6-Azauridine Induces Autophagy-Mediated Cell Death via a p53-and AMPK-Dependent Pathway

被引:12
作者
Cha, Yeo-Eun [1 ]
Park, Rackhyun [1 ]
Jang, Minsu [1 ]
Park, Yea-In [1 ]
Yamamoto, Ayane [1 ]
Oh, Won Keun [2 ]
Lee, Eun-Ju [3 ]
Park, Junsoo [1 ]
机构
[1] Yonsei Univ, Div Biol Sci & Technol, Wonju 26493, South Korea
[2] Seoul Natl Univ, Coll Pharm, Korea Bioact Nat Mat Bank, Res Inst Pharmaceut Sci, Seoul 08826, South Korea
[3] Chung Ang Univ, Sch Med, Dept Obstet & Gynecol, Seoul 06974, South Korea
基金
新加坡国家研究基金会;
关键词
autophagy-mediated cell death; 6-azauridine; autophagy; autophagic flux;
D O I
10.3390/ijms22062947
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1 / 11
页数:10
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