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首页> 外文期刊>Expert opinion on therapeutic targets >Hepatocellular carcinoma treatment over sorafenib: epigenetics, microRNAs and microenvironment. Is there a light at the end of the tunnel?
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Hepatocellular carcinoma treatment over sorafenib: epigenetics, microRNAs and microenvironment. Is there a light at the end of the tunnel?

机译:索拉非尼的肝细胞癌治疗:表观遗传学,microRNA和微环境。隧道尽头有灯吗?

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Introduction: Sorafenib is currently the only approved therapy in hepatocellular carcinoma (HCC). Alternative first- and second-line treatments are a significant unmet medical need, and several biologic agents have been tested in recent years, with poor results. Therefore, angiogenic pathways and the cytokine cascade remain possible targets in HCC. Recent studies suggest a role of epigenetic processes, associated with the initiation and development of HCC. In this field, DNA methylation, micro-RNAs (miRNAs) and tumor microenvironment cells became a possible new target for HCC treatment.Areas covered: This review explains the possible role of DNA methylation and histone deacetylase inhibitors as predictive biomarkers and target therapy, the extensive world of the promising miRNA blockade strategy, and the recent strong evidence of correlation between HCC tumors and peritumoral stroma cells. The literature and preclinic/clinic data were obtained through an electronic search.Expert opinion: Future research should aim to understand how best to identify patient groups that would benefit most from the prescribed therapy. To overcome the therapeutic stranding' of HCC, a possible way out from the current therapeutic tunnel might be to evaluate the major epigenetic and genetic processes involved in HCC carcinogenesis, not underestimating the tumor microenvironment and its actors' (angiogenesis, immune system, platelets). We are only at the start of a long journey towards the elucidation of HCC molecular pathways as therapeutic targets. Yet, currently this path appears to be the only one to cast some light at the end of the tunnel.
机译:简介:索拉非尼是目前唯一批准用于肝细胞癌(HCC)的疗法。替代性的一线和二线治疗是目前尚未满足的重大医疗需求,近年来已经对几种生物制剂进行了测试,但效果较差。因此,血管生成途径和细胞因子级联仍然是肝癌的可能靶标。最近的研究表明表观遗传过程的作用,与肝癌的发生和发展有关。在这一领域,DNA甲基化,微小RNA(miRNA)和肿瘤微环境细胞成为HCC治疗的新靶标。研究领域:本综述解释了DNA甲基化和组蛋白脱乙酰基酶抑制剂作为预测性生物标志物和靶标治疗的可能作用。 miRNA阻断策略的广泛应用,以及HCC肿瘤与肿瘤周围基质细胞之间相关性的最新证据。文献和临床前/临床数据是通过电子搜索获得的。专家意见:未来的研究应旨在了解如何最好地确定将从处方治疗中受益最大的患者群体。为了克服肝癌的治疗难题,从当前治疗隧道中脱颖而出的一种可能方法可能是评估肝癌致癌过程中涉及的主要表观遗传和遗传过程,而不是低估肿瘤的微环境及其参与者(血管生成,免疫系统,血小板) 。我们只是在阐明作为治疗靶点的HCC分子途径的漫长旅程的开始。但是,目前这条路径似乎是在隧道尽头投射光线的唯一路径。

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