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NASA GeneLab Platform Utilized for Biological Response to Space Radiation in Animal Models

McDonald, J. Tyson; Stainforth, Robert; Miller, Jack; Cahill, Thomas; Abraham da Silveira, Willian; Rathi, Komal S.; Hardiman, Gary; Taylor, Deanne; Costes, Sylvain V.; Chauhan, Vinita; Meller, Robert; Beheshti, Afshin

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Authors

J. Tyson McDonald

Robert Stainforth

Jack Miller

Thomas Cahill

Komal S. Rathi

Gary Hardiman

Deanne Taylor

Sylvain V. Costes

Vinita Chauhan

Robert Meller

Afshin Beheshti



Abstract

Background: Ionizing radiation from galactic cosmic rays (GCR) is one of the major risk factors that will impact the health of astronauts on extended missions outside the protective effects of the Earth's magnetic field. The NASA GeneLab project has detailed information on radiation exposure using animal models with curated dosimetry information for spaceflight experiments.

Methods: We analyzed multiple GeneLab omics datasets associated with both ground-based and spaceflight radiation studies that included in vivo and in vitro approaches. A range of ions from protons to iron particles with doses from 0.1 to 1.0 Gy for ground studies, as well as samples flown in low Earth orbit (LEO) with total doses of 1.0 mGy to 30 mGy, were utilized.

Results: From this analysis, we were able to identify distinct biological signatures associating specific ions with specific biological responses due to radiation exposure in space. For example, we discovered changes in mitochondrial function, ribosomal assembly, and immune pathways as a function of dose.

Conclusions: We provided a summary of how the GeneLab's rich database of omics experiments with animal models can be used to generate novel hypotheses to better understand human health risks from GCR exposures.

Journal Article Type Article
Acceptance Date Feb 3, 2020
Online Publication Date Feb 7, 2020
Publication Date Feb 7, 2020
Deposit Date Oct 25, 2024
Publicly Available Date Oct 25, 2024
Journal Cancers
Electronic ISSN 2072-6694
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 12
Issue 2
Article Number 381
DOI https://doi.org/10.3390/cancers12020381
PMID 32045996