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Mutation analysis of the p73 gene in nonastrocytic brain tumours
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  • Regular Article
  • Open access
  • Published: 17 July 2001

Mutation analysis of the p73 gene in nonastrocytic brain tumours

  • M E Alonso1,
  • M J Bello1,
  • P Gonzalez-Gomez1,
  • J Lomas1,
  • D Arjona1,
  • J M de Campos2,
  • M E Kusak2,
  • J L Sarasa3,
  • A Isla4 &
  • …
  • J A Rey1 

British Journal of Cancer volume 85, pages 204–208 (2001)Cite this article

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Abstract

Loss of heterozygosity (LOH) involving the distal chromosome 1 p36 region occurs frequently in nonastrocytic brain tumours, but the tumour suppressor gene targeted by this deletion is unknown. p73 is a novel gene that has high sequence homology and similar gene structure to the p53 gene; it has been mapped to 1 p36, and may thus represent a candidate for this tumour suppressor gene. To determine whether p73 is involved in nonastrocytic brain tumour development, we analysed 65 tumour samples including 26 oligodendrogliomas, 4 ependymomas, 5 medulloblastomas, 10 meningiomas, 2 meningeal haemangiopericytomas, 2 neurofibrosarcomas, 3 primary lymphomas, 8 schwannomas and 5 metastatic tumours to the brain, for p73 alterations. Characterization of allelic loss at 1 p36–p35 showed LOH in about 50% of cases, primarily involving oligodendroglial tumours (22 of 26 cases analysed; 85%) and meningiomas (4 of 10; 40%). PCR-SSCP and direct DNA sequencing of exons 2 to 14 of p73 revealed a missense mutation in one primary lymphoma: a G-to-A transition, with Glu291Lys change. 8 additional cases displayed no tumour-specific alterations, as 3 distinct polymorphic changes were identified: a double polymorphic change of exon 5 was found in one ependymoma and both samples derived from an oligodendroglioma, as follows: a G-to-A transition with no change in Pro 146, and a C-to-T variation with no change in Asn 204: a delG at exon 3/+12 position was identified in 4 samples corresponding to 2 oligodendrogliomas, 1 ependymoma and 1 meningioma, and a C-to-T change at exon 2/+10 position was present in a metastatic tumour. Although both LOH at 1 p36 and p73 sequence changes were evidenced in 4 cases, it is difficult to establish a causal role of the p73 variations and nonastrocytic brain tumours development. © 2001 Cancer Research Campaign www.bjcancer.com

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

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Authors and Affiliations

  1. Departamento de Cirugia Experimental, Laboratorio de Oncogenética Molecular, Unidad de Investigación, Hospital Universitario La Paz, Madrid, 28046, Spain

    M E Alonso, M J Bello, P Gonzalez-Gomez, J Lomas, D Arjona & J A Rey

  2. Departamento de Neurocirugia, Hospital del Rio Hortega, Valladolid, 47010, Spain

    J M de Campos & M E Kusak

  3. Departamento de Anatomia Patológica, Fundación Jiménez Diaz, Madrid, 28040, Spain

    J L Sarasa

  4. Departamento de Neurocirugia, Hospital Universitario La Paz, Madrid, 28046, Spain

    A Isla

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From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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Alonso, M., Bello, M., Gonzalez-Gomez, P. et al. Mutation analysis of the p73 gene in nonastrocytic brain tumours. Br J Cancer 85, 204–208 (2001). https://doi.org/10.1054/bjoc.2001.1855

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  • Received: 18 January 2001

  • Revised: 26 March 2001

  • Accepted: 27 March 2001

  • Published: 17 July 2001

  • Issue date: 20 July 2001

  • DOI: https://doi.org/10.1054/bjoc.2001.1855

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Keywords

  • p73gene
  • nonastrocytic tumours
  • LOH 1p36
  • primary brain lymphoma

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