Role of Genetic Variation in ABC Transporters in Breast Cancer Prognosis and Therapy Response
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
CZ.02.1.01/0.0/0.0/16_013/0001634
Czech Ministry of Education, Youth and Sports
19-03063S
Czech Science Foundation
UNCE/MED/006
Grant Agency of Charles University
17-28470A
Czech Medical Council
PubMed
33334016
PubMed Central
PMC7765380
DOI
10.3390/ijms21249556
PII: ijms21249556
Knihovny.cz E-zdroje
- Klíčová slova
- ABC transporter, breast cancer, competitive allele-specific PCR, disease-free survival, next-generation sequencing, therapy response,
- MeSH
- ABC transportéry genetika MeSH
- alely MeSH
- frekvence genu MeSH
- genetická variace * MeSH
- genotyp MeSH
- jednonukleotidový polymorfismus MeSH
- Kaplanův-Meierův odhad MeSH
- lidé MeSH
- lokus kvantitativního znaku MeSH
- nádorové biomarkery * MeSH
- nádory prsu diagnóza genetika mortalita terapie MeSH
- neoadjuvantní terapie MeSH
- prognóza MeSH
- protokoly antitumorózní kombinované chemoterapie terapeutické užití MeSH
- výsledek terapie MeSH
- vysoce účinné nukleotidové sekvenování MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- ABC transportéry MeSH
- nádorové biomarkery * MeSH
Breast cancer is the most common cancer in women in the world. The role of germline genetic variability in ATP-binding cassette (ABC) transporters in cancer chemoresistance and prognosis still needs to be elucidated. We used next-generation sequencing to assess associations of germline variants in coding and regulatory sequences of all human ABC genes with response of the patients to the neoadjuvant cytotoxic chemotherapy and disease-free survival (n = 105). A total of 43 prioritized variants associating with response or survival in the above testing phase were then analyzed by allelic discrimination in the large validation set (n = 802). Variants in ABCA4, ABCA9, ABCA12, ABCB5, ABCC5, ABCC8, ABCC11, and ABCD4 associated with response and variants in ABCA7, ABCA13, ABCC4, and ABCG8 with survival of the patients. No association passed a false discovery rate test, however, the rs17822931 (Gly180Arg) in ABCC11, associating with response, and the synonymous rs17548783 in ABCA13 (survival) have a strong support in the literature and are, thus, interesting for further research. Although replicated associations have not reached robust statistical significance, the role of ABC transporters in breast cancer should not be ruled out. Future research and careful validation of findings will be essential for assessment of genetic variation which was not in the focus of this study, e.g., non-coding sequences, copy numbers, and structural variations together with somatic mutations.
Biomedical Center Faculty of Medicine in Pilsen Charles University 323 00 Pilsen Czech Republic
Department of Oncosurgery Medicon Services 140 00 Prague Czech Republic
Department of Surgery EUC Hospital and University of Tomas Bata in Zlin 760 01 Zlin Czech Republic
Toxicogenomics Unit National Institute of Public Health 100 42 Prague Czech Republic
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