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Surveillance nanotechnology for multi-organ cancer metastases

The identification and molecular profiling of early metastases remains a major challenge in cancer diagnostics and therapy. Most in vivo imaging methods fail to detect small cancerous lesions, a problem that is compounded by the distinct physical and biological barriers associated with different met...

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Detalles Bibliográficos
Autores principales: Kantamneni, Harini, Zevon, Margot, Donzanti, Michael J., Zhao, Xinyu, Sheng, Yang, Barkund, Shravani R., McCabe, Lucas H., Banach-Petrosky, Whitney, Higgins, Laura M., Ganesan, Shridar, Riman, Richard E., Roth, Charles M., Tan, Mei-Chee, Pierce, Mark C., Ganapathy, Vidya, Moghe, Prabhas V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844578/
https://www.ncbi.nlm.nih.gov/pubmed/29531851
http://dx.doi.org/10.1038/s41551-017-0167-9
Descripción
Sumario:The identification and molecular profiling of early metastases remains a major challenge in cancer diagnostics and therapy. Most in vivo imaging methods fail to detect small cancerous lesions, a problem that is compounded by the distinct physical and biological barriers associated with different metastatic niches. Here, we show that intravenously injected rare-earth-doped albumin-encapsulated nanoparticles emitting short-wave infrared light (SWIR) can detect targeted metastatic lesions in vivo, allowing for the longitudinal tracking of multi-organ metastases. In a murine model of basal human breast cancer, the nanoprobes enabled whole-body SWIR detection of adrenal gland microlesions and bone lesions that were undetectable via contrast-enhanced magnetic resonance imaging (CE-MRI) as early as, respectively, three weeks and five weeks post-inoculation. Whole-body SWIR imaging of nanoprobes functionalized to differentially target distinct metastatic sites and administered to a biomimetic murine model of human breast cancer resolved multi-organ metastases that showed varied molecular profiles at the lungs, adrenal glands and bones. Real-time surveillance of lesions in multiple organs should facilitate pre-therapy and post-therapy monitoring in preclinical settings.