INDUCTION OF C-MYC G-QUADRUPLEX DNA AND CYTOTOXICITY OF A CALIX[]ARENE-CONTAINING BINUCLEAR RUTHENIUM(II) COMPLEX

ABSTRACT Herein, a binuclear ruthenium(II) complex modified by calix[4]arene group has been prepared. The complex as potential inducer and stabilizer of c-myc G-quadruplex DNA and antitumor reagent were studied. Observations revealed that the complex could bind to c-myc Pu27 and Pu22 DNA strongly with constants of 1.18 × 107 (Pu27) and 4.13 × 106 M-1 (Pu22) via groove mode as determined from absorption and luminescence titrations, as well as CD spectra. Results of continuous variation analysis confirmed that the complex interacted with c-myc G-quadruplex DNA through a 1:1 binding stoichiometry. As verified by PCR-stop assay, the replication of c-myc DNA was effectively blocked by the complex with the complete inhibition at the complex concentration of 4.0 μM both for Pu27 and Pu22, suggesting that the complex could efficiently induce the formation of c-myc G-quadruplex DNA. The appearance of blue TMB solution in the visual experiment also proved that the sequences of Pu27 and Pu22 could fold into G-quadruplex under the induction of the complex. Nevertheless, the complex was found to exhibit weak stabilization ability on c-myc G-quadruplex DNA according to FRET assay, which increased the melting point of c-myc DNA only 3-3.5 °C. The experiments on Topoisomerase inhibition and cytotoxicity of the complex showed that it acted as an inhibitor of TopoI and exhibited moderate anticancer activity against MCF-7 and Huh-7 tumor cells.

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Main Authors: Mi,Ya-Xuan, Wang,Shuang, Yan,Shuang-Mei, Cui,Yue, Wang,Ming-He, Zheng,Ze-Bao, Zhao,Xiao-Long
Format: Digital revista
Language:English
Published: Sociedad Chilena de Química 2019
Online Access:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072019000404639
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spelling oai:scielo:S0717-970720190004046392020-02-03INDUCTION OF C-MYC G-QUADRUPLEX DNA AND CYTOTOXICITY OF A CALIX[]ARENE-CONTAINING BINUCLEAR RUTHENIUM(II) COMPLEXMi,Ya-XuanWang,ShuangYan,Shuang-MeiCui,YueWang,Ming-HeZheng,Ze-BaoZhao,Xiao-Long Ruthenium c-myc G-quadruplex DNA Topoisomerase Cytotoxicity ABSTRACT Herein, a binuclear ruthenium(II) complex modified by calix[4]arene group has been prepared. The complex as potential inducer and stabilizer of c-myc G-quadruplex DNA and antitumor reagent were studied. Observations revealed that the complex could bind to c-myc Pu27 and Pu22 DNA strongly with constants of 1.18 × 107 (Pu27) and 4.13 × 106 M-1 (Pu22) via groove mode as determined from absorption and luminescence titrations, as well as CD spectra. Results of continuous variation analysis confirmed that the complex interacted with c-myc G-quadruplex DNA through a 1:1 binding stoichiometry. As verified by PCR-stop assay, the replication of c-myc DNA was effectively blocked by the complex with the complete inhibition at the complex concentration of 4.0 μM both for Pu27 and Pu22, suggesting that the complex could efficiently induce the formation of c-myc G-quadruplex DNA. The appearance of blue TMB solution in the visual experiment also proved that the sequences of Pu27 and Pu22 could fold into G-quadruplex under the induction of the complex. Nevertheless, the complex was found to exhibit weak stabilization ability on c-myc G-quadruplex DNA according to FRET assay, which increased the melting point of c-myc DNA only 3-3.5 °C. The experiments on Topoisomerase inhibition and cytotoxicity of the complex showed that it acted as an inhibitor of TopoI and exhibited moderate anticancer activity against MCF-7 and Huh-7 tumor cells.info:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.64 n.4 20192019-12-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072019000404639en10.4067/S0717-97072019000404639
