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Project Title:  Gamma-Tocotrienol as a Countermeasure against High-Energy Charged Particle-Induced Carcinogenesis, Cardiovascular Disease, and Central Nervous System Effects Reduce
Images: icon  Fiscal Year: FY 2025 
Division: Human Research 
Research Discipline/Element:
HRP SR:Space Radiation
 Start Date: 01/31/2019  
End Date: 10/31/2025  
Task Last Updated: 11/19/2024 		 Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Boerma, Marjan  Ph.D. / University of Arkansas, Little Rock 
Address:  4301 W. Markham Street, Slot 522-10 
Slot 522-10 
Little Rock , AR 72205-7101 		 Email: mboerma@uams.edu 
Phone: 501-686-6599  
Congressional District: 2 
Web:  
 Organization Type: UNIVERSITY 
Organization Name: University of Arkansas, Little Rock 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Weil, Michael  Ph.D. Colorado State University 
Key Personnel Changes / Previous PI: Ed. note - PI addition to Nov 2021 report: We are currently in a phase of the grant in which Drs. Pathak and Landes are no longer Co-Investigators. At this point in the project, only Dr. Weil is a Co-Investigator (CoI). No changes in Principal Investigator (PI) or other key personnel.
Project Information: Grant/Contract No. 80NSSC19K0437 
Responsible Center: NASA JSC 
Grant Monitor: Zawaski, Janice  
Center Contact:  
janice.zawaski@nasa.gov 
Unique ID: 12265  		Solicitation / Funding Source: 2017-2018 HERO 80JSC017N0001-BPBA Topics in Biological, Physiological, and Behavioral Adaptations to Spaceflight. Appendix C 
Grant/Contract No.: 80NSSC19K0437 
Project Type: Ground 
Flight Program:  
TechPort: No  		No. of Post Docs: 0 
No. of PhD Candidates: 0 
No. of Master's Candidates: 0 
No. of Bachelor's Candidates: 0  		No. of PhD Degrees: 0 
No. of Master's Degrees: 0 
No. of Bachelor's Degrees: 0 
Human Research Program Elements: (1) SR:Space Radiation
Human Research Program Risks: None
Human Research Program Gaps: None
Flight Assignment/Project Notes: NOTE: End date changed to 10/31/2025 per NSSC information (Ed., 9/17/24)

NOTE: End date changed to 10/31/2024 per M. Kirby/JSC and NSSC information (Ed., 8/14/23)

NOTE: End date changed to 10/31/2023 per V. Lehman/JSC (Ed., 6/20/23)

NOTE: End date changed to 10/31/2022 per NSSC information (Ed., 5/17/21)

NOTE: End date changed to 3/31/2022 per NSSC information (Ed., 11/4/20)

Task Description: Recent evidence shows that radiation encountered during deep space travel is associated with increased risks of cancer. Administration of a dietary radiation countermeasure before and/or during the mission is an attractive option to reduce the carcinogenesis risk. Gamma-tocotrienol is one of the strongest radiation protectors of all natural compounds tested so far and it has shown cancer prevention properties in human subjects and animal models. It is safe, non-toxic and well tolerated, exhibits no interactions with other medications, and requires no special storage conditions. Altogether, gamma-tocotrienol has high potential as a radiation countermeasure during space travel. In this project, we develop a mouse model of radiation carcinogenesis that may be used to test the protective properties of gamma-tocotrienol and other countermeasures. For this purpose, we are searching for a genetically modified mouse model that shows a low spontaneous cancer rate, but increased tumor incidence in response to low-dose radiation. P53deltaP mice carry a mutation in the P53 gene that makes them more susceptible to carcinogenesis. We obtained P53deltaP mice and created a breeding colony. However, at around 100 days of age, these mice started developing a range of hematologic and solid tumors, and this unexpectedly high rate of tumor formation in untreated animals made the mice unsuitable for studying long-term carcinogenesis from low doses of ionizing radiation. Therefore, a major goal of the project is to cross P53deltaP mice onto different genetic backgrounds that we expect will lower the number of spontaneous tumors. We will monitor survival time and tumor formation with and without low-dose radiation.

Research Impact/Earth Benefits: There is concern about increased carcinogenesis risk after chronic exposures to low-dose ionizing radiation, such as from medical treatments, occupational low-dose exposures, and radiological accidents. This project aims to develop a mouse model of low-dose radiation-induced carcinogenesis that may be used to test gamma-tocotrienol and other countermeasures. This information will not only contribute to reducing the risk of radiation exposure during deep-space travel, but also the risks of carcinogenesis from exposure to low-dose rate radiation on Earth.

Task Progress & Bibliography Information FY2025 
Task Progress: In prior project years, P53deltaP mice on an FVB/Jax genetic background were obtained and used to create a breeding colony. However, at around 100 days of age, these mice started developing a range of hematologic and solid tumors, including lung tumors, mammary tumors, and subcutaneous tumors. The unexpectedly high rate of tumor formation in untreated animals make P53deltaP mice on an FVB/Jax genetic background unsuitable for studying long-term carcinogenesis from low doses of ionizing radiation. Therefore, we crossed P53deltaP mice on a C57BL/6J genetic background and we crossed P53deltaP mice on a mixed C57BL/6J and 129S4/SvJae background. We expect that P53deltaP mice on one or both genetic backgrounds will show low numbers of spontaneous tumors but a wide range of tumor types after low-dose radiation exposure. To create the new mouse lines, we followed a breeding strategy combined with single nucleotide polymorphism (SNP) based assessment of genetic background to select the mice with the most desirable background. P53deltaP mice on both genetic backgrounds were housed for aging. At this time, the average survival time of P53deltaP mice on a C57BL/6J background is 470 days (and counting). The average survival time of P53deltaP mice on a mixed C57BL/6J and 129S4/SvJae background is 431 days (and counting). These results suggest that the background tumor formation in P53deltaP mice on both genetic backgrounds is lower compared to the original line of these mice. Next, we would like to expose these mice to low-dose radiation to determine the rate of radiation-induced tumor formation.

