Biochemical modulation of Cisplatin mechanisms of action: enhancement of antitumor activity and circumvention of drug resistance.
By M. Fuertes, C. Alonso, J. Pérez. Chemical Reviews, 2003
829 citations recorded by the source corpus.
Subfields: Molecular Biology, Oncology, Toxicology
View Paper: https://www.semanticscholar.org/paper/c52aeaae560cc2b720f63e672c41cc99430b528b
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In Oncology
Citations in the corpus
- Cisplatin: The first metal based anticancer drug. (2019, background): “activating factor 1) and ATP (adenosine triphosphate) to form an apoptosome complex which activates caspase-9 [42].”
- Cellular processing of platinum anticancer drugs (2005, background): “Among these many compounds, only one has been approved by the FDA: oxaliplatin, for the treatment of colorectal cance”
- Copper complexes as anticancer agents. (2009, background): “The combined interest in (i) improving the DNA cleavage specificity of (52) type complexes together with their ability to perform double-strand breaks (DSB) and (ii) circumventing drug resistance owing to the use of cisplatin [190-194] inspired the design of bifunctional molecules (53a) and (53b) [1”
- Molecular mechanisms of resistance and toxicity associated with platinating agents. (2007, background): “All crosslinks result in contortion of the DNA (reviewed in [10]).”