Cytotoxicity and mechanism of action of metal complexes: An overview.


Journal

Toxicology
ISSN: 1879-3185
Titre abrégé: Toxicology
Pays: Ireland
ID NLM: 0361055

Informations de publication

Date de publication:
15 06 2023
Historique:
received: 05 04 2023
revised: 18 04 2023
accepted: 19 04 2023
medline: 1 6 2023
pubmed: 23 4 2023
entrez: 22 04 2023
Statut: ppublish

Résumé

After the discovery of cisplatin, many metal compounds were investigated for the therapy of diseases, especially cancer. The high therapeutic potential of metal-based compounds is related to the special properties of these compounds, such as their redox activity and ability to target vital biological sites. The overproduction of ROS and the consequent destruction of the membrane potential of mitochondria and/or the DNA helix is one of the known pathways leading to the induction of apoptosis by metal complexes. The apoptosis process can occur via the death receptor pathway and/or the mitochondrial pathway. The expression of Bcl2 proteins and the caspase family play critical roles in these pathways. In addition to apoptosis, autophagy is another process that regulates the suppression or promotion of various cancers through a dual action. On the other hand, the ability to interact with DNA is an important property found in several metal complexes with potent antiproliferative effects against cancer cells. These interactions were classified into two important categories: covalent/coordinated or subtle, and non-coordinated interactions. The anticancer activity of metal complexes is sometimes achieved by the simultaneous combination of several mechanisms. In this review, the anticancer effect of metal complexes is mechanistically discussed by different pathways, and some effective agents on their antiproliferative properties are explained.

Identifiants

pubmed: 37087063
pii: S0300-483X(23)00102-6
doi: 10.1016/j.tox.2023.153516
pii:
doi:

Substances chimiques

Coordination Complexes 0
Antineoplastic Agents 0
Cisplatin Q20Q21Q62J
DNA 9007-49-2

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

153516

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Sara Abdolmaleki (S)

School of Science and Technology, The University of Georgia, Tbilisi, Georgia. Electronic address: sara.abdolmaleki19@gmail.com.

Samad Khaksar (S)

School of Science and Technology, The University of Georgia, Tbilisi, Georgia. Electronic address: s.khaksar@ug.edu.ge.

Alireza Aliabadi (A)

Pharmaceutical Sciences Research Center, Health Institute, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Akram Panjehpour (A)

Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, P.O. Box 14115-175, Tehran, Iran.

Elham Motieiyan (E)

Department of Chemistry, Payame Noor University, P.O. BOX 19395-4697, Tehran, Iran.

Domenica Marabello (D)

Dipartimento di Chimica, University of Torino, Via P. Giuria 7, 10125 Torino, Italy; Interdepartmental Centre for Crystallography, University of Torino, Italy.

Mohammad Hossein Faraji (MH)

Physiology Division, Department of Basic Science, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.

Maria Beihaghi (M)

School of Science and Technology, The University of Georgia, Tbilisi, Georgia; Department of Biology, Kavian Institute of Higher Education, Mashhad, Iran.

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Classifications MeSH