Kawamura-Akiyama Yoshiko, Kusaba Hitoshi, Kanzawa Fumihiko, Tamura Tomohide, Saijo Nagahiro, Nishio Kazuto
Pharmacology Division, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.
Lung Cancer. 2002 Oct;38(1):43-50. doi: 10.1016/s0169-5002(02)00175-7.
ZD0473 is a new generation platinum agent that, in preclinical studies, shows evidence of an extended spectrum of anti-tumor activity and overcomes platinum resistance mechanisms. The drug contains a bulky methylpyridine ligand at its platinum center, which is responsible for its ability to overcome platinum resistance. We examined the growth inhibitory effects of ZD0473 in human lung cancer cell lines resistant to cisplatin in vitro. Four cisplatin resistant human lung cancer cell lines (PC-14/CDDP, SBC-3/CDDP, PC-9/CDDP, H69/CDDP) showed the expected resistance to cisplatin but were non-cross, or much less, resistant to ZD0473, as determined by an MTT assay. A reduction in the intracellular accumulation of cisplatin, but not of ZD0473, was observed in the PC-14/CDDP cells compared with the levels in PC-14 parental cells. The reduction in cisplatin accumulation is considered a major mechanism of the acquired cisplatin resistance in PC-14/CDDP cells. Therefore, the increase in platinum accumulation is considered a possible mechanism underlying the activity of ZD0473 in cisplatin-resistant cells. Glutathione-mediated resistance to cisplatin was also overcome by ZD0473 in PC-14/CDDP cells. In addition, we showed that the intraperitoneal administration of ZD0473 at its maximum tolerable dose in mice produced a marked in vivo antitumor activity against cisplatin-resistant PC-14/CDDP tumors. These results suggest that ZD0473 may be a potent agent in human lung cancer cells with multifactorial cisplatin resistance.
ZD0473是一种新一代铂类药物,在临床前研究中显示出抗肿瘤活性谱扩展的证据,并能克服铂耐药机制。该药物在其铂中心含有一个庞大的甲基吡啶配体,这使其具备克服铂耐药的能力。我们在体外研究了ZD0473对耐顺铂的人肺癌细胞系的生长抑制作用。通过MTT试验测定,四种耐顺铂的人肺癌细胞系(PC-14/CDDP、SBC-3/CDDP、PC-9/CDDP、H69/CDDP)对顺铂表现出预期的耐药性,但对ZD0473无交叉耐药或耐药性低得多。与PC-14亲代细胞相比,在PC-14/CDDP细胞中观察到顺铂的细胞内蓄积减少,但ZD0473的细胞内蓄积未减少。顺铂蓄积的减少被认为是PC-14/CDDP细胞获得性顺铂耐药的主要机制。因此,铂蓄积的增加被认为是ZD0473在耐顺铂细胞中发挥活性的可能机制。ZD0473在PC-14/CDDP细胞中也克服了谷胱甘肽介导的顺铂耐药性。此外,我们还表明,在小鼠中以最大耐受剂量腹腔注射ZD0473对耐顺铂的PC-14/CDDP肿瘤产生了显著的体内抗肿瘤活性。这些结果表明,ZD0473可能是一种对具有多因素顺铂耐药性的人肺癌细胞有效的药物。