Bibliography: Description: (Last Updated: 11/29/2024) 

Show Cumulative Bibliography
 
Abstracts for Journals and Proceedings Boerma M. "Gamma-Tocotrienol as a countermeasure against high-energy charged particle-induced carcinogenesis, cardiovascular disease, and central nervous system effects." 2024 NASA Human Research Program Investigators’ Workshop in Galveston, TX, February 13-16, 2024. Poster presentation.

Abstracts. 2024 NASA Human Research Program Investigators’ Workshop in Galveston, TX, February 13-16, 2024. , Feb-2024

Back to Search Results    
Project Title:  Gamma-Tocotrienol as a Countermeasure against High-Energy Charged Particle-Induced Carcinogenesis, Cardiovascular Disease, and Central Nervous System Effects Reduce
Images: icon  Fiscal Year: FY 2024 
Division: Human Research 
Research Discipline/Element:
HRP SR:Space Radiation
 Start Date: 01/31/2019  
End Date: 10/31/2025  
Task Last Updated: 08/11/2023 		 Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Boerma, Marjan  Ph.D. / University of Arkansas, Little Rock 
Address:  4301 W. Markham Street, Slot 522-10 
Slot 522-10 
Little Rock , AR 72205-7101 		 Email: mboerma@uams.edu 
Phone: 501-686-6599  
Congressional District: 2 
Web:  
 Organization Type: UNIVERSITY 
Organization Name: University of Arkansas, Little Rock 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Weil, Michael  Ph.D. Colorado State University 
Key Personnel Changes / Previous PI: Ed. note - PI addition to Nov 2021 report: We are currently in a phase of the grant in which Drs. Pathak and Landes are no longer Co-Investigators. At this point in the project, only Dr. Weil is a Co-Investigator (CoI). No changes in Principal Investigator (PI) or other key personnel.
Project Information: Grant/Contract No. 80NSSC19K0437 
Responsible Center: NASA JSC 
Grant Monitor: Zawaski, Janice  
Center Contact:  
janice.zawaski@nasa.gov 
Unique ID: 12265  		Solicitation / Funding Source: 2017-2018 HERO 80JSC017N0001-BPBA Topics in Biological, Physiological, and Behavioral Adaptations to Spaceflight. Appendix C 
Grant/Contract No.: 80NSSC19K0437 
Project Type: Ground 
Flight Program:  
TechPort: No  		No. of Post Docs: 1 
No. of PhD Candidates: 0 
No. of Master's Candidates: 0 
No. of Bachelor's Candidates: 0  		No. of PhD Degrees: 0 
No. of Master's Degrees: 0 
No. of Bachelor's Degrees: 0 
Human Research Program Elements: (1) SR:Space Radiation
Human Research Program Risks: None
Human Research Program Gaps: None
Flight Assignment/Project Notes: NOTE: End date changed to 10/31/2025 per NSSC information (Ed., 9/17/24)

NOTE: End date changed to 10/31/2024 per M. Kirby/JSC and NSSC information (Ed., 8/14/23)

NOTE: End date changed to 10/31/2023 per V. Lehman/JSC (Ed., 6/20/23)

NOTE: End date changed to 10/31/2022 per NSSC information (Ed., 5/17/21)

NOTE: End date changed to 3/31/2022 per NSSC information (Ed., 11/4/20)

Task Description: Recent evidence shows that radiation encountered during deep space travel is associated with increased risks of cancer. Administration of a dietary radiation countermeasure before and/or during the mission is an attractive option to reduce the carcinogenesis risk. Gamma-tocotrienol is one of the strongest radiation protectors of all natural compounds tested so far and it has shown cancer prevention properties in human subjects and animal models. It is safe, non-toxic and well tolerated, exhibits no interactions with other medications, and requires no special storage conditions. Altogether, gamma-tocotrienol has high potential as a radiation countermeasure during space travel. In this project, we develop a mouse model of radiation carcinogenesis that may be used to test the protective properties of gamma-tocotrienol and other countermeasures. For this purpose, we are searching for a genetically modified mouse model that shows a low spontaneous cancer rate, but increased tumor incidence in response to low-dose radiation. P53deltaP mice carry a mutation in the P53 gene that makes them more susceptible to carcinogenesis. We obtained P53deltaP mice and created a breeding colony. However, at around 100 days of age, these mice started developing a range of hematologic and solid tumors, and this unexpectedly high rate of tumor formation in untreated animals made the mice unsuitable for studying long-term carcinogenesis from low doses of ionizing radiation. Therefore, the project is now focused on crossing P53deltaP mice onto a different genetic background that we expect will lower the number of spontaneous tumors.

