Evidence map›Paper›PMID 40430277›Full record

ReviewMolecules (Basel, Switzerland)2025

Innovative Approaches in the Synthesis and Optimization of Copper Complexes for Antitumor Therapies: A Comprehensive Review.

Clara Maria Faria Silva, Ricardo Campos Lino, Mariana Cristina Teixeira de Moura, Anna Paula de Sá Borges, Robson José de Oliveira Júnior

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Copper Complexes: Main Mechanisms as Anticancer Agents.Molecules (Basel, Switzerland) · 2026
    Review
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

5 authors.

Clara Maria Faria SilvaLaboratory of Cytogenetics, Institute of Biotechnology, Federal University of Uberlândia, Campus Umuarama, St. Piaui s/n, Uberlândia 38405-320, MG, Brazil.ORCID 0000-0002-3300-5073
Ricardo Campos LinoLaboratory of Cytogenetics, Institute of Biotechnology, Federal University of Uberlândia, Campus Umuarama, St. Piaui s/n, Uberlândia 38405-320, MG, Brazil.ORCID 0000-0002-7667-0671
Mariana Cristina Teixeira de MouraLaboratory of Cytogenetics, Institute of Biotechnology, Federal University of Uberlândia, Campus Umuarama, St. Piaui s/n, Uberlândia 38405-320, MG, Brazil.
Anna Paula de Sá BorgesAcademic Institute of health and biological Sciencies, State University of Goiás, UnU Itumbiara, Av. Modesto de Carvalho, s/n, District Agro. Industrial, Itumbiara 75536-100, GO, Brazil.
Robson José de Oliveira JúniorLaboratory of Cytogenetics, Institute of Biotechnology, Federal University of Uberlândia, Campus Umuarama, St. Piaui s/n, Uberlândia 38405-320, MG, Brazil.ORCID 0000-0001-8453-3194

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior 0Fundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-00704-21Fundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-01087-21National Council for Scientific and Technological Development 0National Institute of Science, Technology in Theranostics and Nanobiotechnology - INCT - Teranano 0Rede Mineira de Pesquisa Translacional em Imunobiológicos e Biofármacos no Câncer (REMITRIBIC), 0Universidade Estadual de Goiás 0Universidade Federal de Uberlândia 0
6 · The paper itself

Abstract

Cancer is the second leading cause of death worldwide. Late diagnosis, low drug selectivity, high toxicity, and treatment resistance are challenges associated with pharmacological interventions. The commonly used therapies include surgery, radiotherapy, hormonal therapy, immunotherapy, and chemotherapy. Recently, Cu complexes have been studied owing to their biological functions and effects on tumor angiogenesis. In this review, we examined 23 types of cancer and revealed the use of cell lines. The synthesis of Cu complexes with ligands such as phenanthroline and thiosemicarbazones has also been reported. Such co-ligation is promising because of its high cytotoxicity and selectivity. Compared with cisplatin, Cu complexes, especially mixed complexes, showed better interactions with DNA, generating reactive oxygen species and inducing apoptosis. Nanoformulations have also been adopted to improve the pharmacological activity of compounds. They enhance the efficacy of complexes by targeting them to the tumor tissue, thereby improving their safety. Studies have also explored Cu complexes with clinically relevant pharmacophores, suggesting a "hybrid chemotherapy" against resistant tumors. Overall, Cu complexes have demonstrated therapeutic versatility, antitumor efficacy, and reduced adverse effects, showing great potential as alternatives to conventional chemotherapy and justifying future clinical investigations to validate their use.

Indexed as

Antineoplastic AgentsCoordination ComplexesCopperNeoplasmsAnimalsApoptosisHumansAntineoplastic AgentsCoordination ComplexesCopperanticancercopper complexescytotoxic activity

Identifiers

PMID40430277
PMCPMC12114317

What OpenQuestion holds

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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.