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A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome
- Source :
- Cellular oncology (Dordrecht). 37(4)
- Publication Year :
- 2014
-
Abstract
- The CDC73 gene, encoding parafibromin, has been identified as a tumour suppressor gene both in hyperparathyroidism-jaw tumour (HPT-JT) syndrome and in sporadic parathyroid carcinoma. While the vast majority of CDC73 mutations affect the N-terminus or the central core of the encoded protein, as yet few mutations have been reported affecting the C-terminus. Here, we report a case (Caucasian female, 28 years) with an invasive ossifying fibroma of the left mandible and hyperparathyroidism (sCa = 16 mg/dl, PTH = 660 pg/mL) due to a parathyroid lesion of 20 mm, hystologically diagnosed as carcinoma. The whole CDC73 gene was screened for the presence of mutations by Sanger sequencing. Immunohistochemistry, in vitro functional assays, Western blotting, MTT assays and in-silico modelling were performed to assess the effect of the detected mutation. Sequence analysis of the CDC73 gene in the proband revealed the presence of a novel deletion affecting the C-terminus of the encoded protein (c.1379delT/p.L460Lfs*18). Clinical and genetic analyses of the available relatives led to the identification of three additional carriers, one of whom was also affected by a parathyroid lesion. Immunohistochemistry, Western blotting, MTT and in-silico modelling assays revealed that the deletion leads to down-regulation of the mutated protein, most likely through a proteasome-mediated pathway. We also found that the deletion may cause a conformational change in the C-terminus of the protein, possibly affecting its interaction with partner proteins. Finally, we found that the mutant protein enhances cellular growth. We report a novel mutation in the CDC73 gene that may underlie HPT-JT syndrome. This mutation appears to affect the C-terminal moiety of the encoded protein, which is thought to interact with other protein partners. The identification of these partners may be instrumental for our understanding of the CDC73-associated phenotype.
- Subjects :
- Adenoma
Adult
Male
Cancer Research
Pathology
medicine.medical_specialty
Parafibromin
Fibroma
CDC73
Biology
Gene mutation
medicine.disease_cause
Jaw Neoplasm
Protein Structure, Secondary
Cell Line
Germline mutation
Mutant protein
medicine
Humans
Gene
Germ-Line Mutation
Tumor Suppressor Protein
Mutation
Hyperparathyroidism
Medicine (all)
Tumor Suppressor Proteins
General Medicine
medicine.disease
Molecular biology
Jaw Neoplasms
Hyperparathyroidism with jaw tumour
Oncology
Parathyroid carcinoma
Italy
HPT-JT
Molecular Medicine
Female
Human
Subjects
Details
- ISSN :
- 22113436
- Volume :
- 37
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Cellular oncology (Dordrecht)
- Accession number :
- edsair.doi.dedup.....73fb77714fd2e15b149fe9bbdc9533f1