Research Impact/Earth Benefits: There is concern about increased carcinogenesis risk after chronic exposures to low-dose ionizing radiation, such as from medical treatments, occupational low-dose exposures, and radiological accidents. This project aims to develop a mouse model of low-dose radiation-induced carcinogenesis that may be used to test gamma-tocotrienol and other countermeasures. This information will not only contribute to reducing the risk of radiation exposure during deep-space travel, but also the risks of carcinogenesis from exposure to low-dose rate radiation on Earth.

Task Progress & Bibliography Information FY2024 
Task Progress: In prior project years, P53deltaP mice on an FVB/Jax genetic background were obtained and used to create a breeding colony. However, at around 100 days of age, these mice started developing a range of hematologic and solid tumors, including lung tumors, mammary tumors, and subcutaneous tumors. The unexpectedly high rate of tumor formation in untreated animals make P53deltaP mice on an FVB/Jax genetic background unsuitable for studying long-term carcinogenesis from low doses of ionizing radiation. Therefore, we crossed P53deltaP mice onto a C57BL/6J mice and a mixed C57BL/6J and 129S4/SvJae background. We followed a breeding strategy, combined with single nucleotide polymorphism (SNP) based assessment of genetic background to select the mice with the most desirable background. Mice created from both colonies have been housed to the age of 60-200 days with very few tumor formations observed. These results suggest that the background tumor formation in P53deltaP mice on both genetic backgrounds is lower compared to the original line of these mice. Next, we would like to expose these mice to low-dose gamma rays to determine the rate of radiation-induced tumor formation.

Bibliography: Description: (Last Updated: 11/29/2024) 

Show Cumulative Bibliography
 
Abstracts for Journals and Proceedings Boerma M, Sridharan V, Landes RD, Weil MM. "Gamma-tocotrienol as a countermeasure against high-energy charged particle-induced carcinogenesis." 2023 NASA Human Research Program Investigators' Workshop, February 7-9, 2023.

Abstracts. 2021 NASA Human Research Program Investigators' Workshop, February 1-4, 2021. , Feb-2023

Back to Search Results    
Project Title:  Gamma-Tocotrienol as a Countermeasure against High-Energy Charged Particle-Induced Carcinogenesis, Cardiovascular Disease, and Central Nervous System Effects Reduce
Images: icon  Fiscal Year: FY 2023 
Division: Human Research 
Research Discipline/Element:
HRP SR:Space Radiation
 Start Date: 01/31/2019  
End Date: 10/31/2023  
Task Last Updated: 09/14/2022 		 Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Boerma, Marjan  Ph.D. / University of Arkansas, Little Rock 
Address:  4301 W. Markham Street, Slot 522-10 
Slot 522-10 
Little Rock , AR 72205-7101 		 Email: mboerma@uams.edu 
Phone: 501-686-6599  
Congressional District: 2 
Web:  
 Organization Type: UNIVERSITY 
Organization Name: University of Arkansas, Little Rock 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Weil, Michael  Ph.D. Colorado State University 
Key Personnel Changes / Previous PI: Ed. note - PI addition to Nov 2021 report: We are currently in a phase of the grant in which Drs. Pathak and Landes are no longer CoInvestigators. At this point in the project, only Dr. Weil is a CoInvestigator (CoI). No changes in Principal Investigator (PI) or other key personnel.
Project Information: Grant/Contract No. 80NSSC19K0437 
Responsible Center: NASA JSC 
Grant Monitor: Zawaski, Janice  
Center Contact:  
janice.zawaski@nasa.gov 
Unique ID: 12265  		Solicitation / Funding Source: 2017-2018 HERO 80JSC017N0001-BPBA Topics in Biological, Physiological, and Behavioral Adaptations to Spaceflight. Appendix C 
Grant/Contract No.: 80NSSC19K0437 
Project Type: Ground 
Flight Program:  
TechPort: No  		No. of Post Docs: 0 
No. of PhD Candidates: 0 
No. of Master's Candidates: 0 
No. of Bachelor's Candidates: 0  		No. of PhD Degrees: 0 
No. of Master's Degrees: 0 
No. of Bachelor's Degrees: 0 
Human Research Program Elements: (1) SR:Space Radiation
Human Research Program Risks: None
Human Research Program Gaps: None
Flight Assignment/Project Notes: NOTE: End date changed to 10/31/2023 per V. Lehman/JSC (Ed., 6/20/23)

NOTE: End date changed to 10/31/2022 per NSSC information (Ed., 5/17/21)

NOTE: End date changed to 3/31/2022 per NSSC information (Ed., 11/4/20)

Task Description: Recent evidence shows that radiation encountered during deep space travel is associated with increased risks of cancer. Administration of a dietary radiation countermeasure before and/or during the mission is an attractive option to reduce the carcinogenesis risk. Gamma-tocotrienol is one of the strongest radiation protectors of all natural compounds tested so far and it has shown cancer prevention properties in human subjects and animal models. It is safe, non-toxic and well tolerated, exhibits no interactions with other medications, and requires no special storage conditions. Altogether, gamma-tocotrienol has high potential as a radiation countermeasure during space travel. In this project, we develop a mouse model of radiation carcinogenesis that may be used to test the protective properties of gamma-tocotrienol and other countermeasures. For this purpose, we are searching for a genetically modified mouse model that shows a low spontaneous cancer rate, but increased tumor incidence in response to low-dose radiation. P53deltaP mice carry a mutation in the P53 gene that makes them more susceptible to carcinogenesis. We obtained P53deltaP mice and created a breeding colony. However, at around 100 days of age, these mice started developing a range of hematologic and solid tumors, and this unexpectedly high rate of tumor formation in untreated animals made the mice unsuitable for studying long-term carcinogenesis from low doses of ionizing radiation. Therefore, the project is now focused on crossing P53deltaP mice onto a different genetic background that we expect will lower the number of spontaneous tumors.

