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Ultrasound molecular imaging of prostate cancer PSMA-targeted biosynthetic GVs.

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Biomaterials science 📖 저널 OA 15.4% 2021: 0/2 OA 2022: 0/1 OA 2023: 0/1 OA 2024: 0/1 OA 2025: 0/9 OA 2026: 6/23 OA 2021~2026 2026 Vol.14(2) p. 495-505
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Yu K, Wang Y, Wang Z, Li C, Liu C, Wu Q

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: Early diagnosis of prostate cancer is critical for improving prognosis, but current detection techniques face limitations such as low sensitivity, high cost, and radiation risks.

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↓ .bib ↓ .ris
APA Yu K, Wang Y, et al. (2026). Ultrasound molecular imaging of prostate cancer PSMA-targeted biosynthetic GVs.. Biomaterials science, 14(2), 495-505. https://doi.org/10.1039/d5bm01324k
MLA Yu K, et al.. "Ultrasound molecular imaging of prostate cancer PSMA-targeted biosynthetic GVs.." Biomaterials science, vol. 14, no. 2, 2026, pp. 495-505.
PMID 41328620 ↗
DOI 10.1039/d5bm01324k

Abstract

: Early diagnosis of prostate cancer is critical for improving prognosis, but current detection techniques face limitations such as low sensitivity, high cost, and radiation risks. Prostate-specific membrane antigen (PSMA) is a transmembrane protein highly expressed in prostate cancer cells and a promising diagnostic and prognostic indicator. This study aims to develop a PSMA-targeted ultrasound contrast agent based on nanobody-modified gas vesicles (GVs) for early diagnosis of prostate cancer. : GVs were extracted from . PSMA-targeting nanobodies (Nb-PSMA) were synthesized by . PSMA-targeted gas vesicles (PSMA-GVs) were prepared by coupling Nb-PSMA to GVs the intermediate coupling agent Mal-PEG-NHS. Control vesicles were prepared similarly. The targeting specificity of PSMA-GVs towards prostate cancer cells was assessed by flow cytometry and confocal microscopy using PSMA-positive PC-3 cells. contrast-enhanced ultrasound imaging of PSMA-GVs was performed in prostate cancer-bearing mice at early and advanced stages. The biocompatibility of PSMA-GVs was assessed by hemolysis tests, CCK8 cytotoxicity assays, serum biochemical assays and HE staining. : PSMA-GVs exhibited a uniform size, with a hydrodynamic diameter of 267.73 ± 2.86 nm, and showed a high specific binding ability to PC3 cells. ultrasound imaging of prostate cancer-bearing mice showed that PSMA-GVs had significantly slower tumor signal attenuation than Con-GVs. Our and experiments demonstrated that PSMA-GVs could bind to prostate cancer cells with higher specificity, generating stronger and longer-lasting molecular imaging signals in tumors, which presented significant advantages over Con-GVs. Immunofluorescence confirmed that PSMA-GVs crossed the vascular wall, entered the peritumoral vascular space, bound to tumor cells, and enabled PSMA-targeted molecular imaging. Additionally, PSMA-GVs showed good biocompatibility. : Our study provides a new strategy for early ultrasound molecular imaging diagnosis of prostate cancer.

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