Whole exome sequencing analysis of ABCC8 and ABCD2 genes associating with clinical course of breast carcinoma
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
26681085
DOI
10.33549/physiolres.933212
PII: 933212
Knihovny.cz E-resources
- MeSH
- ATP Binding Cassette Transporter, Subfamily D MeSH
- ATP-Binding Cassette Transporters genetics MeSH
- Adult MeSH
- Exome genetics MeSH
- Genetic Association Studies * methods MeSH
- Polymorphism, Single Nucleotide genetics MeSH
- Middle Aged MeSH
- Humans MeSH
- Breast Neoplasms diagnosis genetics MeSH
- Sulfonylurea Receptors genetics MeSH
- Sequence Analysis, DNA * methods MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- ATP Binding Cassette Transporter, Subfamily D MeSH
- ATP-Binding Cassette Transporters MeSH
- ABCC8 protein, human MeSH Browser
- ABCD2 protein, human MeSH Browser
- Sulfonylurea Receptors MeSH
The aim of the present study was to introduce methods for exome sequencing of two ATP-binding cassette (ABC) transporters ABCC8 and ABCD2 recently suggested to play a putative role in breast cancer progression and prognosis of patients. We performed next generation sequencing targeted at analysis of all exons in ABCC8 and ABCD2 genes and surrounding noncoding sequences in blood DNA samples from 24 patients with breast cancer. The revealed alterations were characterized by in silico tools. We then compared the most frequent functionally relevant polymorphism rs757110 in ABCC8 with clinical data of patients. In total, the study identified 113 genetic alterations (>70 % novel ones) in both genes. Of these alterations, 83 were noncoding, 13 synonymous, 10 frameshifts and 7 were missense alterations. Four in silico programs predicted pathogenicity of two polymorphisms and four newly identified alterations. Rs757110 polymorphism in ABCC8 did not significantly associate with clinical data of the patients. In conclusion, exome sequencing identified several functionally relevant alterations in ABCC8 and ABCD2 genes that may further be used for a larger follow-up study aiming to assess their clinical significance.
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