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 [(124)I]I-Sotorasib analog in targeting G12C mutant tumor lesions using PET imaging.
Preclinical Evaluation of [(124)I]-Sotorasib for the Imaging of Kirsten Rat Sarcoma G12C Mutant Tumors.
[(124)I]-Sotorasib 用于 Kirsten 大鼠肉瘤 G12C 突变肿瘤成像的临床前评价
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作者:Artschwager Raik, Kalidindi Teja M, Johnson Delissa, Brennan Christopher, Samuels Zachary V, Lito Piro, Pillarsetty Naga Vara Kishore
| 期刊: | ACS Pharmacology and Translational Science | 影响因子: | 3.700 |
| 时间: | 2024 | 起止号: | 2024 Nov 21; 7(12):3867-3878 |
| doi: | 10.1021/acsptsci.4c00425 | 种属: | Rat |
| 研究方向: | 肿瘤 | ||
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