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Early diagnosis of bladder cancer by photoacoustic imaging of tumor-targeted gold nanorods

Detection and removal of bladder cancer lesions at an early stage is crucial for preventing tumor relapse and progression. This study aimed to develop a new technological platform for the visualization of small and flat urothelial lesions of high-grade bladder carcinoma in situ (CIS). We found that...

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Detalles Bibliográficos
Autores principales: Alchera, Elisa, Monieri, Matteo, Maturi, Mirko, Locatelli, Irene, Locatelli, Erica, Tortorella, Silvia, Sacchi, Angelina, Corti, Angelo, Nebuloni, Manuela, Lucianò, Roberta, Pederzoli, Filippo, Montorsi, Francesco, Salonia, Andrea, Meyer, Sandra, Jose, Jithin, Giustetto, Pierangela, Franchini, Mauro Comes, Curnis, Flavio, Alfano, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649962/
https://www.ncbi.nlm.nih.gov/pubmed/36386292
http://dx.doi.org/10.1016/j.pacs.2022.100400
Descripción
Sumario:Detection and removal of bladder cancer lesions at an early stage is crucial for preventing tumor relapse and progression. This study aimed to develop a new technological platform for the visualization of small and flat urothelial lesions of high-grade bladder carcinoma in situ (CIS). We found that the integrin α5β1, overexpressed in bladder cancer cell lines, murine orthotopic bladder cancer and human bladder CIS, can be exploited as a receptor for targeted delivery of GNRs functionalized with the cyclic CphgisoDGRG peptide (Iso4). The GNRs@Chit-Iso4 was stable in urine and selectively recognized α5β1 positive neoplastic urothelium, while low frequency ultrasound-assisted shaking of intravesically instilled GNRs@Chit-Iso4 allowed the distribution of nanoparticles across the entire volume of the bladder. Photoacoustic imaging of GNRs@Chit-Iso4 bound to tumor cells allowed for the detection of neoplastic lesions smaller than 0.5 mm that were undetectable by ultrasound imaging and bioluminescence.