Increased p53 immunopositivity in anaplastic medulloblastoma and supratentorial PNET is not caused by JC virus

<p>Abstract</p> <p>Background</p> <p>p53 mutations are relatively uncommon in medulloblastoma, but abnormalities in this cell cycle pathway have been associated with anaplasia and worse clinical outcomes. We correlated p53 protein expression with pathological subtype an...

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Main Authors: Shah Keerti V, Khaki Leila, Daniel Richard W, Chaudhry Aneeka, Eberhart Charles G, Gravitt Patti E
Format: Article
Language:English
Published: BMC 2005-02-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/5/19
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author Shah Keerti V
Khaki Leila
Daniel Richard W
Chaudhry Aneeka
Eberhart Charles G
Gravitt Patti E
author_facet Shah Keerti V
Khaki Leila
Daniel Richard W
Chaudhry Aneeka
Eberhart Charles G
Gravitt Patti E
author_sort Shah Keerti V
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>p53 mutations are relatively uncommon in medulloblastoma, but abnormalities in this cell cycle pathway have been associated with anaplasia and worse clinical outcomes. We correlated p53 protein expression with pathological subtype and clinical outcome in 75 embryonal brain tumors. The presence of JC virus, which results in p53 protein accumulation, was also examined.</p> <p>Methods</p> <p>p53 protein levels were evaluated semi-quantitatively in 64 medulloblastomas, 3 atypical teratoid rhabdoid tumors (ATRT), and 8 supratentorial primitive neuroectodermal tumors (sPNET) using immunohistochemistry. JC viral sequences were analyzed in DNA extracted from 33 frozen medulloblastoma and PNET samples using quantitative polymerase chain reaction.</p> <p>Results</p> <p>p53 expression was detected in 18% of non-anaplastic medulloblastomas, 45% of anaplastic medulloblastomas, 67% of ATRT, and 88% of sPNET. The increased p53 immunoreactivity in anaplastic medulloblastoma, ATRT, and sPNET was statistically significant. Log rank analysis of clinical outcome revealed significantly shorter survival in patients with p53 immunopositive embryonal tumors. No JC virus was identified in the embryonal brain tumor samples, while an endogenous human retrovirus (ERV-3) was readily detected.</p> <p>Conclusion</p> <p>Immunoreactivity for p53 protein is more common in anaplastic medulloblastomas, ATRT and sPNET than in non-anaplastic tumors, and is associated with worse clinical outcomes. However, JC virus infection is not responsible for increased levels of p53 protein.</p>
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spelling doaj.art-d205cdf8d5d24e40af42457c8de159072022-12-21T23:27:35ZengBMCBMC Cancer1471-24072005-02-01511910.1186/1471-2407-5-19Increased p53 immunopositivity in anaplastic medulloblastoma and supratentorial PNET is not caused by JC virusShah Keerti VKhaki LeilaDaniel Richard WChaudhry AneekaEberhart Charles GGravitt Patti E<p>Abstract</p> <p>Background</p> <p>p53 mutations are relatively uncommon in medulloblastoma, but abnormalities in this cell cycle pathway have been associated with anaplasia and worse clinical outcomes. We correlated p53 protein expression with pathological subtype and clinical outcome in 75 embryonal brain tumors. The presence of JC virus, which results in p53 protein accumulation, was also examined.</p> <p>Methods</p> <p>p53 protein levels were evaluated semi-quantitatively in 64 medulloblastomas, 3 atypical teratoid rhabdoid tumors (ATRT), and 8 supratentorial primitive neuroectodermal tumors (sPNET) using immunohistochemistry. JC viral sequences were analyzed in DNA extracted from 33 frozen medulloblastoma and PNET samples using quantitative polymerase chain reaction.</p> <p>Results</p> <p>p53 expression was detected in 18% of non-anaplastic medulloblastomas, 45% of anaplastic medulloblastomas, 67% of ATRT, and 88% of sPNET. The increased p53 immunoreactivity in anaplastic medulloblastoma, ATRT, and sPNET was statistically significant. Log rank analysis of clinical outcome revealed significantly shorter survival in patients with p53 immunopositive embryonal tumors. No JC virus was identified in the embryonal brain tumor samples, while an endogenous human retrovirus (ERV-3) was readily detected.</p> <p>Conclusion</p> <p>Immunoreactivity for p53 protein is more common in anaplastic medulloblastomas, ATRT and sPNET than in non-anaplastic tumors, and is associated with worse clinical outcomes. However, JC virus infection is not responsible for increased levels of p53 protein.</p>http://www.biomedcentral.com/1471-2407/5/19
spellingShingle Shah Keerti V
Khaki Leila
Daniel Richard W
Chaudhry Aneeka
Eberhart Charles G
Gravitt Patti E
Increased p53 immunopositivity in anaplastic medulloblastoma and supratentorial PNET is not caused by JC virus
BMC Cancer
title Increased p53 immunopositivity in anaplastic medulloblastoma and supratentorial PNET is not caused by JC virus
title_full Increased p53 immunopositivity in anaplastic medulloblastoma and supratentorial PNET is not caused by JC virus
title_fullStr Increased p53 immunopositivity in anaplastic medulloblastoma and supratentorial PNET is not caused by JC virus
title_full_unstemmed Increased p53 immunopositivity in anaplastic medulloblastoma and supratentorial PNET is not caused by JC virus
title_short Increased p53 immunopositivity in anaplastic medulloblastoma and supratentorial PNET is not caused by JC virus
title_sort increased p53 immunopositivity in anaplastic medulloblastoma and supratentorial pnet is not caused by jc virus
url http://www.biomedcentral.com/1471-2407/5/19
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