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Epidermal growth factor receptor-targeted near-infrared probe cetuximab-IRDye800CW enables stable and tumor-specific fluorescence imaging in colorectal cancer models.

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Journal of biomedical optics 2025 Vol.30(12) p. 126002
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유사 논문
P · Population 대상 환자/모집단
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I · Intervention 중재 / 시술
of the probe intravenously and underwent daily fluorescence imaging for 10 days
C · Comparison 대조 / 비교
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O · Outcome 결과 / 결론
[CONCLUSION] Cetuximab-IRDye800CW provides stable, tumor-specific, high-contrast fluorescence imaging in EGFR-high CRC models. These findings validate its molecular targeting capability and support its translational potential for fluorescence-guided CRC surgery.

Huang Y, Zhang X, Jiang Y, Wang D

📝 환자 설명용 한 줄

[SIGNIFICANCE] Colorectal cancer (CRC) remains a major cause of cancer-related mortality, with incomplete resection contributing to recurrence and poor survival.

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APA Huang Y, Zhang X, et al. (2025). Epidermal growth factor receptor-targeted near-infrared probe cetuximab-IRDye800CW enables stable and tumor-specific fluorescence imaging in colorectal cancer models.. Journal of biomedical optics, 30(12), 126002. https://doi.org/10.1117/1.JBO.30.12.126002
MLA Huang Y, et al.. "Epidermal growth factor receptor-targeted near-infrared probe cetuximab-IRDye800CW enables stable and tumor-specific fluorescence imaging in colorectal cancer models.." Journal of biomedical optics, vol. 30, no. 12, 2025, pp. 126002.
PMID 41346398 ↗

Abstract

[SIGNIFICANCE] Colorectal cancer (CRC) remains a major cause of cancer-related mortality, with incomplete resection contributing to recurrence and poor survival. Improving intraoperative margin detection is critical to enhance surgical precision and patient outcomes.

[AIM] We aim to evaluate the tumor-targeting specificity of cetuximab-IRDye800CW (Cet-IRDye800CW), an epidermal growth factor receptor (EGFR)-specific near-infrared probe, for fluorescence-guided surgery in CRC models.

[APPROACH] Cet-IRDye800CW and IgG-IRDye800CW controls were synthesized and tested in LS174T and SW948 xenografts as well as patient-derived xenografts (PDXs). Mice received of the probe intravenously and underwent daily fluorescence imaging for 10 days. Tumor-to-background ratio (TBR) and mean fluorescence intensity (MFI) were quantified, and EGFR expression was analyzed by Western blot, reverse transcription quantitative polymerase chain reaction, and immunohistochemistry.

[RESULTS] Cetuximab-IRDye800CW significantly enhanced tumor fluorescence compared with controls in all models ( ). TBR increased progressively and peaked on day 10 (LS174T: ; SW948: ), whereas background MFI declined, resulting in improved tumor contrast. Tumor-specific fluorescence was detectable from day 1 and intensified over time. Similar findings were observed in PDX models, consistent with high EGFR expression.

[CONCLUSION] Cetuximab-IRDye800CW provides stable, tumor-specific, high-contrast fluorescence imaging in EGFR-high CRC models. These findings validate its molecular targeting capability and support its translational potential for fluorescence-guided CRC surgery.

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