Abstract | BACKGROUND: METHODS: Seventeen patients diagnosed with insulinoma were recruited along with 30 healthy volunteers who acted as controls for the present study. The patients presented with symptoms of sweating, tremors, drowsiness, palpitations, loss of consciousness, abnormal behavior, seizures and weight gain. Detailed clinical and family history was collected from all the participants along with 5 ml of blood sample after taking informed consent. Genomic DNA isolated from blood was subjected to MEN1 gene amplification followed by direct sequencing. Nucleotide sequences obtained were compared with published MEN1 cDNA sequences. Prediction of functional effects of novel changes was done using various bioinformatics algorithms. RESULTS: Molecular analysis revealed presence of three novel exonic mutations (M561K, Q192K and Q261Q), two novel intronic variations c.445-44G → A and c.913-42G → C in introns two and six respectively and three reported exon SNPs; H433H (rs540012), D418D (rs2071313), A541T (rs2959656) and one intronic SNP (rs669976). CONCLUSIONS: The study identified presence of novel pathogenic MEN1 mutations in sporadic cases of insulinoma. The new mutations identified were in regions involved in defective binding of menin to proteins implicated in genetic and epigenetic mechanisms. The outcome of the study extends the growing list of MEN1 pathogenic mutations even in sporadic cases providing consequential insight into phenotypic heterogeneity and in the expression of individual mutations.
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Authors | Viveka P Jyotsna, Ekta Malik, Shweta Birla, Arundhati Sharma |
Journal | BMC endocrine disorders
(BMC Endocr Disord)
Vol. 15
Pg. 44
(Aug 26 2015)
ISSN: 1472-6823 [Electronic] England |
PMID | 26307114
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- MEN1 protein, human
- Proto-Oncogene Proteins
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Topics |
- Adolescent
- Adult
- Aged
- Case-Control Studies
- Female
- Genetic Variation
- Humans
- Insulinoma
(genetics)
- Male
- Middle Aged
- Mutation
- Pancreatic Neoplasms
(genetics)
- Polymorphism, Single Nucleotide
- Proto-Oncogene Proteins
(genetics)
- Young Adult
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