In the past years, genome wide association studies (GWAS) have provided evidence that inter-individual susceptibility to diverse pathological conditions can reveal a common genetic architecture. Through the analysis of congenital heart disease (CHD) and neuroblastoma (NB) GWAS data, we aimed to dissect the genetic susceptibility shared between these conditions, which are known to arise from neural crest cell (NCC) migration or development abnormalities, via identification and functional characterization of common regions of association. Two loci (2q35 and 3q25.32) harbor single nucleotide polymorphisms (SNPs) that are associated at a p-value < 10−3 with conotruncal malformations and ventricular septal defect respectively, as well as with NB. In addition, the lead SNP in 4p16.2 for atrial septal defect and the lead SNP in 3q25.32 for tetralogy of Fallot are less than 250 Kb distant from the lead SNPs for NB at the same genomic regions. Some of these shared susceptibility loci regulate the expression of relevant genes involved in NCC formation and developmental processes (such as BARD1, MSX1, and SHOX2) and are enriched in several epigenetic markers from NB and fetal heart cell lines. Although the clinical correlation between NB and CHD is unclear, our exploration of a possible common genetic basis between NB and a subset of cardiac malformations can help shed light on their shared embryological origin and pathogenetic mechanisms.

Exploring shared susceptibility between two neural crest cells originating conditions: neuroblastoma and congenital heart disease / Testori, Alessandro; Lasorsa, Vito A.; Cimmino, Flora; Cantalupo, Sueva; Cardinale, Antonella; Avitabile, Marianna; Limongelli, Giuseppe; Russo, Maria Giovanna; Diskin, Sharon; Maris, John; Devoto, Marcella; Keavney, Bernard; Cordell, Heather J.; Iolascon, Achille; Capasso, Mario. - In: GENES. - ISSN 2073-4425. - 10:9(2019). [10.3390/genes10090663]

Exploring shared susceptibility between two neural crest cells originating conditions: neuroblastoma and congenital heart disease

Devoto, Marcella;
2019

Abstract

In the past years, genome wide association studies (GWAS) have provided evidence that inter-individual susceptibility to diverse pathological conditions can reveal a common genetic architecture. Through the analysis of congenital heart disease (CHD) and neuroblastoma (NB) GWAS data, we aimed to dissect the genetic susceptibility shared between these conditions, which are known to arise from neural crest cell (NCC) migration or development abnormalities, via identification and functional characterization of common regions of association. Two loci (2q35 and 3q25.32) harbor single nucleotide polymorphisms (SNPs) that are associated at a p-value < 10−3 with conotruncal malformations and ventricular septal defect respectively, as well as with NB. In addition, the lead SNP in 4p16.2 for atrial septal defect and the lead SNP in 3q25.32 for tetralogy of Fallot are less than 250 Kb distant from the lead SNPs for NB at the same genomic regions. Some of these shared susceptibility loci regulate the expression of relevant genes involved in NCC formation and developmental processes (such as BARD1, MSX1, and SHOX2) and are enriched in several epigenetic markers from NB and fetal heart cell lines. Although the clinical correlation between NB and CHD is unclear, our exploration of a possible common genetic basis between NB and a subset of cardiac malformations can help shed light on their shared embryological origin and pathogenetic mechanisms.
2019
neuroblastoma; congenital heart disease; genome wide association studies
01 Pubblicazione su rivista::01a Articolo in rivista
Exploring shared susceptibility between two neural crest cells originating conditions: neuroblastoma and congenital heart disease / Testori, Alessandro; Lasorsa, Vito A.; Cimmino, Flora; Cantalupo, Sueva; Cardinale, Antonella; Avitabile, Marianna; Limongelli, Giuseppe; Russo, Maria Giovanna; Diskin, Sharon; Maris, John; Devoto, Marcella; Keavney, Bernard; Cordell, Heather J.; Iolascon, Achille; Capasso, Mario. - In: GENES. - ISSN 2073-4425. - 10:9(2019). [10.3390/genes10090663]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1307651
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