CHEK2 mutations and the risk of papillary thyroid cancer

M Siołek, C Cybulski, D Gąsior‐Perczak… - … Journal of Cancer, 2015 - Wiley Online Library
Mutations in the cell cycle checkpoint kinase 2 (CHEK2) tumor suppressor gene are
associated with multi‐organ cancer susceptibility including cancers of the breast and …

The c.470 T > C CHEK2 missense variant increases the risk of differentiated thyroid carcinoma in the Great Poland population

M Kaczmarek-Ryś, K Ziemnicka… - Hereditary cancer in …, 2015 - Springer
Background Differentiated thyroid carcinoma (DTC) originates from thyroid follicular
epithelial cells and belongs to a group of slowly progressing tumors with a relatively good …

CHEK2 is a multiorgan cancer susceptibility gene

C Cybulski, B Gorski, T Huzarski, B Masojć… - The American Journal of …, 2004 - cell.com
A single founder allele of the CHEK2 gene has been associated with predisposition to
breast and prostate cancer in North America and Europe. The CHEK2 protein participates in …

Association of two mutations in the CHEK2 gene with breast cancer

N Bogdanova, N Enβen‐Dubrowinskaja… - … journal of cancer, 2005 - Wiley Online Library
The 1100delC mutation of the cell cycle checkpoint kinase 2 (CHEK2) gene confers an
increased risk for breast cancer, but the clinical impact of other CHEK2 gene variants …

CHEK2 variants in susceptibility to breast cancer and evidence of retention of the wild type allele in tumours

N Sodha, S Bullock, R Taylor, G Mitchell… - British journal of …, 2002 - nature.com
We have recently shown that the CHEK2* 1100delC mutation acts as a low penetrance
breast cancer susceptibility allele. To investigate if other CHEK2 variants confer an …

Frequency of the CHEK2 1100delC Mutation among Women with Breast Cancer: An International Study

S Zhang, CM Phelan, P Zhang, F Rousseau… - Cancer Research, 2008 - AACR
A founder allele in the CHEK2 gene (1100delC) has been associated with an elevated risk
of breast cancer. This allele is responsible for the majority of CHEK2-associated breast …

Increased Risk for Other Cancers in Addition to Breast Cancer for CHEK2*1100delC Heterozygotes Estimated From the Copenhagen General Population Study

C Näslund-Koch, BG Nordestgaard… - Journal of Clinical …, 2016 - ascopubs.org
Purpose CHEK2 is a cell cycle checkpoint regulator, and the CHEK2* 1100delC germline
mutation leads to loss of function and increased breast cancer risk. It seems plausible that …

[HTML][HTML] Breast cancer risk is similar for CHEK2 founder and non-founder mutation carriers

TP Leedom, H LaDuca, R McFarland, S Li, JS Dolinsky… - Cancer genetics, 2016 - Elsevier
Highlights•Compared phenotypes of founder and non-founder CHEK2 mutation carriers.•No
significant phenotypic differences were observed between founders and non …

Correlation of CHEK2 protein expression and c. 1100delC mutation status with tumor characteristics among unselected breast cancer patients

O Kilpivaara, J Bartkova, H Eerola… - … journal of cancer, 2005 - Wiley Online Library
The CHEK2 kinase is a tumor suppressor whose activation in response to DNA double‐
strand breaks contributes to cell cycle arrest or apoptosis. The c. 1100delC mutation is …

CHEK2* 1100delC homozygosity is associated with a high breast cancer risk in women

MA Adank, MA Jonker, I Kluijt, SE van Mil… - Journal of medical …, 2011 - jmg.bmj.com
Background Mutations in the CHEK2 gene confer a moderately increased breast cancer risk.
The risk for female carriers of the CHEK2* 1100delC mutation is twofold increased. Breast …