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Research ArticleExperimental Studies

Effectiveness of Analogs of the GS-Nitroxide, JP4-039, as Total Body Irradiation Mitigators

MICHAEL W. EPPERLY, JOSHUA R. SACHER, TANJA KRAINZ, XIAOLIN ZHANG, PETER WIPF, MARY LIANG, RENEE FISHER, SONG LI, HONG WANG and JOEL S. GREENBERGER
In Vivo January 2017, 31 (1) 39-43;
MICHAEL W. EPPERLY
1Department of Radiation Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, PA, U.S.A.
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JOSHUA R. SACHER
2Department of Chemistry, University of Pittsburgh, Pittsburgh, PA, U.S.A.
3Center for Chemical Methodologies and Library Development, University of Pittsburgh, Pittsburgh, PA, U.S.A.
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TANJA KRAINZ
2Department of Chemistry, University of Pittsburgh, Pittsburgh, PA, U.S.A.
3Center for Chemical Methodologies and Library Development, University of Pittsburgh, Pittsburgh, PA, U.S.A.
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XIAOLIN ZHANG
2Department of Chemistry, University of Pittsburgh, Pittsburgh, PA, U.S.A.
3Center for Chemical Methodologies and Library Development, University of Pittsburgh, Pittsburgh, PA, U.S.A.
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PETER WIPF
2Department of Chemistry, University of Pittsburgh, Pittsburgh, PA, U.S.A.
3Center for Chemical Methodologies and Library Development, University of Pittsburgh, Pittsburgh, PA, U.S.A.
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MARY LIANG
2Department of Chemistry, University of Pittsburgh, Pittsburgh, PA, U.S.A.
3Center for Chemical Methodologies and Library Development, University of Pittsburgh, Pittsburgh, PA, U.S.A.
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RENEE FISHER
1Department of Radiation Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, PA, U.S.A.
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SONG LI
4School of Pharmacy, University of Pittsburgh, Pittsburgh, PA, U.S.A.
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HONG WANG
1Department of Radiation Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, PA, U.S.A.
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JOEL S. GREENBERGER
1Department of Radiation Oncology, University of Pittsburgh Cancer Institute, Pittsburgh, PA, U.S.A.
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  • For correspondence: greenbergerjs{at}upmc.edu
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Abstract

Background/Aim: Mitochondrial-targeted gramicidin S (GS)-nitroxide, JP4-039, has been demonstrated to be a potent radiation mitigator, and safe over a wide dose range. In addition, JP4-039 has organ-specific effectiveness when locally applied. Materials and Methods: We tested the effect of another GS-nitroxide, XJB-5-131, which has more effective mitochondrial localization, and compared these results to those for radiation mitigation against the hematopoietic syndrome, and two analogs of JP4-039, which have the same mitochondrial localization signal, but different chemical payloads: JRS527.084 contains a second nitroxide per molecule, and TK649.030 contains an ester group attached to the nitroxide. Results: The results demonstrate the superiority of JP4-039 as a systemic radiation mitigator. Conclusion: Structure–activity relationships and bioassays demonstrate that JP4-039 is an optimized small-molecule radiation mitigator.

  • Oxidative stress
  • GS-nitroxide
  • radiation mitigation
  • Received November 7, 2016.
  • Revision received December 5, 2016.
  • Accepted December 8, 2016.
  • Copyright © 2017 The Author(s). Published by the International Institute of Anticancer Research.
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Effectiveness of Analogs of the GS-Nitroxide, JP4-039, as Total Body Irradiation Mitigators
MICHAEL W. EPPERLY, JOSHUA R. SACHER, TANJA KRAINZ, XIAOLIN ZHANG, PETER WIPF, MARY LIANG, RENEE FISHER, SONG LI, HONG WANG, JOEL S. GREENBERGER
In Vivo Jan 2017, 31 (1) 39-43;

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Effectiveness of Analogs of the GS-Nitroxide, JP4-039, as Total Body Irradiation Mitigators
MICHAEL W. EPPERLY, JOSHUA R. SACHER, TANJA KRAINZ, XIAOLIN ZHANG, PETER WIPF, MARY LIANG, RENEE FISHER, SONG LI, HONG WANG, JOEL S. GREENBERGER
In Vivo Jan 2017, 31 (1) 39-43;
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Keywords

  • oxidative stress
  • GS-nitroxide
  • radiation mitigation
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