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Review
. 2010 Jun;77(6):887-94.
doi: 10.1124/mol.109.063172. Epub 2010 Feb 16.

Copper transporters and the cellular pharmacology of the platinum-containing cancer drugs

Stephen B Howell  1 , Roohangiz Safaei, Christopher A Larson, Michael J Sailor
Affiliations
Review

Copper transporters and the cellular pharmacology of the platinum-containing cancer drugs

Stephen B Howell et al. Mol Pharmacol. 2010 Jun.

Abstract

Multiple lines of evidence indicate that the platinum-containing cancer drugs enter cells, are distributed to various subcellular compartments, and are exported from cells via transporters that evolved to manage copper homeostasis. The cytotoxicity of the platinum drugs is directly related to how much drug enters the cell, and almost all cells that have acquired resistance to the platinum drugs exhibit reduced drug accumulation. The major copper influx transporter, copper transporter 1 (CTR1), has now been shown to control the tumor cell accumulation and cytotoxic effect of cisplatin, carboplatin, and oxaliplatin. There is a good correlation between change in CTR1 expression and acquired cisplatin resistance among ovarian cancer cell lines, and genetic knockout of CTR1 renders cells resistant to cisplatin in vivo. The expression of CTR1 is regulated at the transcriptional level by copper via Sp1 and at the post-translational level by the proteosome. Copper and cisplatin both trigger the down-regulation of CTR1 via a process that involves ubiquitination and proteosomal degradation and requires the copper chaperone antioxidant protein 1 (ATOX1). The cisplatin-induced degradation of CTR1 can be blocked with the proteosome inhibitor bortezomib, and this increases the cellular uptake and the cytotoxicity of cisplatin in a synergistic manner. Copper and platinum(II) have similar sulfur binding characteristics, and the presence of stacked rings of methionines and cysteines in the CTR1 trimer suggest a mechanism by which CTR1 selectively transports copper and the platinum-containing drugs via sequential transchelation reactions similar to the manner in which copper is passed from ATOX1 to the copper efflux transporters.

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Figures

Fig. 1
Fig. 1
Schematic diagram of the major mammalian copper homeostasis pathways.
Fig. 2
Fig. 2
Schematic illustration of the trimeric pore of CTR1. The diagram illustrates the concept that, when assembled as a trimer, CTR1 provides a series of stacked rings of methionines, histidines, and cysteines that participate in transchelation reactions to ensure the regulated movement of copper through CTR1.
Fig. 3
Fig. 3
Schematic diagram of the movement of copper through the CTR1 pore via transchelation involving Met40, Met45, Met150, and Met154. [Redrawn from De Feo CJ, Aller SG, Siluvai GS, Blackburn NJ, and Unger VM (2009) Three-dimensional structure of the human copper transporter hCTR1. Proc Natl Acad Sci USA 106:4237–4242. Copyright © 2009 National Academy of Sciences of the United States of America. Used with permission.]
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References

    1. Aller SG, Eng ET, De Feo CJ, Unger VM. Eukaryotic CTR copper uptake transporters require two faces of the third transmembrane domain for helix packing, oligomerization, and function. J Biol Chem. 2004;279:53435–53441. - PMC - PubMed
    1. Arredondo M, Muñoz P, Mura CV, Nùñez MT. DMT1, a physiologically relevant apical Cu1+ transporter of intestinal cells. Am J Physiol Cell Physiol. 2003;284:C1525–C1530. - PubMed
    1. Beretta GL, Gatti L, Tinelli S, Corna E, Colangelo D, Zunino F, Perego P. Cellular pharmacology of cisplatin in relation to the expression of human copper transporter CTR1 in different pairs of cisplatin-sensitive and -resistant cells. Biochem Pharmacol. 2004;68:283–291. - PubMed
    1. Boal AK, Rosenzweig AC. Crystal structures of cisplatin bound to a human copper chaperone. J Am Chem Soc. 2009;131:14196–14197. - PMC - PubMed
    1. Dancis A, Haile D, Yuan DS, Klausner RD. The Saccharomyces cerevisiae copper transport protein (Ctr1p). Biochemical characterization, regulation by copper, and physiologic role in copper uptake. J Biol Chem. 1994;269:25660–25667. - PubMed

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