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In vitro Development of Chemotherapy and Targeted Therapy Drug-Resistant Cancer Cell Lines: A Practical Guide with Case Studies

医学 细胞培养 化疗 细胞 肿瘤科 癌症研究 癌症 抗药性 药品 癌细胞 靶向治疗 细胞生长 肺癌 电池类型 黑色素瘤 癌细胞系 后天抵抗 药物开发 内科学 生物信息学 临床试验 乳腺癌 免疫学 靶向给药 药理学 细胞疗法 体外 选择(遗传算法)
作者
Martina S.J. McDermott,Alex J. Eustace,Steven Busschots,Laura Breen,John Crown,Martin Clynes,Norma Oâ€TMDonovan,Britta Stordal
出处
期刊:Frontiers in Oncology [Frontiers Media SA]
卷期号:4: 40-40 被引量:293
标识
DOI:10.3389/fonc.2014.00040
摘要

The development of a drug-resistant cell line can take from 3 to 18 months. However, little is published on the methodology of this development process. This article will discuss key decisions to be made prior to starting resistant cell line development; the choice of parent cell line, dose of selecting agent, treatment interval, and optimizing the dose of drug for the parent cell line. Clinically relevant drug-resistant cell lines are developed by mimicking the conditions cancer patients experience during chemotherapy and cell lines display between two- and eight-fold resistance compared to their parental cell line. Doses of drug administered are low, and a pulsed treatment strategy is often used where the cells recover in drug-free media. High-level laboratory models are developed with the aim of understanding potential mechanisms of resistance to chemotherapy agents. Doses of drug are higher and escalated over time. It is common to have difficulty developing stable clinically relevant drug-resistant cell lines. A comparative selection strategy of multiple cell lines or multiple chemotherapeutic agents mitigates this risk and gives insight into which agents or type of cell line develops resistance easily. Successful selection strategies from our research are presented. Pulsed-selection produced platinum or taxane-resistant large cell lung cancer (H1299 and H460) and temozolomide-resistant melanoma (Malme-3M and HT144) cell lines. Continuous selection produced a lapatinib-resistant breast cancer cell line (HCC1954). Techniques for maintaining drug-resistant cell lines are outlined including; maintaining cells with chemotherapy, pulse treating with chemotherapy, or returning to master drug-resistant stocks. The heterogeneity of drug-resistant models produced from the same parent cell line with the same chemotherapy agent is explored with reference to P-glycoprotein. Heterogeneity in drug-resistant cell lines reflects the heterogeneity that can occur in clinical drug resistance.
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