Our goal is to develop a platform to contribute to deeper understanding of the interplay between radiation physics, chemistry and biology at sub-cellular levels and to facilitate interdisciplinary work on radiobiological research questions. Monte Carlo (MC) methods have been successfully employed to simulate physical properties of radiation, from the macroscopic dose deposition in radiation therapy patients down to the cellular scale to understand relative biological effectiveness. However, no tool currently provides accurate modeling of macroscopic as well as microscopic biological effects of radiation where researchers can define which interactions or structures (organ, cells and sub-cellular structures such as DNA, RNA or cell-membrane) are of interest. Furthermore, MC codes are nearly exclusively used by research physicists because their use requires a learning period that is generally too long for clinical physicists and biological researchers. We thus propose to build on a previously developed MC platform (TOPAS, a TOol for PArticle Simulation) and advance the physical and biological understanding across multiple levels through the detailed modeling of physical and chemical processes. We will offer a new approach to biological modeling by expanding TOPAS to the nanometer scale and include inter- and intra-cellular signaling and radiation response of sub-cellular components. This proposal will lay the foundation for a deeper understanding of the biological effects of radiation in tissues in order to facilitate new research at the boundary between physics and biology. To accomplish this we will: SA1: Customize MC for simulations of fluorescent nuclear track detectors (FNTD) and experimentally validate simulated particle track structures using these FNTDs. SA2: Facilitate chemical tracking of radicals and sub-cellular target (such as DNA, RNA, membrane, mitochondria) response simulation within MC. SA3: Develop a graphical user interface (GUI) and provide an extensible library of sub-cellular geometry components that can be easily exchanged among researchers. SA4: Develop specific model scenarios to carry out foundational research in four selected research topics. The resulting tool, TOPAS-nBio, will facilitate the exchange of ideas and results between physicists and biologists. The flexibility of the proposed TOPAS-nBio, together with open exchange of cell components among researchers, will facilitate communication across fields provide the basis for interdisciplinary collaborations and provide a tool to advance understanding of biological responses to radiation.

Public Health Relevance

In order to understand the effects of radiation on the human body, we need to understand the interplay between radiation physics, chemistry and biology at inter- and intra-cellular levels. The proposed Monte Carlo platform TOPAS-nBio will promote research connecting these three disciplines by providing capability for detailed modeling of physical and chemical processes across multiple temporal and spatial scales. This framework will be invaluable to develop and test new biological ideas and models and encourage cross-disciplinary collaborations. By improving models that describe cell specific responses to radiation through the mechanistic approach in TOPAS-nBio, this novel platform will contribute to the development of fully biologically optimized treatment planning for radiation cancer therapy in the future and facilitate new research at the boundary between physics and biology.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA187003-02
Application #
9042318
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Capala, Jacek
Project Start
2015-04-01
Project End
2019-03-31
Budget Start
2016-04-01
Budget End
2017-03-31
Support Year
2
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
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
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
Sung, Wonmo; Ye, Sung-Joon; McNamara, Aimee L et al. (2017) Dependence of gold nanoparticle radiosensitization on cell geometry. Nanoscale 9:5843-5853
McNamara, A L; Kam, W W Y; Scales, N et al. (2016) Dose enhancement effects to the nucleus and mitochondria from gold nanoparticles in the cytosol. Phys Med Biol 61:5993-6010

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