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Genetic and epigenetic biomarkers for diagnosis, prognosis and treatment of colorectal cancer

机译:用于大肠癌诊断,预后和治疗的遗传和表观生物标志物

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Colorectal cancer (CRC) is one of the most common cancer worldwide and results from the accumulation of mutations and epimutations in colonic mucosa cells ultimately leading to cell proliferation and metastasis. Unfortunately, CRC prognosis is still poor and the search of novel diagnostic and prognostic biomarkers is highly desired to prevent CRC-related deaths. The present article aims to summarize the most recent findings concerning the use of either genetic or epigenetic (mainly related to DNA methylation) biomarkers for CRC diagnosis, prognosis, and response to treatment. Recent large-scale DNA methylation studies suggest that CRC can be divided into several subtypes according to the frequency of DNA methylation and those of mutations in key CRC genes, and that this is reflected by different prognostic outcomes. Increasing evidence suggests that the analysis of DNA methylation in blood or fecal specimens could represent a valuable non-invasive diagnostic tool for CRC. Moreover, a broad spectrum of studies indicates that the inter-individual response to chemotherapeutic treatments depends on both epigenetic modifications and genetic mutations occurring in colorectal cancer cells, thereby opening the way for a personalized medicine. Overall, combining genetic and epigenetic data might represent the most promising tool for a proper diagnostic, prognostic and therapeutic approach. (C) 2014 Baishideng Publishing Group Co., Limited. All rights reserved.
机译:大肠癌(CRC)是全球最常见的癌症之一,其结果是结肠粘膜细胞中突变和表位突变的积累,最终导致细胞增殖和转移。不幸的是,CRC的预后仍然很差,并且迫切需要寻找新的诊断和预后生物标记物以预防CRC相关的死亡。本文旨在总结有关使用遗传或表观遗传标志(主要与DNA甲基化相关)生物标志物进行CRC诊断,预后和治疗反应的最新发现。最近的大规模DNA甲基化研究表明,根据DNA甲基化的频率和关键CRC基因突变的频率,CRC可以分为几种亚型,这反映在不同的预后结果上。越来越多的证据表明,对血液或粪便标本中的DNA甲基化进行分析可能代表了一种有价值的CRC非侵入性诊断工具。此外,广泛的研究表明,个体对化学疗法的反应取决于大肠癌细胞中发生的表观遗传修饰和遗传突变,从而为个性化医学开辟了道路。总体而言,结合遗传和表观遗传数据可能代表正确诊断,预后和治疗方法的最有前途的工具。 (C)2014百事登出版集团有限公司。版权所有。

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