A lack of neuroblastoma in Down syndrome: a study from 11 European countries

Détails

ID Serval
serval:BIB_A2697A55BE3F
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
A lack of neuroblastoma in Down syndrome: a study from 11 European countries
Périodique
Cancer Research
Auteur⸱e⸱s
Satge  D., Sasco  A. J., Carlsen  N. L., Stiller  C. A., Rubie  H., Hero  B., de Bernardi  B., de Kraker  J., Coze  C., Kogner  P., Langmark  F., Hakvoort-Cammel  F. G., Beck  D., von der Weid  N., Parkes  S., Hartmann  O., Lippens  R. J., Kamps  W. A., Sommelet  D.
ISSN
0008-5472 (Print)
Statut éditorial
Publié
Date de publication
02/1998
Volume
58
Numéro
3
Pages
448-52
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Feb 1
Résumé
An epidemiological investigation in 11 European countries comprising a total childhood population of 54.1 million children and using 8 separate data sources was conducted to evaluate the occurrence of neuroblastoma in Down syndrome (DS). No cases of DS were detected among 6724 infants and children with neuroblastoma, although more than five were expected. This highly significant result (P = 0.0045 according to the Poisson test) is consistent with data in the literature, which contains only two poorly detailed cases in epidemiological studies and one ganglioneuroma in a DS mosaic patient. Like other tumors, such as leukemias, testicular germ cell tumors and lymphomas are in excess in DS patients; the lack of neuroblastomas does not reflect a general decreased incidence of cancer but rather a specific underrepresentation of this precise tumor. S-100 b protein, the gene for which maps to the long arm of chromosome 21, (a) is overproduced in DS patients, (b) produces growth inhibition and differentiation of neural cells in vitro, (c) is abundant in good-prognosis neuroblastomas, and (d) has been shown to induce growth inhibition and differentiation and cell death in several human and murine neuroblastoma cell lines and could be responsible for this variation. Additional epidemiological and experimental studies are warranted to confirm our interpretation of these data.
Mots-clé
Adolescent Child Child, Preschool Chromosomes, Human, Pair 21/genetics Comorbidity Down Syndrome/*epidemiology/genetics Europe/epidemiology Female Humans Immunity, Natural Incidence Infant Infant, Newborn Male Neuroblastoma/*epidemiology/genetics S100 Proteins/genetics/physiology
Pubmed
Web of science
Création de la notice
25/01/2008 11:35
Dernière modification de la notice
20/08/2019 16:08
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