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Biological evaluation of novel thiomaltol-based organometallic complexes as topoisomerase II? inhibitors.


ABSTRACT: Topoisomerase II? (topo2?) is an essential nuclear enzyme involved in DNA replication, transcription, recombination, chromosome condensation, and highly expressed in many tumors. Thus, topo2?-targeting has become a very efficient and well-established anticancer strategy. Herein, we investigate the cytotoxic and DNA-damaging activity of thiomaltol-containing ruthenium-, osmium-, rhodium- and iridium-based organometallic complexes in human mammary carcinoma cell lines by means of several biological assays, including knockdown of topo2? expression levels by RNA interference. Results suggest that inhibition of topo2? is a key process in the cytotoxic mechanism for some of the compounds, whereas direct induction of DNA double-strand breaks or other DNA damage is mostly rather minor. In addition, molecular modeling studies performed for two of the compounds (with Ru(II) as the metal center) evinces that these complexes are able to access the DNA-binding pocket of the enzyme, where the hydrophilic environment favors the interaction with highly polar complexes. These findings substantiate the potential of these compounds for application as antitumor metallopharmaceuticals.

SUBMITTER: Legina MS 

PROVIDER: S-EPMC7186247 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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Biological evaluation of novel thiomaltol-based organometallic complexes as topoisomerase IIα inhibitors.

Legina Maria S MS   Nogueira Juan J JJ   Kandioller Wolfgang W   Jakupec Michael A MA   González Leticia L   Keppler Bernhard K BK  

Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry 20200319 3


Topoisomerase IIα (topo2α) is an essential nuclear enzyme involved in DNA replication, transcription, recombination, chromosome condensation, and highly expressed in many tumors. Thus, topo2α-targeting has become a very efficient and well-established anticancer strategy. Herein, we investigate the cytotoxic and DNA-damaging activity of thiomaltol-containing ruthenium-, osmium-, rhodium- and iridium-based organometallic complexes in human mammary carcinoma cell lines by means of several biologica  ...[more]

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