A spatiotemporal multi-scale computational model for FDG PET imaging at different stages of tumor growth and angiogenesis

Bibliographic Details
Title: A spatiotemporal multi-scale computational model for FDG PET imaging at different stages of tumor growth and angiogenesis
Authors: Farshad Moradi Kashkooli, Mohammad Amin Abazari, M. Soltani, Mehran Akbarpour Ghazani, Arman Rahmim
Source: Scientific Reports, Vol 12, Iss 1, Pp 1-16 (2022)
Publisher Information: Nature Portfolio, 2022.
Publication Year: 2022
Collection: LCC:Medicine
LCC:Science
Subject Terms: Medicine, Science
More Details: Abstract A deeper understanding of the tumor microenvironment (TME) and its role in metabolic activity at different stages of vascularized tumors can provide useful insights into cancer progression and better support clinical assessments. In this study, a robust and comprehensive multi-scale computational model for spatiotemporal transport of F-18 fluorodeoxyglucose (FDG) is developed to incorporate important aspects of the TME, spanning subcellular-, cellular-, and tissue-level scales. Our mathematical model includes biophysiological details, such as radiopharmaceutical transport within interstitial space via convection and diffusion mechanisms, radiopharmaceutical exchange between intracellular and extracellular matrices by glucose transporters, cellular uptake of radiopharmaceutical, as well as its intracellular phosphorylation by the enzyme. Further, to examine the effects of tumor size by varying microvascular densities (MVDs) on FDG dynamics, four different capillary networks are generated by angiogenesis modeling. Results demonstrate that as tumor grows, its MVD increases, and hence, the spatiotemporal distribution of total FDG uptake by tumor tissue changes towards a more homogenous distribution. In addition, spatiotemporal distributions in tumor with lower MVD have relatively smaller magnitudes, due to the lower diffusion rate of FDG as well as lower local intravenous FDG release. Since mean standardized uptake value (SUVmean) differs at various stages of microvascular networks with different tumor sizes, it may be meaningful to normalize the measured values by tumor size and the MVD prior to routine clinical reporting. Overall, the present framework has the potential for more accurate investigation of biological phenomena within TME towards personalized medicine.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2045-2322
Relation: https://doaj.org/toc/2045-2322
DOI: 10.1038/s41598-022-13345-4
Access URL: https://doaj.org/article/9dffdaf3ff1c44f89f99441cd66fbbeb
Accession Number: edsdoj.9dffdaf3ff1c44f89f99441cd66fbbeb
Database: Directory of Open Access Journals
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More Details
ISSN:20452322
DOI:10.1038/s41598-022-13345-4
Published in:Scientific Reports
Language:English