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Research ArticleMinireview

Protoporphyrin IX: the Good, the Bad, and the Ugly

Madhav Sachar, Karl E. Anderson and Xiaochao Ma
Journal of Pharmacology and Experimental Therapeutics February 2016, 356 (2) 267-275; DOI: https://doi.org/10.1124/jpet.115.228130
Madhav Sachar
Department of Pharmaceutical Sciences, Center for Pharmacogenetics, School of Pharmacy, University of Pittsburgh, Pittsburgh, Pennsylvania (M.S., X.M.); and Department of Preventive Medicine and Community Health, University of Texas Medical Branch, Galveston, Texas (K.E.A.)
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Karl E. Anderson
Department of Pharmaceutical Sciences, Center for Pharmacogenetics, School of Pharmacy, University of Pittsburgh, Pittsburgh, Pennsylvania (M.S., X.M.); and Department of Preventive Medicine and Community Health, University of Texas Medical Branch, Galveston, Texas (K.E.A.)
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Xiaochao Ma
Department of Pharmaceutical Sciences, Center for Pharmacogenetics, School of Pharmacy, University of Pittsburgh, Pittsburgh, Pennsylvania (M.S., X.M.); and Department of Preventive Medicine and Community Health, University of Texas Medical Branch, Galveston, Texas (K.E.A.)
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Abstract

Protoporphyrin IX (PPIX) is ubiquitously present in all living cells in small amounts as a precursor of heme. PPIX has some biologic functions of its own, and PPIX-based strategies have been used for cancer diagnosis and treatment (the good). PPIX serves as the substrate for ferrochelatase, the final enzyme in heme biosynthesis, and its homeostasis is tightly regulated during heme synthesis. Accumulation of PPIX in human porphyrias can cause skin photosensitivity, biliary stones, hepatobiliary damage, and even liver failure (the bad and the ugly). In this work, we review the mechanisms that are associated with the broad aspects of PPIX. Because PPIX is a hydrophobic molecule, its disposition is by hepatic rather than renal excretion. Large amounts of PPIX are toxic to the liver and can cause cholestatic liver injury. Application of PPIX in cancer diagnosis and treatment is based on its photodynamic effects.

Footnotes

    • Received July 27, 2015.
    • Accepted November 20, 2015.
  • This work was supported in part by the National Institutes of Health National Institute of Diabetes and Digestive and Kidney Diseases [Grant DK090305].

  • dx.doi.org/10.1124/jpet.115.228130.

  • Copyright © 2016 by The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 356 (2)
Journal of Pharmacology and Experimental Therapeutics
Vol. 356, Issue 2
1 Feb 2016
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Research ArticleMinireview

Pharmacology and Toxicology of PPIX

Madhav Sachar, Karl E. Anderson and Xiaochao Ma
Journal of Pharmacology and Experimental Therapeutics February 1, 2016, 356 (2) 267-275; DOI: https://doi.org/10.1124/jpet.115.228130

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Research ArticleMinireview

Pharmacology and Toxicology of PPIX

Madhav Sachar, Karl E. Anderson and Xiaochao Ma
Journal of Pharmacology and Experimental Therapeutics February 1, 2016, 356 (2) 267-275; DOI: https://doi.org/10.1124/jpet.115.228130
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  • Article
    • Abstract
    • Introduction
    • PPIX Biosynthesis
    • Regulation of PPIX Biosynthesis through ALAS
    • Disregulation of PPIX Homeostasis
    • Clinical Manifestations and Management of PPIX Toxicity
    • PPIX-Based Strategies for Diagnosis and Therapy
    • Conclusions
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