Literature DB >> 26778106

The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers.

Yael Laitman1, Lital Boker-Keinan2, Michal Berkenstadt3, Irena Liphsitz4, Daphna Weissglas-Volkov5, Liat Ries-Levavi3, Ifat Sarouk6, Elon Pras3, Eitan Friedman7.   

Abstract

Cancer risks in heterozygous mutation carriers of the ATM, BLM, and FANCC genes are controversial. To shed light on this issue, cancer rates were evaluated by cross referencing asymptomatic Israeli heterozygous mutation carriers in the ATM, BLM, and FANCC genes with cancer diagnoses registered at the Israeli National Cancer Registry (INCR). Comparison of observed to expected Standardized Incidence Rates (SIR) was performed. Overall, 474 individuals participated in the study: 378 females; 25 Arab and 31 Jewish ATM carriers, 152 BLM carriers, and 170 FANCC carriers (all Ashkenazim). Age range at genotyping was 19-53 years (mean + SD 30.6 + 5 years). In addition, 96 males were included; 5, 34, and 57 ATM, BLM, and FANCC mutation carriers, respectively. Over 5-16 years from genotyping (4721 person/years), 15 new cancers were diagnosed in mutation carriers: 5 breast, 4 cervical, 3 melanomas, and one each bone sarcoma, pancreatic, and colorectal cancer. No single cancer diagnosis was more prevalent then expected in all groups combined or per gene analyzed. Specifically breast cancer SIR was 0.02-0.77. We conclude that Israeli ATM, BLM, and FANCC heterozygous mutation carriers are not at an increased risk for developing cancer.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ATM; BLM; Cancer risks; FANCC; autosomal recessive; founder mutations; inherited cancer syndrome

Mesh:

Substances:

Year:  2015        PMID: 26778106     DOI: 10.1016/j.cancergen.2015.12.006

Source DB:  PubMed          Journal:  Cancer Genet


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