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The tubal epigenome - An emerging target for ovarian cancer

机译:输卵管外膜组 - 卵巢癌的新出现靶标

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Ovarian cancer is the most lethal gynecologic malignancy in the United States. The mortality of this disease is primarily attributed to challenges in early detection and therapeutic resistance. Recent studies indicate that the majority of high-grade serous ovarian carcinomas (HGSCs) originate from aberrant fallopian tube epithelial (FTE) cells. This shift in thinking about ovarian cancer pathogenesis has been met with an effort to identify the early genetic and epigenetic changes that underlie the transformation of normal FTE cells and prompt them to migrate and colonize the ovary, ultimately giving rise to aggressive HGSC. While identification of these early changes is important for biomarker discovery, the emergence of epigenetic alterations in FTE chromatin may also provide new opportunities for early detection, prevention, and therapeutic intervention. Here we provide a comprehensive overview of the current knowledge regarding early epigenetic reprogramming that precedes HGSC tumor development, the way that these alterations affect both intrinsic and extrinsic tumor properties, and how the epigenome may be targeted to thwart HGSC tumorigenesis. (C) 2020 Elsevier Inc. All rights reserved.
机译:卵巢癌是美国最致命的妇科恶性肿瘤。该疾病的死亡率主要归因于早期检测和治疗抵抗的挑战。最近的研究表明,大多数高级浆液癌癌(HGSCs)起源于异常输卵管上皮(FTE)细胞。这种转变思考卵巢癌发病机构的努力,努力确定正常FTE细胞的转化并提示他们迁移和殖民卵巢,最终引起侵袭性HGSC的早期遗传和表观遗传变化。虽然鉴定这些早期的变化对于生物标志物发现很重要,但FTE染色质中表观遗传变化的出现也可能为早期检测,预防和治疗干预提供新的机会。在这里,我们全面概述了关于HGSC肿瘤发育的早期表观遗传重编程的目前的知识,这些改变对内在和外在肿瘤性质影响的方式,以及外表组合如何靶向HGSC肿瘤瘤。 (c)2020 Elsevier Inc.保留所有权利。

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