Wang Wanyan, Cui Jiayan, Ma Hui, Lu Weiqiang, Huang Jin
State Key Laboratory of Bioreactor Engineering, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, China.
Shanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, Shanghai, China.
Front Oncol. 2021 May 28;11:684961. doi: 10.3389/fonc.2021.684961. eCollection 2021.
Metabolic rewiring is considered as a primary feature of cancer. Malignant cells reprogram metabolism pathway in response to various intrinsic and extrinsic drawback to fuel cell survival and growth. Among the complex metabolic pathways, pyrimidine biosynthesis is conserved in all living organism and is necessary to maintain cellular fundamental function (i.e. DNA and RNA biosynthesis). A wealth of evidence has demonstrated that dysfunction of pyrimidine metabolism is closely related to cancer progression and numerous drugs targeting pyrimidine metabolism have been approved for multiple types of cancer. However, the non-negligible side effects and limited efficacy warrants a better strategy for negating pyrimidine metabolism in cancer. In recent years, increased studies have evidenced the interplay of oncogenic signaling and pyrimidine synthesis in tumorigenesis. Here, we review the recent conceptual advances on pyrimidine metabolism, especially dihydroorotate dehydrogenase (DHODH), in the framework of precision oncology medicine and prospect how this would guide the development of new drug precisely targeting the pyrimidine metabolism in cancer.
代谢重编程被认为是癌症的一个主要特征。恶性细胞会重新编程代谢途径,以应对各种内在和外在的不利因素,为细胞存活和生长提供能量。在复杂的代谢途径中,嘧啶生物合成在所有生物体中都是保守的,并且是维持细胞基本功能(即DNA和RNA生物合成)所必需的。大量证据表明,嘧啶代谢功能障碍与癌症进展密切相关,许多针对嘧啶代谢的药物已被批准用于多种类型的癌症。然而,不可忽视的副作用和有限的疗效需要一种更好的策略来抑制癌症中的嘧啶代谢。近年来,越来越多的研究证明了致癌信号与嘧啶合成在肿瘤发生中的相互作用。在此,我们在精准肿瘤医学的框架下,综述了嘧啶代谢,尤其是二氢乳清酸脱氢酶(DHODH)的最新概念进展,并展望这将如何指导精确靶向癌症中嘧啶代谢的新药开发。