| Literature DB >> 26233905 |
Saskia Preissner1, Maurizio Simmaco2, Giovanna Gentile2, Robert Preissner3.
Abstract
The individual variability of pharmacokinetics is underestimated and few systematic studies exist in this field. In most cases, this leads to unwanted side effects or toxicity. In polychemotherapy, prodrugs (like ifosfamide), which have to be activated by cytochrome P450 enzymes (CYPs), play an important role. If patients are poor metabolizers for these drugs, the therapy will be ineffective. Furthermore, CYPs and transporters can be (over)expressed in target tissues, which is also not examined and considered in clinical routine. Here, we present a body map showing relevant enzymes in some organs and tissues. Finally, a typical case of a Caucasian chemotherapy patient with breast cancer is presented and discussed regarding a personalized cancer therapy considering the single nucleotide polymorphisms found via genotyping.Entities:
Keywords: Drug cocktail optimization; Drug interactions; Personalized cancer therapy
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Year: 2015 PMID: 26233905 DOI: 10.1016/bs.apha.2015.03.004
Source DB: PubMed Journal: Adv Pharmacol ISSN: 1054-3589