卡铂
紫杉醇
加合物
细胞毒性
化学
药效学
药理学
核苷酸
癌症研究
生物化学
体外
化疗
医学
顺铂
内科学
药代动力学
有机化学
基因
作者
Shuai Jiang,Amy Pan,Tzu‐yin Lin,Hongyong Zhang,Michael Malfatti,Kenneth W. Turteltaub,Paul T. Henderson,Chong-xian Pan
标识
DOI:10.1021/acs.chemrestox.5b00422
摘要
This rapid report focuses on the pharmacodynamic mechanism of the carboplatin/paclitaxel combination and correlates it with its cytotoxicity. Consistent with the synergistic to additive antitumor activity (the combination index ranging from 0.53 to 0.94), cells exposed to this combination had significantly increased carboplatin-DNA adduct formation when compared to that of carboplatin alone (450 ± 30 versus 320 ± 120 adducts per 10(8) nucleotides at 2 h, p = 0.004). Removal of paclitaxel increased the repair of carboplatin-DNA adducts: 39.4 versus 33.1 adducts per 10(8) nucleotides per hour in carboplatin alone (p = 0.021). This rapid report provides the first pharmacodynamics data to support the use of carboplatin/paclitaxel combination in the clinic.
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