TY - JOUR
T1 - Prostate-specific membrane antigen-targeted photoacoustic imaging of prostate cancer in vivo
AU - Zhang, Haichong K.
AU - Chen, Ying
AU - Kang, Jeeun
AU - Lisok, Ala
AU - Minn, Il
AU - Pomper, Martin G.
AU - Boctor, Emad M.
N1 - Funding Information:
National Institutes of Health (US), Grant/Award Numbers: CA202199, EB015638, CA134675; National Science Foundation (US), Grant/Award Number: 1653322
Funding Information:
Financial supports were provided by the NIH grants CA202199, EB021396, EB024495, CA192482, CA184228, and CA134675, CDMRP grant PC171089 and NSF SCH: CAREER grant 1653322.
Publisher Copyright:
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2018/9
Y1 - 2018/9
N2 - A sensitive, noninvasive method to detect localized prostate cancer, particularly for early detection and repetitive study in patients undergoing active surveillance, remains an unmet need. Here, we propose a molecular photoacoustic (PA) imaging approach by targeting the prostate-specific membrane antigen (PSMA), which is over-expressed in the vast majority of prostate cancers. We performed spectroscopic PA imaging in an experimental model of prostate cancer, namely, in immunocompromised mice bearing PSMA+ (PC3 PIP) and PSMA− (PC3 flu) tumors through administration of the known PSMA-targeted fluorescence agent, YC-27. Differences in contrast between PSMA+ and isogenic control tumors were observed upon PA imaging, with PSMA+ tumors showing higher contrast in average of 66.07-fold with 5 mice at the 24-hour postinjection time points. These results were corroborated using standard near-infrared fluorescence imaging with YC-27, and the squared correlation between PA and fluorescence intensities was 0.89. Spectroscopic PA imaging is a new molecular imaging modality with sufficient sensitivity for targeting PSMA in vivo, demonstrating the potential applications for other saturable targets relevant to cancer and other disorders.
AB - A sensitive, noninvasive method to detect localized prostate cancer, particularly for early detection and repetitive study in patients undergoing active surveillance, remains an unmet need. Here, we propose a molecular photoacoustic (PA) imaging approach by targeting the prostate-specific membrane antigen (PSMA), which is over-expressed in the vast majority of prostate cancers. We performed spectroscopic PA imaging in an experimental model of prostate cancer, namely, in immunocompromised mice bearing PSMA+ (PC3 PIP) and PSMA− (PC3 flu) tumors through administration of the known PSMA-targeted fluorescence agent, YC-27. Differences in contrast between PSMA+ and isogenic control tumors were observed upon PA imaging, with PSMA+ tumors showing higher contrast in average of 66.07-fold with 5 mice at the 24-hour postinjection time points. These results were corroborated using standard near-infrared fluorescence imaging with YC-27, and the squared correlation between PA and fluorescence intensities was 0.89. Spectroscopic PA imaging is a new molecular imaging modality with sufficient sensitivity for targeting PSMA in vivo, demonstrating the potential applications for other saturable targets relevant to cancer and other disorders.
KW - molecular imaging
KW - prostate-specific membrane antigen
KW - spectroscopic photoacoustic imaging
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U2 - 10.1002/jbio.201800021
DO - 10.1002/jbio.201800021
M3 - Letter
C2 - 29653029
AN - SCOPUS:85052830304
SN - 1864-063X
VL - 11
JO - Journal of biophotonics
JF - Journal of biophotonics
IS - 9
M1 - e201800021
ER -