首页> 外文期刊>Japanese Journal of Cancer Research >Evaluation of the relative cytotoxic effects of anticancer agents in serum-supplemented versus serum-free media using a tetrazolium colorimetric assay.
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Evaluation of the relative cytotoxic effects of anticancer agents in serum-supplemented versus serum-free media using a tetrazolium colorimetric assay.

机译:使用四氮唑比色测定法评估抗癌剂在补充血清和不含血清的培养基中的相对细胞毒性作用。

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Most cell culture and in vitro drug sensitivity assays utilize serum-supplemented media (SSM). However, fully defined serum-free media (SFM) offer several advantages and are being used increasingly for initiation and maintenance of cell cultures. Because serum inhibits the in vitro cytotoxicity of certain antineoplastic agents, we investigated the inter-relationships between medium type, cell proliferation and cytotoxic effect. Twenty-four human lung cancer cell lines were tested with nine anticancer agents in both media types. A semi-automated tetrazolium (MTT) colorimetric assay was used for assaying cell survival. Cell lines initiated and maintained in SFM preferentially proliferated in that medium type or proliferated equally well in both media types. In contrast, cell lines established in SSM varied considerably in their medium of preference. There appeared to be a direct correlation or trend between cell proliferative rate and cytotoxicity of all drugs with the possible exceptions of methotrexateand carmustine. In general, the cell lines were more sensitive to anticancer agents when they were exposed in the culture medium in which they preferentially proliferated. Therefore, to determine the influence of culture media on cytotoxicity, we analyzed the data only from lines that replicated equally efficiently in both media. After correction for cell proliferative rate, SSM had a negative effect on the cytotoxic action of some drugs (especially methotrexate, 5-fluorouracil and, to a lesser extent, mitomycin-C). Our results demonstrate that fully defined SFM may be suitable for initiating cell lines and for use in in vitro cytotoxicity assays for selection of individualized therapy or for screening of new anti-neoplastic agents, and thus may increase the number of antineoplastic agents that can be tested satisfactorily.
机译:大多数细胞培养和体外药物敏感性测定均利用血清补充培养基(SSM)。但是,完全定义的无血清培养基(SFM)具有许多优点,并且越来越多地用于细胞培养的起始和维持。由于血清会抑制某些抗肿瘤药的体外细胞毒性,因此我们研究了培养基类型,细胞增殖与细胞毒性作用之间的相互关系。在两种培养基类型中,都用9种抗癌药测试了24种人肺癌细胞系。半自动四唑鎓(MTT)比色测定法用于测定细胞存活率。在SFM中启动和维持的细胞系优先在该培养基类型中增殖或在两种培养基类型中均增殖良好。相反,在SSM中建立的细胞系在其偏好的培养基上有很大不同。除甲氨蝶呤和卡莫司汀外,所有药物的细胞增殖率和细胞毒性之间似乎都存在直接的相关性或趋势。通常,当细胞系暴露于优先增殖的培养基中时,它们对抗癌药更敏感。因此,为了确定培养基对细胞毒性的影响,我们仅分析了在两种培养基中均有效复制的品系数据。校正细胞增殖率后,SSM对某些药物(尤其是甲氨蝶呤,5-氟尿嘧啶和较小程度的丝裂霉素-C)的细胞毒性作用具有负面影响。我们的结果表明,完全定义的SFM可能适用于启动细胞系,并适用于体外细胞毒性测定,以选择个性化疗法或筛选新的抗肿瘤药,因此可能会增加可以测试的抗肿瘤药的数量。令人满意。

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