چکیده
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The development of suitable compounds for the effective treatment of cancer is highly demanded. Inorganic complexes based
on cobalt and copper centers have revealed a great potential for the treatment of various cancers. The current study aimed to
develop effective pyrazole-based agents against breast cancer. A pyrazole-based ligand (L: Na[
EtNCSPzMe2]) and its cobalt
and copper complexes were synthesized, and the single crystals of the complexes were prepared for crystallographic analysis.
The X-ray structure of the synthesized complexes indicated both of the complexes were mononuclear and monoclinic.
The synthesized [Co(L)3] complex demonstrated a six-coordinated distorted octahedral geometry around the cobalt center,
while the [Cu(L)2] complex occupied a four-coordinated seesaw geometry with N2S2
environment around the copper center.
The compounds were evaluated for their anticancer activities against the human breast MDA-MB-231 cell lines with the
MTT and flow cytometry assays to investigate the efficacy of these synthesized compounds in the induction of apoptosis and
death in breast cancer cells. The investigated complexes significantly indicated more anticancer activity in compare with the
free ligand and the among them Cu(II) complex showed considerable and higher activity against the tested cell lines. The
molecular docking was carried out to explore the binding modes of these compounds on DNA and epidermal growth factor
receptor precursor (EGFR) proteins. Altogether, in silico and in vitro investigations indicated that coordination of chelating
organic ligand to the metal centers promoted the compounds anticancer activity and these complexes may be used the likely
candidate for further development in cancer treatment after complementary preclinical evaluations.
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