Literature DB >> 9099970

Screening for TP53 mutations in patients and tumours from 109 Swedish breast cancer families.

M Zelada-Hedman1, A L Børresen-Dale, A Claro, J Chen, L Skoog, A Lindblom.   

Abstract

To estimate the prevalence of TP53 mutations in familial breast cancer, constant denaturant gel electrophoresis (CDGE) was used to screen exons 5-8 of the TP53 gene for germline mutations. Genomic DNA from 128 breast cancer patients belonging to 109 families with familial cancer were screened. No germline mutations were found in any of the patients. We also studied TP53 mutations in tumour DNA from 51 of the same individuals and found mutations in 14%. This is similar to what has been reported in sporadic breast cancer.

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Year:  1997        PMID: 9099970      PMCID: PMC2222784          DOI: 10.1038/bjc.1997.205

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  20 in total

1.  Evidence of a hereditary p53 syndrome in cancer-prone families.

Authors:  Q Wang; C Lasset; H Sobol; M Ozturk
Journal:  Int J Cancer       Date:  1996-02-08       Impact factor: 7.396

2.  Improved double-stranded DNA sequencing using the linear polymerase chain reaction.

Authors:  V Murray
Journal:  Nucleic Acids Res       Date:  1989-11-11       Impact factor: 16.971

3.  Alterations of the TP53 gene as a potential prognostic marker in breast carcinomas. Advantages of using constant denaturant gel electrophoresis in mutation detection.

Authors:  T I Andersen; A L Børresen
Journal:  Diagn Mol Pathol       Date:  1995-09

4.  Identification of the breast cancer susceptibility gene BRCA2.

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Journal:  Nature       Date:  1995 Dec 21-28       Impact factor: 49.962

Review 5.  Germline p53 mutations and heritable cancer.

Authors:  D Malkin
Journal:  Annu Rev Genet       Date:  1994       Impact factor: 16.830

6.  Direct sequencing of affinity-captured amplified human DNA application to the detection of apolipoprotein E polymorphism.

Authors:  A C Syvänen; K Aalto-Setälä; K Kontula; H Söderlund
Journal:  FEBS Lett       Date:  1989-11-20       Impact factor: 4.124

7.  Frequent p53 gene mutations and novel alleles in familial breast cancer.

Authors:  O K Glebov; K E McKenzie; C A White; S Sukumar
Journal:  Cancer Res       Date:  1994-07-15       Impact factor: 12.701

8.  Database of p53 gene somatic mutations in human tumors and cell lines.

Authors:  M Hollstein; K Rice; M S Greenblatt; T Soussi; R Fuchs; T Sørlie; E Hovig; B Smith-Sørensen; R Montesano; C C Harris
Journal:  Nucleic Acids Res       Date:  1994-09       Impact factor: 16.971

9.  Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families.

Authors:  J M Birch; A L Hartley; K J Tricker; J Prosser; A Condie; A M Kelsey; M Harris; P H Jones; A Binchy; D Crowther
Journal:  Cancer Res       Date:  1994-03-01       Impact factor: 12.701

10.  Mutations in p53 do not account for heritable breast cancer: a study in five affected families.

Authors:  J Prosser; P A Elder; A Condie; I MacFadyen; C M Steel; H J Evans
Journal:  Br J Cancer       Date:  1991-02       Impact factor: 7.640

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  4 in total

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3.  A hypothesis-generating search for new genetic breast cancer syndromes--a national study in 803 Swedish families.

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4.  The R72P P53 mutation is associated with familial breast cancer in Jewish women.

Authors:  T Ohayon; R Gershoni-Baruch; M Z Papa; T Distelman Menachem; S Eisenberg Barzilai; E Friedman
Journal:  Br J Cancer       Date:  2005-03-28       Impact factor: 7.640

  4 in total

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