Research Impact/Earth Benefits: There is concern about increased carcinogenesis risk after chronic exposures to low-dose ionizing radiation, such as from medical treatments, occupational low-dose exposures, and radiological accidents. This project aims to develop a mouse model of low-dose radiation-induced carcinogenesis that may be used to test gamma-tocotrienol and other countermeasures. This information will not only contribute to reducing the risk of radiation exposure during deep-space travel, but also the risks of carcinogenesis from exposure to low-dose rate radiation on Earth.

Task Progress & Bibliography Information FY2023 
Task Progress: In prior project years, P53deltaP mice on an FVB/Jax genetic background were obtained and used to create a breeding colony. However, at around 100 days of age, these mice started developing a range of hematologic and solid tumors, including lung tumors, mammary tumors, and subcutaneous tumors. The unexpectedly high rate of tumor formation in untreated animals make P53deltaP mice on an FVB/Jax genetic background unsuitable for studying long-term carcinogenesis from low doses of ionizing radiation. Therefore, we began crossing P53deltaP mice onto a mixed C57BL/6J and 129S4/SvJae background. We expect that this genetic background will lower the number of spontaneous tumors. We are following a breeding strategy, combined with single nucleotide polymorphism (SNP) based assessment of genetic background to select the mice with the most desirable background. This reduces the number of generations required to create P53deltaP mice onto the mixed C57BL/6J and 129S4/SvJae background. The crossing onto the C57BL/6J background is complete, and we are currently following a breeding strategy to introduce the 129S4/SvJae genetic background. Colonies of mice on both the C57BL/6J background and the mixed genetic background will be maintained. Then, mice created from both colonies will be exposed to low-dose radiation or control treatment to observe tumor formation.

Bibliography: Description: (Last Updated: 11/29/2024) 

Show Cumulative Bibliography
 
Abstracts for Journals and Proceedings Boerma M, Sridharan V, Landes RD, Weil MM. "Gamma-tocotrienol as a countermeasure against high-energy charged particle-induced carcinogenesis." 2022 NASA Human Research Program Investigators' Workshop, February 7-10, 2022.

Abstract. 2022 NASA Human Research Program Investigators' Workshop, February 7-10, 2022. , Feb-2022

Articles in Peer-reviewed Journals Nemec-Bakk AS, Sridharan V, Landes RD, Singh P, Cao M, Dominic P, Seawright JW, Chancellor JC, Boerma M. "Effects of low-dose oxygen ions on cardiac function and structure in female C57BL/6J mice." Life Sci Space Res (Amst). 2022 Feb;32:105-112. https://doi.org/10.1016/j.lssr.2021.12.004 ; PubMed PMID: 35065756; PubMed Central PMCID: PMC8803400 , Feb-2022
Back to Search Results    
Project Title:  Gamma-Tocotrienol as a Countermeasure against High-Energy Charged Particle-Induced Carcinogenesis, Cardiovascular Disease, and Central Nervous System Effects Reduce
Images: icon  Fiscal Year: FY 2022 
Division: Human Research 
Research Discipline/Element:
HRP SR:Space Radiation
 Start Date: 01/31/2019  
End Date: 10/31/2022  
Task Last Updated: 11/11/2021 		 Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Boerma, Marjan  Ph.D. / University of Arkansas, Little Rock 
Address:  4301 W. Markham Street, Slot 522-10 
Slot 522-10 
Little Rock , AR 72205-7101 		 Email: mboerma@uams.edu 
Phone: 501-686-6599  
Congressional District: 2 
Web:  
 Organization Type: UNIVERSITY 
Organization Name: University of Arkansas, Little Rock 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Weil, Michael  Ph.D. Colorado State University 
Key Personnel Changes / Previous PI: Ed. note - PI addition to Nov 2021 report: We are currently in a phase of the grant in which Drs. Pathak and Landes are no longer CoInvestigators. At this point in the project, only Dr. Weil is a CoInvestigator (CoI). No changes in Principal Investigator (PI) or other key personnel.
Project Information: Grant/Contract No. 80NSSC19K0437 
Responsible Center: NASA JSC 
Grant Monitor: Zawaski, Janice  
Center Contact:  
janice.zawaski@nasa.gov 
Unique ID: 12265  		Solicitation / Funding Source: 2017-2018 HERO 80JSC017N0001-BPBA Topics in Biological, Physiological, and Behavioral Adaptations to Spaceflight. Appendix C 
Grant/Contract No.: 80NSSC19K0437 
Project Type: Ground 
Flight Program:  
TechPort: No  		No. of Post Docs: 0 
No. of PhD Candidates: 0 
No. of Master's Candidates: 0 
No. of Bachelor's Candidates: 0  		No. of PhD Degrees: 0 
No. of Master's Degrees: 0 
No. of Bachelor's Degrees: 0 
Human Research Program Elements: (1) SR:Space Radiation
Human Research Program Risks: None
Human Research Program Gaps: None
Flight Assignment/Project Notes: NOTE: End date changed to 10/31/2022 per NSSC information (Ed., 5/17/21)

