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Synthetic Methods for the Preparation of Platinum Anticancer Complexes

Author(s)
Wilson, Justin J.; Lippard, Stephen J.
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Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.

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Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
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Abstract
The demonstration in the 1960s that cis-diammine-dichloroplatinum(II), or cisplatin, inhibits cellular division of Escherichia coli led to the subsequent discovery that this simple coordination compound is also an effective antitumor agent in mouse models. Subsequent studies validated cisplatin as an effective anticancer agent in humans as well, and FDA approval of cisplatin for the treatment of metastatic ovarian and testicular cancers was granted in 1978. Its introduction as a chemotherapeutic agent significantly improved the survival outlook for many cancer patients; the cure rate for testicular cancer before the approval of cisplatin was less than 10%, significantly lower than the 90% cure rate attained with modern platinum chemotherapy.
Date issued
2013-11
URI
http://hdl.handle.net/1721.1/96862
Department
Massachusetts Institute of Technology. Department of Chemistry
Journal
Chemical Reviews
Publisher
American Chemical Society (ACS)
Citation
Wilson, Justin J., and Stephen J. Lippard. “Synthetic Methods for the Preparation of Platinum Anticancer Complexes.” Chemical Reviews 114, no. 8 (April 23, 2014): 4470–4495.
Version: Author's final manuscript
ISSN
0009-2665
1520-6890

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