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超越葡萄糖与瓦伯格效应:探寻癌症代谢模型中的最佳平衡点

Beyond glucose and Warburg: finding the sweet spot in cancer metabolism models.

作者信息

Hammond Nia G, Cameron Robert B, Faubert Brandon

机构信息

Department of Medicine, Section of Hematology/Oncology, University of Chicago, Chicago, IL, USA.

出版信息

NPJ Metab Health Dis. 2024 Sep 2;2(1):11. doi: 10.1038/s44324-024-00017-2.

Abstract

Advances in cancer biology have highlighted metabolic reprogramming as an essential aspect of tumorigenesis and progression. However, recent efforts to study tumor metabolism in vivo have identified some disconnects between in vitro and in vivo biology. This is due, at least in part, to the simplified nature of cell culture models and highlights a growing need to utilize more physiologically relevant approaches to more accurately assess tumor metabolism. In this review, we outline the evolution of our understanding of cancer metabolism and discuss some discrepancies between in vitro and in vivo conditions. We describe how the development of physiological media, in combination with advanced culturing methods, can bridge the gap between in vitro and in vivo metabolism.

摘要

癌症生物学的进展凸显了代谢重编程是肿瘤发生和发展的一个重要方面。然而,最近在体内研究肿瘤代谢的努力发现了体外和体内生物学之间的一些脱节。这至少部分是由于细胞培养模型的简化性质,并突出了越来越需要利用更具生理相关性的方法来更准确地评估肿瘤代谢。在这篇综述中,我们概述了我们对癌症代谢理解的演变,并讨论了体外和体内条件之间的一些差异。我们描述了生理培养基的发展,结合先进的培养方法,如何能够弥合体外和体内代谢之间的差距。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dab/12118702/4ee42457b64c/44324_2024_17_Fig1_HTML.jpg

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