| Literature DB >> 35151222 |
Lele Zhang1, Jifa Zhang1, Jiaxing Wang2, Changyu Ren3, Pan Tang4, Liang Ouyang1, Yuxi Wang5.
Abstract
Human dihydroorotate dehydrogenase (hDHODH) is a flavin-dependent enzyme catalyzing the fourth step of pyrimidine de novo biosynthesis. Since aberrant pyrimidine metabolism is closely related abnormal cell proliferation, hDHODH is believed to have an intimate linkage with cancers. For instance, hDHODH induces the abrogation of β-catenin degradation and cell proliferation in esophageal squamous cell carcinoma (ESCC). Thus, small molecular inhibitors targeting hDHODH has been considered as a promising strategy for cancer treatment. In recent years, in exploiting novel structural hDHODH inhibitors (hDHODHi), a candidate drug PTC299 has entered clinical trials for treating acute myelocytic leukemia (AML) and other tumors. This review discusses tumor-related research of hDHODH and highlights the structure-activity relationships of hDHODHi, providing insights into new drugs targeting hDHODH for antitumor clinical practice.Entities:
Keywords: Anticancer; Human dihydroorotate dehydrogenase (hDHODH); Small molecule inhibitors; Structure-activity relationships (SARs)
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Year: 2022 PMID: 35151222 DOI: 10.1016/j.ejmech.2022.114176
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514