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肾细胞癌:对当前模型系统中出现的代谢组学生物标志物的批判性分析。

Renal cell carcinoma: a critical analysis of metabolomic biomarkers emerging from current model systems.

作者信息

Rodrigues Daniela, Monteiro Márcia, Jerónimo Carmen, Henrique Rui, Belo Luís, Bastos Maria de Lourdes, Guedes de Pinho Paula, Carvalho Márcia

机构信息

UCIBIO/REQUIMTE, Faculty of Pharmacy, Laboratory of Toxicology, Department of Biological Sciences, University of Porto, Porto, Portugal.

UCIBIO/REQUIMTE, Faculty of Pharmacy, Laboratory of Toxicology, Department of Biological Sciences, University of Porto, Porto, Portugal.

出版信息

Transl Res. 2017 Feb;180:1-11. doi: 10.1016/j.trsl.2016.07.018. Epub 2016 Aug 2.

Abstract

Metabolomics, an emerging field of "omics" sciences, has caught wide scientific attention in the area of biomarker research for cancers in which early diagnostic biomarkers have the potential to greatly improve patient outcome, such as renal cell carcinoma (RCC). Metabolomic approaches have been successfully applied to various human RCC model systems, mostly ex vivo neoplastic renal tissues and biofluids (urine and serum) from patients with RCC. Importantly, in contrast to other cancers, only a few studies have addressed the RCC metabolome using cancer cell culture-based in vitro models. Herein, we first carried out a comprehensive review of current metabolomic data in RCC, with emphasis on metabolite disturbances and dysregulated metabolic pathways identified in each of these experimental models. We then critically analyzed the consistency of evidence in this field and whether metabolites found altered in tumor cell and tissue microenvironment are reflected in biofluids, which constitute the rationale underlying the translation of discovered metabolic biomarkers into noninvasive diagnostic tools. Finally, dominant metabolic pathways and promising metabolites as biomarkers for diagnosis and prognosis of RCC are outlined.

摘要

代谢组学作为“组学”科学的一个新兴领域,在癌症生物标志物研究领域引起了广泛的科学关注,在该领域中,早期诊断生物标志物有可能极大地改善患者的治疗结果,例如肾细胞癌(RCC)。代谢组学方法已成功应用于各种人类肾细胞癌模型系统,主要是离体肿瘤肾组织以及肾细胞癌患者的生物流体(尿液和血清)。重要的是,与其他癌症不同,只有少数研究使用基于癌细胞培养的体外模型研究肾细胞癌的代谢组。在此,我们首先对肾细胞癌当前的代谢组学数据进行了全面综述,重点关注在每种这些实验模型中确定的代谢物紊乱和失调的代谢途径。然后,我们批判性地分析了该领域证据的一致性,以及在肿瘤细胞和组织微环境中发现的改变的代谢物是否在生物流体中得到反映,这构成了将发现的代谢生物标志物转化为非侵入性诊断工具的基本原理。最后,概述了作为肾细胞癌诊断和预后生物标志物的主要代谢途径和有前景的代谢物。

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