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Development of a CLDN18.2-targeting immuno-PET probe for non-invasive imaging in gastrointestinal tumors

Claudin18.2 (CLDN18.2) is a tight junction protein that is overexpressed in a variety of solid tumors such as gastrointestinal cancer and oesophageal cancer. It has been identified as a promising target and a potential biomarker to diagnose tumor, evaluate efficacy, and determine patient prognosis....

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Autores principales: Chen, Yan, Hou, Xingguo, Li, Dapeng, Ding, Jin, Liu, Jiayue, Wang, Zilei, Teng, Fei, Li, Hongjun, Zhang, Fan, Gu, Yi, Yu, Steven, Qian, Xueming, Yang, Zhi, Zhu, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Xi'an Jiaotong University 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173170/
https://www.ncbi.nlm.nih.gov/pubmed/37181294
http://dx.doi.org/10.1016/j.jpha.2023.02.011
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author Chen, Yan
Hou, Xingguo
Li, Dapeng
Ding, Jin
Liu, Jiayue
Wang, Zilei
Teng, Fei
Li, Hongjun
Zhang, Fan
Gu, Yi
Yu, Steven
Qian, Xueming
Yang, Zhi
Zhu, Hua
author_facet Chen, Yan
Hou, Xingguo
Li, Dapeng
Ding, Jin
Liu, Jiayue
Wang, Zilei
Teng, Fei
Li, Hongjun
Zhang, Fan
Gu, Yi
Yu, Steven
Qian, Xueming
Yang, Zhi
Zhu, Hua
author_sort Chen, Yan
collection PubMed
description Claudin18.2 (CLDN18.2) is a tight junction protein that is overexpressed in a variety of solid tumors such as gastrointestinal cancer and oesophageal cancer. It has been identified as a promising target and a potential biomarker to diagnose tumor, evaluate efficacy, and determine patient prognosis. TST001 is a recombinant humanized CLDN18.2 antibody that selectively binds to the extracellular loop of human Claudin18.2. In this study, we constructed a solid target radionuclide zirconium-89 ((89)Zr) labled-TST001 to detect the expression of in the human stomach cancer BGC823(CLDN18.2) cell lines. The [(89)Zr]Zr-desferrioxamine (DFO)-TST001 showed high radiochemical purity (RCP, >99%) and specific activity (24.15 ± 1.34 GBq/μmol), and was stable in 5% human serum albumin, and phosphate buffer saline (>85% RCP at 96 h). The EC(50) values of TST001 and DFO-TST001 were as high as 0.413 ± 0.055 and 0.361 ± 0.058 nM (P > 0.05), respectively. The radiotracer had a significantly higher average standard uptake values in CLDN18.2-positive tumors than in CLDN18.2-negative tumors (1.11 ± 0.02 vs. 0.49 ± 0.03, P = 0.0016) 2 days post injection (p.i.). BGC823(CLDN18.2) mice models showed high tumor/muscle ratios 96 h p.i. with [(89)Zr]Zr-DFO-TST001 was much higher than those of the other imaging groups. Immunohistochemistry results showed that BGC823(CLDN18.2) tumors were highly positive (+++) for CLDN18.2, while those in the BGC823 group did not express CLDN18.2 (−). The results of ex vivo biodistribution studies showed that there was a higher distribution in the BGC823(CLDN18.2) tumor bearing mice (2.05 ± 0.16 %ID/g) than BGC823 mice (0.69 ± 0.02 %ID/g) and blocking group (0.72 ± 0.02 %ID/g). A dosimetry estimation study showed that the effective dose of [(89)Zr]Zr-DFO-TST001 was 0.0705 mSv/MBq, which is within the range of acceptable doses for nuclear medicine research. Taken together, these results suggest that Good Manufacturing Practices produced by this immuno-positron emission tomography probe can detect CLDN18.2-overexpressing tumors.
