ReviewDiscover oncology2025
Advancing cancer therapy: the role of silver(I) phosphine complexes in overcoming resistance and toxicity.
Review in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
4 citing papers in PubMed.
- Quinoline-Based Scaffolds in Anticancer Drug Discovery: Molecular Targets, Synthetic Strategies, and Biological Advances.ChemMedChem · 2026Review
- Novel triphenylphosphonium-hydrazone salts: integrated experimental and computational insights into AChE inhibition and resistance-overcoming antimicrobial and antibiofilm potential.Naunyn-Schmiedeberg's archives of pharmacology · 2026Article
- Silver(I) Complexes Bearing S-Alkyl Thiosalicylic Acid Derivatives: DNA/BSA Binding and Antitumor Activity In Vitro and In Vivo.Pharmaceutics · 2025Article
- Redox-Active Quinazolinone Thioamide Ag(I) Complexes with Potent Antibacterial Activity: Mechanistic Insights and Hydrogel-Enhanced Efficacy.Molecules (Basel, Switzerland) · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Silver(I) phosphine complexes have attracted significant attention recently due to their structural versatility and promising anticancer properties. These complexes exhibit diverse coordination geometries-ranging from tetrahedral and trigonal planar to linear-depending on the ligand environment and metal-to-ligand ratio, directly influencing their biological activity. Notably, they demonstrate substantial cytotoxicity against various cancer cell lines, including oesophageal (SNO), breast (MCF-7), and lung (A549) cancers, with IC₅₀ values in the low micromolar range. A key advantage of these complexes is their selective toxicity toward malignant cells while sparing healthy ones, positioning them as potential alternatives to traditional chemotherapeutics like cisplatin, often associated with severe side effects and drug resistance. The anticancer mechanism of silver(I) phosphine complexes primarily involves apoptosis induction through mitochondrial disruption, phosphatidylserine externalisation, and caspase activation. Additionally, these complexes can overcome common resistance mechanisms encountered in conventional cancer treatments by targeting alternative cellular pathways. This review critically evaluates the structural chemistry, synthesis, and characterisation of silver(I) phosphine complexes and recent advancements in their biological applications. Furthermore, we discuss their potential to address critical limitations in cancer therapies, particularly in overcoming drug resistance and toxicity, while exploring opportunities for ligand optimisation and progress toward clinical applications.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.