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首页> 外文期刊>Journal of molecular cell biology >Non-coding RNAs in cancers with chromosomal rearrangements: the signatures, causes, functions and implications
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Non-coding RNAs in cancers with chromosomal rearrangements: the signatures, causes, functions and implications

机译:在癌症中的非编码RNA具有染色体重排:签名,原因,功能和含义

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摘要

Chromosomal translocation leads to the juxtaposition of two otherwise separate DNA loci, which could result in gene fusion. These rearrangements at the DNA level are catastrophic events and often have causal roles in tumorigenesis. The oncogenic DNA messages are transferred to RNA molecules, which are in most cases translated into cancerous fusion proteins. Gene expression programs and signaling pathways are altered in these cytogenetically abnormal contexts. Notably, non-coding RNAs have attracted increasing attention and are believed to be tightly associated with chromosome-rearranged cancers. These RNAs not only function as modulators in downstream pathways but also directly affect chromosomal translocation or the associated products. This review summarizes recent research advances on the relationship between non-coding RNAs and chromosomal translocations and on diverse functions of non-coding RNAs in cancers with chromosomal rearrangements.
机译:染色体易位导致两种违背其他DNA基因座的并置,这可能导致基因融合。 DNA水平的这些重排是灾难性的事件,并且肿瘤发生中通常具有因果作用。 致癌DNA消息转移到RNA分子,在大多数情况下转化为癌融合蛋白。 基因表达程序和信号通路在这些细胞异常异常的环境中改变。 值得注意的是,非编码RNA引起了越来越多的关注,并且被认为与染色体重排癌紧密相关。 这些RNA不仅用作下游途径的调节剂,而且直接影响染色体易位或相关产品。 本综述总结了最近关于非编码RNA和染色体易位关系的研究进展以及癌症中非编码RNA在具有染色体重排的癌症之间的不同功能。

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