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放射增敏剂:原理与潜力。

Radiosensitizers: rationale and potential.

作者信息

Brown J M

出版信息

Cancer Treat Rep. 1981;65 Suppl 2:95-102.

PMID:7346152
Abstract

This paper briefly reviews agents that are capable of sensitizing hypoxic cells to radiation and chemotherapeutic agents. The first part is a synopsis of the development of hypoxic radiosensitizers, which concludes that misonidazole can be effective against human tumors. Unfortunately, neurotoxicity limits its effectiveness in humans because the dose that can be given in conjunction with daily fractionated radiation is five to ten times lower than is required for full radiosensitization of the hypoxic cells. The second part covers our recent efforts to develop a drug that does not produce such limiting neurotoxicity. The primary rationale of our program was to synthesize a drug with a short plasma half-life that was too hydrophilic to cross the blood-brain barrier but was able to penetrate tumors and radiosensitize hypoxic cells. From this program, a new drug, SR-2508, has been found that is as efficient as misonidazole in its radiosensitizing ability, but is four to ten times less toxic. Finally, the potential of radiosensitizers not only as agents that can sensitize tumor cells to radiation, but also as agents that can specifically sensitize tumors to chemotherapeutic agents, is discussed. In addition, these drugs may be potential cytotoxic agents that produce toxicity only in solid tumors.

摘要

本文简要综述了能够使缺氧细胞对辐射和化疗药物敏感的药物。第一部分是缺氧放射增敏剂的发展概述,得出结论:米索硝唑对人类肿瘤可能有效。不幸的是,神经毒性限制了它在人体中的有效性,因为与每日分次放疗联合使用时所能给予的剂量比使缺氧细胞完全放射增敏所需的剂量低五到十倍。第二部分介绍了我们最近研发一种不会产生这种限制性神经毒性药物的努力。我们项目的主要原理是合成一种血浆半衰期短、亲水性太强以至于无法穿过血脑屏障,但能够穿透肿瘤并使缺氧细胞放射增敏的药物。从这个项目中,发现了一种新药SR - 2508,其放射增敏能力与米索硝唑相当,但毒性低四到十倍。最后,讨论了放射增敏剂不仅作为能使肿瘤细胞对辐射敏感的药物,而且作为能使肿瘤对化疗药物特异性敏感的药物的潜力。此外,这些药物可能是仅在实体瘤中产生毒性的潜在细胞毒性药物。

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