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  4. A novel 111indium-labeled dual carbonic anhydrase 9-targeted probe as a potential SPECT imaging radiotracer for detection of hypoxic colorectal cancer cells
 
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A novel 111indium-labeled dual carbonic anhydrase 9-targeted probe as a potential SPECT imaging radiotracer for detection of hypoxic colorectal cancer cells

Journal
European Journal of Pharmaceutics and Biopharmaceutics
Journal Volume
168
Pages
38
Date Issued
2021-11
Author(s)
Guan, Siao-Syun
Wu, Cheng-Tien
Liao, Tse-Zung
Lin, Kun-Liang
Peng, Cheng-Liang
Shih, Ying-Hsia
Weng, Mao-Feng
Chen, Chun-Tang
Yeh, Chung-Hsin
Wang, Ying-Chieh
SHING-HWA LIU  
DOI
10.1016/j.ejpb.2021.08.004
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/628609
URL
https://api.elsevier.com/content/abstract/scopus_id/85113722064
Abstract
Tumor hypoxia is a common feature in colorectal cancer (CRC), and is associated with resistance to radiotherapy and chemotherapy. Thus, a specifically targeted probe for the detection of hypoxic CRC cells is urgently needed. Carbonic anhydrase 9 (CA9) is considered to be a specific marker for hypoxic CRC diagnosis. Here, a nuclear imaging Indium-111 (111In)-labeled dual CA9-targeted probe was synthesized and evaluated for CA9 detection in in vitro, in vivo, and in human samples. The CA9-targeted peptide (CA9tp) and CA9 inhibitor acetazolamide (AAZ) were combined to form a dual CA9-targeted probe (AAZ-CA9tp) using an automatic microwave peptide synthesizer, which then was conjugated with 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) for radioisotope (111In) labeling (111In-DOTA-AAZ-CA9tp). The assays for cell binding, stability, and toxicity were conducted in hypoxic CRC HCT15 cells. The analyses for imaging and biodistribution were performed in an HCT15 xenograft mouse model. The binding and distribution of 111In-DOTA-AAZ-CA9tp were detected in human CRC samples using microautoradiography. AAZ-CA9tp possessed good CA9-targeting ability in hypoxic HCT15 cells. The dual CA9-targeted radiotracer showed high serum stability, high surface binding, and high affinity in vitro. After exposure of 111In-DOTA-AAZ-CA9tp to the HCT15-bearing xenograft mice, the levels of 111In-DOTA-AAZ-CA9tp were markedly and specifically increased in the hypoxic tumor tissues compared to control mice. 111In-DOTA-AAZ-CA9tp also targeted the areas of CA9 overexpression in human colorectal tumor tissue sections. The results of this study suggest that the novel 111In-DOTA-AAZ-CA9tp nuclear imaging agent may be a useful tool for the detection of hypoxic CRC cells in clinical practice.
Subjects
Carbonic anhydrase 9-targeted probe; Colorectal cancer; Indium-111 label; SPECT imaging; Tumor hypoxia
SDGs

[SDGs]SDG3

Publisher
ELSEVIER
Type
journal article

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