Campling B G, Pym J, Baker H M, Cole S P, Lam Y M
Department of Oncology, Queen's University, Kingston, Ontario, Canada.
Br J Cancer. 1991 Jan;63(1):75-83. doi: 10.1038/bjc.1991.16.
A simple colorimetric test, the MTT assay, has been adapted for chemosensitivity testing of human small cell lung cancer cell lines, and fresh tumour samples. Optimal conditions for clinical chemosensitivity testing were determined using established SCLC lines. Nineteen different chemotherapeutic agents were tested, and sixteen of them were found to be cytotoxic in this assay system. The drug sensitivity of a panel of 16 SCLC cell lines was measured and compared. There was very little intraexperiment variation, but the interexperiment variation was significant. Cell lines which were derived from patients who had not received chemotherapy at the time the cell line was established were more sensitive (to all but one of the drugs) than lines derived from treated patients, and the differences were statistically significant for two of the drugs. One cell line, NCI-H209, which was derived from an untreated patient, stood out as being the most sensitive or among the most sensitive to all of the drugs tested. Another cell line, H69AR, which is a multidrug resistant subline of the cell line NCI-H69, was the most resistant to many of the natural product drugs tested. Multiple drug chemosensitivity testing was performed on eight fresh tumour samples from SCLC patients (five pleural effusions, one lymph node, and two primary tumours). It was possible to perform chemosensitivity testing on all of the clinical samples in which sufficient tumour cells were available. The drug sensitivity of the clinical samples was, in most cases, within the same range as for the cell lines. Since this assay is very rapid and simple to perform, it may have practical applications in clinical drug sensitivity testing of human tumours.
一种简单的比色试验——MTT 法,已被用于人类小细胞肺癌细胞系及新鲜肿瘤样本的化学敏感性测试。利用已建立的小细胞肺癌细胞系确定了临床化学敏感性测试的最佳条件。测试了 19 种不同的化疗药物,其中 16 种在该检测系统中具有细胞毒性。测量并比较了一组 16 个小细胞肺癌细胞系的药物敏感性。实验内变异很小,但实验间变异显著。在建立细胞系时未接受化疗的患者来源的细胞系(对除一种药物外的所有药物)比接受过治疗的患者来源的细胞系更敏感,且两种药物的差异具有统计学意义。一个来自未治疗患者的细胞系 NCI-H209,对所有测试药物均表现出最敏感或最敏感之一。另一个细胞系 H69AR,是细胞系 NCI-H69 的多药耐药亚系,对许多测试的天然产物药物最具抗性。对 8 例小细胞肺癌患者的新鲜肿瘤样本(5 例胸腔积液、1 例淋巴结和 2 例原发性肿瘤)进行了多药化学敏感性测试。在所有有足够肿瘤细胞的临床样本中都可以进行化学敏感性测试。在大多数情况下,临床样本的药物敏感性与细胞系处于相同范围内。由于该检测方法非常快速且易于操作,它可能在人类肿瘤的临床药物敏感性测试中有实际应用。