NOTE: End date changed to 3/31/2022 per NSSC information (Ed., 11/4/20)

Task Description: Recent evidence shows that radiation encountered during deep space travel is associated with increased risks of cancer. Administration of a dietary radiation countermeasure before and/or during the mission is an attractive option to reduce the carcinogenesis risk. Gamma-tocotrienol is one of the strongest radiation protectors of all natural compounds tested so far and it has shown cancer prevention properties in human subjects and animal models. It is safe, non-toxic and well tolerated, exhibits no interactions with other medications, and requires no special storage conditions. Altogether, gamma-tocotrienol has high potential as a radiation countermeasure during space travel. In this project, we develop a mouse model of radiation carcinogenesis that may be used to test the protective properties of gamma-tocotrienol and other countermeasures. For this purpose, we are searching for a genetically modified mouse model that shows a low spontaneous cancer rate, but increased tumor incidence in response to low-dose radiation. P53deltaP mice carry a mutation in the P53 gene that makes them more susceptible to carcinogenesis. We obtained P53deltaP mice and created a breeding colony. However, at around 100 days of age, these mice started developing a range of hematologic and solid tumors, and this unexpectedly high rate of tumor formation in untreated animals made the mice unsuitable for studying long-term carcinogenesis from low doses of ionizing radiation. Therefore, the project is now focused on crossing P53deltaP mice onto a different genetic background that we expect will lower the number of spontaneous tumors.

Research Impact/Earth Benefits: There is concern about increased carcinogenesis risk after chronic exposures to low-dose ionizing radiation, such as from medical treatments, occupational low-dose exposures, and radiological accidents. This project aims to develop a mouse model of low-dose radiation-induced carcinogenesis that may be used to test gamma-tocotrienol and other countermeasures. This information will not only contribute to reducing the risk of radiation exposure during deep-space travel, but also the risks of carcinogenesis from exposure to low-dose rate radiation on Earth.

Task Progress & Bibliography Information FY2022 
Task Progress: In prior project years, P53deltaP mice on an FVB/JAX genetic background were obtained and used to create a breeding colony. However, at around 100 days of age, these mice started developing a range of hematologic and solid tumors, including lung tumors, mammary tumors, and subcutaneous tumors. The unexpectedly high rate of tumor formation in untreated animals make P53deltaP mice on an FVB/JAX genetic background unsuitable for studying long-term carcinogenesis from low doses of ionizing radiation. Therefore, we began crossing P53deltaP mice onto a mixed C57BL/6J and 129S4/SvJae background. We expect that this genetic background will lower the number of spontaneous tumors. We are following a breeding strategy, combined with single nucleotide polymorphism (SNP) based assessment of genetic background, to select the mice with the most desirable background. This reduces the number of generations required to create P53deltaP mice onto the mixed C57BL/6J and 129S4/SvJae background. The crossing onto the C57BL/6J background is almost complete and will be followed by crossing onto the 129S4/SvJae background. Then, mice created from the colony need to be housed for at least 200 days to observe spontaneous tumor formation.

Bibliography: Description: (Last Updated: 11/29/2024) 

Show Cumulative Bibliography
 
Abstracts for Journals and Proceedings Boerma M, Sridharan V, Landes RD, Weil MM. "Gamma-tocotrienol as a countermeasure against high-energy charged particle-induced carcinogenesis." 2021 NASA Human Research Program Investigators’ Workshop, Virtual, February 1-4, 2021.

Abstracts. 2021 NASA Human Research Program Investigators’ Workshop, Virtual, February 1-4, 2021. , Feb-2021

