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首页> 外文期刊>Progress in Artificial Intelligence >Separated Siamese Twins: Intronic Small Nucleolar RNAs and Matched Host Genes May be Altered in Conjunction or Separately in Multiple Cancer Types
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Separated Siamese Twins: Intronic Small Nucleolar RNAs and Matched Host Genes May be Altered in Conjunction or Separately in Multiple Cancer Types

机译:分离的暹罗双胞胎:内肠核核仁RNA和匹配的宿主基因可以在多种癌症类型中结合或单独改变

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摘要

Small nucleolar RNAs (snoRNAs) are non-coding RNAs involved in RNA modification and processing. Approximately half of the so far identified snoRNA genes map within the intronic regions of host genes, and their expression, as well as the expression of their host genes, is dependent on transcript splicing and maturation. Growing evidence indicates that mutations and/or deregulations that affect snoRNAs, as well as host genes, play a significant role in oncogenesis. Among the possible factors underlying snoRNA/host gene expression deregulation is copy number alteration (CNA). We analyzed the data available in The Cancer Genome Atlas database, relative to CNA and expression of 295 snoRNA/host gene couples in 10 cancer types, to understand whether the genetic or expression alteration of snoRNAs and their matched host genes would have overlapping trends. Our results show that, counterintuitively, copy number and expression alterations of snoRNAs and matched host genes are not necessarily coupled. In addition, some snoRNA/host genes are mutated and overexpressed recurrently in multiple cancer types. Our findings suggest that the differential contribution to cancer development of both snoRNAs and host genes should always be considered, and that snoRNAs and their host genes may contribute to cancer development in conjunction or independently.
机译:小核仁RNA(Snornas)是非编码RNA,参与RNA改性和加工。到宿主基因的内部内部区域内的大约一半到宿主基因的内部区域,以及它们的表达以及它们的宿主基因的表达,取决于转录剪接和成熟。日益增长的证据表明,影响翼游毒和宿主基因的突变和/或放松剂,在肿瘤发生中发挥着重要作用。潜水员/宿主基因表达的可能因素中,Dereculation是拷贝数改变(CNA)。我们分析了癌症基因组Atlas数据库中可用的数据,相对于10例癌症类型的CNA和表达295个Snorna /宿主基因夫妇,以了解Snornas的遗传或表达改变是否具有重叠的趋势。我们的结果表明,违反直接性,拷贝数和匹配宿主基因的拷贝数和表达改造不一定耦合。此外,在多种癌症类型中均匀地突变和过表达一些Snorna /宿主基因。我们的研究结果表明,应始终考虑对癌症和宿主基因的癌症开发的差异贡献,并且突袭者及其宿主基因可能与癌症开发结合或独立促进癌症发展。

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