Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
FEBS Lett. 2010 Apr 2;584(7):1417-26. doi: 10.1016/j.febslet.2010.01.009. Epub 2010 Jan 22.
Cell growth is regulated by two antagonistic processes: TOR signaling and autophagy. These processes integrate signals including growth factors, amino acids, and energy status to ensure that cell growth is appropriate to environmental conditions. Autophagy responds indirectly to the cellular milieu as a downstream inhibitory target of TOR signaling and is also directly controlled by nutrient availability, cellular energy status, and cell stress. The control of cell growth by TOR signaling and autophagy are relevant to disease, as altered regulation of either pathway results in tumorigenesis. Here we give an overview of how TOR signaling and autophagy integrate nutritional status to regulate cell growth, how these pathways are coordinately regulated, and how dysfunction of this regulation might result in tumorigenesis.
TOR 信号和自噬。这些过程整合了包括生长因子、氨基酸和能量状态在内的信号,以确保细胞生长与环境条件相适应。自噬作为 TOR 信号的下游抑制靶点,间接响应细胞环境,同时也直接受到营养物质可用性、细胞能量状态和细胞应激的控制。TOR 信号和自噬对细胞生长的控制与疾病有关,因为这两种途径的调节异常会导致肿瘤发生。在这里,我们概述了 TOR 信号和自噬如何整合营养状态来调节细胞生长,这些途径是如何协调调节的,以及这种调节的功能障碍如何导致肿瘤发生。