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首页> 外文期刊>Mass Spectrometry Reviews >PROTEOMICS ANALYSIS OF TUMOR MICROENVIRONMENT: IMPLICATIONS OF METABOLIC AND OXIDATIVE STRESSES IN TUMORIGENESIS
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PROTEOMICS ANALYSIS OF TUMOR MICROENVIRONMENT: IMPLICATIONS OF METABOLIC AND OXIDATIVE STRESSES IN TUMORIGENESIS

机译:肿瘤微环境的蛋白质组学分析:代谢中的氧化应激和氧化应激的意义

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摘要

Tumorigenesis is always concomitant with microenvironmental alterations. The tumor microenvironment is a heterogeneous and complex milieu, which exerts a variety of stresses on tumor cells for proliferation, survival, or death. Recently, accumulated evidence revealed that metabolic and oxidative stresses both play significant roles in tumor development and progression that converge on a common autophagic pathway. Tumor cells display increased metabolic autonomy, and the hallmark is the exploitation of aerobic glycolysis (termed Warburg effect), which increased glucose consumption and decreased oxidative phosphorylation to support growth and proliferation. This characteristic renders cancer cells more aggressive; they devour tremendous amounts of nutrients from microenvironment to result in an ever-growing appetite for new tumor vessel formation and the release of more "waste," including key determinants of cell fate like lactate and reactive oxygen species (ROS). The intracellular ROS level of cancer cells can also be modulated by a variety of stimuli in the tumor microenvironment, such as pro-growth and pro-inflammatory factors. The intracellular redox state serves as a double-edged sword in tumor development and progression: ROS overproduction results in cytotoxic effects and might lead to apoptotic cell death, whereas certain level of ROS can act as a second-messenger for regulation of such cellular processes as cell survival, proliferation, and metastasis. The molecular mechanisms for cancer cell responses to metabolic and oxidative stresses are complex and are likely to involve multiple molecules or signaling pathways. In addition, the expression and modification of these proteins after metabolic or oxidative stress challenge are diverse in different cancer cells and endow them with different functions. Therefore, MS-based high-throughput platforms, such as proteomics, are indispensable in the global analysis of cancer cell responses to metabolic and oxidative stress. Herein, we highlight recent advances in the understanding of the metabolic and oxidative stresses associated with tumor progression with pro-teomics-based systems biology approaches.
机译:肿瘤发生总是伴随着微环境的改变。肿瘤微环境是一种异质且复杂的环境,它对肿瘤细胞施加多种应激以使其增殖,存活或死亡。最近,积累的证据表明,代谢和氧化应激均在肿瘤发展和进展中发挥重要作用,它们在共同的自噬途径上趋于一致。肿瘤细胞显示出更高的代谢自主性,其标志是有氧糖酵解(称为Warburg效应)的利用,这增加了葡萄糖的消耗并减少了氧化磷酸化以支持生长和增殖。这种特性使癌细胞更具攻击性。它们从微环境中吞噬大量营养,导致对新的肿瘤血管形成的食欲不断增长,并释放出更多的“废物”,包括决定细胞命运的关键决定因素,如乳酸和活性氧(ROS)。癌细胞的细胞内ROS水平也可以通过肿瘤微环境中的多种刺激来调节,例如促生长和促炎因子。细胞内的氧化还原状态在肿瘤的发展和进程中起了双刃剑的作用:ROS的过量产生导致细胞毒性作用,并可能导致凋亡性细胞死亡,而一定水平的ROS可以作为调节此类细胞过程的第二信使。细胞存活,增殖和转移。癌细胞对代谢和氧化应激反应的分子机制很复杂,可能涉及多个分子或信号通路。另外,在代谢或氧化应激挑战后,这些蛋白质的表达和修饰在不同的癌细胞中是不同的,并赋予它们不同的功能。因此,基于蛋白质组学的基于MS的高通量平台在癌细胞对代谢和氧化应激反应的全局分析中必不可少。本文中,我们重点介绍了基于蛋白质组学的系统生物学方法在与肿瘤进展相关的代谢和氧化应激理解方面的最新进展。

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