Genetic polymorphism of drug metabolizing enzymes and estrogen receptor in pharmacogenetics of tamoxifen: implication for optimization of breast cancer treatment / Teh Lay Kek and Mohd Zaki Salleh

Introduction: Tamoxifen has been used as a hormonal therapy in breast cancer patients who are positive for estrogen receptor. The drug is metabolized by Cytochrome P450 2D6 (CYP2D6) into several metabolite. Variation in CYP2D6 activity has important therapeutic consequences and can play a significan...

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Main Authors: Lay Kek, Teh, Salleh, Mohd Zaki
Format: Research Reports
Language:English
Published: Research Management Institute (RMI) 2010
Subjects:
Online Access:http://ir.uitm.edu.my/id/eprint/24806/
http://ir.uitm.edu.my/id/eprint/24806/1/LP_TEH%20LAY%20KEK%20RMI%2010_5.pdf
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recordtype eprints
spelling uitm-248062019-07-19T03:09:31Z http://ir.uitm.edu.my/id/eprint/24806/ Genetic polymorphism of drug metabolizing enzymes and estrogen receptor in pharmacogenetics of tamoxifen: implication for optimization of breast cancer treatment / Teh Lay Kek and Mohd Zaki Salleh Lay Kek, Teh Salleh, Mohd Zaki Materia medica Introduction: Tamoxifen has been used as a hormonal therapy in breast cancer patients who are positive for estrogen receptor. The drug is metabolized by Cytochrome P450 2D6 (CYP2D6) into several metabolite. Variation in CYP2D6 activity has important therapeutic consequences and can play a significant role in the development of adverse events or therapeutic failure in susceptible individuals. Beside, variation of drug transporter such as MDRl may alter the accumulation of the drug and cause toxicity in patients. Furthermore, the different expression of receptor-a and estrogen receptor-P may be associated with different therapy outcome. Materials and methods: In subject recruitment, patient samples were collected from HUKM, Hospital Selayang and HTAF. Patients who have received tamoxifen for treatment of breast cancer were recruited according to exclusion and inclusion criteria. Genotyping method for CYP2D6 and MDRl were developed using multiplex allele specific PCR (ASPCR) approach. DHPLC method was developed to detect existing and new alleles in CYP2D6 and estrogen receptors. The expression of estrogen receptor-a and estrogen receptor-p from samples would be quantitated using Real-time PCR. Result: The most common variants detected is CYP2D6*10 with 50% of heterozygous CYP2D6*1/*10 and CYP2D6*5 with 7.8% was detected high in breast cancer patients. Furthermore CYP2D6*l/*4 and CYP2D6*l/*4 was detected but at low frequencies. Research Management Institute (RMI) 2010 Research Reports NonPeerReviewed text en http://ir.uitm.edu.my/id/eprint/24806/1/LP_TEH%20LAY%20KEK%20RMI%2010_5.pdf Lay Kek, Teh and Salleh, Mohd Zaki (2010) Genetic polymorphism of drug metabolizing enzymes and estrogen receptor in pharmacogenetics of tamoxifen: implication for optimization of breast cancer treatment / Teh Lay Kek and Mohd Zaki Salleh. [Research Reports] (Unpublished)
repository_type Digital Repository
institution_category Local University
institution Universiti Teknologi MARA
building UiTM Institutional Repository
collection Online Access
language English
topic Materia medica
spellingShingle Materia medica
Lay Kek, Teh
Salleh, Mohd Zaki
Genetic polymorphism of drug metabolizing enzymes and estrogen receptor in pharmacogenetics of tamoxifen: implication for optimization of breast cancer treatment / Teh Lay Kek and Mohd Zaki Salleh
description Introduction: Tamoxifen has been used as a hormonal therapy in breast cancer patients who are positive for estrogen receptor. The drug is metabolized by Cytochrome P450 2D6 (CYP2D6) into several metabolite. Variation in CYP2D6 activity has important therapeutic consequences and can play a significant role in the development of adverse events or therapeutic failure in susceptible individuals. Beside, variation of drug transporter such as MDRl may alter the accumulation of the drug and cause toxicity in patients. Furthermore, the different expression of receptor-a and estrogen receptor-P may be associated with different therapy outcome. Materials and methods: In subject recruitment, patient samples were collected from HUKM, Hospital Selayang and HTAF. Patients who have received tamoxifen for treatment of breast cancer were recruited according to exclusion and inclusion criteria. Genotyping method for CYP2D6 and MDRl were developed using multiplex allele specific PCR (ASPCR) approach. DHPLC method was developed to detect existing and new alleles in CYP2D6 and estrogen receptors. The expression of estrogen receptor-a and estrogen receptor-p from samples would be quantitated using Real-time PCR. Result: The most common variants detected is CYP2D6*10 with 50% of heterozygous CYP2D6*1/*10 and CYP2D6*5 with 7.8% was detected high in breast cancer patients. Furthermore CYP2D6*l/*4 and CYP2D6*l/*4 was detected but at low frequencies.
format Research Reports
author Lay Kek, Teh
Salleh, Mohd Zaki
author_facet Lay Kek, Teh
Salleh, Mohd Zaki
author_sort Lay Kek, Teh
title Genetic polymorphism of drug metabolizing enzymes and estrogen receptor in pharmacogenetics of tamoxifen: implication for optimization of breast cancer treatment / Teh Lay Kek and Mohd Zaki Salleh
title_short Genetic polymorphism of drug metabolizing enzymes and estrogen receptor in pharmacogenetics of tamoxifen: implication for optimization of breast cancer treatment / Teh Lay Kek and Mohd Zaki Salleh
title_full Genetic polymorphism of drug metabolizing enzymes and estrogen receptor in pharmacogenetics of tamoxifen: implication for optimization of breast cancer treatment / Teh Lay Kek and Mohd Zaki Salleh
title_fullStr Genetic polymorphism of drug metabolizing enzymes and estrogen receptor in pharmacogenetics of tamoxifen: implication for optimization of breast cancer treatment / Teh Lay Kek and Mohd Zaki Salleh
title_full_unstemmed Genetic polymorphism of drug metabolizing enzymes and estrogen receptor in pharmacogenetics of tamoxifen: implication for optimization of breast cancer treatment / Teh Lay Kek and Mohd Zaki Salleh
title_sort genetic polymorphism of drug metabolizing enzymes and estrogen receptor in pharmacogenetics of tamoxifen: implication for optimization of breast cancer treatment / teh lay kek and mohd zaki salleh
publisher Research Management Institute (RMI)
publishDate 2010
url http://ir.uitm.edu.my/id/eprint/24806/
http://ir.uitm.edu.my/id/eprint/24806/1/LP_TEH%20LAY%20KEK%20RMI%2010_5.pdf
first_indexed 2023-09-18T23:13:24Z
last_indexed 2023-09-18T23:13:24Z
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