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体外评估抗癌药物的特异性

Assessing Specificity of Anticancer Drugs In Vitro.

作者信息

Kluwe Lan

机构信息

Department of Maxillofacial Surgery, University Medical Center Hamburg-Eppendorf; Department of Neurology, University Medical Center Hamburg-Eppendorf; Laboratory for Tumor Biology and Regenerative Medicine, University Medical Center Hamburg-Eppendorf;

出版信息

J Vis Exp. 2016 Mar 23(109):e53752. doi: 10.3791/53752.

Abstract

A procedure for assessing specificity of anticancer drugs in vitro using cultures containing both tumor and non-tumor cells is demonstrated. The key element is the quantitative determination of a tumor-specific genetic alteration in relation to a universal sequence using a dual-probe digital PCR assay and the subsequent calculation of the proportion of tumor cells. The assay is carried out on a culture containing tumor cells of an established line and spiked-in non-tumor cells. The mixed culture is treated with a test drug at various concentrations. After the treatment, DNA is prepared directly from the survived adhesive cells in wells of 96-well plates using a simple and inexpensive method, and subjected to a dual-probe digital PCR assay for measuring a tumor-specific genetic alteration and a reference universal sequence. In the present demonstration, a heterozygous deletion of the NF1 gene is used as the tumor-specific genetic alteration and a RPP30 gene as the reference gene. Using the ratio NF1/RPP30, the proportion of tumor cells was calculated. Since the dose-dependent change of the proportion of tumor cells provides an in vitro indication for specificity of the drug, this genetic and cell-based in vitro assay will likely have application potential in drug discovery. Furthermore, for personalized cancer-care, this genetic- and cell-based tool may contribute to optimizing adjuvant chemotherapy by means of testing efficacy and specificity of candidate drugs using primary cultures of individual tumors.

摘要

本文展示了一种使用包含肿瘤细胞和非肿瘤细胞的培养物在体外评估抗癌药物特异性的方法。关键要素是使用双探针数字PCR测定法对与通用序列相关的肿瘤特异性基因改变进行定量测定,并随后计算肿瘤细胞的比例。该测定法在含有既定细胞系的肿瘤细胞和添加的非肿瘤细胞的培养物上进行。将混合培养物用不同浓度的测试药物处理。处理后,使用一种简单且廉价的方法直接从96孔板孔中的存活贴壁细胞制备DNA,并进行双探针数字PCR测定以测量肿瘤特异性基因改变和参考通用序列。在本演示中,NF1基因的杂合缺失用作肿瘤特异性基因改变,RPP30基因用作参考基因。使用NF1/RPP30的比率计算肿瘤细胞的比例。由于肿瘤细胞比例的剂量依赖性变化为药物特异性提供了体外指标,这种基于基因和细胞的体外测定法可能在药物发现中具有应用潜力。此外,对于个性化癌症治疗,这种基于基因和细胞的工具可能有助于通过使用个体肿瘤的原代培养物测试候选药物的疗效和特异性来优化辅助化疗。

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