Yuji Wang, Ming Zhao, Guohui Cui, Chunying Cui, J. Ju, Shiqi Peng
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引用次数: 1
摘要
为了降低顺铂的毒性,研究了N-(2,3,4,5,6-五羟基己基)-N-二硫代氨基甲酸酯- l -异亮氨酸二钠(GID)为基础的联合治疗。27μM GID联合治疗对HepG2、Hela、MES-SA、HL60和H1299细胞的增殖抑制作用与单用顺铂相当。对小鼠植入式肿瘤增殖,1.667μmol/kg GID联合治疗比单用顺铂具有更高的抑制作用。对于接受顺铂治疗的小鼠,这种治疗联合有效地减少了铂在器官中的积累,但不影响肿瘤组织中的铂水平。与单用顺铂相比,这种联合治疗不仅增加尿素和粪便中的铂含量,而且增加尿素排泄。以上结果提示,以GID为基础的联合治疗能够降低顺铂的毒副作用,支持顺铂的抗肿瘤效力。
Therapeutic Alliance: Using N-(2,3,4,5,6-Pentahydroxylhex-1-yl)-NDithiocarbamate-L-Isoleucine Disodium to Improve the Toxicity and Survival of Cisplatin Receiving Mice
To reduce the toxicity of cisplatin N-(2,3,4,5,6-pentahydroxylhex-1-yl)-N-dithiocarbamate-L-isoleucine diso- dium (GID) based therapeutic alliance is investigated. For the proliferation of HepG2, Hela, MES-SA, HL60 and H1299 cells, 27μM of GID based therapeutic alliance gave comparable inhibition to cisplatin alone. For implanted tumor prolif- eration in mice, 1.667μmol/kg of GID based therapeutic alliance gave higher inhibition than cisplatin alone. For cisplatin receiving mice, this therapeutic alliance effectively reduces the platinum accumulations in the organs but does not affect the platinum level in the tumor tissue. Comparing to cisplatin alone, this therapeutic alliance not only increases urea and fecal platinum levels but also increases urea excretion. All the observations imply that GID based therapeutic alliance is capable of reducing the toxicity and supporting the anti-tumor potency of cisplatin.