Department of Science Education, Ewha Womans University, Seoul 03760, Republic of Korea.
Int J Mol Sci. 2024 Jan 26;25(3):1572. doi: 10.3390/ijms25031572.
The most commonly used chemotherapy for colorectal cancer (CRC) is the application of 5-fluorouracil (5-FU). Inhibition of thymidylate synthase (TYMS) expression appears to be a promising strategy to overcome the decreased sensitivity to 5-FU caused by high expression of TYMS, which can be induced by 5-FU treatment. Several compounds have been shown to potentially inhibit the expression of TYMS, but it is unclear whether short-chain fatty acids (SCFAs), which are naturally produced by bacteria in the human intestine, can regulate the expression of TYMS. Sodium butyrate (NaB) is the most widely known SCFA for its beneficial effects. Therefore, we investigated the enhancing effects on inhibition of cell viability and induction of apoptosis after co-treatment of NaB with 5-FU in two CRC cell lines, HCT116 and LoVo. This study suggests that the effect of NaB in improving therapeutic sensitivity to 5-FU in CRC cells may result from a mechanism that strongly inhibits the expression of TYMS. This study also shows that NaB inhibits the migration of CRC cells and can cause cell cycle arrest in the G2/M phase. These results suggest that NaB could be developed as a potential therapeutic adjuvant to improve the therapeutic effect of 5-FU in CRC.
结直肠癌(CRC)最常用的化疗药物是 5-氟尿嘧啶(5-FU)。抑制胸苷酸合成酶(TYMS)的表达似乎是克服由于 TYMS 高表达导致的 5-FU 敏感性降低的一种很有前途的策略,5-FU 治疗可以诱导 TYMS 高表达。已经有几种化合物被证明可能抑制 TYMS 的表达,但目前尚不清楚肠道细菌自然产生的短链脂肪酸(SCFAs)是否可以调节 TYMS 的表达。丁酸钠(NaB)是最广为人知的 SCFA,因其有益的作用。因此,我们研究了在两种 CRC 细胞系 HCT116 和 LoVo 中,NaB 与 5-FU 联合治疗对细胞活力抑制和细胞凋亡诱导的增强作用。本研究表明,NaB 改善 CRC 细胞对 5-FU 治疗敏感性的作用可能是通过一种强烈抑制 TYMS 表达的机制实现的。本研究还表明,NaB 抑制 CRC 细胞的迁移,并能导致细胞周期停滞在 G2/M 期。这些结果表明,NaB 可以开发为一种潜在的治疗佐剂,以提高 5-FU 在 CRC 中的治疗效果。