Abstract
In this study we analyzed the expression of mRNA for PDGF-B and PDGF B-type receptor (PDGFrecB) in 42 biopsy specimens from human astrocytic gliomas and other brain tumors. All gliomas expressed PDGF-B mRNA at higher levels than found in peritumoral and normal nervous tissues. Levels of PDGF-B transcripts correlated strongly with those of mRNA for glial fibrillary acidic protein. Thus, the production of PDGF-B mRNA may be attributed mainly to tumoral glial cells. PDGFrecB transcripts were found in 24 out of 29 gliomas, in agreement with the hypothesis of an autocrine growth stimulation in these tumors. Moreover, mean levels of PDGFrecB expression were higher in glioblastomas than in astrocytomas and over 30-fold higher in meningiomas than in gliomas. This suggests that in gliomas PDGFrecB can be expressed also by vascular elements, in agreement with the hypothesized existence of a paracrine mechanism that may be responsible for the endothelial hyperplasias.
MeSH Terms
Astrocytoma/genetics,pathology
Biopsy
Brain Neoplasms/genetics,pathology
Cerebellar Neoplasms/genetics,pathology
Child
Gene Expression Regulation, Neoplastic/physiology
Glial Fibrillary Acidic Protein/genetics
Glioma/genetics,pathology
Humans
Medulloblastoma/genetics,pathology
Platelet-Derived Growth Factor/genetics
Proto-Oncogene Proteins/genetics
Proto-Oncogene Proteins c-sis
RNA, Messenger/genetics
Receptors, Cell Surface/genetics
Receptors, Platelet-Derived Growth Factor
Transcription, Genetic/genetics
Chemicals
Glial Fibrillary Acidic Protein
Platelet-Derived Growth Factor
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-sis
RNA, Messenger
Receptors, Cell Surface
Receptors, Platelet-Derived Growth Factor
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Mauro A
Second Neurological Clinic, University of Turin, Italy.
Bulfone A
Turco E
Schiffer D
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