体内
乳腺癌
转移性乳腺癌
医学
磁共振成像
病理
全身成像
癌症
分子成像
生物医学工程
转移
癌症研究
放射科
内科学
生物
生物技术
作者
Harini Kantamneni,Margot Zevon,Michael J Donzanti,Xinyu Zhao,Sheng Yang,Shravani Barkund,Lucas H McCabe,Whitney Banach‐Petrosky,Laura M. Higgins,Shridar Ganesan,Richard E. Riman,Charles M. Roth,Mei-Chee Tan,Mark C. Pierce,Vidya Ganapathy,Prabhas V. Moghe
标识
DOI:10.1038/s41551-017-0167-9
摘要
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 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 as early as three and five weeks post-inoculation, respectively. 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 in the lungs, adrenal glands and bones. Real-time surveillance of lesions in multiple organs should facilitate pre- and post-therapy monitoring in preclinical settings. Rare-earth-doped albumin-encapsulated nanoparticles emitting short-wave infrared light enable whole-body real-time tracking of metastatic lesions in multiple organs in mice.
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