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The significance of DNA methylation profile in metastasis-related genes for the progression of colorectal cancer

机译:DNA甲基化谱在结直肠癌进展中的转移相关基因中的重要性

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摘要

DNA methylation, an epigenetic modification plays a role in the pathogenesis of colorectal cancer (CRC). CRC cases, both sporadic and familial, are often characterized by abnormal pattern of the cytosine methylation in CpG dinucleotides in regulatory regions of genes important for cancer transformation. Also genes mutated in CRC can have their epigenetic pattern altered and we suggest that changes in DNA methylation array can be important for CRC metastatic potential. the main reason of CRC-associated mortality. These genes are: KRAS, genes of the Rho family of GTPases, MACC1, Met, MTA1 and RASS1A. In addition, genes encoding miRNA important for epithelial mesenchymal transition and other metastasis-related effects, such as mir-9, miR-34 and miR-210 can be good candidates for associating their DNA methylation profiles with CRC metastasis. Analysis of DNA methylation profile in various stages of CRC along with other genetic/epigenetic changes specific for all main stages of CRC transformation could help in anti-metastatic therapy immediately after CRC diagnosis. However, targeting DNA methylation pattern in CRC therapy is a conception, which requires further work to precisely change DNA methylation array, without affecting genes, whose expression should not be changed.
机译:DNA甲基化,表观遗传学改性在结肠直肠癌(CRC)的发病机制中起作用。 CRC病例,散发性和家族,既经常是CpG二核苷酸中胞嘧啶甲基化异常模式,在对癌症转化的重要基因的调节区域中的调节区域。此外,CRC中突变的基因也可以改变其表观遗传模式,并且我们表明DNA甲基化阵列的变化对于CRC转移潜力来说是重要的。 CRC相关死亡率的主要原因。这些基因是:Kras,Rho的GTP酶,MacC1,Met,MTA1和Rass1a的基因。此外,编码对上皮间充质转变和其他相关效应的miRNA的基因,例如miR-9,miR-34和miR-210可以是良好的候选者,用于将其DNA甲基化谱与CRC转移相关联。 CRC各个阶段的DNA甲基化曲线与CRC转化的所有主要阶段的其他遗传/表观遗传变化的分析有助于CRC诊断后立即有助于抗转移治疗。然而,靶向CRC疗法中的DNA甲基化模式是概念,其需要进一步的工作来精确地改变DNA甲基化阵列,而不会影响其表达不应改变。

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