Breast Cancer Clinical Research Unit, CNIO - Spanish National Cancer Research Center, Madrid, Spain.
Metabolomics Platform, Department of Electronic Engineering, Universitat Rovira i Virgili, Tarragona, Spain.
Nat Commun. 2019 Nov 1;10(1):5011. doi: 10.1038/s41467-019-13028-1.
Upregulation of fatty acid synthase (FASN) is a common event in cancer, although its mechanistic and potential therapeutic roles are not completely understood. In this study, we establish a key role of FASN during transformation. FASN is required for eliciting the anaplerotic shift of the Krebs cycle observed in cancer cells. However, its main role is to consume acetyl-CoA, which unlocks isocitrate dehydrogenase (IDH)-dependent reductive carboxylation, producing the reductive power necessary to quench reactive oxygen species (ROS) originated during the switch from two-dimensional (2D) to three-dimensional (3D) growth (a necessary hallmark of cancer). Upregulation of FASN elicits the 2D-to-3D switch; however, FASN's synthetic product palmitate is dispensable for this process since cells satisfy their fatty acid requirements from the media. In vivo, genetic deletion or pharmacologic inhibition of FASN before oncogenic activation prevents tumor development and invasive growth. These results render FASN as a potential target for cancer prevention studies.
脂肪酸合酶(FASN)的上调是癌症中的常见事件,尽管其机制和潜在的治疗作用尚未完全阐明。在这项研究中,我们确立了 FASN 在转化过程中的关键作用。FASN 是在癌细胞中观察到的克雷布斯循环的回补作用所必需的。然而,其主要作用是消耗乙酰辅酶 A,这会解锁异柠檬酸脱氢酶(IDH)依赖性还原羧化作用,产生在从二维(2D)到三维(3D)生长的转变过程中(这是癌症的一个必要特征)中产生的还原性物质,以消除活性氧(ROS)。FASN 的上调引发了 2D 到 3D 的转变;然而,FASN 的合成产物棕榈酸对于这个过程是可有可无的,因为细胞可以从培养基中满足其脂肪酸需求。在体内,在致癌激活之前遗传删除或药物抑制 FASN 可防止肿瘤的发展和侵袭性生长。这些结果表明 FASN 是癌症预防研究的潜在靶点。