Literature DB >> 7647334

Familial breast cancer and genes involved in breast carcinogenesis.

A Lindblom1.   

Abstract

Breast cancer has often been reported to run in families, and the most important risk factor for the disease is a family history of breast cancer. Numerous pedigrees and segregation analyses have suggested an autosomal dominant transmitted susceptibility to breast cancer. Familial breast cancer occurs alone or associated with other cancers in clinically distinguishable syndromes. Such cases may be characterized by early onset, bilateral disease, prolonged survival, and anticipation, mainly seen as a higher penetrance or earlier onset in subsequent generations. Studies of patients and tumors from these families as well as sporadic cases have led to localization and/or identification of a number of genes implicated in breast carcinogenesis of familial and sporadic breast cancer.

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Year:  1995        PMID: 7647334     DOI: 10.1007/bf00665789

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  133 in total

1.  The hereditary aspect of breast cancer in mother and daughter.

Authors:  D P MORSE
Journal:  Cancer       Date:  1951-07       Impact factor: 6.860

2.  Genetic epidemiology of breast cancer: segregation analysis of 200 Danish pedigrees.

Authors:  W R Williams; D E Anderson
Journal:  Genet Epidemiol       Date:  1984       Impact factor: 2.135

3.  Detection of frequent allelic loss on proximal chromosome 17q in sporadic breast carcinoma using microsatellite length polymorphisms.

Authors:  P A Futreal; P Söderkvist; J R Marks; J D Iglehart; C Cochran; J C Barrett; R W Wiseman
Journal:  Cancer Res       Date:  1992-05-01       Impact factor: 12.701

4.  p53 gene mutations occur in combination with 17p allelic deletions as late events in colorectal tumorigenesis.

Authors:  S J Baker; A C Preisinger; J M Jessup; C Paraskeva; S Markowitz; J K Willson; S Hamilton; B Vogelstein
Journal:  Cancer Res       Date:  1990-12-01       Impact factor: 12.701

5.  Mechanisms of p53 loss in human sarcomas.

Authors:  L M Mulligan; G J Matlashewski; H J Scrable; W K Cavenee
Journal:  Proc Natl Acad Sci U S A       Date:  1990-08       Impact factor: 11.205

6.  Genetic epidemiology of breast cancer and associated cancers in high-risk families. I. Segregation analysis.

Authors:  R C Go; M C King; J Bailey-Wilson; R C Elston; H T Lynch
Journal:  J Natl Cancer Inst       Date:  1983-09       Impact factor: 13.506

7.  Genetic alterations of the tumour suppressor gene regions 3p, 11p, 13q, 17p, and 17q in human breast carcinomas.

Authors:  T I Andersen; A Gaustad; L Ottestad; G W Farrants; J M Nesland; K M Tveit; A L Børresen
Journal:  Genes Chromosomes Cancer       Date:  1992-03       Impact factor: 5.006

Review 8.  TP53 tumor suppressor gene: a model for investigating human mutagenesis.

Authors:  C Caron de Fromentel; T Soussi
Journal:  Genes Chromosomes Cancer       Date:  1992-01       Impact factor: 5.006

9.  Maintenance of p53 alterations throughout breast cancer progression.

Authors:  A M Davidoff; B J Kerns; J D Iglehart; J R Marks
Journal:  Cancer Res       Date:  1991-05-15       Impact factor: 12.701

10.  Partial deletion of chromosome 11p in breast cancer correlates with size of primary tumour and oestrogen receptor level.

Authors:  J Mackay; P A Elder; D J Porteous; C M Steel; R A Hawkins; J J Going; U Chetty
Journal:  Br J Cancer       Date:  1988-12       Impact factor: 7.640

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  1 in total

1.  A population-based study of contralateral breast cancer following a first primary breast cancer (Washington, United States)

Authors:  L S Cook; E White; S M Schwartz; B McKnight; J R Daling; N S Weiss
Journal:  Cancer Causes Control       Date:  1996-05       Impact factor: 2.506

  1 in total

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