Ultrasound molecular imaging of prostate cancer PSMA-targeted biosynthetic GVs.
1/5 보강
: 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.
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 ↗
Abstract 한글 요약
: 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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