Platelet-derived growth factor receptor expression and amplification in choroid plexus carcinomas
Author(s) -
Ni. Nupponen,
Janna Paulsson,
Astrid Jeibmann,
Brigitte Wrede,
Minna Tanner,
Johannes Wolff,
Werner Paulus,
Arne Östman,
Martin Hasselblatt
Publication year - 2007
Publication title -
modern pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.596
H-Index - 153
eISSN - 1530-0285
pISSN - 0893-3952
DOI - 10.1038/modpathol.3800989
Subject(s) - choroid plexus , platelet derived growth factor receptor , pdgfra , cish , pdgfrb , growth factor receptor , pathology , pdgfb , receptor tyrosine kinase , receptor , cancer research , platelet derived growth factor , biology , medicine , in situ hybridization , growth factor , endocrinology , gist , gene expression , central nervous system , stromal cell , biochemistry , gene
Platelet-derived growth factor (PDGF) receptor signaling has been implicated in the development of glial tumors, but not yet been examined in choroid plexus carcinomas, pediatric tumors with dismal prognosis for which novel treatment options would be desirable. Therefore, protein expression of PDGF receptors alpha and beta as well as amplification status of the respective genes, PDGFRA and PDGFRB, were examined in a series of 22 patients harboring choroid plexus carcinoma using immunohistochemistry and chromogenic in situ hybridization (CISH). The majority of choroid plexus carcinomas expressed PDGF receptors with 6 cases (27%) displaying high staining scores for PDGF receptor alpha and 13 cases (59%) showing high staining scores for PDGF receptor beta. Correspondingly, copy-number gains of PDGFRA were observed in 8 cases out of 12 cases available for CISH and 1 case displayed amplification (six or more signals per nucleus). The proportion of choroid plexus carcinomas with amplification of PDGFRB was even higher (5/12 cases). PDGFRB amplification status and PDGF receptor beta protein expression scores were significantly correlated (P=0.01, Spearman). Expression status of PDGF receptor alpha or PDGF receptor beta was not significantly associated with progression-free survival. To conclude, expression and amplification of PDGF receptors, particularly PDGF receptor beta, are frequent in choroid plexus carcinomas, providing a first rationale for the development of treatments targeting PDGF receptor signaling in these rare malignant pediatric tumors.
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