The breast cancer resistance protein protects against a major chlorophyll-derived dietary phototoxin and protoporphyria

  1. Johan W. Jonker*,
  2. Marije Buitelaar*,
  3. Els Wagenaar*,
  4. Martin A. van der Valk,
  5. George L. Scheffer,
  6. Rik J. Scheper,
  7. Torsten Plösch§,
  8. Folkert Kuipers§,
  9. Ronald P. J. Oude Elferink,
  10. Hilde Rosing,
  11. Jos H. Beijnen, and
  12. Alfred H. Schinkel*,**
  1. Divisions of *Experimental Therapy and Experimental Animal Pathology, The Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands Europe; Department of Pathology, Free University Hospital, 1081 HV Amsterdam, The Netherlands Europe; §Center for Liver, Digestive, and Metabolic Diseases, Laboratory of Pediatrics, University Hospital Groningen, 9713 GZ Groningen, The Netherlands Europe; Laboratory of Experimental Hepatology, Academic Medical Center, 1105 AZ Amsterdam, The Netherlands Europe; and Department of Pharmacy and Pharmacology, Slotervaart Hospital, 1066 EC Amsterdam, The Netherlands Europe
  1. Communicated by P. Borst, The Netherlands Cancer Institute, Amsterdam, The Netherlands (received for review September 10, 2002)

Abstract

The breast cancer resistance protein (BCRP/ABCG2) is a member of the ATP-binding cassette family of drug transporters and confers resistance to various anticancer drugs. We show here that mice lacking Bcrp1/Abcg2 become extremely sensitive to the dietary chlorophyll-breakdown product pheophorbide a, resulting in severe, sometimes lethal phototoxic lesions on light-exposed skin. Pheophorbide a occurs in various plant-derived foods and food supplements. Bcrp1 transports pheophorbide a and is highly efficient in limiting its uptake from ingested food. Bcrp1 −/− mice also displayed a previously unknown type of protoporphyria. Erythrocyte levels of the heme precursor and phototoxin protoporphyrin IX, which is structurally related to pheophorbide a, were increased 10-fold. Transplantation with wild-type bone marrow cured the protoporphyria and reduced the phototoxin sensitivity of Bcrp1 −/− mice. These results indicate that humans or animals with low or absent BCRP activity may be at increased risk for developing protoporphyria and diet-dependent phototoxicity and provide a striking illustration of the importance of drug transporters in protection from toxicity of normal food constituents.

Footnotes

  • ** To whom correspondence should be addressed at: Division of Experimental Therapy, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands. E-mail: a.schinkel{at}nki.nl.

  • Abbreviations:
    1. ABC, ATP-binding cassette

    2. BCRP/ABCG2, breast cancer resistance protein

    3. Bcrp1/Abcg2, murine BCRP

    4. PPIX, protoporphyrin IX

« Previous | Next Article »Table of Contents