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5'-氨基-5'-脱氧胸苷对正常小鼠组织和两种人结肠癌异种移植瘤中碘脱氧尿苷代谢及掺入细胞DNA的体内调节作用

In vivo modulation of iododeoxyuridine metabolism and incorporation into cellular DNA by 5'-amino-5'-deoxythymidine in normal mouse tissues and two human colon cancer xenografts.

作者信息

Kinsella T J, Glennon M C, Kunugi K A, Lindstrom M J

机构信息

Departments of Human Oncology and Biostatistics, University of Wisconsin Medical School, Madison, Wisconsin 53792, USA.

出版信息

Clin Cancer Res. 1996 Jun;2(6):981-9.

PMID:9816259
Abstract

This in vivo study examines the ability of 5'-amino-5'-deoxythymidine (5'-AdThd) to modulate 5-iododeoxyuridine (IdUrd) cellular metabolism in two human colon cancer xenografts (HT 29 and HCT-116), two actively proliferating normal mouse tissues (bone marrow and intestine), and a quiescent normal mouse tissue (liver). 5'-AdThd is a thymidine analogue that at low concentrations (<30 micrometer) can increase thymidine kinase activity, which is the rate-limiting enzyme for activation of IdUrd. We reported recently that the in vitro incubation of HT 29 and HCT-116 cells in 5'-AdThd + IdUrd resulted in an enhancement of 5-iodo-2'-dUTP pools, IdUrd DNA incorporation, and subsequent radiosensitization compared with incubation with IdUrd alone (Clin. Cancer Res., 1: 407-416, 1995). These in vitro effects were more significant in the radioresistant cell line HT 29. Using a 6-day continuous infusion of IdUrd (50 or 100 mg/kg/day) and/or 5'-AdThd (200 mg/kg/day), no increase in systemic toxicity (percentage of body weight loss) was observed in athymic nude mice with 5'-AdThd alone or when combined with IdUrd. There was significant dose-dependent, systemic toxicity with IdUrd, which was reversible within 3 days of completing the lower-dose IdUrd infusion. However, a comparison of plasma levels during the 6-day continuous infusion of IdUrd +/- 5'-AdThd showed a significant interaction of IdUrd and 5'-AdThd, resulting in higher plasma levels by day 6 of both compounds and the principal metabolites, iodouracil and deoxyuridine, which is consistent with nonlinear saturating effects on dihydrouracil dehydrogenase. Coadministration of IdUrd and 5'-AdThd resulted in an increase in the percentage of IdUrd DNA incorporation in the two proliferating normal tissues, which was significant only with the lower IdUrd dose. No effect on IdUrd DNA incorporation was found in normal liver at either IdUrd dose +/- 5'-AdThd. Similar to our in vitro data, the continuous infusion of IdUrd and 5'-AdThd showed a significant effect by increasing the percentage of IdUrd DNA incorporation in HT-29 xenografts at both IdUrd doses, whereas coadministration of 5'-AdThd had no such effect in HCT-116 xenografts.

摘要

本体内研究检测了5'-氨基-5'-脱氧胸苷(5'-AdThd)调节5-碘脱氧尿苷(IdUrd)在两种人结肠癌异种移植瘤(HT 29和HCT-116)、两种活跃增殖的正常小鼠组织(骨髓和肠道)以及一种静止的正常小鼠组织(肝脏)中细胞代谢的能力。5'-AdThd是一种胸苷类似物,在低浓度(<30微米)时可增加胸苷激酶活性,而胸苷激酶是激活IdUrd的限速酶。我们最近报道,与单独用IdUrd孵育相比,HT 29和HCT-116细胞在5'-AdThd + IdUrd中进行体外孵育会导致5-碘-2'-dUTP池增加、IdUrd掺入DNA以及随后的放射增敏作用(《临床癌症研究》,1: 407 - 416,1995)。这些体外效应在耐辐射细胞系HT 29中更为显著。通过对无胸腺裸鼠连续6天输注IdUrd(50或100毫克/千克/天)和/或5'-AdThd(200毫克/千克/天),单独使用5'-AdThd或与IdUrd联合使用时,未观察到全身毒性(体重减轻百分比)增加。IdUrd存在显著的剂量依赖性全身毒性,在完成低剂量IdUrd输注后的3天内可逆转。然而,在连续6天输注IdUrd +/- 5'-AdThd期间对血浆水平进行比较显示,IdUrd和5'-AdThd存在显著相互作用,导致两种化合物及其主要代谢产物碘尿嘧啶和脱氧尿苷在第6天时血浆水平升高,这与对二氢尿嘧啶脱氢酶的非线性饱和效应一致。IdUrd和5'-AdThd共同给药导致两种增殖正常组织中IdUrd掺入DNA的百分比增加,仅在较低IdUrd剂量时显著。在正常肝脏中,无论IdUrd剂量 +/- 5'-AdThd如何,均未发现对IdUrd掺入DNA有影响。与我们的体外数据相似,连续输注IdUrd和5'-AdThd显示,在两种IdUrd剂量下,HT-29异种移植瘤中IdUrd掺入DNA的百分比均显著增加,而5'-AdThd与HCT-116异种移植瘤共同给药时则无此效应。

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