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碘化脱氧尿苷增强辐射作用。

Radiation enhancement with iodinated deoxyuridine.

作者信息

Fairchild R G, Brill A B, Ettinger K V

出版信息

Invest Radiol. 1982 Jul-Aug;17(4):407-16. doi: 10.1097/00004424-198207000-00020.

Abstract

A technique, Photon Activation Therapy (PAT), is described in which high Linear Energy Transfer (LET) radiations in the form of Auger electron distributions are generated by a photon beam through photoactivation of stable iodine incorporated as an analog of thymidine (Tyd) in DNA. Of the several halogenated deoxyribonucleosides evaluated, iodinated deoxyuridine (IdUrd) was found to be the only viable choice as a Tyd analog for PAT. Calculations show that 5% replacement of Tyd in tumor DNA multiplies the biologic effectiveness of a given photon radiotherapy dose by a factor of approximately 3. If further therapeutic advantages accorded to high LET radiations are taken into account, as well as repair and regeneration of normal tissues during protracted irradiations, an advantage of approximately 6 is realized. Five percent replacement of Tyd has already been reported for human tumor in vivo. Higher replacements of Tyd with IdUrd would provide proportionately greater advantages. The expectation is that previous clinical results with BrdUrd and high-energy X-rays can be significantly improved upon through the use of IdUrd and suitable lower energy activating photons (35-50 keV). In particular, it is suggested that protracted irradiations with implanted sources such as 145Sm or 145Pm may provide unique advantages at selected sites such as brain or head and neck tumors.

摘要

本文描述了一种光子激活疗法(PAT)技术,该技术通过光子束对作为DNA中胸苷(Tyd)类似物掺入的稳定碘进行光激活,产生俄歇电子分布形式的高线性能量转移(LET)辐射。在所评估的几种卤代脱氧核糖核苷中,碘化脱氧尿苷(IdUrd)被发现是PAT中作为Tyd类似物的唯一可行选择。计算表明,肿瘤DNA中5%的Tyd被取代可使给定光子放疗剂量的生物学有效性提高约3倍。如果考虑到高线性能量转移辐射所带来的进一步治疗优势,以及在长时间照射过程中正常组织的修复和再生,优势约为6倍。体内人类肿瘤中已报道Tyd被取代5%的情况。用IdUrd更高比例地取代Tyd将带来相应更大的优势。预期通过使用IdUrd和合适的较低能量激活光子(35 - 50 keV),可以显著改善先前使用溴脱氧尿苷(BrdUrd)和高能X射线的临床结果。特别是,有人提出用植入源如145Sm或145Pm进行长时间照射,可能在特定部位如脑肿瘤或头颈部肿瘤中提供独特优势。

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