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Prostate Specific Membrane Antigen (PSMA)-Targeted Photoacoustic Imaging of Prostate Cancer In Vivo

机译:前列腺癌体内膜特异性抗原(PSMA)靶向光声成像。

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摘要

A sensitive, non-invasive 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 five mice at the 24-hour post-injection 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.
机译:灵敏的,非侵入性的方法来检测局限性前列腺癌,尤其是在进行主动监测的患者中进行早期发现和重复研究,仍然是未满足的需求。在这里,我们提出一种针对前列腺特异性膜抗原(PSMA)的分子光声(PA)成像方法,该方法在绝大多数前列腺癌中均过表达。我们在前列腺癌的实验模型中,即在患有PSMA +(PC3 PIP)和PSMA-(PC3 flu)肿瘤的免疫受损小鼠中,通过施用已知的靶向PSMA的荧光剂YC-27,进行了光谱PA成像。 PA成像后观察到PSMA +和等基因对照肿瘤之间的对比差异,在注射后24小时内,五只小鼠的PSMA +肿瘤显示出更高的平均对比度,为66.07倍。这些结果得到了使用YC-27的标准近红外荧光成像的证实,PA和荧光强度之间的平方相关为0.89。光谱PA成像是一种新的分子成像方式,具有足够的敏感性,可体内靶向PSMA,证明了与癌症和其他疾病相关的其他可饱和靶标的潜在应用。

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