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Survivin is a negative prognostic marker in medulloblastoma
Author(s) -
Pizem J.,
Cör A.,
ZadravecZaletel L.,
Popovic M.
Publication year - 2005
Publication title -
neuropathology and applied neurobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.538
H-Index - 95
eISSN - 1365-2990
pISSN - 0305-1846
DOI - 10.1111/j.1365-2990.2005.00664.x
Subject(s) - survivin , medulloblastoma , wnt signaling pathway , cancer research , beta catenin , biology , immunohistochemistry , apoptosis , inhibitor of apoptosis , medicine , oncology , pathology , signal transduction , programmed cell death , genetics
Survivin is a member of the inhibitor of apoptosis protein family, which is over‐expressed in many human cancers. Our aim was to analyse survivin expression in medulloblastoma, its association with aberrant activation of the WNT (wingless) pathway and to test the prognostic significance of survivin expression. We immuno histochemically analysed survivin expression and localization of β‐catenin, a downstream mediator of the WNT pathway, in 56 cases of medulloblastoma. Survivin was detected in the nuclei of tumour cells in all cases, but the proportion of positive nuclei varied from 0.5 to 31.3%. Survivin expression tended to be higher in medulloblastomas with an aberrant activation of the WNT pathway (nuclear localization of β‐catenin), but did not correlate with histological type, age group or dissemination via cerebrospinal fluid pathways. Survivin expression and dissemination status were two independent negative prognostic variables for the overall survival of patients with medulloblastoma. In conclusion, survivin is up‐regulated in medulloblastomas. It is a negative prognostic marker and a potential therapeutic target.