顺铂
铂金
体内
体外
铂化合物
药理学
医学
癌症研究
化疗
生物化学
化学
内科学
生物
遗传学
催化作用
作者
José Pérez,Miguel A. Fuertes,Carlos Alonso,Carmen Navarro‐Ranninger
标识
DOI:10.1016/s1040-8428(00)00053-6
摘要
The discovery in the 1990s of several trans-Pt complexes with in vitro and in vivo activity against tumor cells sensitive and/or resistant to cisplatin has forced the re-evaluation of the structure-activity relationships for platinum antitumor drugs. Because the determinant factors of cytotoxic activity of trans-platinum complexes do not follow the same patterns as those found for cisplatin and its analogues, the differences in cellular and biochemical pharmacology between trans-platinum antitumor complexes and cisplatin might be systematically exploited to design novel trans-platinum complexes with a clinical profile complementary to that of cisplatin and related analogues. Therefore, there may exist a novel molecular rationale for new platinum antitumor drugs development in the twenty-first century.
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