Literature DB >> 15488637

Analysis of familial male breast cancer for germline mutations in CHEK2.

Nayanta Sodha1, Charlotte Wilson, Sarah L Bullock, Hazel Phillimore, Richard S Houlston, Rosalind A Eeles.   

Abstract

We have previously shown that the1100delC variant of the cell-cycle-checkpoint kinase gene CHEK2, which is carried by approximately 1% of the population confers a two-fold increase in female breast cancer and a 10-fold increase in male breast cancer. To extend our knowledge on the role of CHEK2 in susceptibility to male breast cancer we have screened a series of 26 breast cancer cases with male representation for germline sequence variation in the CHEK2 gene. One individual was found to harbour the 1100delC variant. No other mutations were identified. Variants other than 1100delC are rare in male breast cancer.

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Year:  2004        PMID: 15488637     DOI: 10.1016/j.canlet.2004.07.002

Source DB:  PubMed          Journal:  Cancer Lett        ISSN: 0304-3835            Impact factor:   8.679


  2 in total

1.  Strictly defined familial male breast cancer.

Authors:  Uwe Güth; Dieter Müller; Dorothy Jane Huang; Ellen Obermann; Hansjakob Müller
Journal:  Fam Cancer       Date:  2011-03       Impact factor: 2.375

2.  A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers.

Authors:  Deborah Thompson; Sheila Seal; Mieke Schutte; Lesley McGuffog; Rita Barfoot; Anthony Renwick; Rosalind Eeles; Nayanta Sodha; Richard Houlston; Susan Shanley; Jan Klijn; Marijke Wasielewski; Jenny Chang-Claude; P Andrew Futreal; Barbara L Weber; Katherine L Nathanson; Michael Stratton; Hanne Meijers-Heijboer; Nazneen Rahman; Douglas F Easton
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2006-12       Impact factor: 4.254

  2 in total

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