Feasibility of Anti-CEA Dye Conjugate for Cancer-Specific Imaging in Gastric Cancer Cell Lines and Mouse Xenograft Models
<b>Purpose:</b> Near-infrared fluorescence-guided surgery (FGS) using cancer-specific tracers is promising for tailored gastric cancer (GC) surgery. Carcinoembryonic antigen (CEA) is a potential target due to its high expression in various digestive cancers, including GC. <b>Materials and Methods:</b> SGM-101, a chimeric anti-CEA monoclonal antibody conjugated with the near-infrared dye BM-104, was evaluated in GC. CEA expression was identified in GC cell lines at the mRNA and protein levels. Xenograft models (MKN-45, SNU-16, SNU-668, 85As2mLuc) were established in mice and injected with SGM-101 or PBS. Biodistribution was monitored using in vivo fluorescence imaging. Tumors were further analyzed by immunofluorescence. In a peritoneal carcinomatosis model, 85As2mLuc cells were injected intraperitoneally, and tumors were evaluated by bioluminescence and fluorescence and histology. <b>Results:</b> MKN-45, SNU-16, and 85As2mLuc were CEA-positive, while SNU-668 was CEA-negative. Flow cytometry confirmed CEA expression: MKN-45 (98%), SNU-16 (85.6%), SNU-668 (6.42%) and 85As2mLuc (78.4%). SGM-101 selectively targeted CEA-expressing tumors, with fluorescence peaking at 48 h, and immunofluorescence verified localization in tumor cells. In the peritoneal models, SGM-101 enabled precise detection of CEA-positive tumors. <b>Conclusions:</b> This study provides the first evidence for the feasibility of SGM-101 in gastric cancer, demonstrating its novelty and translational potential as a cancer-specific imaging agent for fluorescence-guided surgery.
Authors
- Hyun Myong Kim
- Françoise Cailler (ORCID: https://orcid.org/0000-0003-0540-2335)
- Karen Dumas
- Do Joong Park (ORCID: https://orcid.org/0000-0001-9644-6127)
- Yoonjin Kwak (ORCID: https://orcid.org/0000-0001-5314-2465)
- Yun‐Sang Lee (ORCID: https://orcid.org/0000-0003-1640-2090)
- Seong‐Ho Kong (ORCID: https://orcid.org/0000-0002-3929-796X)
- Hyuk‐Joon Lee (ORCID: https://orcid.org/0000-0002-9530-647X)
- Hye Seung Lee (ORCID: https://orcid.org/0000-0002-1667-7986)
- Bérénice Framery
- André Pèlegrin (ORCID: https://orcid.org/0000-0001-9254-2648)
- Yie‐Ri Yoo (ORCID: https://orcid.org/0009-0003-3902-4982)
- Kyoungyun Jeong (ORCID: https://orcid.org/0000-0002-5249-1142)
- Leena Lim
- Ji-Yong Park (ORCID: https://orcid.org/0000-0003-4055-5919)
- Han‐Kwang Yang (ORCID: https://orcid.org/0000-0003-3495-3048)
- Ji‐Yeon Shin (ORCID: https://orcid.org/0009-0005-9054-4064)
- Jaeun Yoo
- Anna P. Koo
Institutions
- Inserm (FR)
- Cancer Research Institute (US)
- Université de Montpellier (FR)
- New Generation University College (ET)
- Seoul National University Hospital (KR)
- Vitzro Tech (South Korea) (KR)
- Institute for Neurosciences of Montpellier (FR)
- Laboratoire National Henri Becquerel (FR)
- Institut de Recherche en Cancérologie de Montpellier (FR)
Publication Details
- Journal
- Cancers
- Published
- 2025-09-08
- DOI
- https://doi.org/10.3390/cancers17172937
- Citations
- 1
- Primary Topic
- Cancer Research and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 1.23
Funders
- Cancer Research Institute
- National Research Foundation
- Seoul National University
- National Research Foundation of Korea
- Seoul National University Hospital
- College of Medicine, Seoul National University