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A Maltol-Containing Ruthenium Polypyridyl Complex as a Potential Anticancer Agent

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F20%3A00559789" target="_blank" >RIV/68378050:_____/20:00559789 - isvavai.cz</a>

  • Result on the web

    <a href="https://chemistry-europe-onlinelibrary-wiley-com.d360prx.biomed.cas.cz/doi/10.1002/chem.201904877" target="_blank" >https://chemistry-europe-onlinelibrary-wiley-com.d360prx.biomed.cas.cz/doi/10.1002/chem.201904877</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/chem.201904877" target="_blank" >10.1002/chem.201904877</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A Maltol-Containing Ruthenium Polypyridyl Complex as a Potential Anticancer Agent

  • Original language description

    Cancer is one of the main causes of death worldwide. Chemotherapy, despite its severe side effects, is to date one of the leading strategies against cancer. Metal-based drugs present several potential advantages when compared to organic compounds and they have gained trust from the scientific community after the approval on the market of the drug cisplatin. Recently, we reported the ruthenium complex ([Ru(DIP)(2)(sq)](PF6) (where DIP is 4,7-diphenyl-1,10-phenantroline and sq is semiquinonate) with a remarkable potential as chemotherapeutic agent against cancer, both in vitro and in vivo. In this work, we analyse a structurally similar compound, namely [Ru(DIP)(2)(mal)](PF6), carrying the flavour-enhancing agent approved by the FDA, maltol (mal). To possess an FDA approved ligand is crucial for a complex, whose mechanism of action might include ligand exchange. Herein, we describe the synthesis and characterisation of [Ru(DIP)(2)(mal)](PF6), its stability in solutions and under conditions that resemble the physiological ones, and its in-depth biological investigation. Cytotoxicity tests on different cell lines in 2D model and on HeLa MultiCellular Tumour Spheroids (MCTS) demonstrated that our compound has higher activity than cisplatin, inspiring further tests. [Ru(DIP)(2)(mal)](PF6) was efficiently internalised by HeLa cells through a passive transport mechanism and severely affected the mitochondrial metabolism.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    <a href="/en/project/GA17-02080S" target="_blank" >GA17-02080S: Study of molecular mechanisms involved in suppression of transcription-associated genomic instability</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2020

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Chemistry - A European Journal

  • ISSN

    0947-6539

  • e-ISSN

    1521-3765

  • Volume of the periodical

    26

  • Issue of the periodical within the volume

    22

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    13

  • Pages from-to

    4997-5009

  • UT code for WoS article

    000521613900001

  • EID of the result in the Scopus database