New Bis copper complex ((Z) -4 - ((4-chlorophenyl) amino) -4-oxobut-2-enoyl) oxy): Cytotoxicity in 4T1 cells and their toxicogenic potential in Swiss mice.

Abstract:

:Copper (II) complexes are promising in the development of new synthetic models for cancer treatment. In this context, we synthesized a new copper complex containing the pharmacophore group 1,4-dioxo-2-butenyl, the Bis(((Z)-4-((4-chlorophenyl) amino)-4-oxobut-2-enoyl)oxy) copper compound and we evaluated its antitumor activity in 4 T1 murine mammary adenocarcinoma cells and their toxicogenic effect in Swiss mice. The compound demonstrated cytotoxicity and genotoxicity to 4 T1 cells, and after cell cycle arrest in G1, which occurred by the increase in ATM and p21 expression, it induced the cells to apoptosis by increasing BAX and caspase-7. In vivo the compound was genotoxic in mice but did not show permanent damage, observed by the absence of increased micronucleus frequency, and did not induce changes in the biometric parameters of the animals. These results indicate that the new copper complex, described firstly in this work, presents therapeutic potential for breast cancer.

journal_name

Toxicol Appl Pharmacol

authors

de Oliveira EJT,Pessatto LR,de Freitas RON,Pelizaro BI,Rabacow APM,Vani JM,Monreal ACD,Mantovani MS,de Azevedo RB,Antoniolli-Silva ACMB,da Silva Gomes R,Oliveira RJ

doi

10.1016/j.taap.2018.08.004

subject

Has Abstract

pub_date

2018-10-01 00:00:00

pages

127-138

eissn

0041-008X

issn

1096-0333

pii

S0041-008X(18)30360-0

journal_volume

356

pub_type

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