International Immunopharmacology, Год журнала: 2024, Номер 145, С. 113698 - 113698
Опубликована: Дек. 6, 2024
Язык: Английский
International Immunopharmacology, Год журнала: 2024, Номер 145, С. 113698 - 113698
Опубликована: Дек. 6, 2024
Язык: Английский
TrAC Trends in Analytical Chemistry, Год журнала: 2025, Номер unknown, С. 118161 - 118161
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
1Advanced Science, Год журнала: 2025, Номер unknown
Опубликована: Фев. 14, 2025
Abstract Designing drugs to intelligently respond different ratio of biological electron donors/receptors in cancer cells and normal is a promising strategy achieve highly effective less toxic chemotherapy. Herein by employing metal center active the selenium‐containing electrophilic drug Ru(phtpy‐NO 2 )(phenSe)Cl ( RuSe ) with strongly polarization characteristics are synthesized which can efficiently shuttle electrons from donors convert oxidative stress. The rate transfer at selenium 1.81 times higher cell environments compared environments. This results being 14.98 more lethal than cells. Experimental demonstrate that transport process carried out via radicals intermediate positively correlated properties atoms. transports bioactive generate large number superoxide anions leading DNA damage decrease mitochondrial membrane potential further activates p53 signaling pathway amplifies cell‐killing effect after transporting electrons. work provides new avenue for design efficient chemotherapeutic agents.
Язык: Английский
Процитировано
1International Journal of Nanomedicine, Год журнала: 2025, Номер Volume 20, С. 2461 - 2473
Опубликована: Фев. 1, 2025
Ferroptosis is a type of iron-dependent programmed cell death characterized by depletion glutathione. Although generally less harmful to normal cells, in tumor the high demand for iron ions provides conditions conducive ferroptosis. In this review, we provide an overview recent progress research on regulation ferroptosis summarizing and assessing current state, trends, applications nanomaterials cells. Given advantages terms targeting, safety, improved drug efficacy, reduced side effects, these materials are considered have potential therapeutic value modulating cells via different mechanisms. respect, describe methods modifying interfering with glutathione activity lipid peroxidation. The development that can be applied induce or inhibit anticipated new options treatment diverse range diseases.
Язык: Английский
Процитировано
1International Journal of Pharmaceutics, Год журнала: 2024, Номер 669, С. 125050 - 125050
Опубликована: Дек. 5, 2024
Язык: Английский
Процитировано
5Microchimica Acta, Год журнала: 2025, Номер 192(5)
Опубликована: Апрель 12, 2025
Язык: Английский
Процитировано
0Colloids and Surfaces B Biointerfaces, Год журнала: 2025, Номер 253, С. 114743 - 114743
Опубликована: Апрель 29, 2025
Язык: Английский
Процитировано
0Journal of Drug Delivery Science and Technology, Год журнала: 2025, Номер unknown, С. 107041 - 107041
Опубликована: Май 1, 2025
Язык: Английский
Процитировано
0Chemical Science, Год журнала: 2025, Номер unknown
Опубликована: Янв. 1, 2025
Glutathione's role in synthesizing functional metal nanomaterials with unique optical properties and nanobiomedical applications.
Язык: Английский
Процитировано
0Analytical Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Март 26, 2025
Amplification of lipid peroxidation with tumor specificity represents a new avenue to boost ferroptosis-mediated anticancer therapeutics but remains challenging. Herein, we proposed metal-phenolic-network (MPN)-coated nanohybrid as microenvironment-responsive amplifier, consisting reactive oxygen species generator MPN, glutathione (GSH) scavenger GSH-P, and peroxidase 4 (GPX4) mRNA gene silencing sequence. The protective MPN shell this amplifier can be specifically disintegrated by acidic adenosine triphosphate (ATP)-rich microenvironments induce oxidative stress through the dual disruption redox homeostasis (Fenton-catalytic accumulation GSH depletion). Furthermore, stress-induced upregulation ferroptosis resistance-related apurinic/apyrimidinic endonuclease 1 (APE1) is further ingeniously employed an amplification element prompt release (AP) site-embedded GPX4 sequence which downregulate level. Based on tandem depletion substrate GPX4, defense system GPX4/GSH heavily devastated enable for effectively improving efficiency. We expect strategy expanded other important regulatory proteins provide mechanism study therapy.
Язык: Английский
Процитировано
0Inorganic Chemistry Communications, Год журнала: 2024, Номер unknown, С. 113835 - 113835
Опубликована: Дек. 1, 2024
Язык: Английский
Процитировано
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