Highlights of New Strategies to Increase the Efficacy of Transition Metal Complexes for Cancer Treatments.
gold compounds
heterobimetallic complexes
metal-based drugs
platinum compounds
targeting strategies
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
29 Dec 2022
29 Dec 2022
Historique:
received:
29
11
2022
revised:
22
12
2022
accepted:
23
12
2022
entrez:
8
1
2023
pubmed:
9
1
2023
medline:
11
1
2023
Statut:
epublish
Résumé
Although important progress has been made, cancer still remains a complex disease to treat. Serious side effects, the insurgence of resistance and poor selectivity are some of the problems associated with the classical metal-based anti-cancer therapies currently in clinical use. New treatment approaches are still needed to increase cancer patient survival without cancer recurrence. Herein, we reviewed two promising-at least in our opinion-new strategies to increase the efficacy of transition metal-based complexes. First, we considered the possibility of assembling two biologically active fragments containing different metal centres into the same molecule, thus obtaining a heterobimetallic complex. A critical comparison with the monometallic counterparts was done. The reviewed literature has been divided into two groups: the case of platinum; the case of gold. Secondly, the conjugation of metal-based complexes to a targeting moiety was discussed. Particularly, we highlighted some interesting examples of compounds targeting cancer cell organelles according to a third-order targeting approach, and complexes targeting the whole cancer cell, according to a second-order targeting strategy.
Identifiants
pubmed: 36615466
pii: molecules28010273
doi: 10.3390/molecules28010273
pmc: PMC9822110
pii:
doi:
Substances chimiques
Coordination Complexes
0
Antineoplastic Agents
0
Transition Elements
0
Gold
7440-57-5
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
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