Literature DB >> 23638818

Impact of metabolizing enzymes on drug response of endocrine therapy in breast cancer.

Pilar H Saladores1, Jana C Precht, Werner Schroth, Hiltrud Brauch, Matthias Schwab.   

Abstract

Estrogen-receptor positive breast cancer accounts for 75% of diagnosed breast cancers worldwide. There are currently two major options for adjuvant treatment: tamoxifen and aromatase inhibitors. Variability in metabolizing enzymes determines their pharmacokinetic profile, possibly affecting treatment response. Therefore, prediction of therapy outcome based on genotypes would enable a more personalized medicine approach, providing optimal therapy for each patient. In this review, the authors will discuss the current evidence on the most important metabolizing enzymes in endocrine therapy, with a special focus on CYP2D6 and its role in tamoxifen metabolism.

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Year:  2013        PMID: 23638818     DOI: 10.1586/erm.13.26

Source DB:  PubMed          Journal:  Expert Rev Mol Diagn        ISSN: 1473-7159            Impact factor:   5.225


  9 in total

1.  Prediction of tamoxifen outcome by genetic variation of CYP2D6 in post-menopausal women with early breast cancer.

Authors:  Hiltrud Brauch; Matthias Schwab
Journal:  Br J Clin Pharmacol       Date:  2014-04       Impact factor: 4.335

2.  A pilot study comparing the effect of flaxseed, aromatase inhibitor, and the combination on breast tumor biomarkers.

Authors:  Susan E McCann; Stephen B Edge; David G Hicks; Lilian U Thompson; Carl D Morrison; Gerald Fetterly; Christopher Andrews; Kim Clark; John Wilton; Swati Kulkarni
Journal:  Nutr Cancer       Date:  2014-03-26       Impact factor: 2.900

3.  Effects of CYP2D6 and CYP3A5 polymorphisms on tamoxifen and its metabolites in Thai breast cancer patients.

Authors:  Wanaporn Charoenchokthavee; Nutthada Areepium; Duangchit Panomvana; Virote Sriuranpong
Journal:  Breast Cancer (Dove Med Press)       Date:  2017-04-15

4.  Addressing Adherence Using Genotype-Specific PBPK Modeling-Impact of Drug Holidays on Tamoxifen and Endoxifen Plasma Levels.

Authors:  Kristin J R Dickschen; Stefan Willmann; Georg Hempel; Michael Block
Journal:  Front Pharmacol       Date:  2017-03-14       Impact factor: 5.810

5.  Nintedanib plus letrozole in early breast cancer: a phase 0/I pharmacodynamic, pharmacokinetic, and safety clinical trial of combined FGFR1 and aromatase inhibition.

Authors:  Miguel Quintela-Fandino; Juan V Apala; Diego Malon; Silvana Mouron; Javier Hornedo; Lucia Gonzalez-Cortijo; Ramon Colomer; Juan Guerra
Journal:  Breast Cancer Res       Date:  2019-05-24       Impact factor: 6.466

6.  Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia.

Authors:  Maroua Boujemaa; Yosr Hamdi; Nesrine Mejri; Lilia Romdhane; Kais Ghedira; Hanen Bouaziz; Houda El Benna; Soumaya Labidi; Hamza Dallali; Olfa Jaidane; Sonia Ben Nasr; Abderrazek Haddaoui; Khaled Rahal; Sonia Abdelhak; Hamouda Boussen; Mohamed Samir Boubaker
Journal:  PLoS One       Date:  2021-01-27       Impact factor: 3.240

Review 7.  The clinical potential of influencing Nrf2 signaling in degenerative and immunological disorders.

Authors:  Bifeng Gao; An Doan; Brooks M Hybertson
Journal:  Clin Pharmacol       Date:  2014-02-03

8.  Prevalence of CYP2D6*2, CYP2D6*4, CYP2D6*10, and CYP3A5*3 in Thai breast cancer patients undergoing tamoxifen treatment.

Authors:  Wanaporn Charoenchokthavee; Duangchit Panomvana; Virote Sriuranpong; Nutthada Areepium
Journal:  Breast Cancer (Dove Med Press)       Date:  2016-08-08

9.  CYP2D6 Genotype Predicts Plasma Concentrations of Tamoxifen Metabolites in Ethiopian Breast Cancer Patients.

Authors:  Jemal Hussien Ahmed; Eyasu Makonnen; Alan Fotoohi; Abraham Aseffa; Rawleigh Howe; Eleni Aklillu
Journal:  Cancers (Basel)       Date:  2019-09-12       Impact factor: 6.639

  9 in total

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