Evidence map›Paper›PMID 40380046›Full record

ReviewDiscover oncology2025

Advancing cancer therapy: the role of silver(I) phosphine complexes in overcoming resistance and toxicity.

Reinout Meijboom, Austine Ofondu Chinomso Iroegbu, Suprakas Sinha Ray

Abstract readReview
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Reinout MeijboomDepartment of Chemical Sciences, University of Johannesburg, Auckland Park, Johannesburg, 2006, South Africa. rmeijboom@uj.ac.za.ORCID http://orcid.org/0000-0003-0901-5690
Austine Ofondu Chinomso IroegbuDepartment of Chemical Sciences, University of Johannesburg, Auckland Park, Johannesburg, 2006, South Africa. aoiroegbu@gmail.com.ORCID http://orcid.org/0000-0001-9235-6554
Suprakas Sinha RayDepartment of Chemical Sciences, University of Johannesburg, Doornfontein, Johannesburg, 2028, South Africa.ORCID http://orcid.org/0000-0002-0007-2595

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Anticancer agentsApoptosisCancer therapyChemotherapy resistanceSilver(I) phosphine complexesStructural chemistry

Identifiers

PMID40380046
PMCPMC12084477

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.