• Title of article

    Quantification of Nanoparticle Enhancement in Polarized Breast Tumor Macrophage Deposits by Spatial Analysis of MRI and Histological Iron Contrast Using Computer Vision

  • Author/Authors

    Leftin, Avigdor Department of Medical Physics - Memorial Sloan Kettering Cancer Center - New York, USA , Koutcher, Jason A Department of Medical Physics - Memorial Sloan Kettering Cancer Center - New York, USA

  • Pages
    9
  • From page
    1
  • To page
    9
  • Abstract
    Magnetic resonance imaging applications utilizing nanoparticle agents for polarized macrophage detection are conventionally analyzed according to iron-dependent parameters averaged over large regions of interest (ROI). However, contributions from macrophage iron deposits are usually obscured in these analyses due to their lower spatial frequency and smaller population size compared with the bulk of the tumor tissue. We hypothesized that, by addressing MRI and histological pixel contrast heterogeneity using computer vision image analysis approaches rather than statistical ROI distribution averages, we could enhance our ability to characterize deposits of polarized tumor-associated macrophages (TAMs). We tested this approach using in vivo iron MRI (FeMRI) and histological detection of macrophage iron in control and ultrasmall superparamagnetic iron oxide (USPIO) enhanced mouse models of breast cancer. Automated spatial proling of the number and size of iron-containing macrophage deposits according to localized high-iron FeMRI or Prussian blue pixel clustering performed better than using distribution averages to evaluate the eects of contrast agent injections. ­is analysis was extended to characterize subpixel contributions to the localized FeMRI measurements with histology that conrmed the association of endogenous and nanoparticle-enhanced iron deposits with macrophages in vascular regions and further allowed us to dene the polarization status of the macrophage iron deposits detected by MRI. ­ese imaging studies demonstrate that characterization of TAMs in breast cancer models can be improved by focusing on spatial distributions of iron deposits rather than ROI averages and indicate that nanoparticle uptake is dependent on the polarization status of the macrophage populations. ­ese ndings have broad implications for nanoparticle-enhanced biomedical imaging especially in cancer.
  • Keywords
    MRI , Tumor , ROI , Histological
  • Journal title
    Contrast Media and Molecular Imaging
  • Serial Year
    2018
  • Record number

    2617613