| Literature DB >> 33971967 |
Yue Zhou1, Lei Tao1, Xia Zhou1, Zeping Zuo2, Jin Gong1, Xiaocong Liu1, Yang Zhou1, Chunqi Liu1, Na Sang1, Huan Liu3, Jiao Zou1, Kun Gou1, Xiaowei Yang1, Yinglan Zhao4,5.
Abstract
Human dihydroorotate dehydrogenase (DHODH) is a flavin-dependent mitochondrial enzyme catalyzing the fourth step in the de novo pyrimidine synthesis pathway. It is originally a target for the treatment of the non-neoplastic diseases involving in rheumatoid arthritis and multiple sclerosis, and is re-emerging as a validated therapeutic target for cancer therapy. In this review, we mainly unravel the biological function of DHODH in tumor progression, including its crucial role in de novo pyrimidine synthesis and mitochondrial respiratory chain in cancer cells. Moreover, various DHODH inhibitors developing in the past decades are also been displayed, and the specific mechanism between DHODH and its additional effects are illustrated. Collectively, we detailly discuss the association between DHODH and tumors in recent years here, and believe it will provide significant evidences and potential strategies for utilizing DHODH as a potential target in preclinical and clinical cancer therapies.Entities:
Keywords: Cancer metabolism; DHODH inhibitors; De novo pyrimidine biosynthesis; Dihydroorotate dehydrogenase; Mitochondria
Year: 2021 PMID: 33971967 DOI: 10.1186/s40170-021-00250-z
Source DB: PubMed Journal: Cancer Metab ISSN: 2049-3002