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放射靶向基因治疗。

Radiotargeted gene therapy.

作者信息

Buchsbaum Donald J, Chaudhuri Tandra R, Zinn Kurt R

机构信息

Department of Radiation Oncology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

J Nucl Med. 2005 Jan;46 Suppl 1:179S-86S.

Abstract

The radiotargeted gene therapy approach to localizing radionuclides at tumor sites involves inducing tumor cells to synthesize a membrane-expressed receptor with a high affinity for injected radiolabeled ligands. A second strategy involves transduction of the sodium iodide symporter (NIS) and free radionuclide therapy. Using the first strategy, induction of high levels of human somatostatin receptor subtype 2 expression and selective tumor uptake, imaging, or growth inhibition with radiolabeled somatostatin analogs has been achieved in human tumor xenograft models. Therapy studies have been performed on several tumor xenograft models with various radionuclides using the NIS radiotargeted gene therapy approach. The use of gene transfer technology to induce expression of high-affinity membrane receptors or transporters can enhance the specificity and extent of radioligand or radionuclide localization in tumors, and the use of radionuclides with appropriate emissions can deliver radiation-absorbed cytotoxic doses across several cell diameters to compensate for limited transduction efficiency. Clinical studies are needed to determine the most promising of these new therapeutic approaches.

摘要

将放射性核素定位在肿瘤部位的放射靶向基因治疗方法,包括诱导肿瘤细胞合成对注射的放射性标记配体具有高亲和力的膜表达受体。第二种策略涉及转导钠碘同向转运体(NIS)和游离放射性核素治疗。使用第一种策略,在人肿瘤异种移植模型中已实现高水平的人类生长抑素受体亚型2表达的诱导以及放射性标记的生长抑素类似物的选择性肿瘤摄取、成像或生长抑制。使用NIS放射靶向基因治疗方法,已在几种肿瘤异种移植模型上使用各种放射性核素进行了治疗研究。利用基因转移技术诱导高亲和力膜受体或转运体的表达,可以提高放射性配体或放射性核素在肿瘤中的定位特异性和程度,并且使用具有适当发射的放射性核素可以将辐射吸收的细胞毒性剂量传递穿过几个细胞直径,以补偿有限的转导效率。需要进行临床研究以确定这些新治疗方法中最有前景的方法。

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