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首页> 外文期刊>Journal of Cancer Research and Therapeutics >The effects of coadministration of tilorone dihydrochloride and culture supernatants from Lactobacillus reuteri on the mouse hepatoma cell line
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The effects of coadministration of tilorone dihydrochloride and culture supernatants from Lactobacillus reuteri on the mouse hepatoma cell line

机译:盐酸替洛龙和罗伊氏乳杆菌培养上清液共同给药对小鼠肝癌细胞系的影响

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Context: Tilorone dihydrochloride is a therapeutic agent with a different mechanism in cancer. The species of Lactobacillus have an important role in cytotoxic effect. Aims: Because of unknown effects of tilorone and culture supernatants from Lactobacillus reuteri on hepatoma, the aim of this study is to evaluate apoptotic, cytotoxic, and therapeutic effects of tilorone on mouse hepatoma cell line with and without culture supernatants from L. reuteri. Materials and Methods: To do so, after cell line culture, cells were divided into different groups such as negative control, treatment with four doses of tilorone, positive control of supernatant (single dose), and combination therapy groups of different doses of tilorone with supernatant (constant doses), for 48 h. All groups were studied with pathologic tests, biochemical study, tetrazolium dye (3-(4, 5- dimethylthiazol -2-yl)-2, 5-diphenyltetrazolium bromide [MTT]) assay, and absolute real-time-polymerase chain reaction (RT-PCR) were done to assess Bax and Bcl-2 genes expression, as molecular studies. Results: MTT assay results revealed that the tilorone tissue culture ICsub50/sub (TCICsub50/sub) on the Hepa1-6 cell line was 50 μg/ml. RT-PCR analysis showed that tilorone dihydrochloride induced upregulation and downregulation in expression of Bax and Bcl-2, respectively. Simultaneous, antioxidant effect has also seen in a way that prevented necrosis, in biochemical analysis. These results were dose dependent and statistically significant compared to the control group. Conclusions: Based on these results, it appeared that this agent could be a good candidate for further evaluation as effective chemotherapy acting through the induction of apoptosis in hepatoma. The cell death caused through bacterial supernatant was rather necrosis than apoptosis.
机译:背景:盐酸噻氯隆是一种具有不同机制的癌症治疗剂。乳酸杆菌的种类在细胞毒性作用中具有重要作用。目的:由于罗瑞氏乳杆菌的tilorone和培养物上清液对肝癌的作用未知,因此本研究的目的是评估替罗酮对有或没有罗伊氏乳杆菌培养物上清液对小鼠肝癌细胞系的凋亡,细胞毒性和治疗作用。材料和方法:为此,在细胞系培养后,将细胞分为不同的组,例如阴性对照,四剂替洛龙治疗,上清液阳性对照(单剂)和不同剂量替洛龙的联合治疗组。上清液(恒定剂量),持续48小时。所有组均进行了病理学检查,生化研究,四唑染料(3-(4,5-二甲基噻唑-2-基)-2,溴化5-二苯基四唑[MTT])测定和绝对实时聚合酶链反应(作为分子研究,进行了RT-PCR以评估Bax和Bcl-2基因的表达。结果:MTT法检测结果显示,Hepa1-6细胞系蒂罗酮组织培养IC 50 (TCIC 50 )为50μg/ ml。 RT-PCR分析表明,盐酸替罗龙分别诱导Bax和Bcl-2表达的上调和下调。在生化分析中,同时还具有抗氧化作用,可以防止坏死。与对照组相比,这些结果是剂量依赖性的,具有统计学意义。结论:基于这些结果,看来该药物可作为通过诱导肝癌细胞凋亡的有效化学疗法而进一步评估的良好候选者。通过细菌上清液引起的细胞死亡不是细胞凋亡而是坏死。

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