Division of Biological Science and Technology, Yonsei University, Wonju 26493, Korea.
Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Korea.
Int J Mol Sci. 2021 Mar 14;22(6):2947. doi: 10.3390/ijms22062947.
6-Azauridine (6-AZA), a pyrimidine nucleoside analogue, is known to exhibit both antitumor and antiviral activities. Although 6-AZA was discovered more than 60 years ago, the cellular effects of this compound are yet to be elucidated. Here, we report that 6-AZA regulates autophagy-mediated cell death in various human cancer cells, where 6-AZA treatment activates autophagic flux through the activation of lysosomal function. Furthermore, 6-AZA exhibited cytotoxicity in all cancer cells studied, although the mechanisms of action were diverse. In H460 cells, 6-AZA treatment induced apoptosis, and the extent of the latter could be reduced by treatment with chloroquine (CQ), a lysosomal inhibitor. However, 6-AZA treatment resulted in cell cycle arrest in H1299 cells, which could not be reversed by CQ. The cytotoxicity associated with 6-AZA treatment could be linearly correlated to the degree of autophagy-mediated cell death. In addition, we demonstrated that the cytotoxic effect of 6-AZA was dependent on AMPK and p53. These results collectively indicate that autophagy-mediated cell death triggered by 6-AZA contributes to its antitumor effect.
6-氮杂尿苷(6-AZA)是一种嘧啶核苷类似物,具有抗肿瘤和抗病毒活性。尽管 6-AZA 是在 60 多年前发现的,但这种化合物的细胞作用仍有待阐明。在这里,我们报告 6-AZA 调节各种人类癌细胞中的自噬介导的细胞死亡,其中 6-AZA 通过激活溶酶体功能来激活自噬通量。此外,6-AZA 在所有研究的癌细胞中均表现出细胞毒性,尽管作用机制不同。在 H460 细胞中,6-AZA 处理诱导细胞凋亡,而氯喹(CQ)处理可减少后者,氯喹是一种溶酶体抑制剂。然而,6-AZA 处理导致 H1299 细胞中的细胞周期停滞,CQ 不能逆转该作用。与 6-AZA 处理相关的细胞毒性与自噬介导的细胞死亡程度呈线性相关。此外,我们证明 6-AZA 的细胞毒性作用依赖于 AMPK 和 p53。这些结果表明,6-AZA 触发的自噬介导的细胞死亡导致其抗肿瘤作用。