Development and Preclinical Evaluation of a Novel EpCAM-Targeted <sup>111</sup> In-Labeled Antibody for SPECT Imaging

High Resolution Image Download MS PowerPoint Slide Epithelial cell adhesion molecule (EpCAM) is overexpressed in various epithelial malignancies and represents an attractive target for molecular imaging and radionuclide therapy. This study aimed to develop and evaluate a novel EpCAM-targeted monoclonal antibody for single-photon emission computed tomography (SPECT) imaging. To this end, Ep4-1, a high-affinity anti-EpCAM monoclonal antibody, was conjugated to the bifunctional chelator p -SCN-Bn-diethylenetriaminepentaacetic acid (DTPA) and radiolabeled with indium-111 ( 111 In). In vitro EpCAM-binding affinity, plasma stability, and cellular internalization were examined using high-EpCAM-expressing DLD-1 cells. In vivo biodistribution, blocking studies, and SPECT/computed tomography (CT) imaging were performed in DLD-1 tumor-bearing mice. Results showed that [ 111 In]In-DTPA-Ep4-1 retained high, EpCAM-specific binding after chelator conjugation and showed excellent plasma stability. The radiolabeled antibody exhibited pronounced cellular internalization; approximately 93% of cell-associated radioactivity was internalized in DLD-1 cells at 6 h, exceeding the reported internalization efficiency of previously described EpCAM-targeted antibodies. In vivo biodistribution indicated progressive and selective tumor uptake, reaching 15.1 ± 1.3% ID/g at 72 h after injection. Co-injection of excess unlabeled Ep4-1 reduced tumor accumulation, consistent with EpCAM-specific targeting. Uptake in the liver and spleen was consistent with the expected pharmacokinetics of intact IgG antibodies. SPECT/CT imaging enabled clear visualization of EpCAM-expressing tumors at 72 h after injection. In conclusion, Ep4-1 is a highly specific and strongly internalizing EpCAM-targeted monoclonal antibody that enables robust SPECT imaging of EpCAM-positive tumors. Given the favorable internalization properties of Ep4-1, it may serve as a promising imaging platform and a potential candidate for future EpCAM-directed radiotheranostics applications, including α-particle-based radionuclide therapy.

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Publication Details

Journal
ACS Omega
Published
2026-07-17
DOI
https://doi.org/10.1021/acsomega.6c04410
Primary Topic
HER2/EGFR in Cancer Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Development and Preclinical Evaluation of a Novel EpCAM-Targeted 111 In-Labeled Antibody for SPECT Imaging

Hidekazu Kawashima, Takashi Kozaka, Takumi Iwasawa, Yuki Naito et al.
ACS Omega
HER2/EGFR in Cancer Research
article

Development and Preclinical Evaluation of a Novel EpCAM-Targeted 111 In-Labeled Antibody for SPECT Imaging

Hidekazu Kawashima, Takashi Kozaka, Takumi Iwasawa, Yuki Naito, Yusuke Yagi, Takiko Daikoku, Marina Omokawa, Hiroyuki Kimura, Kazunori Kato, Hiroyuki Fujimoto, Hiroyuki Yasui, Sato Oshige
article en

Abstract

High Resolution Image Download MS PowerPoint Slide Epithelial cell adhesion molecule (EpCAM) is overexpressed in various epithelial malignancies and represents an attractive target for molecular imaging and radionuclide therapy. This study aimed to develop and evaluate a novel EpCAM-targeted monoclonal antibody for single-photon emission computed tomography (SPECT) imaging. To this end, Ep4-1, a high-affinity anti-EpCAM monoclonal antibody, was conjugated to the bifunctional chelator p -SCN-Bn-diethylenetriaminepentaacetic acid (DTPA) and radiolabeled with indium-111 ( 111 In). In vitro EpCAM-binding affinity, plasma stability, and cellular internalization were examined using high-EpCAM-expressing DLD-1 cells. In vivo biodistribution, blocking studies, and SPECT/computed tomography (CT) imaging were performed in DLD-1 tumor-bearing mice. Results showed that [ 111 In]In-DTPA-Ep4-1 retained high, EpCAM-specific binding after chelator conjugation and showed excellent plasma stability. The radiolabeled antibody exhibited pronounced cellular internalization; approximately 93% of cell-associated radioactivity was internalized in DLD-1 cells at 6 h, exceeding the reported internalization efficiency of previously described EpCAM-targeted antibodies. In vivo biodistribution indicated progressive and selective tumor uptake, reaching 15.1 ± 1.3% ID/g at 72 h after injection. Co-injection of excess unlabeled Ep4-1 reduced tumor accumulation, consistent with EpCAM-specific targeting. Uptake in the liver and spleen was consistent with the expected pharmacokinetics of intact IgG antibodies. SPECT/CT imaging enabled clear visualization of EpCAM-expressing tumors at 72 h after injection. In conclusion, Ep4-1 is a highly specific and strongly internalizing EpCAM-targeted monoclonal antibody that enables robust SPECT imaging of EpCAM-positive tumors. Given the favorable internalization properties of Ep4-1, it may serve as a promising imaging platform and a potential candidate for future EpCAM-directed radiotheranostics applications, including α-particle-based radionuclide therapy.

ACS Omega
Kanazawa University (JP), National Legal Medicine Institute (PT), Toyo University (JP), Okayama University (JP), Environment Agency (GB), Japan Radioisotope Association (JP), Kyoto University (JP), Kyoto Pharmaceutical University (JP), Analytical Services (US), Department of Disease Control (TH), Advanced Pharma (US), Kyoto College of Medical Science (JP), Institute for Learning Innovation (US), Model Animal Research Center (CN), North Medical Center (JP), Institute for Disease Modeling (US), Center for Disease Analysis (US)
Japan Society for the Promotion of Science
Openalex Percentile: Top 11%
HER2/EGFR in Cancer Research
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