Articles in Peer-reviewed Journals Girgis M, Li Y, Jayatilake M, Gill K, Wang S, Makambi K, Sridharan V, Cheema AK. "Short-term metabolic disruptions in urine of mouse models following exposure to low doses of oxygen ion radiation." J Environ Sci Health C Toxicol Carcinog. In special issue on "Overcoming the challenges of space environment," edited by M. Boerma, I. Koturbashhttps. 2021 Apr 27;39(2):234-49. https://doi.org/10.1080/26896583.2020.1868866 ; PMID: 33902388 , Apr-2021
Articles in Peer-reviewed Journals Dissmore T, DeMarco AG, Jayatilake M, Girgis M, Bansal S, Li Y, Mehta K, Sridharan V, Gill K, Bansal S, Tyburski JB, Cheema AK. "Longitudinal metabolic alterations in plasma of rats exposed to low doses of high linear energy transfer radiation." J Environ Sci Health C Toxicol Carcinog. In special issue on "Overcoming the challenges of space environment," edited by M. Boerma, I. Koturbashhttps. 2021 Apr 27;39(2):219-33. https://doi.org/10.1080/26896583.2020.1865027 ; PubMed PMID: 33902389 , Apr-2021
Articles in Peer-reviewed Journals Nemec-Bakk AS, Sridharan V, Landes RD, Singh P, Cao M, Seawright JW, Liu X, Zheng G, Dominic P, Pathak R, Boerma M. "Mitigation of late cardiovascular effects of oxygen ion radiation by gamma-tocotrienol in a mouse model." Life Sci Space Res (Amst). 2021 Nov;31:43-50. https://doi.org/10.1016/j.lssr.2021.07.006 ; PubMed PMID: 34689949; PubMed PMCID: PMC8548672 , Nov-2021
Back to Search Results    
Project Title:  Gamma-Tocotrienol as a Countermeasure against High-Energy Charged Particle-Induced Carcinogenesis, Cardiovascular Disease, and Central Nervous System Effects Reduce
Images: icon  Fiscal Year: FY 2021 
Division: Human Research 
Research Discipline/Element:
HRP SR:Space Radiation
 Start Date: 01/31/2019  
End Date: 10/31/2022  
Task Last Updated: 12/01/2020 		 Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Boerma, Marjan  Ph.D. / University of Arkansas, Little Rock 
Address:  4301 W. Markham Street, Slot 522-10 
Slot 522-10 
Little Rock , AR 72205-7101 		 Email: mboerma@uams.edu 
Phone: 501-686-6599  
Congressional District: 2 
Web:  
 Organization Type: UNIVERSITY 
Organization Name: University of Arkansas, Little Rock 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Landes, Reid  Ph.D. University of Arkansas, Little Rock 
Weil, Michael  Ph.D. Colorado State University 
Pathak, Rupak  Ph.D. University of Arkansas, Little Rock 
Key Personnel Changes / Previous PI: December 2020 report: No changes in PI or other key personnel.
Project Information: Grant/Contract No. 80NSSC19K0437 
Responsible Center: NASA JSC 
Grant Monitor: Zawaski, Janice  
Center Contact:  
janice.zawaski@nasa.gov 
Unique ID: 12265  		Solicitation / Funding Source: 2017-2018 HERO 80JSC017N0001-BPBA Topics in Biological, Physiological, and Behavioral Adaptations to Spaceflight. Appendix C 
Grant/Contract No.: 80NSSC19K0437 
Project Type: Ground 
Flight Program:  
TechPort: No  		No. of Post Docs:  
No. of PhD Candidates:  
No. of Master's Candidates:  
No. of Bachelor's Candidates:   		No. of PhD Degrees:  
No. of Master's Degrees:  
No. of Bachelor's Degrees:  
Human Research Program Elements: (1) SR:Space Radiation
Human Research Program Risks: None
Human Research Program Gaps: None
Flight Assignment/Project Notes: NOTE: End date changed to 10/31/2022 per NSSC information (Ed., 5/17/21)

NOTE: End date changed to 3/31/2022 per NSSC information (Ed., 11/4/20)

Task Description: Recent evidence shows that radiation encountered during deep space travel is associated with increased risks of cancer. Administration of a dietary radiation countermeasure before and/or during the mission is an attractive option to reduce the carcinogenesis risk. Gamma-tocotrienol is one of the strongest radiation protectors of all natural compounds tested so far. It is safe, non-toxic and well tolerated, exhibits no interactions with other medications and requires no special storage conditions. It has anti-oxidant and anti-inflammatory properties and protects against endothelial dysfunction. Moreover, studies with tocotrienol administration in human subjects and animal models have shown cancer prevention. In our preliminary studies, gamma-tocotrienol reduced radiation-induced genomic instability, as detected by studying chromosomal aberrations, in human endothelial cells and in bone marrow cells of gamma-ray exposed mice. Altogether, based on its safety profile, biological properties, and our preliminary results, gamma-tocotrienol has high potential as radiation countermeasure during space travel. Here, we use a mouse model to test whether gamma-tocotrienol protects against radiation-induced carcinogenesis. For this purpose, genetically modified mice will be used that show a low spontaneous cancer rate, but increased tumor incidence in response to low-dose radiation. Male and female adult mice will be exposed to mixed charged particle beams to mimic galactic cosmic rays at the NASA Space Radiation Laboratory. Twenty-four hours before each radiation exposure, mice will be administered gamma-tocotrienol. Mice will be followed for 18 months after irradiation and inspected daily for tumor formation. In addition, bone marrow cells will be collected to assess the effects of gamma-tocotrienol on genomic instability by cytogenetic analysis. These studies will advance the countermeasure readiness level of gamma-tocotrienol against carcinogenesis risks of space radiation.

Research Impact/Earth Benefits: There is concern about increased carcinogenesis risk after chronic exposures to low-dose ionizing radiation, such as from medical treatments, occupational low-dose exposures, and radiological accidents. The current project will provide evidence for gamma-tocotrienol as a safe countermeasure against radiation-induced carcinogenesis. This information will not only contribute to reducing the risk of radiation exposure during deep-space travel, but also the risks of carcinogenesis from exposure to low-dose rate radiation exposures on Earth.

Task Progress & Bibliography Information FY2021 
Task Progress: A total of 387 male and female P53deltaP mice (on an FVB/Jax genetic background) of the age of ~6 months were transported from a breeding colony at the University of Arkansas for Medical Sciences to Brookhaven National Laboratory. A total of 129 mice were assigned to the control group, 129 mice were exposed to a single dose of 0.75 Gy full-spectrum simulated galactic cosmic rays at the NASA Space Radiation Laboratory, and 129 mice were exposed to a single dose of 3 Gy gamma-rays. After irradiation, all mice were transported to Colorado State University where they are being followed for 18 months after irradiation to determine tumor formation. The mice are currently at the age of ~1 year. In all groups, about 50% of all males and 70-80% of all females have developed cancer. It is yet to soon after radiation exposure to draw conclusions on the effects of gamma or galactic cosmic rays on tumorigenesis.

