The breast cancer resistance protein protects against a major chlorophyll-derived dietary phototoxin and protoporphyria
- Johan W. Jonker*,
- Marije Buitelaar*,
- Els Wagenaar*,
- Martin A. van der Valk†,
- George L. Scheffer‡,
- Rik J. Scheper‡,
- Torsten Plösch§,
- Folkert Kuipers§,
- Ronald P. J. Oude Elferink¶,
- Hilde Rosing∥,
- Jos H. Beijnen∥, and
- Alfred H. Schinkel*,**
- 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
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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
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↵ ** 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:
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ABC, ATP-binding cassette
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BCRP/ABCG2, breast cancer resistance protein
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Bcrp1/Abcg2, murine BCRP
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PPIX, protoporphyrin IX
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- Copyright © 2002, The National Academy of Sciences





