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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.
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http://dx.doi.org/10.3390/ijms22062947 | DOI Listing |
Biofactors
September 2025
Department of Pharmacognosy, Faculty of Pharmacy, Gazi University, Ankara, Türkiye.
Alzheimer's disease (AD), a progressive neurodegenerative disorder characterized by amyloid-β (Aβ) aggregation, oxidative stress, and neuroinflammation, remains a significant global health challenge. This study investigates the therapeutic potential of flavonols-quercetin, kaempferol, myricetin, and fisetin-in targeting Aβ aggregation and mitigating AD pathology through diverse molecular mechanisms. Our findings reveal that flavonols effectively inhibit Aβ oligomerization and fibril formation, reduce oxidative stress via Nrf2/HO-1 pathway activation, and suppress neuroinflammation by modulating microglial polarization.
View Article and Find Full Text PDFiScience
September 2025
The Scottish Association for Marine Science, Scottish Marine Institute, Culture Collection for Algae and Protozoa, Oban, Argyll PA37 1QA, Scotland.
Brown algae (Phaeophyta) encompass key primary producers of temperate and cold coastal seas, such as kelps, the cultivation of which is rapidly expanding worldwide. Here, we show that across ten brown algal species, innate resistance against the intracellular oomycete pathogen is mediated by local cell death and accompanied by cell-wide deposition of β1-3 glucans and fluorescent metabolites, the accumulation of reactive oxygen species, and the expression of programmed cell death (PCD) markers. This response also occurs in compatible strains for a fraction of the infected algal cells, which makes it a quantitative trait.
View Article and Find Full Text PDFMater Today Bio
October 2025
School and Hospital of Stomatology, Guangdong Engineering Research Center of Oral Restoration and Reconstruction, Guangzhou Key Laboratory of Basic and Applied Research of Oral Regenerative Medicine, Guangzhou Medical University, Guangzhou, 510182, China.
Rare earth nanomaterials, especially those incorporating neodymium, hold great potential for bone regeneration, but their clinical application is limited by insufficient understanding of immunomodulatory effects and potential toxicity concerns. To address this, we developed neodymium-doped mesoporous silica nanoparticles (NDMSN) to modulate macrophage autophagy and polarization. NDMSN exhibited uniform dispersion with an average size of 103 nm.
View Article and Find Full Text PDFMacromol Biosci
August 2025
Center for Nanotechnology in Drug Delivery and Division of Pharmacoengineering and Molecular Pharmaceutics, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Triple-negative breast cancer (TNBC) remains a formidable clinical challenge due to its molecular heterogeneity and resistance to conventional therapies. This study presents a high-integrity nanoemulsion (NE) formulation designed to enhance the delivery and stability of the Toll-like receptor 7/8 (TLR7/8) agonist resiquimod (R848) for immunotherapy. Neutral and negatively charged NEs were developed with and without the reactive lipophilic compound ricinoleic acid.
View Article and Find Full Text PDFDiscov Oncol
August 2025
Department of Medical Oncology, People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530021, China.
Background: Autophagy plays a critical role in the biology of gastric cancer (GC), influencing tumor progression, drug resistance, and treatment outcomes. This study aims to analyze the bibliometric landscape of autophagy research in GC, identifying key contributors, influential publications, and emerging research themes.
Method: A systematic literature search was conducted using the Web of Science Core Collection, encompassing studies published from 1977 to 2024.