Literature DB >> 1679237

Identification of a germ-line mutation in the p53 gene in a patient with an intracranial ependymoma.

A K Metzger1, V C Sheffield, G Duyk, L Daneshvar, M S Edwards, P H Cogen.   

Abstract

We detected a germ-line mutation of the p53 gene in a patient with a malignant ependymoma of the posterior fossa. This mutation, which was found at codon 242, resulted in an amino acid substitution in a highly conserved site of exon 7 of the p53 gene; the same mutation was found in both the germ-line and the tumor tissue. This is the most common region of previously described somatic p53 mutations in tumor specimens and of the germ-line p53 mutations in patients with the Li-Fraumeni cancer syndrome. Evaluation of the patient's family revealed several direct maternal and paternal relatives who had died at a young age from different types of cancer. The association of a germ-line p53 mutation with an intracranial malignancy and a strong family history of cancer suggests that p53 gene mutations predispose a person to malignancy and, like retinoblastoma mutations, may be inherited.

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Year:  1991        PMID: 1679237      PMCID: PMC52396          DOI: 10.1073/pnas.88.17.7825

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  30 in total

1.  Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes.

Authors:  V C Sheffield; D R Cox; L S Lerman; R M Myers
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

2.  A novel strategy for constructing clustered point mutations.

Authors:  M Haltiner; T Kempe; R Tjian
Journal:  Nucleic Acids Res       Date:  1985-02-11       Impact factor: 16.971

Review 3.  Oncogenes and tumor-suppressing genes.

Authors:  S H Friend; T P Dryja; R A Weinberg
Journal:  N Engl J Med       Date:  1988-03-10       Impact factor: 91.245

4.  Characterization of the human p53 gene.

Authors:  P Lamb; L Crawford
Journal:  Mol Cell Biol       Date:  1986-05       Impact factor: 4.272

5.  Nearly all single base substitutions in DNA fragments joined to a GC-clamp can be detected by denaturing gradient gel electrophoresis.

Authors:  R M Myers; S G Fischer; L S Lerman; T Maniatis
Journal:  Nucleic Acids Res       Date:  1985-05-10       Impact factor: 16.971

6.  High incidence of lung, bone, and lymphoid tumors in transgenic mice overexpressing mutant alleles of the p53 oncogene.

Authors:  A Lavigueur; V Maltby; D Mock; J Rossant; T Pawson; A Bernstein
Journal:  Mol Cell Biol       Date:  1989-09       Impact factor: 4.272

7.  Concerted nonsyntenic allelic loss in human colorectal carcinoma.

Authors:  D J Law; S Olschwang; J P Monpezat; D Lefrançois; D Jagelman; N J Petrelli; G Thomas; A P Feinberg
Journal:  Science       Date:  1988-08-19       Impact factor: 47.728

8.  p53: a frequent target for genetic abnormalities in lung cancer.

Authors:  T Takahashi; M M Nau; I Chiba; M J Birrer; R K Rosenberg; M Vinocour; M Levitt; H Pass; A F Gazdar; J D Minna
Journal:  Science       Date:  1989-10-27       Impact factor: 47.728

9.  P53 expression in breast cancer.

Authors:  G Cattoretti; F Rilke; S Andreola; L D'Amato; D Delia
Journal:  Int J Cancer       Date:  1988-02-15       Impact factor: 7.396

10.  Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas.

Authors:  S J Baker; E R Fearon; J M Nigro; S R Hamilton; A C Preisinger; J M Jessup; P vanTuinen; D H Ledbetter; D F Barker; Y Nakamura; R White; B Vogelstein
Journal:  Science       Date:  1989-04-14       Impact factor: 47.728

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  25 in total

1.  Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesis.

Authors:  P H Cogen; L Daneshvar; A K Metzger; G Duyk; M S Edwards; V C Sheffield
Journal:  Am J Hum Genet       Date:  1992-03       Impact factor: 11.025

Review 2.  Cancer risks from germline p53 mutations.

Authors:  T Frebourg; S H Friend
Journal:  J Clin Invest       Date:  1992-11       Impact factor: 14.808

3.  Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresis.

Authors:  V C Sheffield; J S Beck; B Nichols; A Cousineau; A C Lidral; E M Stone
Journal:  Am J Hum Genet       Date:  1992-03       Impact factor: 11.025

4.  Molecular genetics in the cancer clinic.

Authors:  E H Radany
Journal:  West J Med       Date:  1991-11

5.  Genetic abnormalities and CNS tumors: report of two cases of ependymoma associated with Klinefelter's Syndrome (KS).

Authors:  M L Garrè; V Capra; E Di Battista; L Giampietri; P Nozza; A Raso; A Pezzolo; A Rossi; C Milanaccio; M Pavanello; A Naselli
Journal:  Childs Nerv Syst       Date:  2006-10-13       Impact factor: 1.475

6.  Single base pair germ-line deletion in the p53 gene in a cancer predisposed family.

Authors:  R Hamelin; F Barichard; I Henry; C Junien; G Thomas
Journal:  Hum Genet       Date:  1994-07       Impact factor: 4.132

7.  Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma.

Authors:  L Diller; E Sexsmith; A Gottlieb; F P Li; D Malkin
Journal:  J Clin Invest       Date:  1995-04       Impact factor: 14.808

Review 8.  Tumor suppressor genes and medulloblastoma.

Authors:  P H Cogen; J D McDonald
Journal:  J Neurooncol       Date:  1996-07       Impact factor: 4.130

Review 9.  Biological background of pediatric medulloblastoma and ependymoma: a review from a translational research perspective.

Authors:  Judith M de Bont; Roger J Packer; Erna M Michiels; Monique L den Boer; Rob Pieters
Journal:  Neuro Oncol       Date:  2008-08-01       Impact factor: 12.300

Review 10.  Molecular biology of pediatric gliomas.

Authors:  C Raffel
Journal:  J Neurooncol       Date:  1996 May-Jun       Impact factor: 4.130

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