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6-Azauridine Induces Autophagy-Mediated Cell Death via a p53- and AMPK-Dependent Pathway.
- Source :
-
International journal of molecular sciences [Int J Mol Sci] 2021 Mar 14; Vol. 22 (6). Date of Electronic Publication: 2021 Mar 14. - Publication Year :
- 2021
-
Abstract
- 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.
- Subjects :
- AMP-Activated Protein Kinase Kinases
Antineoplastic Agents pharmacology
Apoptosis drug effects
Autophagic Cell Death drug effects
Autophagy drug effects
Cell Line, Tumor
Cell Proliferation drug effects
Cell Survival drug effects
Drug Synergism
Humans
Lysosomes drug effects
Neoplasms genetics
Neoplasms pathology
Signal Transduction drug effects
Azauridine pharmacology
Chloroquine pharmacology
Neoplasms drug therapy
Protein Kinases genetics
Tumor Suppressor Protein p53 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1422-0067
- Volume :
- 22
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- International journal of molecular sciences
- Publication Type :
- Academic Journal
- Accession number :
- 33799444
- Full Text :
- https://doi.org/10.3390/ijms22062947