Starling J J, Shepard R L, Cao J, Law K L, Norman B H, Kroin J S, Ehlhardt W J, Baughman T M, Winter M A, Bell M G, Shih C, Gruber J, Elmquist W F, Dantzig A H
Lilly Research Laboratories, Lilly Corporate Center, Indianapolis, IN 46285, USA.
Adv Enzyme Regul. 1997;37:335-47. doi: 10.1016/s0065-2571(96)00021-0.
The above data indicate that LY335979 displays the following characteristics of an 'ideal modulator' of Pgp-mediated multidrug resistance: high affinity binding to Pgp, high potency for in vitro reversal of drug resistance, high therapeutic index (activity was demonstrated at doses ranging from 1-30 mg/kg) observed in in vivo antitumor efficacy experiments, and a lack of pharmacokinetic interactions that alter the plasma concentration of coadministered oncolytic agents. These desirable features strongly suggest that LY335979 is an exciting new clinical agent to test the hypothesis that inhibition of P-glycoprotein activity will result in reversal of multidrug resistance in human tumors.
上述数据表明,LY335979展现出作为P-糖蛋白介导的多药耐药“理想调节剂”的以下特性:与P-糖蛋白的高亲和力结合、体外逆转耐药性的高效能、在体内抗肿瘤疗效实验中观察到的高治疗指数(在1-30mg/kg剂量范围内表现出活性),以及不存在改变同时给药的溶瘤剂血浆浓度的药代动力学相互作用。这些理想特性有力地表明,LY335979是一种令人兴奋的新型临床药物,可用于验证抑制P-糖蛋白活性将导致人类肿瘤多药耐药逆转这一假说。