Enhanced Antitumor Activity against Melanoma Cancer Cells by Nitric Oxide Release and Photosensitized Generation of Singlet Oxygen from Ruthenium Complexes

被引:24
|
作者
Ramos, Loyanne C. B. [1 ]
Pereira Marchesi, Mario Sergio [1 ]
Callejon, Daniel [1 ]
Baruffi, Marcelo Dias [1 ]
Lunardi, Claure N. [2 ]
Slep, Leonardo D. [3 ,4 ]
Bendhack, Lusiane M. [1 ]
da Silva, Roberto Santana [1 ]
机构
[1] Fac Ciencias Farmaceut Ribeirao Preto USP, Av Cafe S-N, BR-14040903 Ribeirao Preto, SP, Brazil
[2] Univ Brasilia, Fac Ceilandia, Brasilia, DF, Brazil
[3] Univ Buenos Aires, Dept Quim Inorgan Analit & Quim Fis, Pabellon 2,Ciudad Univ,C1428EHA, Buenos Aires, DF, Argentina
[4] Univ Buenos Aires, INQUIMAE, CONICET, Fac Ciencias Exactas & Nat, Pabellon 2,Ciudad Univ,C1428EHA, Buenos Aires, DF, Argentina
基金
巴西圣保罗研究基金会;
关键词
Ruthenium; Toxicity; Antitumor agents; Nitrogen oxides; Singlet oxygen; APOPTOSIS; CALCIUM; LIGHT; MECHANISMS; PHOTOLYSIS; BCL-2;
D O I
10.1002/ejic.201600217
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
We have investigated the synergistic effect of nitric oxide and singlet oxygen originating from stimulated ruthenium complexes and their photodynamic action against a melanoma cancer cell line. In aqueous solution, the photosensitizer [Ru(NH3)(5)pz](2+) (I; pz = pyrazine) and the nitrosylruthenium complex trans-[RuCl([15]aneN(4))NO](2+) (II; [15]aneN(4) = 1,4,8,12-tetrazacyclopentadecane) can produce singlet oxygen and nitric oxide, respectively. The phototoxicity of complex I does not correlate with the singlet oxygen quantum yields unless it is mediated by nitric oxide release from complex II. This effect is around 70 and 50 % higher than the effect prompted by compounds I and II, respectively, in isolation in the presence of light. It was found that the number of hypodiploid cells in the melanoma cancer cells increased, which indicates that a mixture of compounds I and II induces apoptosis of tumorigenic cell lines. Both singlet oxygen and nitric oxide produced by the ruthenium complexes enhance the photodynamic efficacy in melanoma cancer cells.
引用
收藏
页码:3592 / 3597
页数:6
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