bcl-2 protein expression in astrocytomas in relation to patient survival and p53 gene status

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ID: 114016
1970
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Abstract
bcl-2 protein expression was characterized in a series of 58 astrocytomas from 21 pediatric and 37 adult patients. As part of a continuing attempt to define relevant prognostic factors which may predict clinical outcome, we have determined the impact of bcl-2 accumulation in malignant astrocytes on the length of patient survival. Aberrant overexpression of bcl-2 protein in tumor cells was detected in 57% (12 of 21) of pediatric and 73% (27 of 37) of the adult cases. Among pediatric patients, the median survival in months showed no relationship with the incidence of bcl-2-positive tumors. Among the adult patients, a favorable prognostic indicator was low-tumor grade (P = 0.05). bcl-2-positive tumors occurred with similar frequencies in WHO grades III and IV of malignancy. When bcl-2 expression in tumor cells was tested as a variable to predict for patient survival, the 6 patients without bcl-2 expression among 23 adult patients with grade IV tumors had a shorter median survival. The same 58 tumors had been previously analyzed for alterations of p53: 4 pediatric and 16 adult tumors had p53 gene mutations. There was no significant difference in median survival related to p53 gene status. There was no relationship between bcl-2 expression and p53 gene status: approximately equal numbers of tumors with either wild-type or mutant p53 were bcl-2 negative or bcl-2 positive. bcl-2 expression is high (40–100%) among other tumors of the central nervous system which also show low malignant potential. Up-regulation of bcl-2 in malignant astrocytes or constitutive expression in some tumor types may be a factor leading to a more favorable clinical outcome.
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newcomb1970actabcl-2 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors E. W. Newcomb;Sandhya K. Bhalla;Clarissa L. Parrish;Roberta L. Hayes;Henry Cohen;Douglas C. Miller;E. W. Newcomb;Sandhya K. Bhalla;Clarissa L. Parrish;Roberta L. Hayes;Henry Cohen;Douglas C. Miller;
Journal acta neuropathologica
Year 1970
DOI
doi:10.1007/s004010050721
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