[Ru(pipe)(dppb)(bipy)]PF6: A novel ruthenium complex that effectively inhibits ERK activation and cyclin D1 expression in A549 cells
| Autor: | Marco A. Banionis, Felipe T. Martins, Marília I.F. Barbosa, Jaqueline Carvalho de Oliveira, Júlia Scaff Moreira Dias, Marina M. Ortega, Marisa Ionta, Graciana Y. Garavelli, Antonio C. Doriguetto, Guilherme Álvaro Ferreira-Silva, Claudio Viegas, Fabio B. do Nascimento |
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| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
A549 cell education.field_of_study Cell cycle checkpoint Stereochemistry Chemistry Cell growth education Population General Medicine Toxicology 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Cyclin D1 Apoptosis 030220 oncology & carcinogenesis Cancer research Cytotoxic T cell Cytotoxicity |
| Zdroj: | Toxicology in Vitro. 44:382-391 |
| ISSN: | 0887-2333 |
| Popis: | Lung cancer is the most frequent type of cancer worldwide. In Brazil, only 14% of the patients diagnosed with lung cancer survived 5years in the last decades. Although improvements in the therapeutic approach, it is relevant to identify new chemotherapeutic agents. In this framework, ruthenium metal compounds emerge as a promising alternative to platinum-based compounds once they displayed lower cytotoxicity and more selectivity for tumor cells. The present study aimed to evaluate the antitumor potential of innovative ruthenium(II) complex, [Ru(pipe)(dppb)(bipy)]PF6 (PIPE) on A549 cells, which is derived from non-small cell lung cancer. Results demonstrated that PIPE effectively reduced the viability and proliferation rate of A549 cells. When PIPE was used at 9μM there was increase in G0/G1 cell population with concomitant reduction in frequency of cells in S-phase, indicating cell cycle arrest in G1/S transition. Antiproliferative activity of PIPE was associated to its ability of reducing cyclin D1 expression and ERK phosphorylation levels. Cytotoxic activity of PIPE on A549 cells was observed when PIPE was used at 18μM, which was associated to its ability of inducing apoptosis by intrinsic pathway. Taken together, the data demonstrated that PIPE is a promising antitumor agent and further in vivo studies should be performed. |
| Databáze: | OpenAIRE |
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