School of Pharmacy, Memorial University of Newfoundland, 300 Prince Philip Dr., A1B 3V6 St. John's, Newfoundland, Canada.
School of Pharmacy, Memorial University of Newfoundland, 300 Prince Philip Dr., A1B 3V6 St. John's, Newfoundland, Canada; Department of Chemistry, Memorial University of Newfoundland, A1B 3X7 St. John's, Newfoundland, Canada.
Int J Pharm. 2018 Oct 5;549(1-2):133-149. doi: 10.1016/j.ijpharm.2018.07.046. Epub 2018 Jul 21.
Many studies have shown that toxicities of anticancer drugs and their adverse effects are related to their chemical structure and high molecular weight that may result in a number of metabolites interacting with drug off-target networks. These factors require further attention for advancing cancer treatment and decreasing toxicities caused by the molecular complexity of antineoplastic agents. Providing more target-selective and tolerable cancer therapy with fewer side effects would not only improve patients' compliance, but also would decrease cancer-remission rates. This review presents several antineoplastic agents and their metabolites with molecular weights greater than 500 g/mol, which reportedly cause more than fifteen types of adverse reactions during breast cancer therapy.
许多研究表明,抗癌药物的毒性及其不良反应与其化学结构和高分子量有关,这可能导致许多代谢物与药物非靶标网络相互作用。这些因素需要进一步关注,以推进癌症治疗并降低抗肿瘤药物分子复杂性引起的毒性。提供更具靶向性和耐受性的癌症治疗方法,副作用更少,不仅可以提高患者的依从性,还可以降低癌症缓解率。本综述介绍了几种分子量大于 500g/mol 的抗肿瘤药物及其代谢物,据报道,这些药物在乳腺癌治疗中会引起超过十五种不良反应。