4.6 Article

Anticancer Activity of Some Ruthenium(III) Complexes with Quinolone Antibiotics: In Vitro Cytotoxicity, Cell Cycle Modulation, and Apoptosis-Inducing Properties in LoVo Colon Cancer Cell Line

Journal

APPLIED SCIENCES-BASEL
Volume 11, Issue 18, Pages -

Publisher

MDPI
DOI: 10.3390/app11188594

Keywords

ruthenium complexes; quinolones; cancer drug resistance; colon cancer; cytotoxicity; apoptosis; cell cycle

Funding

  1. Ministry of Research, the Executive Unit for Financing Higher Education, Research, Development and Innovation (UEFISCDI) [PCCA PN-II 136/2012, PN-III-P2-2.1-PED-2019-5143, PED 383/2020]

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Our study focused on the anticancer activity of several ruthenium (Ru) complexes with quinolone antibiotics in colon tumor cell cultures. The results showed dose-dependent increased levels of cell lysis and induction of apoptosis in LoVo cancer cells treated with the Ru(III) complexes. Additionally, a major decrease in cell proliferation, with a G0/G1 cell arrest and modulation of cell cycle phases, was observed, indicating the potential for the Ru(III) complexes in future chemotherapeutic approaches.
Cisplatin is one of the most effective anticancer agents used to treat colon cancer, which is the third malignancy between the most common human cancers in the world, but the resistance developed represents an obstacle against the full success of chemotherapy. An emerging interest appeared in finding other metallic compounds, such as ruthenium(III) complexes, for chemotherapeutic application in cancer. Our study focused on the anticancer activity of several ruthenium (Ru) complexes with quinolone antibiotics in colon tumor cell cultures. Real-time cell analysis and drug-mediated cytotoxicity tests monitored the inhibitory effects in the drug-treated LoVo colon cancer cells. Flow cytometry assays were performed to evaluate cell cycle phases distribution and apoptotic events. The obtained results showed dose-dependent increased levels of cell lysis and induction of apoptosis in LoVo cancer cells treated with the Ru(III) complexes. In addition, data showed a major decrease in cell proliferation, since the percentages of cells distributed in the S cell cycle phase diminished, and a G0/G1 cell arrest was observed. Therefore, our results strongly suggest that the newly synthesized Ru(III) complexes might play an important role in future chemotherapeutic approaches, since their activity is based on diminishing cell proliferation, induction of apoptosis, and modulation of cell cycle phases.

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