Bibliography: Description: (Last Updated: 11/29/2024) 

Show Cumulative Bibliography
 
Articles in Peer-reviewed Journals Upadhyay M, Rajagopal M, Gill K, Li Y, Bansal S, Sridharan V, Tyburski JB, Boerma M, Cheema AK. "Identification of plasma lipidome changes associated with low dose space-type radiation exposure in a murine model." Metabolites. 2020 Jun 17;10(6):E252. https://doi.org/10.3390/metabo10060252 ; PMID: 32560360; PMCID: PMC7345467 , Jun-2020
Articles in Peer-reviewed Journals Sridharan V, Seawright JW, Landes RD, Cao M, Singh P, Davis CM, Mao XW, Singh SP, Zhang X, Nelson GA, Boerma M. "Effects of single-dose protons or oxygen ions on function and structure of the cardiovascular system in male Long Evans rats." Life Sci Space Res (Amst). 2020 Aug;26:62-8. https://doi.org/10.1016/j.lssr.2020.04.002 ; PMID: 32718688; PMCID: PMC7387753 , Aug-2020
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Project Title:  Gamma-Tocotrienol as a Countermeasure against High-Energy Charged Particle-Induced Carcinogenesis, Cardiovascular Disease, and Central Nervous System Effects Reduce
Images: icon  Fiscal Year: FY 2020 
Division: Human Research 
Research Discipline/Element:
HRP SR:Space Radiation
 Start Date: 01/31/2019  
End Date: 03/31/2022  
Task Last Updated: 11/12/2019 		 Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Boerma, Marjan  Ph.D. / University of Arkansas, Little Rock 
Address:  4301 W. Markham Street, Slot 522-10 
Slot 522-10 
Little Rock , AR 72205-7101 		 Email: mboerma@uams.edu 
Phone: 501-686-6599  
Congressional District: 2 
Web:  
 Organization Type: UNIVERSITY 
Organization Name: University of Arkansas, Little Rock 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Landes, Reid  Ph.D. University of Arkansas, Little Rock 
Weil, Michael  Ph.D. Colorado State University 
Pathak, Rupak  Ph.D. University of Arkansas, Little Rock 
Key Personnel Changes / Previous PI: November 2019 report: No changes.
Project Information: Grant/Contract No. 80NSSC19K0437 
Responsible Center: NASA JSC 
Grant Monitor:  
Center Contact:   
Unique ID: 12265  		Solicitation / Funding Source: 2017-2018 HERO 80JSC017N0001-BPBA Topics in Biological, Physiological, and Behavioral Adaptations to Spaceflight. Appendix C 
Grant/Contract No.: 80NSSC19K0437 
Project Type: Ground 
Flight Program:  
TechPort: No  		No. of Post Docs:  
No. of PhD Candidates:  
No. of Master's Candidates:  
No. of Bachelor's Candidates:   		No. of PhD Degrees:  
No. of Master's Degrees:  
No. of Bachelor's Degrees:  
Human Research Program Elements: (1) SR:Space Radiation
Human Research Program Risks: None
Human Research Program Gaps: None
Flight Assignment/Project Notes: NOTE: End date changed to 3/31/2022 per NSSC information (Ed., 11/4/20)

Task Description: Recent evidence shows that radiation encountered during deep space travel is associated with increased risks of cancer. Administration of a dietary radiation countermeasure before and/or during the mission is an attractive option to reduce the carcinogenesis risk. Gamma-tocotrienol is one of the strongest radiation protectors of all natural compounds tested so far. It is safe, non-toxic and well tolerated, exhibits no interactions with other medications and requires no special storage conditions. It has anti-oxidant and anti-inflammatory properties and protects against endothelial dysfunction. Moreover, studies with tocotrienol administration in human subjects and animal models have shown cancer prevention. In our preliminary studies, gamma-tocotrienol reduced radiation-induced genomic instability, as detected by studying chromosomal aberrations, in human endothelial cells and in bone marrow cells of gamma-ray exposed mice. Altogether, based on its safety profile, biological properties, and our preliminary results, gamma-tocotrienol has high potential as radiation countermeasure during space travel. Here, we use a mouse model to test whether gamma-tocotrienol protects against radiation-induced carcinogenesis. For this purpose, genetically modified mice will be used that show a low spontaneous cancer rate, but increased tumor incidence in response to low-dose radiation. Male and female adult mice will be exposed to mixed charged particle beams to mimic galactic cosmic rays at the NASA Space Radiation Laboratory. Twenty-four hours before each radiation exposure, mice will be administered gamma-tocotrienol. Mice will be followed for 18 months after irradiation and inspected daily for tumor formation. In addition, bone marrow cells will be collected to assess the effects of gamma-tocotrienol on genomic instability by cytogenetic analysis. These studies will advance the countermeasure readiness level of gamma-tocotrienol against carcinogenesis risks of space radiation.

Research Impact/Earth Benefits: There is concern about increased carcinogenesis risk after chronic exposures to low-dose ionizing radiation, such as from medical treatments, occupational low-dose exposures, and radiological accidents. The current project will provide evidence for gamma-tocotrienol as a safe countermeasure against radiation-induced carcinogenesis. This information will not only contribute to reducing the risk of radiation exposure during deep-space travel, but also the risks of carcinogenesis from exposure to low-dose rate radiation exposures on Earth.

Task Progress & Bibliography Information FY2020 
Task Progress: This is the progress report of year 1 of this project. The project is on schedule.

This project makes use of a transgenic mouse model with a mutation in the p53 gene (P53 deltaP mice) on a mixed 129/SvJ and C57BL/6J background. These mice are not commercially available and need to be bred in-house. A breeding colony was established and is on schedule to produce >500 male and female mice as required for this project in year 2.

