 (DNMT1) genetic polymorphism[J].J Int Adv Otol,2017,13:313.
10 Matos TD,Sim?es-Teixeira H,Caria H,et al.Assessing noncoding sequence variants of,GJB2,for hearing loss association[J].Genetics Research International,2011,24:25.
11 Yin T,Huang F,Ren J,et al.Bilateral sudden hearing loss following habitual abortion:a case report and review of literature[J].Int J Clin Exp Med,2013,6:720.
12 Lin C,Lee K,Yu S,et al.Effect of comorbid diabetes and hypercholesterolemia on the prognosis of idiopathic sudden sensorineural hearing loss[J].Laryngoscope,2016,126:142.
13 Uchida Y,Teranishi M,Nishio N,et al.Endothelin-1 gene polymorphism in sudden sensorineural hearing loss[J].Laryngoscope,2013,123:E59.
14 Cho SH,Chen H,Kim IS,et al.Association of the 4 g/5 g polymorphism of plasminogen activator inhibitor-1 gene with sudden sensorineural hearing loss.A case control study[J].Bmc Ear Nose Throat Disord,2012,12:5.
15 Rhee I,Bachman KE,Park BH,et al.DNMT1 and DNMT3b cooperate to silence genes in human cancer cells[J].Nature,2002,416:552.
16 Kullmann K,Deryal M,Ong MF,et al.DNMT1 genetic polymorphisms affect breast cancer risk in the central;European Caucasian population[J].Clin Epigenetics,2013,5:7.
17 张吉才,余宗涛,吕军,等.肝癌组织中HBV感染与甲基化转移酶表达的关系[J].临床肝胆病杂志,2013,29:620.
18 Demille D,Carlston CM,Tam OH,et al.Three novel GJB2 (connexin 26) variants associated with autosomal dominant syndromic and nonsyndromic hearing loss[J].Am J Med Genet A,2018,176:945.
19 Bakhchane A,Bousfiha A,Charoute H,et al.Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss[J].Eur J Med Genet,2016,59:325.