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采用MTT法对人肺癌细胞系进行化学敏感性测试。

Chemosensitivity testing of human lung cancer cell lines using the MTT assay.

作者信息

Carmichael J, Mitchell J B, DeGraff W G, Gamson J, Gazdar A F, Johnson B E, Glatstein E, Minna J D

机构信息

NCI-Navy Medical Oncology Branch, Bethesda, Maryland 20814.

出版信息

Br J Cancer. 1988 Jun;57(6):540-7. doi: 10.1038/bjc.1988.125.

DOI:10.1038/bjc.1988.125
PMID:2841961
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2246465/
Abstract

Thirty human lung cancer cell lines were tested for chemosensitivity using the semi-automated, non-clonogenic MTT assay. The tumour cell lines came from three major categories of patients: untreated small cell lung cancer (SCLC); SCLC relapsing on chemotherapy; and non-SCLC predominantly from untreated patients. From these data IC50 values were derived for each drug in each cell line. While some inter-experimental variability was observed, the rank order of chemosensitivity of each cell line within this panel was significantly correlated between experiments. These results show that tumour cell lines derived from untreated small cell lung cancer patients were the most chemosensitive for adriamycin, melphalan, vincristine and VP16 compared to the other cell types. In addition, untreated SCLC was more sensitive than non-SCLC to BCNU and cis-platin, while vincristine was the only drug to which treated SCLC was more sensitive compared to the non-SCLC lines. In contrast, no significant differences between the lung cancer types were observed for vinblastine. Thus, this panel of lung cancer cells exhibited a drug sensitivity profile paralleling that observed in clinical practice. These results suggest that this lung cancer cell line panel in combination with a relatively simple but reproducible chemosensitivity assay, such as the MTT assay, has potential for the testing of drug combinations and evaluating new anti-cancer agents in vitro.

摘要

使用半自动、非克隆形成的MTT法对30种人肺癌细胞系进行化学敏感性测试。这些肿瘤细胞系来自三类主要患者:未经治疗的小细胞肺癌(SCLC);化疗后复发的SCLC;以及主要来自未经治疗患者的非小细胞肺癌(NSCLC)。根据这些数据得出每种细胞系中每种药物的IC50值。虽然观察到一些实验间的变异性,但该组中每个细胞系的化学敏感性排序在实验之间显著相关。这些结果表明,与其他细胞类型相比,来自未经治疗的小细胞肺癌患者的肿瘤细胞系对阿霉素、美法仑、长春新碱和依托泊苷最敏感。此外,未经治疗的SCLC对卡莫司汀和顺铂比NSCLC更敏感,而长春新碱是唯一一种治疗后的SCLC比NSCLC系更敏感的药物。相比之下,对于长春花碱,未观察到肺癌类型之间的显著差异。因此,该组肺癌细胞表现出与临床实践中观察到的药物敏感性特征相似的情况。这些结果表明,该组肺癌细胞系与相对简单但可重复的化学敏感性测定法(如MTT法)相结合,具有在体外测试药物组合和评估新抗癌药物的潜力。

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