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Tissue factor-specific ultra-bright SERRS nanostars for Raman detection of pulmonary micrometastases.


ABSTRACT: Here we demonstrate a novel application of 'surface enhanced resonance Raman scattering nanoparticles' (SERRS NPs) for imaging breast cancer lung metastases with much higher precision than currently feasible. A breast cancer lung metastasis mouse model was established by intravenous injection of LM2 cells. These mice were intravenously administered SERRS NPs conjugated with ALT-836, an anti-tissue factor (TF) monoclonal antibody, and subjected to Raman imaging to visualize the expression of TF both in vivo and ex vivo. Raman imaging indicated marked uptake of ?TF-SERRS-NPs by the lung metastases compared to isotype and blocking controls. Conversely, little uptake of ?TF-SERRS-NPs was observed in the lungs of healthy mice. Successful detection and delineation of pulmonary micrometastatic lesions as small as 200 ?m, corroborated by histology, immunohistochemistry, and bioluminescence imaging confirmed the suitability of both TF as a target and ?TF-SERRS-NPs as an effective contrast agent for imaging breast cancer lung metastases. Further advancements of this technique in the form of Raman endoscopes coupled with ultrabright SERRS NPs developed in this work could lead to minimally invasive detection and resection of lung metastases.

SUBMITTER: Nayak TR 

PROVIDER: S-EPMC5438878 | biostudies-literature | 2017 Jan

REPOSITORIES: biostudies-literature

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Tissue factor-specific ultra-bright SERRS nanostars for Raman detection of pulmonary micrometastases.

Nayak Tapas R TR   Andreou Chrysafis C   Oseledchyk Anton A   Marcus Warren D WD   Wong Hing C HC   Massagué Joan J   Kircher Moritz F MF  

Nanoscale 20170101 3


Here we demonstrate a novel application of 'surface enhanced resonance Raman scattering nanoparticles' (SERRS NPs) for imaging breast cancer lung metastases with much higher precision than currently feasible. A breast cancer lung metastasis mouse model was established by intravenous injection of LM2 cells. These mice were intravenously administered SERRS NPs conjugated with ALT-836, an anti-tissue factor (TF) monoclonal antibody, and subjected to Raman imaging to visualize the expression of TF b  ...[more]

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