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spelling pubmed-101731702023-05-12 Development of a CLDN18.2-targeting immuno-PET probe for non-invasive imaging in gastrointestinal tumors Chen, Yan Hou, Xingguo Li, Dapeng Ding, Jin Liu, Jiayue Wang, Zilei Teng, Fei Li, Hongjun Zhang, Fan Gu, Yi Yu, Steven Qian, Xueming Yang, Zhi Zhu, Hua J Pharm Anal Original Article Claudin18.2 (CLDN18.2) is a tight junction protein that is overexpressed in a variety of solid tumors such as gastrointestinal cancer and oesophageal cancer. It has been identified as a promising target and a potential biomarker to diagnose tumor, evaluate efficacy, and determine patient prognosis. TST001 is a recombinant humanized CLDN18.2 antibody that selectively binds to the extracellular loop of human Claudin18.2. In this study, we constructed a solid target radionuclide zirconium-89 ((89)Zr) labled-TST001 to detect the expression of in the human stomach cancer BGC823(CLDN18.2) cell lines. The [(89)Zr]Zr-desferrioxamine (DFO)-TST001 showed high radiochemical purity (RCP, >99%) and specific activity (24.15 ± 1.34 GBq/μmol), and was stable in 5% human serum albumin, and phosphate buffer saline (>85% RCP at 96 h). The EC(50) values of TST001 and DFO-TST001 were as high as 0.413 ± 0.055 and 0.361 ± 0.058 nM (P > 0.05), respectively. The radiotracer had a significantly higher average standard uptake values in CLDN18.2-positive tumors than in CLDN18.2-negative tumors (1.11 ± 0.02 vs. 0.49 ± 0.03, P = 0.0016) 2 days post injection (p.i.). BGC823(CLDN18.2) mice models showed high tumor/muscle ratios 96 h p.i. with [(89)Zr]Zr-DFO-TST001 was much higher than those of the other imaging groups. Immunohistochemistry results showed that BGC823(CLDN18.2) tumors were highly positive (+++) for CLDN18.2, while those in the BGC823 group did not express CLDN18.2 (−). The results of ex vivo biodistribution studies showed that there was a higher distribution in the BGC823(CLDN18.2) tumor bearing mice (2.05 ± 0.16 %ID/g) than BGC823 mice (0.69 ± 0.02 %ID/g) and blocking group (0.72 ± 0.02 %ID/g). A dosimetry estimation study showed that the effective dose of [(89)Zr]Zr-DFO-TST001 was 0.0705 mSv/MBq, which is within the range of acceptable doses for nuclear medicine research. Taken together, these results suggest that Good Manufacturing Practices produced by this immuno-positron emission tomography probe can detect CLDN18.2-overexpressing tumors. Xi'an Jiaotong University 2023-04 2023-02-28 /pmc/articles/PMC10173170/ /pubmed/37181294 http://dx.doi.org/10.1016/j.jpha.2023.02.011 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Chen, Yan
Hou, Xingguo
Li, Dapeng
Ding, Jin
Liu, Jiayue
Wang, Zilei
Teng, Fei
Li, Hongjun
Zhang, Fan
Gu, Yi
Yu, Steven
Qian, Xueming
Yang, Zhi
Zhu, Hua
Development of a CLDN18.2-targeting immuno-PET probe for non-invasive imaging in gastrointestinal tumors
title Development of a CLDN18.2-targeting immuno-PET probe for non-invasive imaging in gastrointestinal tumors
title_full Development of a CLDN18.2-targeting immuno-PET probe for non-invasive imaging in gastrointestinal tumors
title_fullStr Development of a CLDN18.2-targeting immuno-PET probe for non-invasive imaging in gastrointestinal tumors
title_full_unstemmed Development of a CLDN18.2-targeting immuno-PET probe for non-invasive imaging in gastrointestinal tumors
title_short Development of a CLDN18.2-targeting immuno-PET probe for non-invasive imaging in gastrointestinal tumors
title_sort development of a cldn18.2-targeting immuno-pet probe for non-invasive imaging in gastrointestinal tumors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173170/
https://www.ncbi.nlm.nih.gov/pubmed/37181294
http://dx.doi.org/10.1016/j.jpha.2023.02.011
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