Chengyue Wu

Assistant Professor


Curriculum vitae



Imaging Physics

The University of Texas MD Anderson Cancer Center



Biologically-Based Mathematical Modeling of Tumor Vasculature and Angiogenesis via Time-Resolved Imaging Data


Journal article


D. Hormuth, C. Phillips, Chengyue Wu, E. Lima, G. Lorenzo, P. Jha, A. M. Jarrett, J. Oden, T. Yankeelov
Cancers, 2021

Semantic Scholar DOI PubMedCentral PubMed
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APA   Click to copy
Hormuth, D., Phillips, C., Wu, C., Lima, E., Lorenzo, G., Jha, P., … Yankeelov, T. (2021). Biologically-Based Mathematical Modeling of Tumor Vasculature and Angiogenesis via Time-Resolved Imaging Data. Cancers.


Chicago/Turabian   Click to copy
Hormuth, D., C. Phillips, Chengyue Wu, E. Lima, G. Lorenzo, P. Jha, A. M. Jarrett, J. Oden, and T. Yankeelov. “Biologically-Based Mathematical Modeling of Tumor Vasculature and Angiogenesis via Time-Resolved Imaging Data.” Cancers (2021).


MLA   Click to copy
Hormuth, D., et al. “Biologically-Based Mathematical Modeling of Tumor Vasculature and Angiogenesis via Time-Resolved Imaging Data.” Cancers, 2021.


BibTeX   Click to copy

@article{d2021a,
  title = {Biologically-Based Mathematical Modeling of Tumor Vasculature and Angiogenesis via Time-Resolved Imaging Data},
  year = {2021},
  journal = {Cancers},
  author = {Hormuth, D. and Phillips, C. and Wu, Chengyue and Lima, E. and Lorenzo, G. and Jha, P. and Jarrett, A. M. and Oden, J. and Yankeelov, T.}
}

Abstract

Simple Summary The recruitment of new vasculature via angiogenesis is a critical component of tumor development, which fundamentally influences tumor growth and response to treatment. The characterization of tumor-induced angiogenesis via mathematical models could enable approaches to forecast tumor response and improve patient care. In this review, we discuss how time-resolved imaging data integrated with mathematical modeling can be used to systematically investigate angiogenesis from the cell to tissue scale and ultimately forecast response to therapy. Abstract Tumor-associated vasculature is responsible for the delivery of nutrients, removal of waste, and allowing growth beyond 2–3 mm3. Additionally, the vascular network, which is changing in both space and time, fundamentally influences tumor response to both systemic and radiation therapy. Thus, a robust understanding of vascular dynamics is necessary to accurately predict tumor growth, as well as establish optimal treatment protocols to achieve optimal tumor control. Such a goal requires the intimate integration of both theory and experiment. Quantitative and time-resolved imaging methods have emerged as technologies able to visualize and characterize tumor vascular properties before and during therapy at the tissue and cell scale. Parallel to, but separate from those developments, mathematical modeling techniques have been developed to enable in silico investigations into theoretical tumor and vascular dynamics. In particular, recent efforts have sought to integrate both theory and experiment to enable data-driven mathematical modeling. Such mathematical models are calibrated by data obtained from individual tumor-vascular systems to predict future vascular growth, delivery of systemic agents, and response to radiotherapy. In this review, we discuss experimental techniques for visualizing and quantifying vascular dynamics including magnetic resonance imaging, microfluidic devices, and confocal microscopy. We then focus on the integration of these experimental measures with biologically based mathematical models to generate testable predictions.


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