Takano H, Kohno K, Shiraishi N, Sato S, Asoh K, Yakushiniji M, Ono M, Kuwano M
Department of Biochemistry, Oita Medical School.
Jpn J Cancer Res. 1989 Apr;80(4):373-9. doi: 10.1111/j.1349-7006.1989.tb02322.x.
A variant clone resistant to high doses of colchicine (KB-C1) derived from human cancer KB cell line is resistant to various anticancer agents. The KB-C1 cells were much more resistant to epidermal growth factor and a chimeric toxin, EGF-Pseudomonas exotoxin (PE), than the parental KB cells. KB-C1 cells have decreased numbers of EGF-receptors, though the affinity of the receptors is similar to that in the parental KB cells. A drug-sensitive revertant (C1-R2) partially recovered its EGF-receptor activity. Northern blot analysis showed a decreased level of EGF-receptor mRNA in KB-C1 cells, while the multidrug-resistance gene, mdr-1, was expressed at very high levels in KB-C1 cells, but not in KB or C1-R2 cells. The drug-resistant cells were less tumorigenic than the parental cells when injected into nude mice. A decreased expression of EGF-receptor in these cells may be one of the pleiotropic properties of multidrug-resistant cells and may perhaps represent the basis for their reduced tumorigenicity.
从人癌KB细胞系衍生而来的对高剂量秋水仙碱具有抗性的变异克隆(KB - C1)对多种抗癌药物具有抗性。与亲本KB细胞相比,KB - C1细胞对表皮生长因子和一种嵌合毒素——表皮生长因子-绿脓杆菌外毒素(PE)具有更强的抗性。KB - C1细胞的表皮生长因子受体数量减少,尽管受体的亲和力与亲本KB细胞中的相似。一种药物敏感回复株(C1 - R2)部分恢复了其表皮生长因子受体活性。Northern印迹分析显示KB - C1细胞中表皮生长因子受体mRNA水平降低,而多药耐药基因mdr - 1在KB - C1细胞中高水平表达,但在KB或C1 - R2细胞中不表达。当将耐药细胞注射到裸鼠体内时,其致瘤性低于亲本细胞。这些细胞中表皮生长因子受体表达的降低可能是多药耐药细胞的多效性特性之一,也许代表了其致瘤性降低的基础。