In year 2 of the project, we plan to transport >500 mice to Brookhaven National Laboratory for exposure to simulated galactic cosmic rays at the NASA Space Radiation Laboratory. Twenty-four hours before irradiation, mice will be administered gamma-tocotrienol or vehicle. After irradiation, mice will be shipped to Colorado State University and the University of Arkansas for Medical Sciences for follow-up.

Bibliography: Description: (Last Updated: 11/29/2024) 

Show Cumulative Bibliography
 
 None in FY 2020
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Project Title:  Gamma-Tocotrienol as a Countermeasure against High-Energy Charged Particle-Induced Carcinogenesis, Cardiovascular Disease, and Central Nervous System Effects Reduce
Images: icon  Fiscal Year: FY 2019 
Division: Human Research 
Research Discipline/Element:
HRP SR:Space Radiation
 Start Date: 01/31/2019  
End Date: 01/30/2021  
Task Last Updated: 03/29/2019 		 Download Task Book report in PDF pdf
Principal Investigator/Affiliation:   Boerma, Marjan  Ph.D. / University of Arkansas, Little Rock 
Address:  4301 W. Markham Street, Slot 522-10 
Slot 522-10 
Little Rock , AR 72205-7101 		 Email: mboerma@uams.edu 
Phone: 501-686-6599  
Congressional District: 2 
Web:  
 Organization Type: UNIVERSITY 
Organization Name: University of Arkansas, Little Rock 
Joint Agency:  
Comments:  
Co-Investigator(s)
Affiliation: 
Landes, Reid  Ph.D. University of Arkansas, Little Rock 
Weil, Michael  Ph.D. Colorado State University 
Pathak, Rupak  Ph.D. University of Arkansas, Little Rock 
Project Information: Grant/Contract No. 80NSSC19K0437 
Responsible Center: NASA JSC 
Grant Monitor: Simonsen, Lisa  
Center Contact:  
lisa.c.simonsen@nasa.gov 
Unique ID: 12265  		Solicitation / Funding Source: 2017-2018 HERO 80JSC017N0001-BPBA Topics in Biological, Physiological, and Behavioral Adaptations to Spaceflight. Appendix C 
Grant/Contract No.: 80NSSC19K0437 
Project Type: Ground 
Flight Program:  
TechPort: No  		No. of Post Docs:  
No. of PhD Candidates:  
No. of Master's Candidates:  
No. of Bachelor's Candidates:   		No. of PhD Degrees:  
No. of Master's Degrees:  
No. of Bachelor's Degrees:  
Human Research Program Elements: (1) SR:Space Radiation
Human Research Program Risks: None
Human Research Program Gaps: None
Task Description: Recent evidence shows that radiation encountered during deep space travel is associated with increased risks of cancer, cardiovascular disease, and adverse effects in the central nervous system. Administration of a dietary radiation countermeasure before and/or during the mission is an attractive option to reduce the risk of carcinogenesis and degenerative effects in the heart and brain. Gamma-tocotrienol is one of the strongest radiation protectors of all natural compounds tested so far. It is safe, non-toxic and well tolerated, exhibits no interactions with other medications and requires no special storage conditions. It has anti-oxidant and anti-inflammatory properties and protects against endothelial dysfunction. Moreover, studies with tocotrienol administration in human subjects and animal models have shown cancer prevention and protection against brain white matter lesions. In our preliminary studies, gamma-tocotrienol reduced radiation-induced genomic instability, as detected by studying chromosomal aberrations, in human endothelial cells and in bone marrow cells of gamma-ray exposed mice. Moreover, gamma-tocotrienol reduced changes in behavior and cardiac function in a mouse model of exposure to high-energy oxygen ions. Altogether, based on its safety profile, biological properties, and our preliminary results, gamma-tocotrienol has high potential as radiation countermeasure during space travel. Here, we aim to use a mouse model of exposure to modeled galactic cosmic rays to test whether gamma-tocotrienol protects against 1) carcinogenesis, 2) changes in behavior, dendritic morphology, and synaptic plasticity, and 3) changes in cardiac and vascular function and structure. Carcinogenesis will be assessed in genetically modified mice that show a low spontaneous cancer rate but increased tumor incidence in response to low-dose radiation. Degenerative tissue effects will be assessed in wild-type mice. Male and female adult mice will be exposed to mixed charged particle beams or gamma-rays as a reference radiation, in five once-a-day fractions at the NASA Space Radiation Laboratory. Twenty-four hours before each radiation exposure, mice will receive an oral dose of gamma-tocotrienol. Mice will be followed for 18 months after irradiation and inspected daily for tumor formation. Bone marrow cells will be collected to assess the effects of gamma-tocotrienol on genomic instability by cytogenetic analysis. Additional cohorts of mice will be used to assess cognitive and cardiovascular function. At 12 months after irradiation, mice in these subcohorts will be sacrificed to collect blood samples, and brain and heart tissue for histological analysis. These studies will advance the countermeasure readiness level of gamma-tocotrienol against risks of both carcinogenesis and degenerative tissue effects of space radiation.

Research Impact/Earth Benefits:

Task Progress & Bibliography Information FY2019 
Task Progress: New project for FY2019.

Bibliography: Description: (Last Updated: 11/29/2024) 

Show Cumulative Bibliography
 
 None in FY 2019
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