Role of Genetic Variation in Cytochromes P450 in Breast Cancer Prognosis and Therapy Response
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu klinické zkoušky, časopisecké články
Grantová podpora
NV19-08-00113
Czech Medical Council
INTER-EXCELLENCE LTA-USA no. 19032
Czech Ministry of Education, Youth and Sports
Progress Q39
Charles University Research Fund
PubMed
33802237
PubMed Central
PMC8001203
DOI
10.3390/ijms22062826
PII: ijms22062826
Knihovny.cz E-zdroje
- Klíčová slova
- breast cancer, cytochrome P450, next-generation sequencing, prognosis, response, survival, therapy,
- MeSH
- genetická variace * MeSH
- lidé středního věku MeSH
- lidé MeSH
- míra přežití MeSH
- nádorové proteiny * genetika metabolismus MeSH
- nádory prsu * farmakoterapie enzymologie genetika mortalita MeSH
- neoadjuvantní terapie * MeSH
- přežití po terapii bez příznaků nemoci MeSH
- systém (enzymů) cytochromů P-450 * genetika metabolismus MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky MeSH
- Názvy látek
- nádorové proteiny * MeSH
- systém (enzymů) cytochromů P-450 * MeSH
Breast cancer is the most frequent cancer in the female population worldwide. The role of germline genetic variability in cytochromes P450 (CYP) in breast cancer prognosis and individualized therapy awaits detailed elucidation. In the present study, we used the next-generation sequencing to assess associations of germline variants in the coding and regulatory sequences of all human CYP genes with response of the patients to the neoadjuvant cytotoxic chemotherapy and disease-free survival (n = 105). A total of 22 prioritized variants associating with a response or survival in the above evaluation phase were then analyzed by allelic discrimination in the large confirmation set (n = 802). Associations of variants in CYP1B1, CYP4F12, CYP4X1, and TBXAS1 with the response to the neoadjuvant cytotoxic chemotherapy were replicated by the confirmation phase. However, just association of variant rs17102977 in CYP4X1 passed the correction for multiple testing and can be considered clinically and statistically validated. Replicated associations for variants in CYP4X1, CYP24A1, and CYP26B1 with disease-free survival of all patients or patients stratified to subgroups according to therapy type have not passed a false discovery rate test. Although statistically not confirmed by the present study, the role of CYP genes in breast cancer prognosis should not be ruled out. In conclusion, the present study brings replicated association of variant rs17102977 in CYP4X1 with the response of patients to the neoadjuvant cytotoxic chemotherapy and warrants further research of genetic variation CYPs in breast cancer.
Biomedical Center Faculty of Medicine in Pilsen Charles University 301 00 Pilsen Czech Republic
Comprehensive Cancer Center Novy Jicin Hospital Novy Jicin 741 01 Novy Jicin Czech Republic
Department of Oncosurgery MEDICON 140 00 Prague Czech Republic
Department of Surgery EUC Hospital Zlin and Tomas Bata University in Zlin 763 02 Zlin Czech Republic
Toxicogenomics Unit National Institute of Public Health 100 00 Prague Czech Republic
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