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Impact of cyp2d6 polymorphisms on tamoxifen responses of women with breast cancer: A microarray-based study in thailand

dc.contributor.authorChonlaphat Sukasemen_US
dc.contributor.authorEkaphop Sirachainanen_US
dc.contributor.authorMontri Chamnanphonen_US
dc.contributor.authorKhunthong Pechatananen_US
dc.contributor.authorThitiya Sirisinhaen_US
dc.contributor.authorTouch Ativitavasen_US
dc.contributor.authorRavat Panvichianen_US
dc.contributor.authorVorachai Ratanatharathornen_US
dc.contributor.authorNarumol Trachuen_US
dc.contributor.authorWasun Chantratitaen_US
dc.contributor.otherDivision of Pharmacogenomics and Personalized Medicineen_US
dc.contributor.otherDivision of Virologyen_US
dc.contributor.otherDivision of Gynecologic Oncologyen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-11T04:40:44Z
dc.date.available2018-06-11T04:40:44Z
dc.date.issued2012-01-01en_US
dc.description.abstractThis study was designed to investigate the frequency of CYP2D6 polymorphisms and evaluate the association between genetic polymorphisms of CYP2D6 and tamoxifen therapeutic outcome in Thai breast cancer patients. We recruited 48 breast cancer patients who received adjuvant tamoxifen for evaluating CYP2D6 genetic polymorphisms using microarray-based technology. Associations between genotypes-phenotypes and disease free survival were analyzed. Median follow up time was 5.6 years. The mean age of the subjects was 50 years. The 3 common allelic frequencies were 43.8% (*10), 36.5 (*1) and 10.4% (*2) which are related to extensive metabolizer (EM) and intermediate metabolizer (IM) with 70.8% and 29.2 %, respectively. No association between CYP2D6 genotypes and DFS was demonstrated. Nevertheless, exploratory analysis showed statistically significant shorter DFS in the IM group of post-menopause patients (HR, 6.85; 95%CI, 1.48-31.69; P=0.005). Furthermore, we observed statistically significant shorter DFS of homozygous CYP2D6*10 when compared with heterozygous CYP2D6*10 and other genotypes (P=0.005). CYP2D6*10 was the most common genotype in our subjects. Post-menopause patients with homozygous CYP2D6*10 and IM have shorter DFS. To confirm this re lationship, larger samples and comprehensively designed trials in Thailand are required.en_US
dc.identifier.citationAsian Pacific Journal of Cancer Prevention. Vol.13, No.9 (2012), 4549-4553en_US
dc.identifier.doi10.7314/APJCP.2012.13.9.4549en_US
dc.identifier.issn2476762Xen_US
dc.identifier.issn15137368en_US
dc.identifier.other2-s2.0-84874017348en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/13867
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84874017348&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleImpact of cyp2d6 polymorphisms on tamoxifen responses of women with breast cancer: A microarray-based study in thailanden_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84874017348&origin=inwarden_US

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