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新型癌症治疗化学增敏剂。

Novel chemoradiosensitizers for cancer therapy.

机构信息

1Radiobiology Laboratory, California Pacific Medical Center Research Institute, San Francisco, CA 94118, USA.

出版信息

Anticancer Res. 2010 Sep;30(9):3675-82.

Abstract

Combined modality therapy using both chemotherapy and radiation has proved superior over radiation therapy alone for a variety of cancer types. While the locoregional control and survival benefits have been established, there is still much room for improvement both in terms of cancer control and normal tissue toxicity, i.e. the therapeutic ratio. Recently, the pace of research and development of both conventional cytotoxic and molecularly targeted radiosensitizers has been staggering. The aim of this paper is to bring the reader up to date on the clinical status of four promising new radiosensitizers: novel camptothecin analogs and inhibitors of poly(ADP-ribose) polymerase, histone deacetylase, and heat-shock protein 90.

摘要

联合使用化疗和放疗的综合治疗方法已被证明优于单纯放疗,可用于多种癌症类型。虽然已经确定了局部区域控制和生存获益,但在癌症控制和正常组织毒性(即治疗比率)方面仍有很大的改进空间。最近,传统细胞毒性药物和分子靶向放射增敏剂的研究和开发步伐令人瞩目。本文的目的是使读者了解四种有前途的新型放射增敏剂的临床现状:新型喜树碱类似物以及聚(ADP-核糖)聚合酶、组蛋白去乙酰化酶和热休克蛋白 90 的抑制剂。

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