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Arene Ru(II) Complexes Acted as Potential KRAS G-Quadruplex DNA Stabilizer Induced DNA Damage Mediated Apoptosis to Inhibit Breast Cancer Progress.


ABSTRACT: A series of arene Ru(II) complexes, [(η6-MeC6H5)Ru(L)Cl]Cl, (L=o-ClPIP, 1; m-ClPIP, 2 and p-ClPIP, 3) (o-ClPIP=2-(2-chlorophenyl)imidazo[4,5-f][1,10]phenanthroline; m-ClPIP=2-(3-chlorophenyl)imidazo[4,5-f][1,10]phenanthroline; p-ClPIP=2-(4-chlorophenyl)imidazo[4,5-f][1,10]phenanthroline) was synthesized and investigated as a potential apoptosis inducer in chemotherapy. Spectroscopy and molecular docking simulations show that 1 exhibits moderated binding affinity to KRAS G-quadruplex DNA by groove mode. Further, in vitro studies reveal that 1 displays inhibitory activity against MCF-7 growth with IC50 = 3.7 ± 0.2 μM. Flow cytometric analysis, comet assay, and immunofluorescence confirm that 1 can induce the apoptosis of MCF-7 cells and G0/G1 phase arrest through DNA damage. In summary, the prepared arene Ru(II) complexes can be developed as a promising candidate for targeting G-quadruplex structure to induce the apoptosis of breast cancer cells via binding and stabilizing KRAS G-quadruplex conformation on oncogene promoter.

SUBMITTER: Qian J 

PROVIDER: S-EPMC9146995 | biostudies-literature | 2022 May

REPOSITORIES: biostudies-literature

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Arene Ru(II) Complexes Acted as Potential <i>KRAS</i> G-Quadruplex DNA Stabilizer Induced DNA Damage Mediated Apoptosis to Inhibit Breast Cancer Progress.

Qian Jiayi J   Liu Ruotong R   Liu Ningzhi N   Yuan Chanling C   Wu Qiong Q   Chen Yanhua Y   Tan Weijun W   Mei Wenjie W  

Molecules (Basel, Switzerland) 20220510 10


A series of arene Ru(II) complexes, [(<i>η</i><sup>6</sup>-MeC<sub>6</sub>H<sub>5</sub>)Ru(L)Cl]Cl, (L=<i>o</i>-ClPIP, <b>1</b>; <i>m</i>-ClPIP, <b>2</b> and <i>p</i>-ClPIP, <b>3</b>) (<i>o</i>-ClPIP=2-(2-chlorophenyl)imidazo[4,5-f][1,10]phenanthroline; <i>m</i>-ClPIP=2-(3-chlorophenyl)imidazo[4,5-f][1,10]phenanthroline; <i>p</i>-ClPIP=2-(4-chlorophenyl)imidazo[4,5-f][1,10]phenanthroline) was synthesized and investigated as a potential apoptosis inducer in chemotherapy. Spectroscopy and molecula  ...[more]

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