Co(II)和Sn(IV)配位化合物在人类癌细胞系中抗增殖潜能的生物学特性:比较蛋白质组学方法。

Ana Silva, Daniel Luís, Susana Santos, Joana Silva, Ana Soraia Mendo, Lidia Coito, Telma F S Silva, Maria Fatima C Guedes da Silva, Luísa M D R S Martins, Armando J L Pombeiro, Pedro M Borralho, Cecília M P Rodrigues, Maria Guadalupe Cabral, Paula A Videira, Carolino Monteiro, Alexandra R Fernandes
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引用次数: 43

摘要

背景:顺铂抗肿瘤活性的发现引起了人们对配合物作为化疗药物的潜在应用的极大兴趣。发现选择性抑制肿瘤增殖的新化合物,避免与化疗药物相关的继发性效应和耐药性是至关重要的。方法:利用结直肠癌、肝癌、乳腺腺癌细胞系和人成纤维细胞,对有机锡(IV)化合物的体外抗增殖潜能进行了评价。用荧光显微镜和流式细胞术评估了Sn(IV)化合物和以1,10-菲罗啉-5,6-二酮为配体的Co(II)化合物的肿瘤细胞死亡情况。在结直肠癌细胞系中对这两种化合物进行了比较蛋白质组学分析。结果:Sn(IV)化合物对结直肠癌和肝癌细胞系具有较高的细胞毒作用(IC50分别为0.238±0.011 μM、0.199±0.003 μM),对人成纤维细胞具有较低的细胞毒性。两种化合物均诱导细胞凋亡,并促进氧化应激相关酶超氧化物歧化酶[Cu-Zn] (SODC)的过度表达。Co(II)化合物诱导抗凋亡蛋白(翻译控制肿瘤蛋白和内质酶)的表达降低,Sn(IV)化合物降低微管稳定蛋白、TCTP和cofilin-1的表达。结论:我们的数据揭示了Sn(IV)化合物对癌细胞具有高的体外抗增殖潜力和中等选择性。结直肠癌细胞系中Sn(IV)和Co(II)化合物的蛋白质组学分析使我们能够深入了解它们的作用机制,特别是通过影响癌症中通常不受调节的蛋白质的表达,并且也表明这两种化合物具有良好的治疗潜力。
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Biological characterization of the antiproliferative potential of Co(II) and Sn(IV) coordination compounds in human cancer cell lines: a comparative proteomic approach.

Background: The discovery of cisplatin's antitumor activity led to a great interest in the potential application of coordination compounds as chemotherapeutic agents. It is essential to identify new compounds that selectively inhibit tumor proliferation, evading secondary effects and resistance associated with chemotherapeutics.

Methods: The in vitro antiproliferative potential of an organotin(IV) compound was evaluated using colorectal and hepatocellular carcinoma, mammary gland adenocarcinoma cell lines, and human fibroblasts. Tumor cell death was evaluated by fluorescence microscopy and flow cytometry for the Sn(IV) compound and also for a Co(II) compound bearing 1,10-phenanthroline-5,6-dione as ligand. Comparative proteomic analysis for both compounds was assessed in the colorectal cancer cell line.

Results: The Sn(IV) compound presented a high cytotoxic effect in colorectal and hepatocellular carcinoma cell lines (IC50 of 0.238 ± 0.011 μM, 0.199 ± 0.003 μM, respectively), and a lower cytotoxicity in human fibroblasts. Both compounds induced cell apoptosis and promoted the overexpression of oxidative stress-related enzyme superoxide dismutase [Cu-Zn] (SODC). The Co(II) compound induced a decreased expression of anti-apoptotic proteins (translationally-controlled tumor protein and endoplasmin), and the Sn(IV) compound decreased expression of proteins involved in microtubule stabilization, TCTP, and cofilin-1.

Conclusions: Our data reveals a high in vitro antiproliferative potential against cancer cell lines and a moderate selectivity promoted by the Sn(IV) compound. Proteomic analysis of Sn(IV) and Co(II) compounds in the colorectal cancer cell line allowed an insight to their mechanisms of action, particularly by affecting the expression of proteins typically deregulated in cancer, and also suggesting a promising therapeutic potential for both compounds.

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