Sandvold Marit Liland, Galmarini Carlos, Myhren Finn, Peters Godefridus
Clavis Pharma, Oslo, Norway.
Nucleosides Nucleotides Nucleic Acids. 2010 Jun;29(4-6):386-93. doi: 10.1080/15257771003729625.
The clinical activity of pyrimidine analogues (araC and gemcitabine) is impaired by different mechanisms of resistance and several efforts to overcome this problem have been undertaken. Elacytarabine (CP-4055, araC-5'elaidic acid ester) and CP-4126 (gemcitabine-5'elaidic acid ester) are lipophilic fatty acid derivatives of the nucleoside analogues araC and gemcitabine, respectively, that are currently investigated in clinical trials in solid tumors and hematological malignancies. Here, we present results on the activity of elacytarabine and CP-4126 in a panel of tumor cell lines that are resistant to araC and gemcitabine and we discuss the potential use of these agents in the treatment of patients with drug resistance phenotypes. We conclude that elacytarabine and CP-4126 are active in cells with deficient nucleoside membrane transport and altered mismatch repair. These results should be taking into consideration for future clinical development of elacyatrabine and CP-4126.
嘧啶类似物(阿糖胞苷和吉西他滨)的临床活性因不同的耐药机制而受损,人们已采取多种措施来克服这一问题。依拉阿糖胞苷(CP - 4055,阿糖胞苷 - 5'反油酸酯)和CP - 4126(吉西他滨 - 5'反油酸酯)分别是核苷类似物阿糖胞苷和吉西他滨的亲脂性脂肪酸衍生物,目前正在实体瘤和血液系统恶性肿瘤的临床试验中进行研究。在此,我们展示了依拉阿糖胞苷和CP - 4126在一组对阿糖胞苷和吉西他滨耐药的肿瘤细胞系中的活性结果,并讨论了这些药物在治疗具有耐药表型患者中的潜在用途。我们得出结论,依拉阿糖胞苷和CP - 4126在核苷膜转运缺陷和错配修复改变的细胞中具有活性。在依拉阿糖胞苷和CP - 4126未来的临床开发中应考虑这些结果。