Suppr超能文献

放射性标记的(R)-(-)-5-碘-3'-O-[2-(ε-胍基己酰基)-2-苯基乙酰基]-2'-脱氧尿苷:一种用于神经母细胞瘤的新型诊疗药物。

Radiolabeled (R)-(-)-5-iodo-3'-O-[2-(ε-guanidinohexanoyl)-2-phenylacetyl]-2'-deoxyuridine: A new theranostic for neuroblastoma.

作者信息

Kortylewicz Zbigniew P, Coulter Don W, Han Guang, Baranowska-Kortylewicz Janina

机构信息

Department of Radiation Oncology, J. Bruce Henriksen Cancer Research Laboratories, University of Nebraska Medical Center, Omaha, Nebraska, USA.

Department of Pediatrics, Division of Hematology and Oncology, University of Nebraska Medical Center, Omaha, Nebraska, USA.

出版信息

J Labelled Comp Radiopharm. 2020 Mar 9. doi: 10.1002/jlcr.3836.

Abstract

Neuroblastoma, the most common extracranial solid tumor in children, accounts for nearly 8% of childhood cancers in the United States. It is a disease with pronounced clinical and biological heterogeneities. The amplification of MYCN, whose key tumorigenic functions include the promotion of proliferation, facilitation of the cell's entry into the S phase, and prevention of cells from leaving the cell cycle, correlates with poor prognosis. Patients with a high proliferation index disease have low survival rates. Neuroblastoma is one of the most radioresponsive of all human tumors. To exploit this radiosensitivity, radioactive guanidine (R)-(-)-5-[ I]iodo-3'-O-[2-(ε-guanidinohexanoyl)-2-phenylacetyl]-2'-deoxyuridine (9, GPAID) was designed. This compound enters neuroblastoma cells much like metaiodobenzylguanidine (MIBG). Additionally, it cotargets DNA of proliferating cells, an attribute especially advantageous in the treatment of MYCN-amplified tumors. GPAID was synthesized from the trimethylstannyl precursor with an average yield of >90% at the no-carrier-added specific activities. The norepinephrine transporter-aided delivery of GPAID to neuroblastoma cells was established in the competitive uptake studies with nonradioactive MIBG. The intracellular processing and DNA targeting properties were confirmed in the subcellular distribution experiments. Studies in a mouse model of neuroblastoma demonstrated the therapeutic potential of GPAID. The tin precursor of GPAID can be used to prepare compounds radiolabeled with single-photon emission computed tomography (SPECT)- and positron-emission tomography (PET)-compatible radionuclides. Accordingly, these reagents can function as theranostics useful in the individualized and comprehensive treatment strategies comprising treatment planning and the assessment of tumor responses as well as the targeted molecular radiotherapy employing treatment doses derived from the imaging data.

摘要

神经母细胞瘤是儿童最常见的颅外实体瘤,在美国儿童癌症中占近8%。它是一种具有明显临床和生物学异质性的疾病。MYCN基因的扩增与预后不良相关,其关键的致瘤功能包括促进增殖、促使细胞进入S期以及阻止细胞离开细胞周期。增殖指数高的疾病患者生存率低。神经母细胞瘤是所有人类肿瘤中对放疗最敏感的肿瘤之一。为了利用这种放射敏感性,设计了放射性胍(R)-(-)-5-[I]碘-3'-O-[2-(ε-胍基己酰基)-2-苯基乙酰基]-2'-脱氧尿苷(9,GPAID)。该化合物进入神经母细胞瘤细胞的方式与间碘苄胍(MIBG)非常相似。此外,它共同靶向增殖细胞的DNA,这一特性在治疗MYCN扩增的肿瘤中特别有利。GPAID由三甲基锡前体合成,在无载体添加的比活下平均产率>90%。在与非放射性MIBG的竞争性摄取研究中,证实了去甲肾上腺素转运体辅助GPAID向神经母细胞瘤细胞的递送。在亚细胞分布实验中证实了其细胞内加工和DNA靶向特性。在神经母细胞瘤小鼠模型中的研究证明了GPAID的治疗潜力。GPAID的锡前体可用于制备用单光子发射计算机断层扫描(SPECT)和正电子发射断层扫描(PET)兼容的放射性核素标记的化合物。因此,这些试剂可作为治疗诊断剂,用于个性化和综合治疗策略,包括治疗计划和肿瘤反应评估,以及采用从成像数据得出的治疗剂量的靶向分子放疗。

相似文献

6
Radiolabeled metaiodobenzylguanidine for the treatment of neuroblastoma.用于治疗神经母细胞瘤的放射性标记间碘苄胍
Nucl Med Biol. 2008 Aug;35 Suppl 1(Suppl 1):S35-48. doi: 10.1016/j.nucmedbio.2008.05.002.

本文引用的文献

5

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验