Author/Authors :
Lin, Gigin Department of Medical Imaging and Intervention - Imaging Core Laboratory - Institute for Radiological Research - Chang Gung Memorial Hospital at Linkou and Chang Gung University - Taoyuan, Taiwan , Keshari, Kayvan R Department of Radiology - Memorial Sloan Kettering Cancer Center - New York, USA , Park, Jae Mo Department of Radiology - University of Texas Southwestern Medical Center - Dallas, USA
Abstract :
Cancer cells reprogram their metabolism to maintain viability via genetic mutations and epigenetic alterations, expressing overall
dynamic heterogeneity. The complex relaxation mechanisms of nuclear spins provide unique and convertible tissue contrasts,
making magnetic resonance imaging (MRI) and magnetic resonance spectroscopy (MRS) pertinent imaging tools in both clinics
and research. In this review, we summarized MR methods that visualize tumor characteristics and its metabolic phenotypes on
an anatomical, microvascular, microstructural, microenvironmental, and metabolomics scale. The review will progress from the
utilities of basic spin-relaxation contrasts in cancer imaging to more advanced imaging methods that measure tumor-distinctive
parameters such as perfusion, water diffusion, magnetic susceptibility, oxygenation, acidosis, redox state, and cell death. Analytical
methods to assess tumor heterogeneity are also reviewed in brief. Although the clinical utility of tumor heterogeneity from imaging
is debatable, the quantification of tumor heterogeneity using functional and metabolic MR images with development of robust
analytical methods and improved MR methods may offer more critical roles of tumor heterogeneity data in clinics. MRI/MRS
can also provide insightful information on pharmacometabolomics, biomarker discovery, disease diagnosis and prognosis, and
treatment response. With these future directions in mind, we anticipate the widespread utilization of these MR-based techniques
in studying in vivo cancer biology to better address significant clinical needs.
Keywords :
Tumor , MR , MRI , MRI/MRS