Journal
CURRENT MEDICINAL CHEMISTRY
Volume 25, Issue 4, Pages 462-477Publisher
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/0929867324666171110141311
Keywords
Platinum anticancer drugs; copper chaperones; copper ATPases; drug resistance; NMR spectroscopy; mass spectrometry
Funding
- University of Bari Aldo Moro
- Consorzio Interuniversitario di Ricerca in Chimica dei Metalli nei Sistemi Biologici (CIRCMSB)
Ask authors/readers for more resources
Background: Resistance, either at the onset of the treatment or developed after an initial positive response, is a major limitation of antitumor therapy. In the case of platinum-based drugs, copper transporters have been found to interfere with drug trafficking by facilitating the import or favoring the platinum export and inactivation. Methods: The use of powerful spectroscopic, spectrometric and computational methods has allowed a deep structural insight into the mode of interaction of platinum drugs with the metal-binding domains of the transporter proteins. Results: This review article focuses on the mode in which platinum drugs can compete with copper ion for binding to transport proteins and consequent structural and biological effects. Three types of transporters are discussed in detail: copper transporter 1 (Ctrl), the major responsible for Cu+ uptake; antioxidant-1 copper chaperone (Atoxl), responsible for copper transfer within the cytoplasm; and copper ATPases (ATP7A/B), responsible for copper export into specific subcellular compartments and outside the cell. Conclusion: The body of knowledge summarized in this review can help in shaping current chemotherapy to optimize the efficacy of platinum drugs (particularly in relation to resistance) and to mitigate adverse effects on copper metabolism.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available