Jiang Wei, Mautner Victor F, Friedrich Reinhard E, Kluwe Lan
Department of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Department of Oral and Maxillofacial Surgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
J Clin Neurol. 2015 Apr;11(2):172-7. doi: 10.3988/jcn.2015.11.2.172.
Individualized drug testing for tumors using a strategy analogous to antibiotic tests for infectious diseases would be highly desirable for personalized and individualized cancer care.
Primary cultures containing tumor and nontumor stromal cells were utilized in a novel strategy to test drug responses with respect to both efficacy and specificity. The strategy tested in this pilot study was implemented using four primary cultures derived from plexiform neurofibromas. Responses to two cytotoxic drugs (nilotinib and imatinib) were measured by following dose-dependent changes in the proportions of tumor and nontumor cells, determined by staining them with cell-type-specific antibodies. The viability of the cultured cells and the cytotoxic effect of the drugs were also measured using proliferation and cytotoxicity assays.
The total number of cells decreased after the drug treatment, in accordance with the observed reduction in proliferation and increased cytotoxic effect upon incubation with the two anticancer drugs. The proportions of Schwann cells and fibroblasts changed dose-dependently, although the patterns of change varied between the tumor samples (from different sources) and between the two drugs. The highly variable in vitro drug responses probably reflect the large variations in the responses of tumors to therapies between individual patients in vivo.
These preliminary results suggest that the concept of assessing in vitro drug responses using primary cultures is feasible, but demands the extensive further development of an application for preclinical drug selection and drug discovery.
采用类似于针对传染病进行抗生素检测的策略对肿瘤进行个体化药物检测,对于个性化癌症治疗而言将非常理想。
利用包含肿瘤和非肿瘤基质细胞的原代培养物,采用一种新策略来测试药物在疗效和特异性方面的反应。在这项初步研究中测试的策略是使用源自丛状神经纤维瘤的四种原代培养物来实施的。通过用细胞类型特异性抗体对肿瘤细胞和非肿瘤细胞进行染色,跟踪它们比例的剂量依赖性变化,来测量对两种细胞毒性药物(尼洛替尼和伊马替尼)的反应。还使用增殖和细胞毒性测定法测量培养细胞的活力以及药物的细胞毒性作用。
药物处理后细胞总数减少,这与观察到的增殖减少以及与两种抗癌药物孵育后细胞毒性作用增加一致。施万细胞和成纤维细胞的比例呈剂量依赖性变化,尽管不同肿瘤样本(来自不同来源)之间以及两种药物之间的变化模式有所不同。体外药物反应的高度变异性可能反映了体内个体患者肿瘤对治疗反应的巨大差异。
这些初步结果表明,使用原代培养物评估体外药物反应的概念是可行的,但需要对临床前药物选择和药物发现的应用进行广泛的进一步开发。