Nanozyme-mediated glutathione depletion for enhanced ROS-based cancer therapies: a comprehensive review DOI
Xinyu Wang,

Nan Wei,

Yang Zhang

и другие.

Nanomedicine, Год журнала: 2024, Номер 20(3), С. 279 - 290

Опубликована: Дек. 27, 2024

Nanozymes can improve reactive oxygen species (ROS)-based cancer therapies by targeting cells' antioxidant defense mechanisms, particularly glutathione (GSH) depletion, to overcome ROS-resistant cells. Nanozymes, innovative enzyme-mimetic nanomaterials, generate ROS, alter the tumor microenvironment (TME), and synergize with photodynamic therapy (PDT), chemodynamic (CDT), radiotherapy, immunotherapy. This review shows how nanozymes catalyze ROS generation, selectively deplete GSH, target elimination, offering clear advantages over standard therapies. defenses PDT, CDT, radiation To maximize nanozyme-based treatment efficacy, biodistribution, biocompatibility, heterogeneity must be assessed. treatment, multifunctional, stimuli-responsive synergistic combination drugs should developed.

Язык: Английский

Microencapsulation of glutathione through water/oil emulsification and complex coacervation: Improved encapsulation efficiency, physicochemical stability, and sustained release effect DOI

Jingyang Yu,

Ge Du,

Yishun Yao

и другие.

Food Research International, Год журнала: 2025, Номер 202, С. 115723 - 115723

Опубликована: Янв. 10, 2025

Язык: Английский

Процитировано

1

Red emitting carbon dots for detection of endogenous glutathione with fluorescence enhancement and cell imaging DOI
Tongtong Zhao, Huilin Chen,

Ziyan Song

и другие.

Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy, Год журнала: 2025, Номер 333, С. 125901 - 125901

Опубликована: Фев. 13, 2025

Язык: Английский

Процитировано

0

Magnesium ions enhance biogenic amine degradation by Pichia kudriavzevii MZ5: Insights from transcriptomics and novel recombinant enzyme expression DOI

Cuicui Zhu,

Ying Xu, Dongfeng Wang

и другие.

International Journal of Biological Macromolecules, Год журнала: 2025, Номер unknown, С. 141617 - 141617

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

Carotenoids for Antiaging: Nutraceutical, Pharmaceutical, and Cosmeceutical Applications DOI Creative Commons
Mariia Shanaida, Olha Мykhailenko, Roman Lysiuk

и другие.

Pharmaceuticals, Год журнала: 2025, Номер 18(3), С. 403 - 403

Опубликована: Март 13, 2025

Background: Carotenoids are bioactive tetraterpenoid C40 pigments that actively synthesized by plants, bacteria, and fungi. Compounds such as α-carotene, β-carotene, lycopene, lutein, astaxanthin, β-cryptoxanthin, fucoxanthin, zeaxanthin have attracted increasing attention for their antiaging properties. They exhibit antioxidant, neuroprotective, anti-inflammatory properties, contributing to the prevention treatment of age-related diseases. Objectives: The aim this study was comprehensively analyze pharmacological potential biological mechanisms carotenoids associated with disorders evaluate application in nutraceuticals, pharmaceuticals, cosmeceuticals. Methods: A systematic review studies published over past two decades conducted using databases PubMed, Scopus, Web Science. selection criteria included clinical, silico, vivo, vitro investigating therapeutic effects carotenoids. Results: demonstrate a variety health benefits, including macular degeneration, cancer, cognitive decline, metabolic disorders, skin aging. Their role nutraceuticals is well supported ability modulate oxidative stress inflammatory pathways. In show promising results formulations targeting neurodegenerative diseases disorders. cosmeceuticals, they improve protecting it against UV radiation damage. However, bioavailability, optimal dosages, toxicity, interactions other compounds remain critical factors maximize efficacy still require careful evaluation scientists. Conclusions: interventions applications fields. Further research needed optimize formulas, confirm long-term safety effectiveness, especially aging population.

Язык: Английский

Процитировано

0

A new one-pot technique for obtaining potential indapamide metabolites by oxidation and conjugation on MALDI target DOI Creative Commons
Olga A. Keltsieva, A. A. Afanasyeva,

S. K. Ilyushonok

и другие.

Опубликована: Март 22, 2025

Introduction. Metabolic activation of xenobiotics, including pharma drugs, is considered to be one the main mechanisms for development idiosyncratic reactions. Accordingly, potential bioactivation a xenobiotic should carefully evaluated in early stages drug development. In this regard, search new rapid and effective screening techniques reactive metabolites xenobiotics presents particular interest. Objective . Development technique modeling processes biotransformation vitro identify indapamide. Materials methods Non-enzymatic instrumental methods, such as electrochemical oxidation (ECO) photocatalytic (PCO) volume, were used comparison methods. The second phase metabolism was modeled by incubating products indapamide with trapping agent (glutathione, GSH). products, well their conjugates GSH, then analyzed high-performance liquid chromatography–tandem mass spectrometry (HPLC–MS/MS). developed one-pot based on UV-induced PCO presence GSH surface target functionalized titanium dioxide followed detection matrix-assisted laser desorption/ionization (MALDI). Results. use ECO resulted 5 3 adducts while volume allowed 7 1 adduct GSH. detected 8 addition number known total 4 previously unstudied each three Conclusions. proposed analytical showed its higher informativity combined simplicity rapidity, which makes it promising candidate preclinical studies drugs predicting toxicity pharmaceutical objects, studying various xenobiotics.

