Overview
My laboratory is focused on the development of imaging biomarkers for diagnosis, prognosis, staging, and therapeutic efficacy in cancer and neurologic diseases. A major emphasis of our recent activities has been the development of rapid in vivo and in vitro magnetic resonance imaging techniques at microscopic spatial resolution. Our results have been validated and applied in the study of hippocampal volume changes in the brain of genetically altered mice. The methods have allowed a non-invasive measure of small morphometric changes in the brain that present a number of advantages when compared to conventional analysis of histologic slices.
We have also developed new methods for whole-body imaging of metastatic disease in oncology. Specifically, we introduced a rapid, whole-body magnetic resonance imaging technique for leukemia and metastatic cancers including prostate and breast cancer. The method is based in part upon measurements of intracellular water self-diffusion coefficients. It requires no introduced contrast agents, can be performed in less than twenty minutes at a spatial resolution of 75 mm3, and is well suited to comparison with other whole body assays such as PET and Tc-99m bone scanning. Major applications include screening for disease, disease staging, therapeutic monitoring, and understanding the mechanisms of drug delivery. Unlike conventional bone scanning, which is an indirect measure of tumor activity, this technique is specifically sensitive to the presence of intact disease versus cells whose membranes have been compromised by cytotoxic therapy.
An area of very active research in our group at this time concerns the development of multi-component imaging biomarkers for the assessment of disease severity and therapeutic response in a uniformly fatal pediatric neurodegenerative disease known as late infantile neuronal ceroid lipofuscinosis, or Batten disease. This multidisciplinary project has a pre-clinical phase focused on the introduction of viral vector mediated gene therapy into the brain via intra-arterial delivery routes.
Finally, an important component of our research effort is devoted to hardware and software design specific to high-sensitivity image acquisition. Recently we developed a new class of high-sensitivity radiofrequency resonators for neuroimaging and magnetic resonance microscopy. In exploring the physics of these resonators it became clear that they also have applications in areas beyond biomedical imaging.
Highlights
- 1Human gene therapy · 2020
- 2Molecular therapy : the journal of the American Society of Gene Therapy · 2025
Publications
Funding
Active
5 grants- PIC06OD036045-01Modernization and Expansion of the Citigroup Biomedical Imaging Center at Weill Cornell Medical CollegeOffice of the Director, NIH · 2023–2027
- KPUL1TR002384-06Clinical and Translational Science Center - UL1National Center for Advancing Translational Sciences · 2017–2027· 2 renewals
- MPIR01NS121544-04Unified Shim-RF Coil Technology for Improved Whole-Brain Spectroscopic MRI for Neurological DisordersNational Institute of Neurological Disorders and Stroke · 2024–2027
- MPIR01EB031820-04A Self-Tuning Liquid Metal Coil Conforming to Movement for High-Resolution Brachial Plexus MRINational Institute of Biomedical Imaging and Bioengineering · 2022–2027
- PIS10OD034271-01New PET/CT System for Human and Non-human Primate ImagingOffice of the Director, NIH · 2023–2026
Completed grants (12)
- KPS10OD027039-01A17T Magnetic Resonance Imaging System for Basic, Translational and Clinical ResearchOffice of the Director, NIH · 2021–2025
- MPIR01EB027918-03Rapid Noninvasive Whole-body Imaging of AAV Gene Transfer VectorsNational Institute of Biomedical Imaging and Bioengineering · 2019–2025
- Co-IR01CA160620-08Active Contrast Encoding MRI for Breast CancerNational Cancer Institute · 2021–2025
- PISRA 203204-01BioMarin Pharmaceutical Inc. 190-203BioMarin Pharmaceuticals, Inc. · 2020–2024Contract
- Co-IODCUP 214052-01Comparison of Brain Biodistribution of Two CDKL5 Gene Therapy Vector LeadsOrphan Disease Center at University of Pennsylvania · 2021–2022No publications yet
- Sub-PIU54NS065768-10LDN: Biomarkers for Disease Severity and Therapeutic Response in LINCLNational Institute of Neurological Disorders and Stroke · 2009–2019 · via University of Minnesota· 2 renewals
- PIR56NS082655-01A1Intra-Arterial Gene Therapy for LINCLNational Institute of Neurological Disorders and Stroke · 2015–2018
- KPR01HD051912-05EWOMechanisms of Recovery Following Severe Brain InjuryEunice Kennedy Shriver National Institute of Child Health and Human Development · 2008–2014
- PIS10RR023020-01Small Animal 7.0 Tesla Magnetic Resonance Imaging and Spectroscopy SystemNCRR · 2007–2009 · via NIH RePORTER
- PIR01EB002070-09MAGNETIC RESONANCE STUDIES OF BONE MARROW HEMATOPOIESISNIBIB · 1994–2007 · via NIH RePORTER
- PIR01HL050139-08MAGNETIC RESONANCE STUDIES OF BONE MARROW HEMATOPOIESISNHLBI · 1994–2003 · via NIH RePORTER
Available technologies
Mentoring
- XZXuanyu ZhuPostdoc mentee · 2024–2025