Fan Kexin, Liu Zhan, Gao Min, Tu Kangsheng, Xu Qiuran, Zhang Yilei
The Institute of Molecular and Translational Medicine, Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Xinjiang Second Medical College, Karamay, China.
Front Oncol. 2022 Feb 1;12:820173. doi: 10.3389/fonc.2022.820173. eCollection 2022.
Metabolic reprogramming is one of the hallmarks of tumor. Growing evidence suggests metabolic changes that support oncogenic progression may cause selective vulnerabilities that can be exploited for cancer treatment. Increasing demands for certain nutrients under genetic determination or environmental challenge enhance dependency of tumor cells on specific nutrient, which could be therapeutically developed through targeting such nutrient dependency. Various nutrients including several amino acids and glucose have been found to induce dependency in genetic alteration- or context-dependent manners. In this review, we discuss the extensively studied nutrient dependency and the biological mechanisms behind such vulnerabilities. Besides, existing applications and strategies to target nutrient dependency in different cancer types, accompanied with remaining challenges to further exploit these metabolic vulnerabilities to improve cancer therapies, are reviewed.
代谢重编程是肿瘤的特征之一。越来越多的证据表明,支持致癌进展的代谢变化可能导致选择性脆弱性,可被用于癌症治疗。在基因决定或环境挑战下对某些营养素的需求增加,增强了肿瘤细胞对特定营养素的依赖性,这可以通过靶向这种营养素依赖性进行治疗开发。包括几种氨基酸和葡萄糖在内的各种营养素已被发现以基因改变或背景依赖的方式诱导依赖性。在这篇综述中,我们讨论了广泛研究的营养素依赖性及其背后的生物学机制。此外,还综述了针对不同癌症类型的营养素依赖性的现有应用和策略,以及进一步利用这些代谢脆弱性以改善癌症治疗所面临的挑战。