http://www.cnr.it/ontology/cnr/individuo/prodotto/ID308011
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. (Articolo in rivista)
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- Label
- A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/jbmr.542 (literal)
- Alternative label
Gianfrancesco F, Rendina D, Di Stefano M, Mingione A, Esposito T, Merlotti D, Gallone S, Magliocca S, Goode A, Formicola D, Morello G, Layfield R, Frattini A, De Filippo G, Nuti R, Searle M, Strazzullo P, Isaia GC, Mossetti G, Gennari L. (2012)
A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease.
in Journal of bone and mineral research
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Gianfrancesco F, Rendina D, Di Stefano M, Mingione A, Esposito T, Merlotti D, Gallone S, Magliocca S, Goode A, Formicola D, Morello G, Layfield R, Frattini A, De Filippo G, Nuti R, Searle M, Strazzullo P, Isaia GC, Mossetti G, Gennari L. (literal)
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- Gianfrancesco Fernando Corresponding Author (literal)
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- ISI Web of Science (WOS) (literal)
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- 1Institute of Genetics and Biophysics ''Adriano Buzzati-Traverso,'' National Research Council of Italy, Naples, Italy
2Department of Clinical and Experimental Medicine, Federico II University Medical School, Naples, Italy
3Department of Internal Medicine, University of Turin, Turin, Italy
4Department of Internal Medicine, Endocrine-Metabolic Sciences and Biochemistry, University of Siena, Siena, Italy
5Department of Neuroscience, University of Turin, Turin, Italy
6School of Biomedical Sciences, University of Nottingham Medical School, Queen's Medical Centre, Nottingham, United Kingdom
7Institute for Biomedical Technologies, CNR, Segrate, Milan, Italy
8Centre for Biomolecular Sciences, School of Chemistry, University Park, Nottingham, United Kingdom (literal)
- Titolo
- A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. (literal)
- Abstract
- Mutations in the SQSTM1 gene were identified as a common cause of Paget's disease of bone (PDB) but experimental evidence
demonstrated that SQSTM1 mutation is not sufficient to induce PDB in vivo. Here, we identified two nonsynonymous single nucleotide
polymorphisms (SNPs) (C421T, H141Y and T575C, V192A) in the TNFRSF11A gene, associated with PDB and with the severity of
phenotype in a large population of 654 unrelated patients that were previously screened for SQSTM1 gene mutations. The largest effect
was found for the T575C variant, yielding an odds ratio of 1.29 (p¼0.003), with the C allele as the risk allele. Moreover, an even more
significant p-value (p¼0.0002) was observed in the subgroup of patients with SQSTM1 mutation, with an odds ratio of 1.71. Interestingly,
patients with the C allele also showed an increased prevalence of polyostotic disease (68%, 53%, and 51% in patients with CC, CT, and TT
genotypes, respectively; p¼0.01), as well as an increased number of affected skeletal sites (2.9, 2.5, and 2.0 in patients with CC, CT, and TT
genotypes, respectively, p¼0.008). These differences increased when analyses were restricted to cases with SQSTM1 mutation. In human
cell lines, cotrasfection with mutated SQSTM1 and TNFRSF11AA192 produced a level of activation of NFkB signaling greater than
cotrasfection with wild-type SQSTM1 and TNFRSF11AV192, confirming genetics and clinical evidences. These results provide the first
evidence that genetic variation within the OPG/RANK/RANKL system influences the severity of PBD in synergistic action with SQSTM1
gene mutations. ? 2012 American Society for Bone and Mineral Research. (literal)
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