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Analysis of the p21 gene in gliomas
Authors:Li  You-Jun  Hoang-Xuan  Khê  Hoang-Xuan  Khê  Zhou  Xiao-Ping  Sanson  Marc  Mokhtari  Karima  Faillot  Thierry  Cornu  Philippe  Poisson  Michel  Thomas  Gilles  Hamelin  Richard
Institution:(1) INSERM U434, Génétique des Tumeurs, CEPH, Paris, France;(2) Department of Neurology and, INSERM, U495;(3) Neuropathology, Hôpital Pitié Salpétrière, Paris, France;(4) Neurosurgery, Hôpital Pitié Salpétrière, Paris, France
Abstract:The p21 gene encodes a cyclin dependent kinase inhibitor protein (p21) which has a tumor suppressive activity in a variety of tumor cell lines. Since, the p21 gene is up-regulated by the p53 tumor suppressor gene, which is frequently mutated in gliomas, acting therefore in the same control pathway, it constitutes a good candidate gene to be also inactivated in these tumors. To test this hypothesis, DNAs from 81 gliomas (48 glioblastomas, 11 anaplastic astrocytomas, 10 low-grade astrocytomas, 12 oligodendrogliomas and mixed gliomas), were investigated for mutations in the p21 coding sequence by denaturant gradient gel electrophoresis followed by sequencing. All these tumors have been previously screened for p53 mutations. Three different DNA variants were identified on codon 31 (17 cases), 27 (1 case) and 117 (1 case) and shown to be also present in matching constitutional DNA, suggesting they were polymorphisms. None of the tumors demonstrated a somatic mutation. No significant correlation between the presence of a p21 variant and the p53 mutation tumor status was observed. In conclusion, mutation in the p21 gene unlikely contributes to the development of gliomas.
Keywords:glioma  p21  p53  WAF1  CIP1
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