Life sciences · Journal article
Bulletin of Science and Practice · October 15, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Journal article.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Excessive accumulation of reactive oxygen species (ROS), which disrupts intracellular redox homeostasis, leads to oxidative stress and DNA strand damage, representing one of the major triggering factors of carcinogenesis. The high systemic toxicity of conventional chemotherapeutic agents and the development of multidrug resistance in tumor cells have increased interest in the application of plant-derived antioxidants in cancer therapy. This review aims to comprehensively analyze, based on scientific literature published between 2020 and 2026, the molecular anticancer mechanisms of antioxidant phytocompounds, their role in the induction of mitochondrial apoptosis, the modulation of signaling pathways, the targeting of oncomiRNAs, and their therapeutic application through green-synthesized nanocarrier systems. Plant-derived polyphenols (e.g., chlorogenic acid), diterpenes (e.g., carnosic acid), stilbenoids (e.g., oxyresveratrol), and enriched extracts activate the caspase-3/9 cascade in cancer cells, suppress the AKT/mTOR signaling pathway, and modulate Nrf2-mediated redox mechanisms. Green-synthesized silver (AgNPs) and gold (AuNPs) nanoparticles, as well as polymeric carrier systems, enhance the bioavailability of these compounds and demonstrate promising potential for improving the efficacy of targeted cancer therapy.