Yu Yong, Nie Qingzhu, Wang Ziyi, Di Yu, Chen Xiaolong, Ren Kaiming
Department of Ophthalmology, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.
Department of Thoracic Surgery, First Hospital of China Medical University, Shenyang, Liaoning, China.
Front Pharmacol. 2023 Feb 10;14:1129010. doi: 10.3389/fphar.2023.1129010. eCollection 2023.
Metabolic adaptation is an emerging hallmark of tumors. fatty acid synthesis is an important metabolic process to produce metabolic intermediates for energy storage, biosynthesis of membrane lipids and generation of signaling molecules. Acetyl-CoA carboxylase 1 (ACC1) is a critical enzyme in the fatty acid synthesis, which carboxylates acetyl-CoA carboxylic acid to form malonyl-CoA. The role of acetyl-CoA carboxylase 1 in fatty acid synthesis makes it a promising therapeutic target for various metabolic diseases such as non-alcoholic fatty liver disease, obesity and diabetes. Tumors have a high energy flow and a strong dependence on fatty acid synthesis. Thus, acetyl-CoA carboxylase inhibition has become a potential choice for anti-tumor therapy. In this review, we first introduced the structure and expression pattern of Acetyl-CoA carboxylase 1. We also discussed the molecular mechanisms of acetyl-CoA carboxylase 1 in the initiation and progression of various cancer types. Furthermore, acetyl-CoA carboxylase1 inhibitors has also been discussed. Collectively, we summarized the interplay between acetyl-CoA carboxylase 1 and tumorigenesis, indicating acetyl-CoA carboxylase 1 as a promising therapeutic target for tumor management.
代谢适应是肿瘤新出现的一个特征。脂肪酸合成是一个重要的代谢过程,用于产生能量储存的代谢中间体、膜脂的生物合成以及信号分子的生成。乙酰辅酶A羧化酶1(ACC1)是脂肪酸合成中的关键酶,它将乙酰辅酶A羧化为丙二酰辅酶A。乙酰辅酶A羧化酶1在脂肪酸合成中的作用使其成为非酒精性脂肪性肝病、肥胖症和糖尿病等各种代谢性疾病的一个有前景的治疗靶点。肿瘤具有高能量流且对脂肪酸合成有很强的依赖性。因此,抑制乙酰辅酶A羧化酶已成为抗肿瘤治疗的一个潜在选择。在本综述中,我们首先介绍了乙酰辅酶A羧化酶1的结构和表达模式。我们还讨论了乙酰辅酶A羧化酶1在各种癌症类型的发生和发展中的分子机制。此外,还讨论了乙酰辅酶A羧化酶1抑制剂。总的来说,我们总结了乙酰辅酶A羧化酶1与肿瘤发生之间的相互作用,表明乙酰辅酶A羧化酶1是肿瘤治疗的一个有前景的靶点。