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Targeted imaging of orthotopic prostate cancer by using clinical transformable photoacoustic molecular probe

To obtain high-yield histological samples by targeted prostate cancer (PCa) biopsy is the current trend compared with transrectal ultrasound (TRUS)-guided systematic histological biopsy, which is regarded as the gold standard for prostate cancer (PCa) diagnosis. In this paper, we present a targeted...

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Bibliographic Details
Published in:BMC cancer 2020-05, Vol.20 (1), p.419-419, Article 419
Main Authors: Qiu, Chen, Bai, Yuanyuan, Yin, Tinghui, Miao, Xiaoyan, Gao, Rongkang, Zhou, Huichao, Ren, Jie, Song, Liang, Liu, Chengbo, Zheng, Hairong, Zheng, Rongqin
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Language:English
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Summary:To obtain high-yield histological samples by targeted prostate cancer (PCa) biopsy is the current trend compared with transrectal ultrasound (TRUS)-guided systematic histological biopsy, which is regarded as the gold standard for prostate cancer (PCa) diagnosis. In this paper, we present a targeted PCa imaging strategy using a real-time molecular photoacoustic imaging system integrated with a handheld US probe (PAI/US) and synthesized an integrin α β targeted probe based on ICG (cRGD-ICG). To prepare cRGD-ICG, ICG-NHS was linked to cRGD through carboxyl-co-reaction. In vitro PA imaging ability of cRGD-ICG was tested. Orthotopic PCa-bearing rats were used as animal models. After injected with either cRGD-ICG or non-targeted probe, rats were implemented with PA imaging to confirm the specific accumulation of cRGD-ICG at tumor region. Moreover, pathological frozen slices were made to observe distribution of the probe in prostate tissue ex vivo. A small molecular PAI probe was synthesized and exhibited excellent targeted imaging ability in vitro. In vivo photoacoustic imaging was carried out after intravenous injection of cRGD-ICG in orthotopic PCa-bearing rats under the facilitation of the PAI/US system. Maximum molecular photoacoustic signals were observed in the tumor area in vivo after the probe injection, which showed 3.8-fold higher signal enhancement than that in the control group (P 
ISSN:1471-2407
1471-2407
DOI:10.1186/s12885-020-06801-9