Hill B T, Bellamy A S, Metcalfe S, Hepburn P J, Masters J R, Whelan R D
Invest New Drugs. 1984;2(1):29-33. doi: 10.1007/BF00173784.
A series of continuous human tumour cell lines, derived from various tumour types, were used to establish whether the combination of spirogermanium (SP) with other 'standard' antitumour drugs proved superior to these as single agents in reducing cell survival in vitro. A non-cytotoxic concentration of SP was selected and when combined with a range of concentrations of cisplatin or 5-fluorouracil (5-FU), definite synergistic cell kill was noted in all lines tested. In contrast, the combination of SP with various other antitumor drugs, including adriamycin, methotrexate and the vinca alkaloids and with X-irradiation did not enhance cytotoxicity. These pre-clinical in vitro studies suggest that benefit may accrue from combining SP with either 5-FU or cisplatin and provide a basis for their clinical evaluation in colo-rectal tumours or transitional cell cancer of the bladder, respectively.
使用一系列源自各种肿瘤类型的连续人肿瘤细胞系,来确定螺旋锗(SP)与其他“标准”抗肿瘤药物联合使用在体外降低细胞存活率方面是否优于这些药物单独使用。选择了非细胞毒性浓度的SP,当与一系列浓度的顺铂或5-氟尿嘧啶(5-FU)联合使用时,在所有测试的细胞系中均观察到明确的协同细胞杀伤作用。相比之下,SP与其他各种抗肿瘤药物(包括阿霉素、甲氨蝶呤和长春花生物碱)以及与X射线照射联合使用时,并未增强细胞毒性。这些临床前体外研究表明,将SP与5-FU或顺铂联合使用可能会带来益处,并分别为它们在结直肠癌或膀胱移行细胞癌中的临床评估提供了依据。