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首页> 外文期刊>Online journal of biological sciences >CYTOTOXICITY AND MODE OF CELL DEATH INDUCED BY TRIPHENYLTIN (IV) COMPOUNDS IN VITRO
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CYTOTOXICITY AND MODE OF CELL DEATH INDUCED BY TRIPHENYLTIN (IV) COMPOUNDS IN VITRO

机译:三苯甲基锡(IV)化合物体外诱导的细胞死亡和细胞死亡模式

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摘要

A series of newly synthesized organotin (IV) with JV-alkyl-Af-phenyldithiocarbamate ligands namely triphenyltin (IV) ethylphenyldithiocarbamate (compound 1) and triphenyltin (IV) butylphenyldithiocarbamate (compound 2) were assessed for their cytotoxic effect against HT-29 human colon adenocarcinoma cells and human CCD-I8C0 normal colon cells. The cytotoxicity of these organotins in both cells was assessed using 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazholium bromide (MTT) assay upon 24 h treatment. Both compounds demonstrated potent cytotoxicity towards HT-29 cells with the IC50 of 0.18 uM for compound 1 and 0.20 iM for compound 2. Interestingly, compound 1 exhibited lower cytotoxicity towards CCD-I8C0 with IC50 of 1.55 uM whereas no IC50 was detected for compound 2 up to 2 uM treatment. The mode of cell death was determined based on the externalization of phosphatidylserine using flow cytometry. Cells treated with compound 1 and compound 2 were mainly viable and the apoptotic cell death was around 10% which suggests that both compounds induced growth arrest. In conclusion, this study demonstrated that both compounds were selective towards human colorectal cells by giving a strong cytotoxicity to cancer cells and low toxicity towards normal cells. Both compounds were suggested to induce growth arrest in HT-29 cells.
机译:评估了一系列新的具有JV-烷基-Af-苯基二硫代氨基甲酸酯配体的有机锡(IV),即三苯基锡(IV)乙基苯基二硫代氨基甲酸酯(化合物1)和三苯基锡(IV)丁基苯基二硫代氨基甲酸酯(化合物2)对HT-29人结肠的细胞毒性作用腺癌细胞和人CCD-I8C0正常结肠细胞。在处理24小时后,使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氢噻吩(MTT)法评估了两种细胞中这些有机素的细胞毒性。两种化合物均表现出对HT-29细胞的有效细胞毒性,化合物1的IC50为0.18 uM,化合物2的IC50为0.20 iM。有趣的是,化合物1对CCD-I8C0的细胞毒性较低,IC50为1.55 uM,而未检测到IC50。 2至2 uM处理。使用流式细胞术基于磷脂酰丝氨酸的外在化确定细胞死亡的模式。用化合物1和化合物2处理的细胞主要是存活的,并且凋亡细胞死亡为约10%,这表明这两种化合物诱导生长停滞。总之,这项研究证明了这两种化合物对人结肠直肠细胞具有选择性,因为它们对癌细胞具有很强的细胞毒性,而对正常细胞则具有低毒性。两种化合物均被认为可诱导HT-29细胞生长停滞。

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