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State of the science: An update on renal cell carcinoma

机译:科学状态:肾细胞癌的最新进展

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Renal cell carcinomas (RCC) are emerging as a complex set of diseases that are having a major socioeconomic impact and showing a continued rise in incidence throughout the world. As the field of urologic oncology faces these trends, several major genomic and mechanistic discoveries are altering our core understanding of this multitude of cancers, including several new rare subtypes of renal cancers. In this review, these new findings are examined and placed in the context of the well-established association of clear cell RCC (ccRCC) with mutations in the von Hippel-Lindau (VHL) gene and resultant aberrant hypoxia inducible factor (HIF) signaling. The impact of novel ccRCC-associated genetic lesions on chromatin remodeling and epigenetic regulation is explored. The effects of VHL mutation on primary ciliary function, extracellular matrix homeostasis, and tumor metabolism are discussed. Studies ofVHLproteostasis, with the goal of harnessing the proteostatic machinery to refunctionalize mutant VHL, are reviewed. Translational efforts using molecular tools to elucidate discriminating features of ccRCC tumors and develop improved prognostic and predictive algorithms are presented, and new therapeutics arising from the earliest molecular discoveries in ccRCC are summarized. By creating an integrated review of the key genomic and molecular biological disease characteristics of ccRCC and placing these data in the context of the evolving therapeutic landscape, we intend to facilitate interaction among basic, translational, and clinical researchers involved in the treatment of this devastating disease, and accelerate progress toward its ultimate eradication.
机译:肾细胞癌(RCC)作为一种复杂的疾病正在出现,正在对社会经济产生重大影响,并且在世界范围内发病率持续上升。随着泌尿外科肿瘤学领域面临这些趋势,一些主要的基因组学和机制发现正在改变我们对多种癌症的核心理解,包括几种新的罕见的肾癌亚型。在这篇综述中,我们对这些新发现进行了检查,并将其置于透明细胞RCC(ccRCC)与von Hippel-Lindau(VHL)基因突变以及由此产生的异常缺氧诱导因子(HIF)信号传导之间的公认关联中。探索了新型ccRCC相关的遗传损伤对染色质重塑和表观遗传调控的影响。讨论了VHL突变对初级睫状功能,细胞外基质稳态和肿瘤代谢的影响。综述了VHL蛋白稳态的研究,其目的是利用蛋白稳定机制使突变型VHL重新功能化。介绍了使用分子工具阐明ccRCC肿瘤的特征并开发改进的预后和预测算法的翻译工作,并总结了ccRCC最早的分子发现产生的新疗法。通过创建ccRCC的关键基因组和分子生物学疾病特征的综合综述并将这些数据置于不断发展的治疗领域中,我们打算促进参与治疗这种毁灭性疾病的基础,转化和临床研究人员之间的互动,并加速朝着最终根除目标迈进。

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