Язык: Английский

Процитировано

0

Knockdown of SLC7A5 inhibits malignant progression and attenuates oxaliplatin resistance in gastric cancer by suppressing glycolysis DOI Creative Commons
Yan Zhang, Jian Cao,

Zheng Yuan

и другие.

Molecular Medicine, Год журнала: 2025, Номер 31(1)

Опубликована: Март 25, 2025

Abstract Background Chemotherapy resistance is a major challenge in the treatment of intermediate and advanced gastric cancer (GC). This study aimed to recognize oxaliplatin resistance-related genes (OXARGs) GC explore their role mechanism GC. Methods OXARGs with prognostic value were analyzed using data from GEO TCGA databases. RT-qPCR WB assay applied verify expression MT2A, NOTCH1 SLC7A5 oxaliplatin-resistant cells (HGC27R MKN45R). The effect on malignant phenotype was verified by CCK-8, EDU, TUNEL, colony formation, wound healing, transwell assay, tumor bearing experiments assay. Results Bioinformatics analysis experimental validation indicate that target for oxaliplatin-resistance Knockdown obviously decreased viability, migration, invasion vitro growth vivo. It also increased apoptosis levels BAX expression, reduced BCL2, MMP 2 MMP9. Additionally, knockdown enhanced sensitivity both Furthermore, downregulated HK2, LDHA, Glut1, PDK1 vivo vitro, leading extracellular glucose lactate levels. However, glutathione significantly attenuated regulatory cells. Trial registration Not Applicable. Conclusion inhibits progression attenuates suppressing glycolysis.

Язык: Английский

Процитировано

0

Alcohol exposure alters the diversity and composition of oral microbiome DOI Creative Commons
Zirui Zhao, Jiaxin Li, Juan Liu

и другие.

Frontiers in Cellular and Infection Microbiology, Год журнала: 2025, Номер 15

Опубликована: Апрель 7, 2025

Introduction Alcohol exposure has been shown to have complex, and sometimes paradoxical, associations with various serious diseases. Currently, there is no knowledge about the effects of alcohol on dynamics oral microbial communities. Objective The study aims investigate chronic consumption diversity composition rat microbiota using 16S rRNA gene amplicon sequencing. Methods In our study, were 2 groups, including a control group (C group) an (A group), 10 rats in every group. For ten weeks, A treated intragastrically day, whereas C got water. After serum levels alanine aminotransferase (ALT) aspartate (AST) measured. Oral swabs taken from both total DNA was extracted for high-throughput sequencing gene. Results According results obtained significant differences observed relative abundances Alpha measures statistically significantly higher (P < 0.05) compared At genus level, altered abundance several microbes, increased unidentified_Chloroplast, Acinetobacter, Vibrio, Romboutsia, Pseudoalteromonas, Aeromonas, Ralstonia, Turicibacter, Shewanella , Bacteroides . Conversely, Haemophilus Streptococcus less abundant Conclusion associated microbiome. These findings contribute understanding potential role bacteria alcohol-related systemic diseases, providing foundational work future prevention intervention studies.

Язык: Английский

Процитировано

0

Identification of QTLs and candidate genes screening for hypoxia tolerance in Pacific white shrimp (Litopenaeus vannamei) DOI

Xiawen Li,

Yian Zhu,

Zhixiang Yuan

и другие.

Aquaculture Reports, Год журнала: 2025, Номер 42, С. 102824 - 102824

Опубликована: Апрель 19, 2025

Язык: Английский

Процитировано

0

Nanozyme-mediated glutathione depletion for enhanced ROS-based cancer therapies: a comprehensive review DOI
Xinyu Wang,

Nan Wei,

Yang Zhang

и другие.

Nanomedicine, Год журнала: 2024, Номер 20(3), С. 279 - 290

Опубликована: Дек. 27, 2024

Nanozymes can improve reactive oxygen species (ROS)-based cancer therapies by targeting cells' antioxidant defense mechanisms, particularly glutathione (GSH) depletion, to overcome ROS-resistant cells. Nanozymes, innovative enzyme-mimetic nanomaterials, generate ROS, alter the tumor microenvironment (TME), and synergize with photodynamic therapy (PDT), chemodynamic (CDT), radiotherapy, immunotherapy. This review shows how nanozymes catalyze ROS generation, selectively deplete GSH, target elimination, offering clear advantages over standard therapies. defenses PDT, CDT, radiation To maximize nanozyme-based treatment efficacy, biodistribution, biocompatibility, heterogeneity must be assessed. treatment, multifunctional, stimuli-responsive synergistic combination drugs should developed.

Язык: Английский

Процитировано

1