The goal of this proposal is to continue our successful development of TOPAS-nBio, a Monte Carlo simulation toolkit specifically designed to connect research disciplines. TOPAS-nBio simulates the initial energy deposition events (physics), then follows the diffusion and reaction of chemical species (chemistry) to infer biological observables at the cell and organelle scale (biology). The developed application already lays the foundation to investigate biological ef- fects of radiation in cell organelles using a mechanistic systems biology modeling approach. However, with constant advances in our understanding of cellular repair processes, the ques- tions asked by the radiation biology community are increasing in complexity. These advances, including more detailed information of various cells lines/types, deficiencies in DNA repair pathways and potential contributions of non-nuclear cell components, need to be considered to correctly describe cell response to radiation damages. Accordingly, in this renewal application, we focus on improving the accuracy of the simulations by including more representative chem- ical reactions and transitioning towards a predictive model that can be applied to specific cell types. To further extend the reach of TOPAS-nBio, we will include changes in the microenvi- ronment across tumor volumes and move towards mechanistic modeling of radiation effects in vivo. Thus, the new developments of TOPAS-nBio will offer predictions of biological outcome from the initial radiation track structure for various cell types for in vitro and in vivo experiments, and thereby drive hypothesis generation at the forefront of bio-physical research. TOPAS-nBio provides an ideal framework to include and test new effect models, cell lines or microenviron- mental conditions. Overall, TOPAS-nBio will continue the mission to advance our under- standing of the fundamental response of tissue to radiation.

Public Health Relevance

With constant advances in our understanding of cellular repair processes, the questions asked by the radiation biology community are increasing in complexity, creating a dire need for a multi-disciplinary computational tool to help a) interpret existing experimental results and b) design promising new ex- periments. TOPAS-nBio is a Monte Carlo platform specifically developed to connect research disci- plines, to simulate the initial energy deposition events (physics), followed by the diffusion and reaction of chemical species (chemistry) to infer biological observables at the cell and organelle scale (biolo- gy). The TOPAS-nBio features developed in the previous funding cycle have already been well re- ceived by the research community. The new developments of TOPAS-nBio will offer mechanistic out- come predictions from the initial radiation track structure for various cell types for in vitro and in vivo experiments, and thereby drive hypothesis generation at the forefront of bio-physical research.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA187003-06
Application #
10104448
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Obcemea, Ceferino H
Project Start
2015-04-01
Project End
2025-01-31
Budget Start
2021-02-01
Budget End
2022-01-31
Support Year
6
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02114
McNamara, Aimee L; Ramos-Méndez, José; Perl, Joseph et al. (2018) Geometrical structures for radiation biology research as implemented in the TOPAS-nBio toolkit. Phys Med Biol 63:175018
Sung, Wonmo; Jeong, Yoon; Kim, Hyejin et al. (2018) Computational Modeling and Clonogenic Assay for Radioenhancement of Gold Nanoparticles Using 3D Live Cell Images. Radiat Res 190:558-564
Ramos-Méndez, J; Perl, J; Schuemann, J et al. (2018) Monte Carlo simulation of chemistry following radiolysis with TOPAS-nBio. Phys Med Biol 63:105014
Yang, Celina; Bromma, Kyle; Sung, Wonmo et al. (2018) Determining the Radiation Enhancement Effects of Gold Nanoparticles in Cells in a Combined Treatment with Cisplatin and Radiation at Therapeutic Megavoltage Energies. Cancers (Basel) 10:
Sung, Wonmo; Schuemann, Jan (2018) Energy optimization in gold nanoparticle enhanced radiation therapy. Phys Med Biol 63:135001
Sung, Wonmo; Ye, Sung-Joon; McNamara, Aimee L et al. (2017) Dependence of gold nanoparticle radiosensitization on cell geometry. Nanoscale 9:5843-5853
Underwood, T S A; Sung, W; McFadden, C H et al. (2017) Comparing stochastic proton interactions simulated using TOPAS-nBio to experimental data from fluorescent nuclear track detectors. Phys Med Biol 62:3237-3249
Ramos-Méndez, José; Schuemann, Jan; Incerti, Sebastien et al. (2017) Flagged uniform particle splitting for variance reduction in proton and carbon ion track-structure simulations. Phys Med Biol 62:5908-5925
McNamara, Aimee; Geng, Changran; Turner, Robert et al. (2017) Validation of the radiobiology toolkit TOPAS-nBio in simple DNA geometries. Phys Med 33:207-215
Schuemann, Jan; Berbeco, Ross; Chithrani, Devika B et al. (2016) Roadmap to Clinical Use of Gold Nanoparticles for Radiation Sensitization. Int J Radiat Oncol Biol Phys 94:189-205

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