Abstract 2132: Near-Infrared Claudin-1 antibody enables accurate detection of primary and metastatic colorectal tumors in mice.

Abstract Background: Claudin-1, a tight-junction protein frequently overexpressed in colorectal cancer (CRC), is an attractive target for antibody-mediated near-infrared (NIR) fluorescence imaging. This study evaluates an anti-Claudin-1 antibody conjugated to IRDye800CW for detecting and validating colorectal tumors using bioluminescence correlation in orthotopic and metastatic mouse models. Methods: Luciferase-expressing LS174T human colon cancer cells were implanted into athymic nude mice to establish orthotopic (n = 10) and hepatic (n = 9) tumor models. Mice received 50 µg of Claudin-1-IRDye800CW intravenously 48 hours before imaging. In vivo imaging was performed using both the Pearl Trilogy Small Animal Imaging System and the Arthrex Synergy Vision System equipped for 800 nm fluorescence. Mean fluorescence intensity (mFI) was used to calculate tumor-to-background (TBR) and tumor-to-liver (TLR) ratios. Co-registration with luciferase bioluminescence was used to confirm probe specificity, and ex vivo imaging validated biodistribution. Results: In the orthotopic model, Claudin-1-IRDye800CW achieved a mean TBR of 3.92, clearly delineating tumor margins, while sub-millimeter peritoneal metastases (< 1 mm) produced a mean TBR of 2.9. In the hepatic model, the mean TLR was 3.42, confirming selective tumor contrast over surrounding tissue. Ex vivo analysis further increased contrast (TBR = 16.4; TLR = 4.78). Fluorescent signals consistently co-localized with luciferase activity, confirming targeting specificity. Both imaging systems demonstrated high-resolution detection, and the Arthrex clinical laparoscope enabled real-time intraoperative visualization under clinically relevant conditions. Conclusion: The anti-Claudin-1-IRDye800CW conjugate selectively and accurately identifies both primary and metastatic colorectal tumors in vivo. Strong tumor contrast and spatial concordance with bioluminescence validate its specificity, while compatibility with a clinical laparoscopic platform underscores the translational promise of Claudin-1-targeted NIR fluorescence imaging for colorectal cancer detection and fluorescence-guided surgery. Citation Format: Javier Bravo, Shanglei Liu, Siamak Amirfakhri, Blackberrie Eddins, Keita Kobayashi, Jasmin Zaker, Robert Hoffman, Sumbal Talib, Aaron M. Mohs, Punita Dhawan, Michael Bouvet. Near-Infrared Claudin-1 antibody enables accurate detection of primary and metastatic colorectal tumors in mice [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2132.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-2132
Primary Topic
Cancer Research and Treatments
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article
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article

Abstract 2132: Near-Infrared Claudin-1 antibody enables accurate detection of primary and metastatic colorectal tumors in mice.

Sumbal Talib, Michael Bouvet, Punita Dhawan, Blackberrie Eddins et al.
Cancer Research
Cancer Research and Treatments
article

Abstract 2132: Near-Infrared Claudin-1 antibody enables accurate detection of primary and metastatic colorectal tumors in mice.

Sumbal Talib, Michael Bouvet, Punita Dhawan, Blackberrie Eddins, Shanglei Liu, Aaron M. Mohs, Siamak Amirfakhri, Javier Bravo, Jasmin Zaker, Keita Kobayashi, Robert Hoffman
article en

Abstract

Abstract Background: Claudin-1, a tight-junction protein frequently overexpressed in colorectal cancer (CRC), is an attractive target for antibody-mediated near-infrared (NIR) fluorescence imaging. This study evaluates an anti-Claudin-1 antibody conjugated to IRDye800CW for detecting and validating colorectal tumors using bioluminescence correlation in orthotopic and metastatic mouse models. Methods: Luciferase-expressing LS174T human colon cancer cells were implanted into athymic nude mice to establish orthotopic (n = 10) and hepatic (n = 9) tumor models. Mice received 50 µg of Claudin-1-IRDye800CW intravenously 48 hours before imaging. In vivo imaging was performed using both the Pearl Trilogy Small Animal Imaging System and the Arthrex Synergy Vision System equipped for 800 nm fluorescence. Mean fluorescence intensity (mFI) was used to calculate tumor-to-background (TBR) and tumor-to-liver (TLR) ratios. Co-registration with luciferase bioluminescence was used to confirm probe specificity, and ex vivo imaging validated biodistribution. Results: In the orthotopic model, Claudin-1-IRDye800CW achieved a mean TBR of 3.92, clearly delineating tumor margins, while sub-millimeter peritoneal metastases (< 1 mm) produced a mean TBR of 2.9. In the hepatic model, the mean TLR was 3.42, confirming selective tumor contrast over surrounding tissue. Ex vivo analysis further increased contrast (TBR = 16.4; TLR = 4.78). Fluorescent signals consistently co-localized with luciferase activity, confirming targeting specificity. Both imaging systems demonstrated high-resolution detection, and the Arthrex clinical laparoscope enabled real-time intraoperative visualization under clinically relevant conditions. Conclusion: The anti-Claudin-1-IRDye800CW conjugate selectively and accurately identifies both primary and metastatic colorectal tumors in vivo. Strong tumor contrast and spatial concordance with bioluminescence validate its specificity, while compatibility with a clinical laparoscopic platform underscores the translational promise of Claudin-1-targeted NIR fluorescence imaging for colorectal cancer detection and fluorescence-guided surgery. Citation Format: Javier Bravo, Shanglei Liu, Siamak Amirfakhri, Blackberrie Eddins, Keita Kobayashi, Jasmin Zaker, Robert Hoffman, Sumbal Talib, Aaron M. Mohs, Punita Dhawan, Michael Bouvet. Near-Infrared Claudin-1 antibody enables accurate detection of primary and metastatic colorectal tumors in mice [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2132.

Cancer ResearchVol. 86(7_Supplement)
Nebraska Medical Center (US), UC San Diego Health System (US), University of Kansas Medical Center (US), University of Nebraska Medical Center (US)
Good health and well-being
Openalex Percentile: Top 29%
Cancer Research and Treatments
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