首页 > 期刊 > 自然科学与工程技术 > 医药卫生科技 > 肿瘤学 > 中国肺癌 > Application of GLAD-PCR Assay for Study on DNA Methylation in Regulatory Regions of Some Tumor-Suppressor Genes in Lung Cancer 【正文】

Application of GLAD-PCR Assay for Study on DNA Methylation in Regulatory Regions of Some Tumor-Suppressor Genes in Lung Cancer

N.A.Smetannikova; A.A.Evdokimov; N.A.Netesova; M.A.Abdurashitov; A.G.Akishev; E.V.Dubinin; P.I.Pozdnyakov; I.V.Vihlyanov; M.K.Nikitin; E.B.Topolnitsky; A.B.Karpov; S.A.Kolomiets; S.Kh.Degtyarev State; Research; Center; of; Virology; and; Biotechnology; Koltsovo; Russia; EpiGene; LLC; Novosibirsk; Russia; Altai; RegionalOncology; Center; Barnaul; Russia; Tomsk; Regional; Clinical; Hospital; Tomsk; Russia; Seversk; Biophysical; Research; Centre; Seversk; Russia; Regional; Clinical; Oncology; Center; Kemerovo; Russia
  • lung
  • neoplasms
  • dna
  • methylation
  • diagnostics

摘要:Hypermethylation of the gene regulatory regions are common for many cancer diseases. In this work we applied GLAD-PCR assay for identificating of the aberrantly methylated RCGY sites in the regulatory regions of some downregulated genes in tissue samples of lung cancer(LC). This list includes EFEMP1, EPHA5, HOXA5, HOXA9, LHX1, MYF6, NID2, OTX1, PAX9, RARB, RASSF1 A, RXRG, SIX6, SKOR1 and TERT genes. The results of DNA samples from 40 cancer and 25 normal lung tissues showed a good diagnostic potential of selected RCGY sites in regulatory regions of MYF6, SIX6, RXRG, LHX1, RASSF1 A and TERT genes with relatively high sensitivity(80.0 %) and specificity(88.0 %) of LC detection in tumor DNA.

注:因版权方要求,不能公开全文,如需全文,请咨询杂志社

投稿咨询 文秘咨询

中国肺癌

  • 预计1-3个月 预计审稿周期
  • 3.17 影响因子
  • 医学 快捷分类
  • 月刊 出版周期

主管单位:中国科学技术协会;主办单位:中国抗癌协会;中国防痨协会;天津医科大学总医院

我们提供的服务

服务流程: 确定期刊 支付定金 完成服务 支付尾款 在线咨询