MASURI, Sebastiano, Petr VAŇHARA, Maria Grazia CABIDDU, Lukáš MORÁŇ, Josef HAVEL, Enzo CADONI and Tiziana PIVETTA. Copper(II) Phenanthroline-Based Complexes as Potential AntiCancer Drugs: A Walkthrough on the Mechanisms of Action. Molecules. Basel: MDPI, 2022, vol. 27, No 1, p. 1-26. ISSN 1420-3049. Available from: https://dx.doi.org/10.3390/molecules27010049.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Copper(II) Phenanthroline-Based Complexes as Potential AntiCancer Drugs: A Walkthrough on the Mechanisms of Action
Authors MASURI, Sebastiano (guarantor), Petr VAŇHARA (203 Czech Republic, belonging to the institution), Maria Grazia CABIDDU, Lukáš MORÁŇ (203 Czech Republic, belonging to the institution), Josef HAVEL (203 Czech Republic, belonging to the institution), Enzo CADONI and Tiziana PIVETTA.
Edition Molecules, Basel, MDPI, 2022, 1420-3049.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10401 Organic chemistry
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.600
RIV identification code RIV/00216224:14110/22:00125429
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.3390/molecules27010049
UT WoS 000755482700001
Keywords in English cancer; coordination compounds; copper; 1-10-phenanthroline; anticancer chemotherapy; chemoresistance; cell stress response
Tags 14110517, rivok
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 2/2/2023 13:41.
Abstract
Copper is an endogenous metal ion that has been studied to prepare a new antitumoral agent with less side-effects. Copper is involved as a cofactor in several enzymes, in ROS production, in the promotion of tumor progression, metastasis, and angiogenesis, and has been found at high levels in serum and tissues of several types of human cancers. Under these circumstances, two strategies are commonly followed in the development of novel anticancer Copper-based drugs: the sequestration of free Copper ions and the synthesis of Copper complexes that trigger cell death. The latter strategy has been followed in the last 40 years and many reviews have covered the anticancer properties of a broad spectrum of Copper complexes, showing that the activity of these compounds is often multi factored. In this work, we would like to focus on the anticancer properties of mixed Cu(II) complexes bearing substituted or unsubstituted 1,10-phenanthroline based ligands and different classes of inorganic and organic auxiliary ligands. For each metal complex, information regarding the tested cell lines and the mechanistic studies will be reported and discussed. The exerted action mechanisms were presented according to the auxiliary ligand/s, the metallic centers, and the increasing complexity of the compound structures.
Links
MUNI/A/1390/2020, interní kód MUName: Analytická a fyzikální chemie ve výzkumu biologických, geologických a syntetických materiálů (Acronym: BIOGEOSYNT)
Investor: Masaryk University
MUNI/A/1689/2020, interní kód MUName: Zdroje pro tkáňové inženýrství 11 (Acronym: TissueEng 11)
Investor: Masaryk University
ROZV/28/LF23/2020, interní kód MUName: Objasněni vlivu ztráty TUSC3 na změnu fenotypových vlastnosti buněk ovariálního povrchového epitelu.
Investor: Ministry of Education, Youth and Sports of the CR, Internal development projects
PrintDisplayed: 28/7/2024 22:22