<i>cis</i> -Diammine(pyridine)chloroplatinum(II), a monofunctional platinum(II) antitumor agent: Uptake, structure, function, and prospects
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- Katherine S. Lovejoy
- *Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139;
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- Ryan C. Todd
- *Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139;
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- Shuzhong Zhang
- Department of Biopharmaceutical Sciences, University of California, San Francisco, CA 94143;
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- Michael S. McCormick
- *Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139;
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- J. Alejandro D'Aquino
- Rosenstiel Basic Medical Sciences Research Center, Brandeis University, Waltham, MA 02454; and
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- Joyce T. Reardon
- Department of Biochemistry and Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC 27599
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- Aziz Sancar
- Department of Biochemistry and Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC 27599
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- Kathleen M. Giacomini
- Department of Biopharmaceutical Sciences, University of California, San Francisco, CA 94143;
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- Stephen J. Lippard
- *Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139;
書誌事項
- 公開日
- 2008-07
- DOI
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- 10.1073/pnas.0803441105
- 公開者
- Proceedings of the National Academy of Sciences
この論文をさがす
説明
<jats:p> We have identified unique chemical and biological properties of a cationic monofunctional platinum(II) complex, <jats:italic>cis</jats:italic> -diammine(pyridine)chloroplatinum(II), <jats:italic>cis</jats:italic> -[Pt(NH <jats:sub>3</jats:sub> ) <jats:sub>2</jats:sub> (py)Cl] <jats:sup>+</jats:sup> or cDPCP, a coordination compound previously identified to have significant anticancer activity in a mouse tumor model. This compound is an excellent substrate for organic cation transporters 1 and 2, also designated SLC22A1 and SLC22A2, respectively. These transporters are abundantly expressed in human colorectal cancers, where they mediate uptake of oxaliplatin, <jats:italic>cis</jats:italic> -[Pt(DACH)(oxalate)] (DACH = <jats:italic>trans-R</jats:italic> , <jats:italic>R</jats:italic> -1,2-diaminocyclohexane), an FDA-approved first-line therapy for colorectal cancer. Unlike oxaliplatin, however, cDPCP binds DNA monofunctionally, as revealed by an x-ray crystal structure of <jats:italic>cis</jats:italic> -{Pt(NH <jats:sub>3</jats:sub> ) <jats:sub>2</jats:sub> (py)} <jats:sup>2+</jats:sup> bound to the N7 atom of a single guanosine residue in a DNA dodecamer duplex. Although the quaternary structure resembles that of B-form DNA, there is a base-pair step to the 5′ side of the Pt adduct with abnormally large shift and slide values, features characteristic of cisplatin intrastrand cross-links. cDPCP effectively blocks transcription from DNA templates carrying adducts of the complex, unlike DNA lesions of other monofunctional platinum(II) compounds like {Pt(dien)} <jats:sup>2+</jats:sup> . cDPCP–DNA adducts are removed by the nucleotide excision repair apparatus, albeit much less efficiently than bifunctional platinum–DNA intrastrand cross-links. These exceptional characteristics indicate that cDPCP and related complexes merit consideration as therapeutic options for treating colorectal and other cancers bearing appropriate cation transporters. </jats:p>
収録刊行物
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- Proceedings of the National Academy of Sciences
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Proceedings of the National Academy of Sciences 105 (26), 8902-8907, 2008-07
Proceedings of the National Academy of Sciences
