CHEK2*1100DELC Variant and Breast Cancer Risk
Abstract
We propose to examine the association between the CHEK2*1 lOOdeIC gene variant and breast cancer among BRCAi/2- negative families. Vital to DNA replication and normal growth of breast cells (like all other cells in the body) is their ability to detect aberrations/damage in the DNA and subsequently to halt the replication process correct errors if possible and either resume normal cell replication or initiate cell death. The CHEK2 gene the human ortholog of yeast Cds1 and Rad53 encodes a cell-cycle checkpoint kinase that plays a role in DNA repair processes involving BRCA1 and p53 and is thus a candidate gene for familial breast cancer and Li-Fraumeni Syndromes (LFS). The proposed study by examining CHEK2 in familial breast cancer will provide additional knowledge to enhance our understanding of the role of CHEK2 gene in breast cancer. By estimating the absolute and relative risk of breast cancer in relation to the CHEK2*i 1 00delC variant the proposed study will offer direct evidence on assessing genetic risk of familial breast cancer.
Document Details
- Document Type
- Technical Report
- Publication Date
- Oct 01, 2006
- Accession Number
- ADA471716
Entities
People
- Habibul Ahsan
Organizations
- Columbia University