Kelner Michael J, McMorris Trevor C, Rojas Rafael J, Estes Leita A, Suthipinijtham Pharnuk
Department of Pathology, University of California, San Diego, USA.
Invest New Drugs. 2008 Oct;26(5):407-15. doi: 10.1007/s10637-008-9113-8. Epub 2008 Jan 29.
The novel agent Irofulven (HMAF, NSC 683863) has demonstrated significant antitumor activity against solid tumors in various xenograft models and human clinical trials. The antitumor potential of combining irofulven with 72 different anti-metabolite, enzyme inhibiting, and miscellaneous agents was investigated in this study. The human lung carcinoma MV522 cell line and its corresponding xenograft model were used to evaluate the activity of irofulven in combination with these different agents. Irofulven in combination with select anti-metabolites, notably cytidine or adenine-derived agents, displayed strong synergistic activity in both in vitro and in vivo studies. Agents demonstrating strong synergistic interaction with irofulven included gemcitabine, cyclocytidine, cytarabine, fludarabine phosphate, cladribine, and 5-fluorouracil. Other anti-metabolites, enzyme inhibitors, and a variety of miscellaneous agents failed to interact beneficially when administered in combination with irofulven. The therapeutic activity of irofulven is enhanced considerably when irofulven is combined with select anti-metabolite agents, and further clinical evaluation of these combinations is warranted. The synergistic interaction with these combinations may stem from a variety of actions including inhibition of the nucleotide excision repair (NER) pathway, topoisomerase I activity, and caspase-dependent and independent induction of apoptosis.
新型药物irofulven(HMAF,NSC 683863)在多种异种移植模型和人体临床试验中已显示出对实体瘤具有显著的抗肿瘤活性。本研究调查了irofulven与72种不同的抗代谢药、酶抑制剂及其他各类药物联合使用时的抗肿瘤潜力。使用人肺癌MV522细胞系及其相应的异种移植模型来评估irofulven与这些不同药物联合使用时的活性。Irofulven与某些抗代谢药联合使用,尤其是胞嘧啶或腺嘌呤衍生的药物,在体外和体内研究中均显示出强大的协同活性。与irofulven表现出强烈协同相互作用的药物包括吉西他滨、环胞苷、阿糖胞苷、磷酸氟达拉滨、克拉屈滨和5-氟尿嘧啶。其他抗代谢药、酶抑制剂以及各类其他药物与irofulven联合使用时未能产生有益的相互作用。当irofulven与某些抗代谢药联合使用时,其治疗活性会显著增强,因此有必要对这些联合用药进行进一步的临床评估。与这些联合用药的协同相互作用可能源于多种作用,包括抑制核苷酸切除修复(NER)途径、拓扑异构酶I活性以及半胱天冬酶依赖性和非依赖性诱导凋亡。