Müller Marco, Georgiev Tony, Mock Jacqueline, Neri Dario, Cazzamalli Samuele, Oehler Sebastian
Philochem AG, 8112 Otelfingen, Switzerland.
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH Zurich), 8093 Zurich, Switzerland.
J Am Chem Soc. 2025 May 28;147(21):18230-18239. doi: 10.1021/jacs.5c05198. Epub 2025 May 16.
Carbonic anhydrase IX (CAIX) is a membrane protein that is highly expressed in clear cell renal cell carcinoma (ccRCC) and in hypoxic tumors. Being virtually absent in most healthy tissues, CAIX became an attractive target for the selective delivery of diagnostic and therapeutic payloads. Here, we report the discovery and characterization of DNA-encoded chemical library (DEL)-derived CAIX ligands for radionuclide-based imaging applications.
DELs were screened against CAIX and CAII to prioritize hits based on their selectivity and enrichment against CAIX. characterization of hits was performed by fluorescence polarization (FP), surface plasmon resonance (SPR), and flow cytometry. biodistribution studies of Lutetium-177 and Gallium-68-radiolabeled compounds were performed in SK-RC-52 tumor-bearing mice.
DEL-based CAIX ligands with different affinities and selectivities could be identified. Selectivity and high affinity toward the target correlated with higher tumor-to-organ ratios and improved tumor retention. The best candidate, named OncoCAIX, reached up to ∼55% injected dose per gram in SK-RC-52 lesions at early time points with very low healthy organ uptake (tumor-to-kidney ratio of >23).
OncoCAIX demonstrated rapid and selective tumor uptake, which is a key feature for the development of radionuclide-based imaging agents for early and late-stage ccRCC and hypoxic tumors.
碳酸酐酶IX(CAIX)是一种膜蛋白,在透明细胞肾细胞癌(ccRCC)和缺氧肿瘤中高度表达。在大多数健康组织中几乎不存在,CAIX成为诊断和治疗有效载荷选择性递送的有吸引力的靶点。在此,我们报告了用于基于放射性核素成像应用的DNA编码化学库(DEL)衍生的CAIX配体的发现和表征。
针对CAIX和CAII筛选DEL,以根据其对CAIX的选择性和富集程度对命中物进行优先级排序。通过荧光偏振(FP)、表面等离子体共振(SPR)和流式细胞术对命中物进行表征。在携带SK-RC-52肿瘤的小鼠中进行了镥-177和镓-68放射性标记化合物的生物分布研究。
可以鉴定出具有不同亲和力和选择性的基于DEL的CAIX配体。对靶标的选择性和高亲和力与更高的肿瘤与器官比率和改善的肿瘤滞留相关。最佳候选物名为OncoCAIX,在早期时间点,SK-RC-52病变中每克达到约55%的注射剂量,健康器官摄取非常低(肿瘤与肾脏比率>23)。
OncoCAIX表现出快速且选择性的肿瘤摄取,这是开发用于早期和晚期ccRCC及缺氧肿瘤的基于放射性核素的成像剂的关键特征。