Pharmacogenetics of tamoxifen in breast cancer patients of African descent: Lack of data

Author:

Kruger Bianca12ORCID,Shamley Delva3ORCID,Soko Nyarai Desiree124ORCID,Dandara Collet12ORCID

Affiliation:

1. Platform for Pharmacogenomics Research and Translation (PREMED) South African Medical Research Council Cape Town South Africa

2. Pharmacogenomics and Drug Metabolism Research Group, Division of Human Genetics, Department of Pathology and Institute of Infectious Diseases and Molecular Medicine, Faculty of Health Sciences University of Cape Town Cape Town South Africa

3. Division of Clinical Anatomy and Biological Anthropology, Department of Human Biology, Faculty of Health Sciences University of Cape Town Cape Town South Africa

4. Department of Pharmaceutical Technology, School of Allied Health Sciences Harare Institute of Technology Harare Zimbabwe

Abstract

AbstractTamoxifen, a selective estrogen receptor modulator, is used to treat hormone receptor‐positive breast cancer. Tamoxifen acts as a prodrug, with its primary therapeutic effect mediated by its principal metabolite, endoxifen. However, tamoxifen has complex pharmacokinetics involving several drug‐metabolizing enzymes and transporters influencing its disposition. Genes encoding enzymes involved in tamoxifen disposition exhibit genetic polymorphisms which vary widely across world populations. This review highlights the lack of data on tamoxifen pharmacogenetics among African populations. Gaps in data are described in this study with the purpose that future research can address this dearth of research on the pharmacogenetics of tamoxifen among African breast cancer patients. Initiatives such as the African Pharmacogenomics Network (APN) are crucial in promoting comprehensive pharmacogenetics studies to pinpoint important variants in pharmacogenes that could be used to reduce toxicity and improve efficacy.

Funder

University of Cape Town

South African Medical Research Council

Human Resource Development Centre, Council of Scientific And Industrial Research

Publisher

Wiley

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