Artschwager Raik, Kalidindi Teja M, Johnson Delissa, Brennan Christopher, Samuels Zachary V, Lito Piro, Pillarsetty Naga Vara Kishore
Department of Radiology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, New York 10065, United States.
Department of Chemistry, Hunter College, City University of New York, New York, New York 10065, United States.
ACS Pharmacol Transl Sci. 2024 Nov 21;7(12):3867-3878. doi: 10.1021/acsptsci.4c00425. eCollection 2024 Dec 13.
Kirsten rat sarcoma (KRAS) is a frequently mutated oncogene responsible for several oncogenic KRAS variants and for driving tumor proliferation. Some nonsmall cell lung cancer (NSCLC) tumors exhibit KRAS G12C mutations, which can be targeted for inhibition using covalent and more recently noncovalent inhibitors. Sotorasib was the first FDA-approved G12C inhibitor that has shown efficacy in lung cancer patients, but with mixed responses. The lack of efficacy can be attributed to tumor heterogeneity (lack of G12C mutations) and/or inefficient delivery. Targeted KRAS G12C imaging has potential to identify NSCLC lesions with the targeted mutation and elucidate the oncogene's role in driving tumor growth and correlating responses to treatment. Toward this goal, we have developed a sotorasib-based molecular agent for PET imaging and tested its efficacy in targeting tumor lesions with KRAS G12C mutations. Here, we describe the synthesis, in vitro and in vivo evaluation of an [I]I-Sotorasib analog in targeting G12C mutant tumor lesions using PET imaging.
Kirsten大鼠肉瘤(KRAS)是一种经常发生突变的致癌基因,它导致了多种致癌性KRAS变体并推动肿瘤增殖。一些非小细胞肺癌(NSCLC)肿瘤表现出KRAS G12C突变,可使用共价抑制剂以及最近出现的非共价抑制剂对其进行靶向抑制。索托拉西布是首个获得美国食品药品监督管理局(FDA)批准的G12C抑制剂,已在肺癌患者中显示出疗效,但反应不一。疗效欠佳可归因于肿瘤异质性(缺乏G12C突变)和/或递送效率低下。靶向KRAS G12C成像有潜力识别具有靶向突变的NSCLC病变,并阐明致癌基因在推动肿瘤生长以及与治疗反应相关性方面的作用。为实现这一目标,我们开发了一种基于索托拉西布的分子探针用于正电子发射断层扫描(PET)成像,并测试了其靶向具有KRAS G12C突变的肿瘤病变的效果。在此,我们描述了一种[I]I-索托拉西布类似物的合成、体外和体内评估,该类似物利用PET成像靶向G12C突变肿瘤病变。