Pharmacogenetics in breast cancer: steps toward personalized medicine in breast cancer management

Sarah Rofaiel1, Esther N Muo1, Shaker A Mousa1,21The Pharmaceutical Research Institute, Albany College of Pharmacy and Health Sciences, Albany, New York, USA; 2King Saud University, Riyadh, Saudi ArabiaAbstract: There is wide individual variability in the pharmacokinetics, pharmacodynamics, and tole...

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Main Authors: Sarah Rofaiel, Esther N Muo, Shaker A Mousa
Format: Article
Language:English
Published: Dove Medical Press 2010-09-01
Series:Pharmacogenomics and Personalized Medicine
Online Access:http://www.dovepress.com/pharmacogenetics-in-breast-cancer-steps-toward-personalized-medicine-i-a5307
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spelling doaj-d4098f4d399848e19511d2b3a3e85e052020-11-25T01:30:17ZengDove Medical PressPharmacogenomics and Personalized Medicine1178-70662010-09-012010default129143Pharmacogenetics in breast cancer: steps toward personalized medicine in breast cancer managementSarah RofaielEsther N MuoShaker A MousaSarah Rofaiel1, Esther N Muo1, Shaker A Mousa1,21The Pharmaceutical Research Institute, Albany College of Pharmacy and Health Sciences, Albany, New York, USA; 2King Saud University, Riyadh, Saudi ArabiaAbstract: There is wide individual variability in the pharmacokinetics, pharmacodynamics, and tolerance to anticancer drugs within the same ethnic group and even greater variability among different ethnicities. Pharmacogenomics (PG) has the potential to provide personalized therapy based on individual genetic variability in an effort to maximize efficacy and reduce adverse effects. The benefits of PG include improved therapeutic index, improved dose regimen, and selection of optimal types of drug for an individual or set of individuals. Advanced or metastatic breast cancer is typically treated with single or multiple combinations of chemotherapy regimens including anthracyclines, taxanes, antimetabolites, alkylating agents, platinum drugs, vinca alkaloids, and others. In this review, the PG of breast cancer therapeutics, including tamoxifen, which is the most widely used therapeutic for the treatment of hormone-dependent breast cancer, is reviewed. The pharmacological activity of tamoxifen depends on its conversion by cytochrome P450 2D6 (CYP2D6) to its abundant active metabolite, endoxifen. Patients with reduced CYP2D6 activity, as a result of either their genotype or induction by the coadministration of other drugs that inhibit CYP2D6 function, produce little endoxifen and hence derive limited therapeutic benefit from tamoxifen; the same can be said about the different classes of therapeutics in breast cancer. PG studies of breast cancer therapeutics should provide patients with breast cancer with optimal and personalized therapy.Keywords: pharmacogenomics, genetic, pharmacokinetic, pharmacodynamic, personalized medicine, pharmacotherapy, anticancer drugs, efficacy, safety http://www.dovepress.com/pharmacogenetics-in-breast-cancer-steps-toward-personalized-medicine-i-a5307
collection DOAJ
language English
format Article
sources DOAJ
author Sarah Rofaiel
Esther N Muo
Shaker A Mousa
spellingShingle Sarah Rofaiel
Esther N Muo
Shaker A Mousa
Pharmacogenetics in breast cancer: steps toward personalized medicine in breast cancer management
Pharmacogenomics and Personalized Medicine
author_facet Sarah Rofaiel
Esther N Muo
Shaker A Mousa
author_sort Sarah Rofaiel
title Pharmacogenetics in breast cancer: steps toward personalized medicine in breast cancer management
title_short Pharmacogenetics in breast cancer: steps toward personalized medicine in breast cancer management
title_full Pharmacogenetics in breast cancer: steps toward personalized medicine in breast cancer management
title_fullStr Pharmacogenetics in breast cancer: steps toward personalized medicine in breast cancer management
title_full_unstemmed Pharmacogenetics in breast cancer: steps toward personalized medicine in breast cancer management
title_sort pharmacogenetics in breast cancer: steps toward personalized medicine in breast cancer management
publisher Dove Medical Press
series Pharmacogenomics and Personalized Medicine
issn 1178-7066
publishDate 2010-09-01
description Sarah Rofaiel1, Esther N Muo1, Shaker A Mousa1,21The Pharmaceutical Research Institute, Albany College of Pharmacy and Health Sciences, Albany, New York, USA; 2King Saud University, Riyadh, Saudi ArabiaAbstract: There is wide individual variability in the pharmacokinetics, pharmacodynamics, and tolerance to anticancer drugs within the same ethnic group and even greater variability among different ethnicities. Pharmacogenomics (PG) has the potential to provide personalized therapy based on individual genetic variability in an effort to maximize efficacy and reduce adverse effects. The benefits of PG include improved therapeutic index, improved dose regimen, and selection of optimal types of drug for an individual or set of individuals. Advanced or metastatic breast cancer is typically treated with single or multiple combinations of chemotherapy regimens including anthracyclines, taxanes, antimetabolites, alkylating agents, platinum drugs, vinca alkaloids, and others. In this review, the PG of breast cancer therapeutics, including tamoxifen, which is the most widely used therapeutic for the treatment of hormone-dependent breast cancer, is reviewed. The pharmacological activity of tamoxifen depends on its conversion by cytochrome P450 2D6 (CYP2D6) to its abundant active metabolite, endoxifen. Patients with reduced CYP2D6 activity, as a result of either their genotype or induction by the coadministration of other drugs that inhibit CYP2D6 function, produce little endoxifen and hence derive limited therapeutic benefit from tamoxifen; the same can be said about the different classes of therapeutics in breast cancer. PG studies of breast cancer therapeutics should provide patients with breast cancer with optimal and personalized therapy.Keywords: pharmacogenomics, genetic, pharmacokinetic, pharmacodynamic, personalized medicine, pharmacotherapy, anticancer drugs, efficacy, safety
url http://www.dovepress.com/pharmacogenetics-in-breast-cancer-steps-toward-personalized-medicine-i-a5307
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