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Gold nanorod-assisted theranostic solution for nonvisible residual disease in bladder cancer.

Authors :
Armanetti, Paolo
Locatelli, Irene
Venegoni, Chiara
Alchera, Elisa
Campanella, Beatrice
Pederzoli, Filippo
Maturi, Mirko
Locatelli, Erica
Tortorella, Silvia
Curnis, Flavio
Corti, Angelo
Lucianò, Roberta
Onor, Massimo
Salonia, Andrea
Montorsi, Francesco
Moschini, Marco
Popov, Viktor
Jose, Jithin
Franchini, Mauro Comes
Ean Hin Ooi
Source :
Proceedings of the National Academy of Sciences of the United States of America; 9/10/2024, Vol. 121 Issue 37, p1-12, 42p
Publication Year :
2024

Abstract

Residual nonvisible bladder cancer after proper treatment caused by technological and therapeutic limitations is responsible for tumor relapse and progression. This study aimed to demonstrate the feasibility of a solution for simultaneous detection and treatment of bladder cancer lesions smaller than one millimeter. The α5β1 integrin was identified as a specific marker in 81% of human high-grade nonmuscle invasive bladder cancers and used as a target for the delivery of targeted gold nanorods (GNRs). In a preclinical model of orthotopic bladder cancer expressing the α5β1 integrin, the photoacoustic imaging of targeted GNRs visualized lesions smaller than one millimeter, and their irradiation with continuous laser was used to induce GNR-assisted hyperthermia. Necrosis of the tumor mass, improved survival, and computational modeling were applied to demonstrate the efficacy and safety of this solution. Our study highlights the potential of the GNR-assisted theranostic strategy as a complementary solution in clinical practice to reduce the risk of nonvisible residual bladder cancer after current treatment. Further validation through clinical studies will support the findings of the present study. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278424
Volume :
121
Issue :
37
Database :
Complementary Index
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
179698063
Full Text :
https://doi.org/10.1073/pnas.2411583121