Discovery of novel thymidylate synthase (TS) inhibitors that influence cancer angiogenesis and metabolic reprogramming in NSCLC cells

• Published in: European journal of medicinal chemistry 2023-10, Vol.258, p.115600-115600, Article 115600
• Main Authors: Dong, Gang, Li, Yu-heng, Guo, Jing-si, Lin, Qi-qi, Deng, Mei-yan, Xue, Wen-han, Li, Xin-yang, Meng, Fan-hao
• Format: Article
• Language: English
• Subjects: Angiogenesis; Animals; Carcinoma, Non-Small-Cell Lung - metabolism; Cell Line, Tumor; Enzyme Inhibitors - chemistry; Enzyme Inhibitors - pharmacology; Glucose metabolism; Humans; Lung Neoplasms - metabolism; Mice; NSCLC; Thymidylate Synthase
• ISSN: 0223-5234; 1768-3254
• DOI: 10.1016/j.ejmech.2023.115600

Based on previous work, further search for more effective and less damaging thymidylate synthase (TS) inhibitors was the focus of this study. After further optimization of the structure, in this study, a series of (E)-N-(2-benzyl hydrazine-1-carbonyl) phenyl-2,4-deoxy-1,2,3,4-tetrahydro pyrimidine-5-sulfonamide derivatives were synthesized and reported for the first time. All target compounds were screened by enzyme activity assay and cell viability inhibition assay. On the one hand, the hit compound DG1 could bind directly to TS proteins intracellularly and promote apoptosis in A549 and H1975 cells. Simultaneously, DG1 could inhibit cancer tissue proliferation more effectively than Pemetrexed (PTX) in the A549 xenograft mouse model. On the other hand, the inhibitory effect of DG1 on NSCLC angiogenesis was verified both in vivo and in vitro. In parallel, DG1 was further uncovered to inhibit the expression of CD26, ET-1, FGF-1, and EGF by angiogenic factor antibody microarray. Moreover, RNA-seq and PCR-array assays revealed that DG1 could inhibit NSCLC proliferation by affecting metabolic reprogramming. Collectively, these data demonstrated that DG1as a TS inhibitor could be promising in treating NSCLC angiogenesis, deserving further investigation. [Display omitted] •DG1 was able to bind directly to TS proteins intracellularly and promote apoptosis in A549 and H1975 cells.•DG1 could inhibit NSCLC angiogenesis in vivo and in vitro.•DG1 could influence the metabolic reprogramming of NSCLC cells.