Longitudinal anatomical and metabolic MRI characterization of orthotopic xenograft prostate tumors in nude mice

J Magn Reson Imaging. 2014 Oct;40(4):848-56. doi: 10.1002/jmri.24433. Epub 2013 Nov 4.

Abstract

Purpose: To assess anatomic and functional magnetic resonance imaging (MRI) for monitoring of tumor volume and metabolism of orthotopic xenograft prostate cancer tumors.

Materials and methods: Human-derived PC-3M cells were implanted into the prostate in 22 nude mice. Tumor volume and MRI appearance were monitored for up to 29 days. Histology was performed to detect metastases. Hyperpolarized [1-(13) C]pyruvate MRI was used to measure tumor metabolism on day 22.

Results: Tumors were visible by MRI 9 days after tumor cell implantation. Tumor volume increased to 720 ± 190 mm(3) on day 29 of imaging. Metastasis was seen in the iliac lymph nodes at all timepoints, and in more distant lymph nodes at later timepoints, but was not detectable by MRI. Regions with low pyruvate uptake corresponded to regions with necrosis and had a higher lactate/pyruvate ratio (0.98 ± 0.4 vs. 1.6 ± 1.1).

Conclusion: MRI using the balanced steady-state free precession (bSSFP) sequence can be used to monitor tumor growth in orthotopic PC-3M tumors as early as 9 days post-injection. Hyperpolarized pyruvate MRI has potential to assess tumor metabolism and necrosis.

Keywords: bSSFP; hyperpolarized pyruvate; metastasis; prostate cancer.

MeSH terms

  • Animals
  • Carbon Isotopes / pharmacokinetics
  • Cell Line, Tumor
  • Computer Simulation
  • Contrast Media / pharmacokinetics
  • Humans
  • Image Interpretation, Computer-Assisted / methods*
  • Longitudinal Studies
  • Magnetic Resonance Imaging / methods*
  • Male
  • Metabolic Clearance Rate
  • Mice
  • Mice, Nude
  • Models, Biological
  • Prostatic Neoplasms / metabolism*
  • Prostatic Neoplasms / pathology*
  • Pyruvic Acid / pharmacokinetics*
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Tumor Burden

Substances

  • Carbon Isotopes
  • Contrast Media
  • Pyruvic Acid