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Novel ImmunoPET Probes [Cu]Cu-NOTA-GGB02-F9 for Small-Cell Lung Cancer Derived from a SEZ6-Targeting Antibody.

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Journal of medicinal chemistry 📖 저널 OA 13.8% 2023: 1/1 OA 2024: 1/8 OA 2025: 14/81 OA 2026: 14/134 OA 2023~2026 2026 Vol.69(3) p. 2968-2975
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출처

Wang G, Zheng L, Yang X, Wang X, Zhou Z, Kan Y

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Seizure-related 6 homologue (SEZ6) is a highly expressed transmembrane protein that has emerged as a promising therapeutic target for small-cell lung cancer (SCLC).

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APA Wang G, Zheng L, et al. (2026). Novel ImmunoPET Probes [Cu]Cu-NOTA-GGB02-F9 for Small-Cell Lung Cancer Derived from a SEZ6-Targeting Antibody.. Journal of medicinal chemistry, 69(3), 2968-2975. https://doi.org/10.1021/acs.jmedchem.5c02806
MLA Wang G, et al.. "Novel ImmunoPET Probes [Cu]Cu-NOTA-GGB02-F9 for Small-Cell Lung Cancer Derived from a SEZ6-Targeting Antibody.." Journal of medicinal chemistry, vol. 69, no. 3, 2026, pp. 2968-2975.
PMID 41589586 ↗

Abstract

Seizure-related 6 homologue (SEZ6) is a highly expressed transmembrane protein that has emerged as a promising therapeutic target for small-cell lung cancer (SCLC). In this study, we developed a novel immuno-positron emission tomography probe ([Cu]Cu-NOTA-GGB02-F9) based on the SEZ6-targeting antibody, GGB02-F9, for use in preclinical mouse models of SCLC. The diagnostic potential of [Cu]Cu-NOTA-GGB02-F9 was evaluated in preclinical SCLC models with varying levels of SEZ6 expression. The H69 tumors exhibited a distinct accumulation of tracer uptake in the tumor xenograft mice, reaching a maximum uptake at 72 h postinjection, which was significantly higher than that in the H69 GGB02-F9-blocked and H460 groups ( < 0.01) at 24, 48, and 72 h postinjection. The uptake of the tumor tracer in mice was found to be associated with SEZ6 expression, as determined by immunohistochemical analysis. Our study demonstrated that [Cu]Cu-NOTA-GGB02-F9 can noninvasively evaluate SEZ6 expression in preclinical SCLC mouse models.

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