Further Approaches in the Design of Antitumor Agents with Response to Cell Resistance: Looking toward Aza Crown Ether-dtc Complexes

被引:8
作者
Arenaza-Corona, Antonino [1 ,2 ,3 ]
Delfina Couce-Fortunez, M. [4 ]
de Blas, Andres [1 ,2 ]
Morales-Morales, David [5 ]
Santillan, Rosa [6 ]
Hopfl, Herbert [3 ]
Rodriguez-Blas, Teresa [1 ,2 ]
Barba, Victor [3 ]
机构
[1] Univ A Coruna, Grp METMED, Dept Quim, La Coruna 15071, Spain
[2] Univ A Coruna, Ctr Invest Cient Avanzadas CICA, La Coruna 15071, Spain
[3] Univ Autonoma Estado Morelos, Ctr Invest Quim IICBA, Cuernavaca 62209, Morelos, Mexico
[4] Univ Vigo, Dept Quim Inorgan, Inst Invest Sanitaria Galicia Sur, Fac Quim, Vigo 36310, Spain
[5] Univ Nacl Autonoma Mexico, Inst Quim, Ciudad De Mexico 04510, Mexico
[6] IPN, Ctr Invest & Estudios Avanzados, Dept Quim, Ciudad De Mexico 07000, Mexico
关键词
CISPLATIN NEPHROTOXICITY; PLATINUM(II) COMPLEX; DNA-DAMAGE; PSEUDOPOTENTIALS; MECHANISM; DINUCLEAR; PALLADIUM(II); POTENTIALS; CHEMISTRY; TITANIUM;
D O I
10.1021/acs.inorgchem.0c02068
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The dianionic aza crown ether-dtc N,N'-bis-(dithiocarbamate)-1,10-diaza-18-crown-6 (L2-) is a versatile ligand capable of yielding binuclear complexes with group 10 elements, also known as Ni-triade, [mu-(kappa(2) -S,-S'-L)M-2(PPh3)(4)]Cl-2 (M = Pd (1), Pt (2)), [mu-(kappa(2)-S,-S'-L)M-2(PPh3)(4)](BPh4)(2) (M = Pd (3), Pt (4)), and mu-(kappa-S,-S'-L)Ni,(PPh3)(2)Cl-2 (5), and has proven to be an excellent option to the design of metal-based drugs able to provide multiple response to cell resistance. Palladium and platinum complexes, 1 and 2, were tested for cytotoxicity in the human cervix carcinoma cell line HeLa-229, the human ovarian carcinoma cell line A2780, and the cisplatin-resistant mutant A2780cis, finding significant activity toward all three cancer cell lines, with low micromolar IC so values, comparable to cisplatin. Markedly, against the cisplatin resistant cell line A2780cis, compound 2 exhibits better cytotoxic activity than the clinical drug (IC50 = 2.3 +/- 0.2 mu M for 2 versus 3.6 +/- 0.5 mu M for cisplatin). Moreover, an enhancement of the antitumor response is achieved when adding an equimolar amount of alkali metal chloride (NaCl or KCl) to the medium, for instance, testing compound 1 against the cisplatin-resistant A2780cis cells, the IC50 decreases from 9.3 +/- 0.4 to 7.4 +/- 0.3 and 5.4 +/- 0.1 mu M, respectively, after addition of the salt solution. For the platinum derivative 2, the IC50 improves by ca. 40% reaching 1.3 +/- 0.1 mu M when potassium chloride is added. Likewise, the resistant factor found for 2 (RF = 1) confirms that this complex circumvents cisplatin-resistance in A2780cis and is improved with the addition of potassium chloride (RF = 0.65). The presence of the aza crown ether moiety as linker in the systems studied herein is a key point since, in addition to allowing and facilitating interaction with alkali metal ions, this unit is flexible enough to adapt to a variety of environments, as confirmed by the X-ray crystal structures described, where different conformations and ways to fold in are found. In order to gain insight into the electronic and structural facts involved in the interaction of complex 2 with the alkali metal ions, a DFT study was performed, and the description of the molecular electrostatic potentials (MEPs) is also presented.
引用
收藏
页码:15120 / 15134
页数:15
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