Literature DB >> 11562180

Molecular and pathological characterization of inherited breast cancer.

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Abstract

The two major breast cancer susceptibility genes, BRCA1 and BRCA2, account for the majority of familial breast-ovarian cancer, but only a modest proportion of breast cancer families without ovarian or male breast cancer. Search for additional breast cancer genes with traditional linkage analysis has so far been unsuccessful, probably due to genetic heterogeneity. Pooling of families of different ethnical, cultural, and geographical origin proved to be a useful approach when identifying BRCA1 and BRCA2, but for genes mutated only in specific populations it is important not to introduce locus heterogeneity by pooling. Genetic heterogeneity can possibly be circumvented by using objective means, such as tumour histopathology or gene expression profiling, for subclassification of families prior to linkage analysis. Also, additional breast cancer genes can be identified by further characterization of the function of BRCA1 and BRCA2 and their interacting proteins. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11562180     DOI: 10.1006/scbi.2001.0393

Source DB:  PubMed          Journal:  Semin Cancer Biol        ISSN: 1044-579X            Impact factor:   15.707


  1 in total

1.  Breast cancer-associated Abraxas mutation disrupts nuclear localization and DNA damage response functions.

Authors:  Szilvia Solyom; Bernadette Aressy; Katri Pylkäs; Jeffrey Patterson-Fortin; Jaana M Hartikainen; Anne Kallioniemi; Saila Kauppila; Jenni Nikkilä; Veli-Matti Kosma; Arto Mannermaa; Roger A Greenberg; Robert Winqvist
Journal:  Sci Transl Med       Date:  2012-02-22       Impact factor: 17.956

  1 in total

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