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叶酸受体靶向放射性核素治疗的前景。

Prospects in folate receptor-targeted radionuclide therapy.

作者信息

Müller Cristina, Schibli Roger

机构信息

Center for Radiopharmaceutical Sciences ETH-PSI-USZ, Paul Scherrer Institute , Villigen-PSI , Switzerland.

出版信息

Front Oncol. 2013 Sep 24;3:249. doi: 10.3389/fonc.2013.00249.

Abstract

Targeted radionuclide therapy is based on systemic application of particle-emitting radiopharmaceuticals which are directed toward a specific tumor-associated target. Accumulation of the radiopharmaceutical in targeted cancer cells results in high doses of absorbed radiation energy whereas toxicity to non-targeted healthy tissue is limited. This strategy has found widespread application in the palliative treatment of neuroendocrine tumors using somatostatin-based radiopeptides. The folate receptor (FR) has been identified as a target associated with a variety of frequent tumor types (e.g., ovarian, lung, brain, renal, and colorectal cancer). In healthy organs and tissue FR-expression is restricted to only a few sites such as for instance the kidneys. This demonstrates why FR-targeting is an attractive strategy for the development of new therapy concepts. Due to its high FR-binding affinity (K D < 10(-9) M) the vitamin folic acid has emerged as an almost ideal targeting agent. Therefore, a variety of folic acid radioconjugates for nuclear imaging have been developed. However, in spite of the large number of cancer patients who could benefit of a folate-based radionuclide therapy, a therapeutic concept with folate radioconjugates has not yet been envisaged for clinical application. The reason is the generally high accumulation of folate radioconjugates in the kidneys where emission of particle-radiation may result in damage to the renal tissue. Therefore, the design of more sophisticated folate radioconjugates providing improved tissue distribution profiles are needed. This review article summarizes recent developments with regard to a therapeutic application of folate radioconjugates. A new construct of a folate radioconjugate and an application protocol which makes use of a pharmacological interaction allowed the first preclinical therapy experiments with radiofolates. These results raise hope for future application of such new concepts also in the clinic.

摘要

靶向放射性核素治疗基于发射粒子的放射性药物的全身应用,这些药物靶向特定的肿瘤相关靶点。放射性药物在靶向癌细胞中的积累导致高剂量的吸收辐射能量,而对非靶向健康组织的毒性有限。这种策略已在使用基于生长抑素的放射性肽对神经内分泌肿瘤进行姑息治疗中得到广泛应用。叶酸受体(FR)已被确定为与多种常见肿瘤类型(如卵巢癌、肺癌、脑癌、肾癌和结直肠癌)相关的靶点。在健康器官和组织中,FR的表达仅限于少数部位,如肾脏。这说明了为什么靶向FR是开发新治疗概念的一个有吸引力的策略。由于其高FR结合亲和力(KD < 10(-9) M),维生素叶酸已成为一种几乎理想的靶向剂。因此,已经开发了多种用于核成像的叶酸放射性缀合物。然而,尽管有大量癌症患者可能从基于叶酸的放射性核素治疗中受益,但尚未设想将叶酸放射性缀合物的治疗概念应用于临床。原因是叶酸放射性缀合物通常在肾脏中大量积累,在那里粒子辐射的发射可能导致肾组织损伤。因此,需要设计更复杂的叶酸放射性缀合物,以提供改善的组织分布情况。这篇综述文章总结了叶酸放射性缀合物治疗应用方面的最新进展。一种新的叶酸放射性缀合物构建体和利用药理相互作用的应用方案使得首次使用放射性叶酸进行临床前治疗实验成为可能。这些结果为这类新概念在临床中的未来应用带来了希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6543/3781362/4bdf4df6988e/fonc-03-00249-g001.jpg

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