Department of Clinical and Molecular Medicine, Sapienza University of Rome, 00161, Rome, Italy.
Division of Medical Oncology 2, "Regina Elena" National Cancer Institute, Via Elio Chianesi 53, 00144, Rome, Italy.
Oncogene. 2018 May;37(18):2367-2378. doi: 10.1038/s41388-018-0141-3. Epub 2018 Feb 15.
Cancer stem cells (CSCs) are an uncommon subset of tumor cells capable of self-renewal, differentiating, and recreating the parental tumor when transplanted into the murine background. Over the past two decades, efforts toward understanding CSC biology culminated into identifying a set of signaling pathways sustaining "stemness". Nevertheless, while metabolic rewiring is nowadays considered a hallmark of cancer, no consensus has been reached on the metabolic features underlying the plastic nature of CSCs, which are capable of residing in a dormant state, and able to rapidly proliferate when the need to repopulate the tumor mass arises. An emerging concept in the field of CSC metabolism is that these cells are extremely reliant on the activity of enzymes involved in lipid metabolism, such as stearoyl-CoA desaturase 1 (SCD1) and 3-hydroxy-3-methylglutharyl-coenzyme A reductase (HMG-CoAR). Indeed, SCD1 and HMG-CoAR have been described as key factors for the correct function of a number of concatenated pathways involved in CSC fate decision, such as Hippo and Wnt. In the present review, we describe metabolic futures of CSCs with a special focus on lipid metabolism, which until now represents an underappreciated force in maintaining CSCs and an attractive therapeutic target.
癌症干细胞(CSC)是一种罕见的肿瘤细胞亚群,能够自我更新、分化,并在移植到小鼠背景中时重新创建原始肿瘤。在过去的二十年中,人们努力理解 CSC 生物学,最终确定了一组维持“干性”的信号通路。然而,尽管代谢重编程现在被认为是癌症的一个标志,但对于支持 CSC 可塑性的代谢特征尚未达成共识,这些特征使 CSC 能够处于休眠状态,并在需要重新填充肿瘤时迅速增殖。CSC 代谢领域的一个新兴概念是,这些细胞非常依赖于参与脂质代谢的酶的活性,例如硬脂酰辅酶 A 去饱和酶 1(SCD1)和 3-羟基-3-甲基戊二酰辅酶 A 还原酶(HMG-CoAR)。事实上,SCD1 和 HMG-CoAR 已被描述为涉及 CSC 命运决定的多个串联途径的正确功能的关键因素,例如 Hippo 和 Wnt。在本综述中,我们描述了 CSC 的代谢未来,特别关注脂质代谢,这迄今为止是维持 CSC 的一个被低估的因素,也是一个有吸引力的治疗靶点。