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Marine anticancer drugs in modulating miRNAs and antioxidant signaling.
- Source :
-
Chemico-Biological Interactions . Aug2024, Vol. 399, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- Several marine drugs exert anticancer effects by inducing oxidative stress, which becomes overloaded and kills cancer cells when redox homeostasis is imbalanced. The downregulation of antioxidant signaling induces oxidative stress, while its upregulation attenuates oxidative stress. Marine drugs have miRNA-modulating effects against cancer cells. However, the potential antioxidant targets of such drugs have been rarely explored. This review aims to categorize the marine-drug-modulated miRNAs that downregulate their antioxidant targets, causing oxidative stress in anticancer treatments. We also categorize the downregulation of oxidative-stress-inducing miRNAs in antioxidant protection among non-cancer cells. We summarize the putative antioxidant targets of miRNA-modulating marine drugs by introducing a bioinformatics tool (miRDB). Finally, the marine drugs affecting antioxidant targets are surveyed. In this way, the connections between marine drugs and their modulating miRNA and antioxidant targets are innovatively categorized to provide a precise network for exploring their potential anticancer functions and protective effects on non-cancer cells. • The downregulation of antioxidant signaling induces oxidative stress. • The upregulation of antioxidant signaling attenuates oxidative stress. • This review categorizes marine-drugs, miRNAs, antioxidant targets, and ROS in anticancer treatments. • Antioxidant targets of miRNA-modulating marine drugs are retrieved bioinformatically. • Marine drugs, miRNA, and antioxidant targets are innovatively connected. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00092797
- Volume :
- 399
- Database :
- Academic Search Index
- Journal :
- Chemico-Biological Interactions
- Publication Type :
- Academic Journal
- Accession number :
- 178681756
- Full Text :
- https://doi.org/10.1016/j.cbi.2024.111142