超越葡萄糖和沃伯格:寻找癌症代谢模型的甜蜜点

Nia G. Hammond, Robert B. Cameron, Brandon Faubert
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引用次数: 0

摘要

癌症生物学的进展突出表明,代谢重编程是肿瘤发生和发展的一个重要方面。然而,最近对体内肿瘤代谢的研究发现,体外和体内生物学之间存在一些脱节。这至少部分归因于细胞培养模型的简化性,并凸显出人们越来越需要利用更贴近生理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新陈代谢认识的演变,并讨论了体外和体内条件之间的一些差异。我们将介绍生理培养基的开发如何与先进的培养方法相结合,从而缩小体外和体内代谢之间的差距。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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