摘要
Thiarabine表现了非常好的抗肿瘤活性,优于吉西他滨、氯法拉滨或阿糖胞苷,可以抵抗小鼠体内的人体肿瘤移植。那与阿糖胞苷不同,thiarabine显示了较强的抗实体瘤移植的活性,这种药物在动物模型表现的强大活性,使其进一步在临床上得到利用。Thiarabine口服有效(生物利用度约16%),给药剂量为每天一次:其与阿糖胞苷的区分主要在两大特征。虽然thiarabine的结构和基本作用机制都与阿糖胞苷比较相似,但是这两种药物在生物药理方面的定量差异也说明了thiarabine有更强的抗肿瘤活性。两大重要属性是thiarabine的5’-三磷酸盐在肿瘤细胞中的较长保留时间以及对DNA合成的潜在抑制。Thiarabine的生物药理指标也不同于吉西他滨。Thiarabine的三期临床I阶段试验表明其对难治性恶性血液病和实体瘤患者有活性。因为其在小鼠体内有抗多种肿瘤移植的活性、它独特的生化活性以及在第I阶段试验令人鼓舞的临床效果,我们认为应该对thiarabine临床治疗血液的和/或实体瘤的效果继续评估。目前为止的临床前试验结果(较优的体内抗肿瘤活性、口服生物利用度 并且每天给药一次),表明thiarabine治疗急性骨髓性白血病方面能够代替阿糖胞苷。
关键词: Thiarabine,阿糖胞苷,吉西他滨,和苷类似物,抗癌治疗
Current Medicinal Chemistry
Title:Thiarabine, 1-(4-Thio-β-D-arabinofuranosyl)cytosine. A Deoxycytidine Analog With Excellent Anticancer Activity
Volume: 22 Issue: 34
Author(s): W.B. Parker, W.R. Waud and J.A. Secrist III
Affiliation:
关键词: Thiarabine,阿糖胞苷,吉西他滨,和苷类似物,抗癌治疗
摘要: Thiarabine has demonstrated exceptional antitumor activity against numerous human tumor xenografts in mice, being superior to gemcitabine, clofarabine, or cytarabine. Unlike cytarabine, thiarabine demonstrated excellent activity against solid tumor xenografts, suggesting that this agent has the kind of robust activity in animal models that leads to clinical utility. Thiarabine is effective orally (bioavailability of approximately 16%) and with once per day dosing: Two characteristics that distinguish it from cytarabine. Although both the structure and basic mechanism of action of thiarabine are similar to that of cytarabine, there are many quantitative differences in the biochemical pharmacology of these two agents that can explain the superior antitumor activity of thiarabine. Two important attributes are the long retention time of the 5’-triphosphate of thiarabine in tumor cells and its potent inhibition of DNA synthesis. The biochemical pharmacology of thiarabine is also different from that of gemcitabine. Thiarabine has been evaluated in three phase I clinical trials, where it has demonstrated some activity in heavily pretreated patients with hematologic malignancies and solid tumors. Because of its impressive activity against numerous human tumor xenografts in mice, its unique biochemical activity, and encouraging clinical results in phase I clinical trials, we believe thiarabine should continue to be evaluated in the clinic for treatment of hematologic and/or solid tumors. The preclinical results to date (superior in vivo antitumor activity, oral bioavailability, and once per day dosing), suggest that thiarabine could replace cytarabine in the treatment of acute myelogenous leukemia.
Export Options
About this article
Cite this article as:
W.B. Parker, W.R. Waud and J.A. Secrist III , Thiarabine, 1-(4-Thio-β-D-arabinofuranosyl)cytosine. A Deoxycytidine Analog With Excellent Anticancer Activity, Current Medicinal Chemistry 2015; 22 (34) . https://dx.doi.org/10.2174/092986732234151119153534
DOI https://dx.doi.org/10.2174/092986732234151119153534 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
- Announcements