Anticancer Effect of a Novel Palladium-Saccharinate Complex of Terpyridine by Inducing Apoptosis on Ehrlich Ascites Carcinoma (EAC) in Balb-C Mice

被引:0
作者
Ikitimur-Armutak, Elif Ilkay [1 ]
Sonmez, Kivilcim [2 ]
Akgun-Dar, Kadriye [3 ]
Sennazli, Gulbin [2 ]
Kapucu, Aysegul [4 ]
Yigit, Funda [1 ]
Yilmaz, Veysel Turan [5 ]
Ulukaya, Engin [6 ]
机构
[1] Istanbul Univ, Dept Histol & Embryol, Istanbul, Turkey
[2] Istanbul Univ, Fac Vet Med, Pathol, Istanbul, Turkey
[3] Istanbul Univ, Fac Sci, Dept Biol, Sect Zool, Istanbul, Turkey
[4] Istanbul Univ, Fac Sci, Dept Biol, Sect Bot, Istanbul, Turkey
[5] Uludag Univ, Fac Chem, Dept Inorgan Chem, TR-16059 Bursa, Turkey
[6] Uludag Univ, Fac Med, Dept Biochem, TR-16059 Bursa, Turkey
关键词
Pd(II) complex; EAC; in vivo; tumor; PCNA; apoptosis; BIOLOGICAL EVALUATION; CRYSTAL-STRUCTURE; CANCER; P53; EXPRESSION; MECHANISMS; MUTATIONS;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: [Pd(sac)(terpy)](sac)center dot 4H(2)O (sac=saccharinate and terpy=2,2':6',2 ''-terpyridine) is newly-synthesized palladium(II) (Pd) complex. We investigated the antiproliferative and apoptotic effects of this complex on Ehrlich ascites carcinoma (EAC). Materials and Methods: EAC cells were administered to 33 Balb/c mice. Mice were divided randomly into four groups: control, cisplatin. Pd(II) complex and paclitaxel. Control group animals received 0.9% NaCl; other groups received treatments cisplatin, Pd(II) complex and paclitaxel on days 7 and 12. At day 14, animals were sacrificed. Expression of active caspase-3, p53 and proliferating cell nuclear antigen (PCNA) was investigated and apoptosis was evaluated by terminal deoxynucleotidyltransferase (TdT)-mediated nick-end labelling (TUNEL) technique. Results: Expression of p53 and PCNA were found to be decreased (p<0.0001), cells with active caspase-3 and TUNEL-positive cells were found to be increased (p<0.0001) in all treatment groups. Conclusion: Like cisplatin and paclitaxel, this Pd(II) complex has a strong anticancer activity against EAC by inducing apoptosis and suppressing proliferation in vivo.
引用
收藏
页码:1491 / 1497
页数:7
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