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氧化应激、肿瘤微环境与代谢重编程:一种邪恶的联系。

Oxidative stress, tumor microenvironment, and metabolic reprogramming: a diabolic liaison.

作者信息

Fiaschi Tania, Chiarugi Paola

机构信息

Department of Biochemical Sciences, University of Florence, 50134 Florence, Italy.

出版信息

Int J Cell Biol. 2012;2012:762825. doi: 10.1155/2012/762825. Epub 2012 May 13.

Abstract

Conversely to normal cells, where deregulated oxidative stress drives the activation of death pathways, malignant cells exploit oxidative milieu for its advantage. Cancer cells are located in a very complex microenvironment together with stromal components that participate to enhance oxidative stress to promote tumor progression. Indeed, convincing experimental and clinical evidence underline the key role of oxidative stress in several tumor aspects thus affecting several characteristics of cancer cells. Oxidants influence the DNA mutational potential, intracellular signaling pathways controlling cell proliferation and survival and cell motility and invasiveness as well as control the reactivity of stromal components that is fundamental for cancer development and dissemination, inflammation, tissue repair, and de novo angiogenesis. This paper is focused on the role of oxidant species in the acquisition of two mandatory features for aggressive neoplastic cells, recently defined by Hanahan and Weinberg as new "hallmarks of cancer": tumor microenvironment and metabolic reprogramming of cancer cells.

摘要

与正常细胞相反,在正常细胞中氧化应激失调会驱动死亡途径的激活,而恶性细胞则利用氧化环境为自身谋利。癌细胞与基质成分共同处于非常复杂的微环境中,基质成分会加剧氧化应激以促进肿瘤进展。的确,令人信服的实验和临床证据强调了氧化应激在肿瘤多个方面的关键作用,从而影响癌细胞的多个特性。氧化剂会影响DNA的突变潜能、控制细胞增殖和存活的细胞内信号通路以及细胞运动性和侵袭性,还会控制基质成分的反应性,而基质成分的反应性对于癌症发展、扩散、炎症、组织修复和新生血管形成至关重要。本文重点关注氧化物种在侵袭性肿瘤细胞获得两个必需特征过程中的作用,这两个特征最近被哈纳汉和温伯格定义为新的“癌症标志”:肿瘤微环境和癌细胞的代谢重编程。

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