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Biological and clinical significance of epigenetic silencing of MARVELD1 gene in lung cancer

机译:MARVELD1 基因表观遗传沉默在肺癌中的生物学和临床意义

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Epigenetic silence in cancer frequently altered signal-transduction pathways during the early stages of tumor development. Recent progress in the field of cancer epigenetics has led to new opportunities for diagnosis and treatment of cancer. We previously demonstrated that novel identified nuclear factor MARVELD1 was widely expressed in human tissues, but down-regulated by promoter methylation in multiple cancers. This study was carried out to determine the biological and clinical significance of MARVELD1 gene silencing in lung cancer. Here, we found the reduced MARVELD1 expression significantly correlated with diagnostic histopathology and malignant degree of lung cancers. DNA hypermethylation and histone deacetylation synergistically inactivated MARVELD1 gene in lung cancer cells. Moreover, MARVELD1 modulated the efficiency of nonsense-mediated mRNA decay (NMD) through interaction with NMD core factor SMG1. The decreased MARVELD1 level in lung cancer reduces NMD efficiency through diminishing the association between NMD complex component UPF1/SMG1 and premature termination codons containing mRNA (PTC-mRNA). The results suggested that MARVELD1 silencing is an appealing diagnostic biomarker for lung cancer and epigenetic silencing of MARVELD1 gene links with the regulatory mechanism of NMD pathway in lung cancer, which may be required for tumorigenesis.
机译:癌症的表观遗传沉默在肿瘤发展的早期阶段经常改变信号传导途径。癌症表观遗传学领域的最新进展为癌症的诊断和治疗带来了新的机遇。我们先前证明,新型鉴定出的核因子MARVELD1在人类组织中广泛表达,但在多种癌症中被启动子甲基化下调。进行这项研究来确定MARVELD1基因沉默在肺癌中的生物学和临床意义。在这里,我们发现降低的MARVELD1表达与肺癌的诊断组织病理学和恶性程度显着相关。 DNA高甲基化和组蛋白去乙酰化协同灭活肺癌细胞中的MARVELD1基因。此外,MARVELD1通过与NMD核心因子SMG1相互作用调节了无义介导的mRNA衰变(NMD)的效率。肺癌中降低的MARVELD1水平通过减少NMD复杂成分UPF1 / SMG1与包含mRNA的过早终止密码子(PTC-mRNA)之间的联系而降低了NMD效率。结果表明,MARVELD1沉默是一种有吸引力的肺癌诊断生物标志物,MARVELD1基因的表观遗传沉默与肺癌中NMD通路的调控机制有关,这可能是肿瘤发生所必需的。

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