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The risk for developing cancer in Israeli ATM, BLM, and FANCC heterozygous mutation carriers.
Laitman, Yael; Boker-Keinan, Lital; Berkenstadt, Michal; Liphsitz, Irena; Weissglas-Volkov, Daphna; Ries-Levavi, Liat; Sarouk, Ifat; Pras, Elon; Friedman, Eitan.
Afiliación
  • Laitman Y; Susanne Levy Gertner Oncogenetics Unit, Sheba Medical Center, Tel-Hashomer, Israel.
  • Boker-Keinan L; Israel National Cancer Registry (INCR), Ministry of Health, Jerusalem, Israel; School of Public Health, Haifa University, Haifa, Israel.
  • Berkenstadt M; Institute of Human Genetics, Sheba Medical Center, Tel-Hashomer, Israel.
  • Liphsitz I; Israel National Cancer Registry (INCR), Ministry of Health, Jerusalem, Israel.
  • Weissglas-Volkov D; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Ries-Levavi L; Institute of Human Genetics, Sheba Medical Center, Tel-Hashomer, Israel.
  • Sarouk I; National AT Clinic, Sheba Medical Center, Tel-Hashomer, Israel.
  • Pras E; Institute of Human Genetics, Sheba Medical Center, Tel-Hashomer, Israel.
  • Friedman E; Susanne Levy Gertner Oncogenetics Unit, Sheba Medical Center, Tel-Hashomer, Israel; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel. Electronic address: eitan.friedman@sheba.health.gov.il.
Cancer Genet ; 209(3): 70-4, 2016 Mar.
Article en En | MEDLINE | ID: mdl-26778106
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Proteína del Grupo de Complementación C de la Anemia de Fanconi / RecQ Helicasas / Proteínas de la Ataxia Telangiectasia Mutada / Heterocigoto / Mutación / Neoplasias Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Genet Año: 2016 Tipo del documento: Article País de afiliación: Israel

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Proteína del Grupo de Complementación C de la Anemia de Fanconi / RecQ Helicasas / Proteínas de la Ataxia Telangiectasia Mutada / Heterocigoto / Mutación / Neoplasias Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Genet Año: 2016 Tipo del documento: Article País de afiliación: Israel