用放射性标记分子靶向过表达的肿瘤细胞受体:生物学靶点、临床应用和转化挑战。

IF 5.1 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Bioorganic Chemistry Pub Date : 2026-10-15 Epub Date: 2026-09-18 DOI:10.1016/j.bioorg.2026.110519
Seyed Jalal Hosseinimehr
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引用次数: 0

摘要

癌症仍然是世界范围内死亡的主要原因,早期诊断和有效的靶向治疗往往受到缺乏肿瘤特异性生物标志物的限制。过表达的细胞表面受体为精确分子成像和放射性核素治疗提供了可接近的靶标,实现了恶性肿瘤的选择性可视化和治疗,同时最大限度地减少了正常组织中的脱靶效应。本文综述了生物标志物靶向放射性药物的现状,重点介绍了临床批准的药物,新兴的分子支架,以及最佳靶向和成像性能的关键标准。临床批准的PSMA和sstr2靶向放射性示踪剂证明了这种方法的成功,分别实现了前列腺癌和神经内分泌肿瘤的高灵敏度和特异性检测。相比之下,许多其他放射性标记分子在监管批准和临床转化方面面临着重大挑战。总的来说,利用过表达的肿瘤生物标志物进行靶向成像和治疗,对于通过精确分子医学改变肿瘤诊断和改善患者预后具有相当大的希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting overexpressed tumor cell receptors with radiolabeled molecules: Biological targets, clinical applications, and translational challenges.

Cancer remains a leading cause of mortality worldwide, and early diagnosis and effective targeted therapy are often constrained by the lack of tumor-specific biomarkers. Overexpressed cell-surface receptors provide accessible targets for precision molecular imaging and radionuclide therapy, enabling selective visualization and treatment of malignancies while minimizing off-target effects in normal tissues. This review synthesizes the current landscape of biomarker-targeted radiopharmaceuticals, highlighting clinically approved agents, emerging molecular scaffolds, and key criteria for optimal targeting and imaging performance. Clinically approved PSMA- and SSTR2-targeted radiotracers exemplify the success of this approach, enabling highly sensitive and specific detection of prostate cancer and neuroendocrine tumors, respectively. In contrast, many other radiolabeled molecules face substantial challenges in regulatory approval and clinical translation. Overall, exploitation of overexpressed tumor biomarkers for targeted imaging and therapy holds considerable promise for transforming oncology diagnostics and improving patient outcomes through precision molecular medicine.

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来源期刊
Bioorganic Chemistry
Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
9.70
自引率
3.90%
发文量
679
审稿时长
31 days
期刊介绍: Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry. For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature. The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.
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