Literature DB >> 18674656

Gynecologic malignancies in Ashkenazi families with the MSH2 A636P founder mutation.

Ofer Lavie1, Stephen B Gruber, Flavio Lejbkowicz, Sara Dishon, Gad Rennert.   

Abstract

OBJECTIVE: A founder mutation A636P in the MSH2 gene was found to be related to hereditary nonpolyposis colorectal cancer in Ashkenazi Jews. Although the incidence of colorectal cancer in carriers is relatively well established, the frequency of other tumors is less clear. STUDY
DESIGN: We studied a consecutive series of 19 carrier families that were cared for by the Clalit Health Studies National Familial Cancer Consultation Service, most of whom were identified through a population-based case-control study of colorectal cancer in northern Israel.
RESULTS: Gynecologic cancers, 88% of which (28 cases) were endometrial cancers, were diagnosed in 78.9% of the carrier families and in 26.2% of the women who were at risk, with a mean age at diagnosis of 51.2 years. Forty-six percent of the women with endometrial cancer reported at least 1 other primary tumor.
CONCLUSION: Genetic counseling and testing for the MSH2 A636P mutation is indicated for Ashkenazi Jewish women with an endometrial cancer, especially if the cancer is detected before the age of 70 years in women with a personal or family history of colorectal cancer.

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Year:  2008        PMID: 18674656     DOI: 10.1016/j.ajog.2008.02.018

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN: 0002-9378            Impact factor:   8.661


  3 in total

1.  High risk of colorectal and endometrial cancer in Ashkenazi families with the MSH2 A636P founder mutation.

Authors:  Bhramar Mukherjee; Gad Rennert; Jaeil Ahn; Sara Dishon; Flavio Lejbkowicz; Hedy S Rennert; Stacey Shiovitz; Victor Moreno; Stephen B Gruber
Journal:  Gastroenterology       Date:  2011-03-16       Impact factor: 22.682

2.  Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome.

Authors:  L Raskin; F Schwenter; M Freytsis; M Tischkowitz; N Wong; G Chong; S A Narod; D A Levine; F Bogomolniy; M Aronson; S N Thibodeau; K S Hunt; G Rennert; S Gallinger; S B Gruber; W D Foulkes
Journal:  Clin Genet       Date:  2010-12-14       Impact factor: 4.438

Review 3.  Hereditary cancer screening: Case reports and review of literature on ten Ashkenazi Jewish founder mutations.

Authors:  Devin M Cox; Katherine L Nelson; Meera Clytone; Debra L Collins
Journal:  Mol Genet Genomic Med       Date:  2018-08-27       Impact factor: 2.183

  3 in total

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