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Differentiation of Normal and Radioresistant Prostate Cancer Xenografts Using Magnetization Transfer-Prepared MRI.
Lam, Wilfred W; Oakden, Wendy; Murray, Leedan; Klein, Jonathan; Iorio, Caterina; Screaton, Robert A; Koletar, Margaret M; Chu, William; Liu, Stanley K; Stanisz, Greg J.
Affiliation
  • Lam WW; Physical Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada. lamw@sri.utoronto.ca.
  • Oakden W; Physical Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada.
  • Murray L; Physical Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada.
  • Klein J; Physical Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada.
  • Iorio C; Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
  • Screaton RA; Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.
  • Koletar MM; Biological Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada.
  • Chu W; Biological Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada.
  • Liu SK; Biochemistry, University of Toronto, Toronto, Ontario, Canada.
  • Stanisz GJ; Physical Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada.
Sci Rep ; 8(1): 10447, 2018 Jul 11.
Article in En | MEDLINE | ID: mdl-29992999
The ability of MRI to differentiate between normal and radioresistant cancer was investigated in prostate tumour xenografts in mice. Specifically, the process of magnetization exchange between water and other molecules was studied. It was found that magnetization transfer from semisolid macromolecules (MT) and chemical exchange saturation transfer (CEST) combined were significantly different between groups (p < 0.01). Further, the T2 relaxation of the semisolid macromolecular pool (T2,B), a parameter specific to MT, was found to be significantly different (p < 0.01). Also significantly different were the rNOE contributions associated with methine groups at -0.9 ppm with a saturation B1 of 0.5 µT (p < 0.01) and with other aliphatic groups at -3.3 ppm with 0.5 and 2 µT (both p < 0.05). Independently, using a live-cell metabolic assay, normal cells were found to have a greater metabolic rate than radioresistant ones. Thus, MRI provides a novel, in vivo method to quantify the metabolic rate of tumours and predict their radiosensitivity.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Radiation Tolerance / Magnetic Resonance Imaging Type of study: Diagnostic_studies / Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: Sci Rep Year: 2018 Document type: Article Affiliation country: Canada Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Radiation Tolerance / Magnetic Resonance Imaging Type of study: Diagnostic_studies / Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: Sci Rep Year: 2018 Document type: Article Affiliation country: Canada Country of publication: United kingdom