Yayın:
Cationic Pd(II)/Pt(II) 5,5-diethylbarbiturate complexes with bis(2-pyridylmethyl)amine and terpyridine: Synthesis, structures,DNA/BSA interactions, intracellular distribution, cytotoxic activity and induction of apoptosis

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Tarih

2015-11

Kurum Yazarları

İçsel, Ceyda
Yılmaz, Veysel Turan
Kaya, Yunus
Durmuş, Selvi
Sarımahmut, Mehmet
Ulukaya, Engin

Yazarlar

Büyükgüngör, Orhan

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayımcı

Elsevier Science

Araştırma Projeleri

Akademik Birimler

Dergi Sayısı

Özet

Four new cationic Pd(II) and Pt(II) 5,5-diethylbarbiturate (barb) complexes, [M(barb)(bpma)]X center dot H2O [M = pd(II), X = Cl (1); M = Pt-II, X = NO3- (2)] and [M(barb)(terPY)]NO3 center dot 0.5H(2)O [M = Pd-II (3); M = Pt-II (4)], where bpma = bis(2-pyridylmethyl)amine and terpy = terpyridine, were synthesized and characterized by elemental analysis, IR, UV-vis, NMR, ESI-MS and X-ray crystallography. The DNA binding properties of the cationic complexes were investigated by spectroscopic titrations, displacement experiments, viscosity, DNA melting and electrophoresis measurements. The results revealed that the complexes effectively bind to FS-DNA (fish sperm DNA) via intercalative/minor groove binding modes with intrinsic binding constants (Kb) in the range of 0.50 x 10(4) - 1.67 x 10(5) M-1. Absorption, emission and synchronous fluorescence measurements showed strong association of the complexes with protein (BSA) through a static mechanism. The mode of interaction of complexes towards DNA and protein was also supported by molecular docking. Complexes 1 and 3 showed significant nuclear uptake in HT-29 cells. In addition, 1 and 3 showed higher inhibition than cisplatin on the growth of MCF-7 and HT-29 cells and induced apoptosis on these cells much more effectively than the rest of the complexes as evidenced by pyknotic nuclear morphology. The levels of caspase-cleaved cytokeratin 18 (M30 antigen) in HT-29 cells treated with 1 and 3 increased in a dose-dependent manner, suggesting apoptosis. Moreover, qRT-PCR experiments showed that I and 3 caused significant increases in the expression of TNFRSF10B in HT-29 cells, indicating the initiation of apoptosis via cell surface death receptors.

Açıklama

Anahtar kelimeler

Anticancer activity, DNA/BSA binding, Electrophoresis, Nuclear uptake, Pd(II)/Pt(II) 5,5-Diethylbarbiturate complexes, Human serum-albumin, Intrastrand cross-link, Dna dodecamer duplex, Cells in-vitro, Crystal-structure, Platinum(II) complexes, Coordination-compounds, Biological evaluation, Anticancer activity, Molecular docking, Biochemistry & molecular biology, Chemistry

Alıntı

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