Novel anti-CEA affibody for rapid tumor-targeting and molecular imaging diagnosis in mice bearing gastrointestinal cancer cell lines

Gastrointestinal cancer is a common malignant tumor with a high incidence worldwide. Despite continuous improvements in diagnosis and treatment strategies, the overall prognosis of gastrointestinal tumors remains poor. Carcinoembryonic antigen (CEA) is highly expressed in various types of cancers, especially in gastrointestinal cancers, making it a potential target for therapeutic intervention. Therefore, the expression of CEA can be used as an indication of the existence of tumors, chosen as a target for molecular imaging diagnosis, and effectively utilized in the targeted therapy of gastrointestinal cancers. In this study, we report the selection and characterization of affibody molecules (Z<sub>CEA</sub>539, Z<sub>CEA</sub>546, and Z<sub>CEA</sub>919) specific to the CEA protein. Their ability to bind to recombinant and native CEA protein has been confirmed by surface plasmon resonance (SPR), immunofluorescence, and immunohistochemistry assays. Furthermore, Dylight755-labeled Z<sub>CEA</sub> affibody showed accumulation within the tumor site 1 h post injection and was continuously enhanced for 4 h. The Dylight755-labeled Z<sub>CEA</sub> affibody exhibited high tumor-targeting specificity in CEA+ xenograft-bearing mice and possesses promising characteristics for tumor-targeting imaging. Overall, our results suggest the potential use of Z<sub>CEA</sub> affibodies as fluorescent molecular imaging probes for detecting CEA expression in gastrointestinal cancer.

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Publication Details

Journal
Frontiers in Microbiology
Published
2024-10-09
DOI
https://doi.org/10.3389/fmicb.2024.1464088
Citations
2
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
0.81
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article

Novel anti-CEA affibody for rapid tumor-targeting and molecular imaging diagnosis in mice bearing gastrointestinal cancer cell lines

Saidu Kamara, Jinji Jin, Kaiji Lv, Yiqi Cai et al.
2 citations
Frontiers in Microbiology
Monoclonal and Polyclonal Antibodies Research
0.81
article

Novel anti-CEA affibody for rapid tumor-targeting and molecular imaging diagnosis in mice bearing gastrointestinal cancer cell lines

Saidu Kamara, Jinji Jin, Kaiji Lv, Yiqi Cai, Huanyi Shao, Shanli Zhu, Jun Chen, Lifang Zhang, Guanbao Zhu, Pengfei Wang
article en
2 citations

Abstract

Gastrointestinal cancer is a common malignant tumor with a high incidence worldwide. Despite continuous improvements in diagnosis and treatment strategies, the overall prognosis of gastrointestinal tumors remains poor. Carcinoembryonic antigen (CEA) is highly expressed in various types of cancers, especially in gastrointestinal cancers, making it a potential target for therapeutic intervention. Therefore, the expression of CEA can be used as an indication of the existence of tumors, chosen as a target for molecular imaging diagnosis, and effectively utilized in the targeted therapy of gastrointestinal cancers. In this study, we report the selection and characterization of affibody molecules (Z<sub>CEA</sub>539, Z<sub>CEA</sub>546, and Z<sub>CEA</sub>919) specific to the CEA protein. Their ability to bind to recombinant and native CEA protein has been confirmed by surface plasmon resonance (SPR), immunofluorescence, and immunohistochemistry assays. Furthermore, Dylight755-labeled Z<sub>CEA</sub> affibody showed accumulation within the tumor site 1 h post injection and was continuously enhanced for 4 h. The Dylight755-labeled Z<sub>CEA</sub> affibody exhibited high tumor-targeting specificity in CEA+ xenograft-bearing mice and possesses promising characteristics for tumor-targeting imaging. Overall, our results suggest the potential use of Z<sub>CEA</sub> affibodies as fluorescent molecular imaging probes for detecting CEA expression in gastrointestinal cancer.

Frontiers in MicrobiologyVol. 15
Wenzhou Medical University (CN), First Affiliated Hospital of Wenzhou Medical University (CN)
No poverty
Openalex Percentile: Top 25%
Monoclonal and Polyclonal Antibodies Research
0.81
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