Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA 19104, USA.
Mol Cell. 2010 Oct 22;40(2):323-32. doi: 10.1016/j.molcel.2010.10.004.
Nutrient stress is generally considered from the standpoint of how cells detect and respond to an insufficient supply of nutrients to meet their bioenergetic needs. However, cells also experience stress as a result of nutrient excess, during which reactive oxygen species (ROS) production exceeds that required for normal physiological responses. This may occur as a result of oncogene activation or chronic exposure to growth factors combined with high levels of nutrients. As a result, multiple mechanisms have evolved to allow cells to detect and adapt to elevated levels of intracellular metabolites, including promotion of signaling and proliferation by ROS, amino acid-dependent mTOR activation, and regulation of signaling and transcription through metabolite-sensitive protein modifications. We discuss how each of these responses can contribute to the development and/or progression of cancer under conditions of cellular nutrient excess and their potential roles in linking chronic organismal over-nutrition (obesity) with cancer.
营养压力通常从细胞如何检测和响应营养供应不足以满足其生物能量需求的角度来考虑。然而,细胞也会因营养过剩而感到压力,在此期间,活性氧 (ROS) 的产生超过了正常生理反应所需的水平。这种情况可能是由于癌基因激活或慢性暴露于生长因子以及高水平的营养物质引起的。因此,已经进化出多种机制来允许细胞检测和适应细胞内代谢物的升高水平,包括 ROS 促进信号转导和增殖、氨基酸依赖性 mTOR 激活以及通过代谢物敏感的蛋白质修饰来调节信号转导和转录。我们讨论了这些反应中的每一种如何在细胞营养过剩的情况下促进癌症的发展和/或进展,以及它们在将慢性机体过度营养(肥胖)与癌症联系起来的潜在作用。