DNA/HSA Interactions and Anticancer Activity of a Palladium(II) Saccharinate Complex Bearing Ethyldiphenylphosphine

Ceyda Icsel
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Abstract

The binding interactions of cis-[Pd(sac)2(PPh2Et)2] with DNA and HSA were comprehensively studied by a number of experimental methods and molecular docking studies. The Pd(II) complex bound to AT-rich sites in the major groove of DNA, and interacted with the hydrophobic cavity of the subdomain IIA of HSA. These experimental findings were supported by molecular docking studies. The Pd(II) complex had shown strong cytotoxic activity against different cancer cell lines and it also had selectivity especially for MCF-7 breast cancer cells higher than cisplatin.
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含乙基二苯基膦的钯(II)糖化配合物的DNA/HSA相互作用及抗癌活性
通过多种实验方法和分子对接研究,全面研究了顺式-[Pd(sac)2(PPh2Et)2]与DNA和HSA的结合相互作用。Pd(II)复合物结合到DNA主槽中富含at的位点上,并与HSA亚结构域IIA的疏水空腔相互作用。这些实验结果得到了分子对接研究的支持。Pd(II)复合物对不同的癌细胞系显示出很强的细胞毒活性,并且对MCF-7乳腺癌细胞的选择性高于顺铂。
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