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首页> 外文期刊>International Journal of Molecular Sciences >From General Aberrant Alternative Splicing in Cancers and Its Therapeutic Application to the Discovery of an Oncogenic DMTF1 Isoform
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From General Aberrant Alternative Splicing in Cancers and Its Therapeutic Application to the Discovery of an Oncogenic DMTF1 Isoform

机译:从癌症中的一般异常替代剪接及其治疗应用到致癌性DMTF1亚型的发现

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摘要

Alternative pre-mRNA splicing is a crucial process that allows the generation of diversified RNA and protein products from a multi-exon gene. In tumor cells, this mechanism can facilitate cancer development and progression through both creating oncogenic isoforms and reducing the expression of normal or controllable protein species. We recently demonstrated that an alternative cyclin D-binding myb-like transcription factor 1 (DMTF1) pre-mRNA splicing isoform, DMTF1β, is increasingly expressed in breast cancer and promotes mammary tumorigenesis in a transgenic mouse model. Aberrant pre-mRNA splicing is a typical event occurring for many cancer-related functional proteins. In this review, we introduce general aberrant pre-mRNA splicing in cancers and discuss its therapeutic application using our recent discovery of the oncogenic DMTF1 isoform as an example. We also summarize new insights in designing novel targeting strategies of cancer therapies based on the understanding of deregulated pre-mRNA splicing mechanisms.
机译:替代性的pre-mRNA剪接是至关重要的过程,它允许从多外显子基因产生多样化的RNA和蛋白质产物。在肿瘤细胞中,这种机制可通过产生致癌同工型并减少正常或可控制蛋白质种类的表达来促进癌症的发展和进展。我们最近证明,替代的细胞周期蛋白D结合myb样转录因子1(DMTF1)前mRNA剪接的同工型DMTF1β在乳腺癌中越来越多地表达,并在转基因小鼠模型中促进了乳腺肿瘤的发生。 mRNA前异常剪接是许多与癌症相关的功能蛋白发生的典型事件。在本文中,我们介绍了癌症中一般的异常mRNA剪接,并以我们最近发现的致癌性DMTF1亚型为例,讨论了其在治疗中的应用。我们还将基于对放松的前mRNA剪接机制的理解,总结在设计新颖的癌症治疗靶向策略方面的新见解。

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