Guffy M M, North J A, Burns C P
Cancer Res. 1984 May;44(5):1863-6.
We have investigated the effect of cellular fatty acid alteration on Adriamycin cytotoxicity using the L1210 lymphoblastic leukemia cell line. Cells growing in Roswell Park Memorial Institute Medium 1640 with 5% fetal bovine serum were modified with respect to fatty acid composition by supplementing their growth medium with 32 microM docosahexaenoic acid (22:6) or oleic acid (18:1). A soft agar clonogenic assay was then used to assess survival following incubation with Adriamycin. When exposed to the drug at a concentration of 0.4 microM, cells grown in the 22:6-supplemented medium were more sensitive (min of drug treatment required to reduce survival by 63% on the exponential portion of the survival curve, 64.9 +/- 4.2 min) to the cytotoxic effects of Adriamycin than cells grown in unsupplemented medium (min of drug treatment required to reduce survival by 63% on the exponential part of the survival curve, 106 +/- 9.7 min) (p less than 0.005). Cytotoxicity of L1210 cells grown in 18:1-supplemented medium was similar to that of cells grown in unsupplemented medium (min of drug treatment required to reduce survival by 63% on the exponential part of the survival curve, 126.6 +/- 9.1 min). The heightened sensitivity to Adriamycin of cells whose medium contained 22:6 increased as the concentration of fatty acid used to supplement the growth medium was increased. The cytotoxicity was also a function of the concentration of Adriamycin from 0.1 to 1.6 microM. When compared to cells grown in unsupplemented medium, those grown in 22:6-supplemented medium contained 3- to 4-fold more polyunsaturated fatty acids in their phospholipids, with a resultant doubling in the mean number of double bonds per fatty acid molecule. These data demonstrate that modification of cellular fatty acid composition may dramatically affect the sensitivity of a tumor cell to Adriamycin.
我们使用L1210淋巴细胞白血病细胞系研究了细胞脂肪酸改变对阿霉素细胞毒性的影响。在含有5%胎牛血清的罗斯威尔帕克纪念研究所培养基1640中生长的细胞,通过在其生长培养基中添加32微摩尔二十二碳六烯酸(22:6)或油酸(18:1),对脂肪酸组成进行了修饰。然后使用软琼脂克隆形成试验来评估与阿霉素孵育后的存活率。当以0.4微摩尔的浓度暴露于该药物时,在添加22:6的培养基中生长的细胞比在未添加培养基中生长的细胞对阿霉素的细胞毒性更敏感(在存活曲线的指数部分使存活率降低63%所需的药物处理最短时间,添加22:6的培养基中为64.9±4.2分钟,未添加培养基中为106±9.7分钟)(p<0.005)。在添加18:1的培养基中生长的L1210细胞的细胞毒性与在未添加培养基中生长的细胞相似(在存活曲线的指数部分使存活率降低63%所需的药物处理最短时间,为126.6±9.1分钟)。培养基中含有22:6的细胞对阿霉素的敏感性增强,且随着用于补充生长培养基的脂肪酸浓度增加而增加。细胞毒性也是阿霉素浓度从0.1到1.6微摩尔的函数。与在未添加培养基中生长的细胞相比,在添加22:6的培养基中生长的细胞其磷脂中的多不饱和脂肪酸含量多3至4倍,每个脂肪酸分子的双键平均数相应增加一倍。这些数据表明,细胞脂肪酸组成的改变可能会显著影响肿瘤细胞对阿霉素的敏感性。