Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1990-1-26
pubmed:abstractText
Seventy-one tumors of the central nervous system in children were studied immunohistologically. Thirty-seven were classified histologically as PNETs, of which 35 were located in the cerebellum (medulloblastomas), one in the cerebrum, and one in the spinal cord. The 34 non-PNETs included five ependymomas, seven gangliogliomas, 15 astrocytomas, and seven tumors of other histology. We used monoclonal antibodies specific for neurofilament (NF) triplet proteins, for microtubule associated protein 2 and tau protein and for glial fibrillary acidic protein (GFAP) and myelin basic protein. In addition, a monoclonal antibody to epithelial membrane antigen was applied. The presence or absence of these antigens defined four major groups of PNETs: 1) PNETs not otherwise specified (10 cases), 2) PNETs with neuronal differentiation (eight cases), 3) PNETs with astrocytic differentiation (six cases), and 4) PNETs with both neuronal and astrocytic differentiation (12 cases). One case showed ependymal differentiation. The pattern of expression of NF isoforms in PNETs was reminiscent of that seen during normal mammalian development, such that phosphorylated NF-H was only present in combination with NF-M and NF-L. Among the other central nervous system tumors, all astrocytomas and gangliogliomas were positive for GFAP, and the gangliogliomas also expressed all NF isoforms. Three atypical teratoid tumors and two rhabdoid tumors showed strong positivity for epithelial membrane antigen and also for GFAP. We conclude that the differentiation antigens described here serve to distinguish PNETs from other pediatric central nervous system tumors and to identify subsets of PNETs. Accordingly, PNETs represent a heterogeneous group of pediatric brain tumors capable of neuronal and glial differentiation.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0023-6837
pubmed:author
pubmed:issnType
Print
pubmed:volume
61
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
635-43
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:2557487-Adolescent, pubmed-meshheading:2557487-Adult, pubmed-meshheading:2557487-Antibodies, Monoclonal, pubmed-meshheading:2557487-Antigens, Neoplasm, pubmed-meshheading:2557487-Astrocytoma, pubmed-meshheading:2557487-Cell Transformation, Neoplastic, pubmed-meshheading:2557487-Central Nervous System Diseases, pubmed-meshheading:2557487-Child, pubmed-meshheading:2557487-Child, Preschool, pubmed-meshheading:2557487-Ependymoma, pubmed-meshheading:2557487-Female, pubmed-meshheading:2557487-Glial Fibrillary Acidic Protein, pubmed-meshheading:2557487-Humans, pubmed-meshheading:2557487-Immunohistochemistry, pubmed-meshheading:2557487-Infant, pubmed-meshheading:2557487-Male, pubmed-meshheading:2557487-Microtubule-Associated Proteins, pubmed-meshheading:2557487-Neoplasms, Germ Cell and Embryonal, pubmed-meshheading:2557487-Neuroblastoma, pubmed-meshheading:2557487-Neurons, pubmed-meshheading:2557487-Prospective Studies, pubmed-meshheading:2557487-Tumor Markers, Biological, pubmed-meshheading:2557487-tau Proteins
pubmed:year
1989
pubmed:articleTitle
Molecular markers of primitive neuroectodermal tumors and other pediatric central nervous system tumors. Monoclonal antibodies to neuronal and glial antigens distinguish subsets of primitive neuroectodermal tumors.
pubmed:affiliation
Department of Pathology, University of Pennsylvania Hospital, Philadelphia.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S.