Micro-MRI at 11.7 T of a murine brain tumor model using delayed contrast enhancement

Rex A Moats1, Sendhil Velan-Mullan, Russell Jacobs

  • 1USC Keck School of Medicine, Los Angeles, CA 90027, USA. moats@hsc.usc.edu

Molecular Imaging
|December 3, 2003
PubMed

Insights

Serial micro-MRI in mice enables non-invasive tracking of brain tumor growth and treatment response. This imaging technique visualizes tumor volume and enhancement variability, aiding in understanding anti-cancer peptide efficacy.

Area of Science:

  • * Biomedical imaging
  • * Oncology research
  • * Preclinical cancer models

Background:

  • * In vivo imaging allows for serial tumor measurement, avoiding animal sacrifice.
  • * Orthotopic brain tumor models in mice present challenges for direct tumor assessment.
  • * Micro-Magnetic Resonance Imaging (micro-MRI) offers a solution for visualizing and measuring these inaccessible tumors.

Purpose of the Study:

  • * To evaluate contrast-enhanced micro-MRI with intraperitoneal administration for monitoring brain tumor growth in mice.
  • * To develop a method for assessing tumor volume and variability in enhancement.
  • * To investigate the efficacy of the anti-angiogenic peptide EMD 121974 in a xenograft brain tumor model.

Main Methods:

  • * Orthotopic murine brain tumor models were established in nude mice.
  • * Serial contrast-enhanced micro-MRI was performed weekly for 7 weeks post-implantation.
  • * Tumor volume and enhancement patterns were analyzed using post-processed 3-D intensity models.

Main Results:

  • * The methodology allowed for serial monitoring of tumor growth and response to treatment.
  • * High-resolution 3-D imaging facilitated qualitative assessment of variable tumor enhancement.
  • * Differences in enhancement patterns were observed, potentially related to vascular factors and tumor age.

Conclusions:

  • * Contrast-enhanced micro-MRI is a viable method for non-invasive, serial assessment of brain tumors in vivo.
  • * The technique effectively visualizes tumor growth and treatment response, including variable enhancement.
  • * This approach aids in understanding the impact of anti-angiogenic therapies on tumor characteristics.

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