Feasibility of Anti-CEA Dye Conjugate for Cancer-Specific Imaging in Gastric Cancer Cell Lines and Mouse Xenograft Models

  • Cancers (Basel). 2025 Sep 8;17(17):2937. doi: 10.3390/cancers17172937.
Kyoungyun Jeong  1 Annie Eunhee Koo  1 Jaeun Yoo  1 Ji-Yeon Shin  1 Leena Lim  1 Hyun Myong Kim  1 Ji-Yong Park  2 Yun-Sang Lee  2 Yoon-Jin Kwak  3 Hye Seung Lee  1  3 Yie-Ri Yoo  1 Bérénice Framery  4 Karen Dumas  4 Françoise Cailler  4 André Pèlegrin  4  5 Do-Joong Park  1  6 Han-Kwang Yang  1  6 Seong-Ho Kong  1  6  7 Hyuk-Joon Lee  1  6
Affiliations
  • 1. Cancer Research Institute, College of Medicine, Seoul National University, 101 Daehak-ro, Jongro-gu, Seoul 03080, Republic of Korea.
  • 2. Department of Nuclear Medicine, Seoul National University Hospital, 101 Daehak-ro, Jongro-gu, Seoul 03080, Republic of Korea.
  • 3. Department of Pathology, Seoul National University Hospital, Seoul National University College of Medicine, 101 Daehak-ro, Jongro-gu, Seoul 03080, Republic of Korea.
  • 4. SurgiMAb, 10 Parc Club du Millénaire, 1025 Avenue Henri Becquerel, 34000 Montpellier, France.
  • 5. IRCM, Université de Montpellier, Inserm, ICM, 208 Rue des Apothicaires, 34298 Montpellier CEDEX 5, France.
  • 6. Department of Surgery, Seoul National University Hospital, 101 Daehak-ro, Jongro-gu, Seoul 03080, Republic of Korea.
  • 7. VITCAL, Co., Ltd., 101 Daehak-ro, Jongro-gu, Seoul 03080, Republic of Korea.
Abstract

Purpose: 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. Materials and Methods: 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. Results: 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. Conclusions: 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.

Keywords
carcinoembryonic antigen; fluorescence; heterografts; immunoconjugates; laparoscopy; stomach neoplasms.
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