Stewart Clinton F, Leggas Markos, Schuetz John D, Panetta John C, Cheshire Pamela J, Peterson Jennifer, Daw Najat, Jenkins Jesse J, Gilbertson Richard, Germain Glen S, Harwood Franklin C, Houghton Peter J
Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Cancer Res. 2004 Oct 15;64(20):7491-9. doi: 10.1158/0008-5472.CAN-04-0096.
As a single agent the ERBB1 inhibitor, gefitinib (Iressa; ZD1839) showed minimal activity against a panel of 10 pediatric tumor xenografts that do not express the ERBB1 receptor. However, combined with irinotecan (CPT-11), significantly greater than additive activity was observed in four of eight models (P < 0.05), and the combination showed enhanced activity against three additional tumor lines. Breast cancer resistance protein (ABCG2), a transporter that confers resistance to SN-38 (the active metabolite of irinotecan), was readily detected in six of nine xenograft models examined by immunohistochemistry. In vitro gefitinib potently reversed resistance to SN-38 only in a cell line that overexpressed functional ABCG2. However, overexpression of ABCG2 did not decrease accumulation nor increase the rate of efflux of [(14)C]gefitinib. On the basis of these results and the distribution of Abcg2 in mouse tissues, we assessed the ability of gefitinib to modulate irinotecan pharmacokinetics. Oral gefitinib coadministration resulted in no change in clearance of intravenously administered irinotecan. However, gefitinib treatment dramatically increased the oral bioavailability of irinotecan after simultaneous oral administration. It is concluded that gefitinib may modulate SN-38 activity at the cellular level to reverse tumor resistance mediated by ABCG2 through inhibiting drug efflux and may be used potentially in humans to modulate the oral bioavailability of a poorly absorbed camptothecin such as irinotecan.
作为单一药物,表皮生长因子受体1(ERBB1)抑制剂吉非替尼(易瑞沙;ZD1839)对一组10种不表达ERBB1受体的儿童肿瘤异种移植模型显示出极小的活性。然而,与伊立替康(CPT - 11)联合使用时,在8个模型中的4个模型中观察到显著大于相加的活性(P < 0.05),并且该联合用药对另外3种肿瘤细胞系显示出增强的活性。乳腺癌耐药蛋白(ABCG2)是一种赋予对SN - 38(伊立替康的活性代谢物)耐药性的转运蛋白,通过免疫组织化学在9个异种移植模型中的6个模型中很容易检测到。在体外,吉非替尼仅在过表达功能性ABCG2的细胞系中有效逆转对SN - 38的耐药性。然而,ABCG2的过表达既没有减少[(14)C]吉非替尼的蓄积,也没有增加其外排速率。基于这些结果以及Abcg2在小鼠组织中的分布,我们评估了吉非替尼调节伊立替康药代动力学的能力。口服吉非替尼共同给药并未导致静脉注射伊立替康的清除率发生变化。然而,吉非替尼治疗在同时口服给药后显著提高了伊立替康的口服生物利用度。得出的结论是,吉非替尼可能在细胞水平调节SN - 38的活性,通过抑制药物外排来逆转由ABCG2介导的肿瘤耐药性,并且可能潜在地用于人类调节如伊立替康这种吸收不良的喜树碱的口服生物利用度。