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. 1996 Feb;27(2):101-9.
doi: 10.1007/BF00177472.

Bcl-2 distribution in neuroepithelial tumors: an immunohistochemical study

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Bcl-2 distribution in neuroepithelial tumors: an immunohistochemical study

D Schiffer et al. J Neurooncol. 1996 Feb.

Abstract

Bcl-2 proto-oncogene prevents apoptosis in many conditions. First detected in lymphomas, it has been also described in non-lymphoid tissues. The immunohistochemical distribution of bcl-2 protein in 100 neuroepithelial tumors is presented. Bcl-2 was positive in some neurons of normal nervous tissue, in reactive astrocytes and variably in all neuroepithelial tumor. The reaction product was either diffuse or granular, due to bcl-21 protein localization on cytoplasmic, nuclear and mitochondrial membranes. The positivity was high in medulloblastomas and in astrocytic tumors. In the latter, the strongest staining was found in cells retaining the astrocytic aspect. Oligodendroglial cells were minimally stained. No correlation of bcl-2 staining with survival was found in each tumor type. The interpretation of the results is based on the one side on the constitutive role played by bcl-2 in the nervous tissue and its neoplastic derivatives. On the other side, in tumors bcl-2 acts by preventing tumor cells from undergoing apoptosis. BCl-2 expression in brain tumors, therefore, receives a dual interpretation. For this reason and for the lacking of correlation with survival, bcl-2 expression cannot be regarded as a prognostic factor.

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References

    1. Cell Growth Differ. 1994 Apr;5(4):411-7 - PubMed
    1. J Histochem Cytochem. 1992 Dec;40(12):1819-25 - PubMed
    1. Nature. 1970 Aug 15;227(5259):680-5 - PubMed
    1. Mol Cell Biol. 1993 Apr;13(4):2432-40 - PubMed
    1. Proc Natl Acad Sci U S A. 1991 Aug 15;88(16):6961-5 - PubMed

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