institution SCIELO
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country Chile
countrycode CL
component Revista
access En linea
databasecode rev-scielo-cl
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region America del Sur
libraryname SciELO
language English
format Digital
author Mi,Ya-Xuan
Wang,Shuang
Yan,Shuang-Mei
Cui,Yue
Wang,Ming-He
Zheng,Ze-Bao
Zhao,Xiao-Long
spellingShingle Mi,Ya-Xuan
Wang,Shuang
Yan,Shuang-Mei
Cui,Yue
Wang,Ming-He
Zheng,Ze-Bao
Zhao,Xiao-Long
INDUCTION OF C-MYC G-QUADRUPLEX DNA AND CYTOTOXICITY OF A CALIX[]ARENE-CONTAINING BINUCLEAR RUTHENIUM(II) COMPLEX
author_facet Mi,Ya-Xuan
Wang,Shuang
Yan,Shuang-Mei
Cui,Yue
Wang,Ming-He
Zheng,Ze-Bao
Zhao,Xiao-Long
author_sort Mi,Ya-Xuan
title INDUCTION OF C-MYC G-QUADRUPLEX DNA AND CYTOTOXICITY OF A CALIX[]ARENE-CONTAINING BINUCLEAR RUTHENIUM(II) COMPLEX
title_short INDUCTION OF C-MYC G-QUADRUPLEX DNA AND CYTOTOXICITY OF A CALIX[]ARENE-CONTAINING BINUCLEAR RUTHENIUM(II) COMPLEX
title_full INDUCTION OF C-MYC G-QUADRUPLEX DNA AND CYTOTOXICITY OF A CALIX[]ARENE-CONTAINING BINUCLEAR RUTHENIUM(II) COMPLEX
title_fullStr INDUCTION OF C-MYC G-QUADRUPLEX DNA AND CYTOTOXICITY OF A CALIX[]ARENE-CONTAINING BINUCLEAR RUTHENIUM(II) COMPLEX
title_full_unstemmed INDUCTION OF C-MYC G-QUADRUPLEX DNA AND CYTOTOXICITY OF A CALIX[]ARENE-CONTAINING BINUCLEAR RUTHENIUM(II) COMPLEX
title_sort induction of c-myc g-quadruplex dna and cytotoxicity of a calix[]arene-containing binuclear ruthenium(ii) complex
description ABSTRACT Herein, a binuclear ruthenium(II) complex modified by calix[4]arene group has been prepared. The complex as potential inducer and stabilizer of c-myc G-quadruplex DNA and antitumor reagent were studied. Observations revealed that the complex could bind to c-myc Pu27 and Pu22 DNA strongly with constants of 1.18 × 107 (Pu27) and 4.13 × 106 M-1 (Pu22) via groove mode as determined from absorption and luminescence titrations, as well as CD spectra. Results of continuous variation analysis confirmed that the complex interacted with c-myc G-quadruplex DNA through a 1:1 binding stoichiometry. As verified by PCR-stop assay, the replication of c-myc DNA was effectively blocked by the complex with the complete inhibition at the complex concentration of 4.0 μM both for Pu27 and Pu22, suggesting that the complex could efficiently induce the formation of c-myc G-quadruplex DNA. The appearance of blue TMB solution in the visual experiment also proved that the sequences of Pu27 and Pu22 could fold into G-quadruplex under the induction of the complex. Nevertheless, the complex was found to exhibit weak stabilization ability on c-myc G-quadruplex DNA according to FRET assay, which increased the melting point of c-myc DNA only 3-3.5 °C. The experiments on Topoisomerase inhibition and cytotoxicity of the complex showed that it acted as an inhibitor of TopoI and exhibited moderate anticancer activity against MCF-7 and Huh-7 tumor cells.
publisher Sociedad Chilena de Química
publishDate 2019
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072019000404639
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