Development of a Dual‐Factor Activatable Covalent Targeted Photoacoustic Imaging Probe for Tumor Imaging

Author:

Song Jiho1ORCID,Zhai Tianqu2ORCID,Hahm Heung Sik1ORCID,Li Yuancheng3ORCID,Mao Hui3ORCID,Wang Xueding2ORCID,Jo Janggun2ORCID,Chang Jae Won145ORCID

Affiliation:

1. Department of Pharmacology and Chemical Biology Emory University Atlanta, Georgia 30322 United States

2. Department of Biomedical Engineering University of Michigan Ann Arbor MI 48109 USA

3. Department of Radiology and Imaging Science Emory University Atlanta, Georgia 30322 United States

4. Department of Hematology and Medical Oncology Emory University Atlanta, Georgia 30322 United States

5. Winship Cancer Institute Emory University Atlanta, Georgia 30322 United States

Abstract

AbstractPhotoacoustic imaging (PAI) is an emerging modality in biomedical imaging with superior imaging depth and specificity. However, PAI still has significant limitations, such as the background noise from endogenous chromophores. To overcome these limitations, we developed a covalent activity‐based PAI probe, NOx‐JS013, targeting NCEH1. NCEH1, a highly expressed and activated serine hydrolase in aggressive cancers, has the potential to be employed for the diagnosis of cancers. We show that NOx‐JS013 labels active NCEH1 in live cells with high selectivity relative to other serine hydrolases. NOx‐JS013 also presents its efficacy as a hypoxia‐responsive imaging probe in live cells. Finally, NOx‐JS013 successfully visualizes aggressive prostate cancer tumors in mouse models of PC3, while being negligibly detected in tumors of non‐aggressive LNCaP mouse models. These findings show that NOx‐JS013 has the potential to be used to develop precision PAI reagents for detecting metastatic progression in various cancers.

Funder

Division of Cancer Epidemiology and Genetics, National Cancer Institute

Prostate Cancer Foundation

Winship Cancer Institute

Publisher

Wiley

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