Literature DB >> 26510986

CYP2D6 Genetic Polymorphisms and Phenotypes in Different Ethnicities of Malaysian Breast Cancer Patients.

Fee Wai Chin1, Soon Choy Chan2, Sabariah Abdul Rahman3,4, Sharifah Noor Akmal5, Rozita Rosli1,6.   

Abstract

The cytochrome P450, family 2, subfamily D, polypeptide 6 (CYP2D6) is an enzyme that is predominantly involved in the metabolism of tamoxifen. Genetic polymorphisms of the CYP2D6 gene may contribute to inter-individual variability in tamoxifen metabolism, which leads to the differences in clinical response to tamoxifen among breast cancer patients. In Malaysia, the knowledge on CYP2D6 genetic polymorphisms as well as metabolizer status in Malaysian breast cancer patients remains unknown. Hence, this study aimed to comprehensively identify CYP2D6 genetic polymorphisms among 80 Malaysian breast cancer patients. The genetic polymorphisms of all the 9 exons of CYP2D6 gene were identified using high-resolution melting analysis and confirmed by DNA sequencing. Seven CYP2D6 alleles consisting of CYP2D6*1, CYP2D6*2, CYP2D6*4, CYP2D6*10, CYP2D6*39, CYP2D6*49, and CYP2D6*75 were identified in this study. Among these alleles, CYP2D6*10 is the most common allele in both Malaysian Malay (54.8%) and Chinese (71.4%) breast cancer patients, whereas CYP2D6*4 in Malaysian Indian (28.6%) breast cancer patients. In relation to CYP2D6 genotype, CYP2D6*10/*10 is more frequently observed in both Malaysian Malay (28.9%) and Chinese (57.1%) breast cancer patients, whereas CYP2D6*4/*10 is more frequently observed in Malaysian Indian (42.8%) breast cancer patients. In terms of CYP2D6 phenotype, 61.5% of Malaysian Malay breast cancer patients are predicted as extensive metabolizers in which they are most likely to respond well to tamoxifen therapy. However, 57.1% of Chinese as well as Indian breast cancer patients are predicted as intermediate metabolizers and they are less likely to gain optimal benefit from the tamoxifen therapy. This is the first report of CYP2D6 genetic polymorphisms and phenotypes in Malaysian breast cancer patients for different ethnicities. These data may aid clinicians in selecting an optimal drug therapy for Malaysian breast cancer patients, hence improve the clinical outcome of the patients.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  CYP2D6; Malaysian breast cancer patients; genetic polymorphisms; tamoxifen

Mesh:

Substances:

Year:  2015        PMID: 26510986     DOI: 10.1111/tbj.12518

Source DB:  PubMed          Journal:  Breast J        ISSN: 1075-122X            Impact factor:   2.431


  7 in total

Review 1.  Precision medicine: does ethnicity information complement genotype-based prescribing decisions?

Authors:  Rashmi R Shah; Andrea Gaedigk
Journal:  Ther Adv Drug Saf       Date:  2017-12-01

2.  CYP2D6*3 (A2549del), *4 (G1846A), *10 (C100T) and *17 (C1023T) genetic polymorphisms in Iranian breast cancer patients treated with adjuvant tamoxifen.

Authors:  Fatemeh Saghafi; Ebrahim Salehifar; Ghasem Janbabai; Ehsan Zaboli; Akbar Hedayatizadeh-Omran; Omolbanin Amjadi; Siavash Moradi
Journal:  Biomed Rep       Date:  2018-09-07

Review 3.  Health-related quality of life in Asian patients with breast cancer: a systematic review.

Authors:  Peh Joo Ho; Sofie A M Gernaat; Mikael Hartman; Helena M Verkooijen
Journal:  BMJ Open       Date:  2018-04-20       Impact factor: 2.692

4.  Prevalence of pharmacogenomic variants in 100 pharmacogenes among Southeast Asian populations under the collaboration of the Southeast Asian Pharmacogenomics Research Network (SEAPharm).

Authors:  Chakkaphan Runcharoen; Koya Fukunaga; Insee Sensorn; Nareenart Iemwimangsa; Sommon Klumsathian; Hang Tong; Nam Sy Vo; Ly Le; Tin Maung Hlaing; Myo Thant; Shamsul Mohd Zain; Zahurin Mohamed; Yuh-Fen Pung; Francis Capule; Jose Nevado; Catherine Lynn Silao; Zeina N Al-Mahayri; Bassam R Ali; Rika Yuliwulandari; Kinasih Prayuni; Hilyatuz Zahroh; Dzul Azri Mohamed Noor; Phonepadith Xangsayarath; Dalouny Xayavong; Sengchanh Kounnavong; Somphou Sayasone; Zoe Kordou; Ioannis Liopetas; Athina Tsikrika; Evangelia-Eirini Tsermpini; Maria Koromina; Christina Mitropoulou; George P Patrinos; Aumpika Kesornsit; Angkana Charoenyingwattana; Sukanya Wattanapokayakit; Surakameth Mahasirimongkol; Taisei Mushiroda; Wasun Chantratita
Journal:  Hum Genome Var       Date:  2021-02-04

5.  Computational Treatment Simulations to Assess the Need for Personalized Tamoxifen Dosing in Breast Cancer Patients of Different Biogeographical Groups.

Authors:  Anna Mueller-Schoell; Robin Michelet; Lena Klopp-Schulze; Madelé van Dyk; Thomas E Mürdter; Matthias Schwab; Markus Joerger; Wilhelm Huisinga; Gerd Mikus; Charlotte Kloft
Journal:  Cancers (Basel)       Date:  2021-05-18       Impact factor: 6.639

6.  Copy number variation of CCL3L1 among three major ethnic groups in Malaysia.

Authors:  Jalilah Jamaluddin; Nur Khairina Mohd Khair; Shameni Devi Vinodamaney; Zulkefley Othman; Suhaili Abubakar
Journal:  BMC Genet       Date:  2020-01-03       Impact factor: 2.797

7.  Tamoxifen side effects: pharmacogenetic and clinical approach in Mexican mestizos.

Authors:  Jorge-Aarón Rangel-Méndez; Rodrigo Rubi-Castellanos; Juan-Francisco Sánchez-Cruz; Rosa Esther Moo-Puc
Journal:  Transl Cancer Res       Date:  2019-02       Impact factor: 1.241

  7 in total

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