Advances in radiopharmaceuticals for cancer radiotheranostics: CCK2R targeting as a paradigm for translational innovation.

IF 24.9 1区 医学 Q1 ONCOLOGY
Jing Li, Xuejun Wen, Rebeka Rita Reszegi, Hemavarshini Kamalrhaj, Wolfgang J Parak, Xiaoyuan Chen, Jingjing Zhang
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Abstract

Radiopharmaceuticals are reshaping the landscape of cancer therapy, offering a unique theranostic advantage that is becoming increasingly central to precision medicine. By labeling the same molecular scaffold with different radionuclides, these agents enable seamless integration of diagnostic imaging and targeted therapy. Clinical breakthroughs with somatostatin receptor subtype 2 (SSTR2)- and prostate-specific membrane antigen (PSMA)-targeted radiopharmaceuticals have significantly enhanced both tumor visualization and therapeutic efficacy, establishing new benchmarks in oncology. Ongoing research is exploring novel molecular targets such as cholecystokinin-2 receptor (CCK2R), fibroblast activation protein (FAP), and C-X-C chemokine receptor type 4 (CXCR4). In parallel, there is growing interest in utilizing alternative radionuclides, including alpha-particle emitters and Auger electron emitters, beyond the commonly used beta-emitters, to improve therapeutic outcomes. Simultaneously, advances in ligand and linker design are being leveraged to optimize in vivo pharmacokinetics and tissue distribution. Among the emerging targets, CCK2R has attracted notable attention due to its overexpression in multiple malignancies. Research efforts have focused on improving ligand stability, receptor-binding affinity, and tumor retention, while also exploring strategies to enhance CCK2R expression on cancer cells. This review offers a comprehensive overview of the current landscape in cancer radiotheranostics, exploring the role of CCK2R in cancer biology and summarizing the latest advancements in the development of CCK2R-targeted radiopharmaceuticals. Using these advancements as a case study, we systematically examine key aspects of next-generation radiopharmaceutical design, from target selection and ligand engineering to pharmacokinetic optimization and clinical translation, providing a multidimensional framework for future innovation in cancer radiotheranostics.

癌症放射治疗的放射药物进展:CCK2R靶向作为转化创新的范例。
放射性药物正在重塑癌症治疗的格局,它提供的独特治疗优势正日益成为精准医疗的核心。通过用不同的放射性核素标记相同的分子支架,这些药物可以实现诊断成像和靶向治疗的无缝集成。生长抑素受体亚型2 (SSTR2)和前列腺特异性膜抗原(PSMA)靶向放射药物的临床突破,显著提高了肿瘤的可视化和治疗效果,为肿瘤学建立了新的标杆。正在进行的研究正在探索新的分子靶点,如胆囊收缩素-2受体(CCK2R)、成纤维细胞激活蛋白(FAP)和C-X-C趋化因子受体4型(CXCR4)。与此同时,除了常用的β -辐射源外,人们对利用替代放射性核素(包括α粒子辐射源和俄歇电子辐射源)来改善治疗效果的兴趣也越来越大。同时,配体和连接体设计的进步也被用于优化体内药代动力学和组织分布。在新兴的靶点中,CCK2R因其在多种恶性肿瘤中的过表达而引起了人们的关注。研究工作主要集中在提高配体稳定性、受体结合亲和力和肿瘤保留率,同时探索增强CCK2R在癌细胞上表达的策略。本文综述了肿瘤放射治疗的现状,探讨了CCK2R在肿瘤生物学中的作用,并总结了以CCK2R为靶点的放射药物的最新进展。以这些进展为例,我们系统地研究了下一代放射药物设计的关键方面,从靶点选择和配体工程到药代动力学优化和临床翻译,为未来癌症放射治疗学的创新提供了一个多维框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer Communications
Cancer Communications Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
25.50
自引率
4.30%
发文量
153
审稿时长
4 weeks
期刊介绍: Cancer Communications is an open access, peer-reviewed online journal that encompasses basic, clinical, and translational cancer research. The journal welcomes submissions concerning clinical trials, epidemiology, molecular and cellular biology, and genetics.
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