首页> 外文期刊>Journal of Rubber Research >Cytotoxicity and genotoxicity ofHevea brasiliensislatex C-serum DCS sub-fraction as anticancer agents
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Cytotoxicity and genotoxicity ofHevea brasiliensislatex C-serum DCS sub-fraction as anticancer agents

机译:Hevea Brasiliensislatex C-血清DCS亚馏分作为抗癌剂的细胞毒性和基因毒性

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Dialysed latex C-serum supernatant (DCS) sub-fraction from the rubber tree (Hevea brasiliensis) was reported to exert significant anti-proliferative effect on specific cancer cell lines, especially in human triple negative breast cancer (MDA-MB-231) and human liver carcinoma (HepG2) cells. In the present study, two human non-cancer origin cell lines, MCF-10A (human breast epithelial cells) and HDFa (human adult dermal fibroblast cells), showed least susceptibility when treated with DCS sub-fraction at concentration range 0-100 mu g/mL using 2,5-diphenyl tetrazolium bromide (MTT) assay. Genotoxicity of DCS sub-fraction was assessed through Ames test, in vitro mouse lymphoma assay, and in vitro micronucleus assay. All genotoxicity experiments were tested with the presence and absence of S9 mixture as metabolic activation system. Ames test results showed negative result of mutagenicity as no clear dose-dependent relationship was observed despite mutagenic potential was detected in frame shift-based TA98 and TA1535Salmonella typhimuriumstrains. Mouse lymphoma assay produced non-linear dose-dependent effect in experiments without the presence of S9. Meanwhile, experiment with the presence of S9 resulted in an inverse effect of the dose-dependent relationship. In micronucleus assay, the dose-dependent cytotoxicity effect of DCS sub-fraction showed no correlation with the increase number of cells containing micronuclei but appeared to be time-dependent. In conclusion, DCS sub-fraction showed no significant positive results in genotoxicity assays. In vivo genotoxicity assays should be conducted to ensure the safe use of DCS sub-fraction in further exploration for biological applications.
机译:据报道,来自橡胶树(Hevea brasiliensis)的透析乳胶C-血清上清液(DCS)亚组分对特定癌细胞系,尤其是对人类三阴性乳腺癌(MDA-MB-231)和人类肝癌(HepG2)细胞具有显著的抗增殖作用。在本研究中,当使用浓度范围为0-100μg/mL的2,5-二苯基四唑溴化铵(MTT)分析法处理DCS亚组分时,两种人类非癌症来源细胞系MCF-10A(人类乳腺上皮细胞)和HDFa(人类成体真皮成纤维细胞)的敏感性最低。通过Ames试验、体外小鼠淋巴瘤试验和体外微核试验评估DCS亚组分的遗传毒性。所有的遗传毒性实验都是在有无S9混合物作为代谢激活系统的情况下进行的。Ames试验结果显示,尽管在基于移帧的TA98和TA1535鼠伤寒沙门氏菌菌株中检测到致突变性,但未观察到明显的剂量依赖关系,因此致突变性结果为阴性。在不存在S9的实验中,小鼠淋巴瘤试验产生非线性剂量依赖性效应。同时,S9存在的实验结果与剂量依赖关系相反。在微核试验中,DCS亚组分的剂量依赖性细胞毒性效应与含有微核的细胞数量的增加无关,但似乎具有时间依赖性。综上所述,DCS亚组分在遗传毒性试验中未显示出显著的阳性结果。应进行体内遗传毒性试验,以确保DCS亚组分在进一步探索生物应用时的安全使用。

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