Literature DB >> 12702560

Heterozygosity for the BLM(Ash) mutation and cancer risk.

Sean P Cleary1, William Zhang, Nando Di Nicola, Melyssa Aronson, Jennifer Aube, Amanda Steinman, Riad Haddad, Mark Redston, Steven Gallinger, Steven A Narod, Robert Gryfe.   

Abstract

Bloom syndrome is an autosomal recessive disorder whose characteristics include an increased risk for many types of cancers. In contrast to the homozygous mutations of Bloom syndrome, heterozygous carriers of BLM mutations may be at increased risk for developing colorectal cancer. We have screened 2,333 Jewish individuals, including 497 individuals with colorectal cancer, 125 with adenomatous polyps, 767 with noncolorectal cancers and 944 controls for the truncating BLM(Ash) founder mutation. The BLM(Ash) mutation was carried by 0.80% of individuals with colorectal neoplasia, 0.87% of those with any type of cancer and 0.85% of controls. In addition to case-control data, we found no evidence to support a significant relationship between increased cancer risk and heterozygous BLM(Ash) mutations with respect to age of cancer diagnosis, tumor multiplicity or family cancer history.

Entities:  

Mesh:

Year:  2003        PMID: 12702560

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  18 in total

1.  Undefined familial colorectal cancer.

Authors:  Constantinos Pantelis Zambirinis; George Theodoropoulos; Maria Gazouli
Journal:  World J Gastrointest Oncol       Date:  2009-10-15

Review 2.  Genetic factors and colorectal cancer in Ashkenazi Jews.

Authors:  Gershon Y Locker; Henry T Lynch
Journal:  Fam Cancer       Date:  2004       Impact factor: 2.375

Review 3.  Bloom's Syndrome: Clinical Spectrum, Molecular Pathogenesis, and Cancer Predisposition.

Authors:  Christopher Cunniff; Jennifer A Bassetti; Nathan A Ellis
Journal:  Mol Syndromol       Date:  2016-11-05

4.  The Swedish family-cancer database: update, application to colorectal cancer and clinical relevance.

Authors:  Kari Hemminki; Charlotta Granström; Bowang Chen
Journal:  Hered Cancer Clin Pract       Date:  2005-01-15       Impact factor: 2.857

5.  Non-Bloom syndrome-associated partial and total loss-of-function variants of BLM helicase.

Authors:  Hamed Mirzaei; Kristina H Schmidt
Journal:  Proc Natl Acad Sci U S A       Date:  2012-11-05       Impact factor: 11.205

Review 6.  Human RecQ Helicases in DNA Double-Strand Break Repair.

Authors:  Huiming Lu; Anthony J Davis
Journal:  Front Cell Dev Biol       Date:  2021-02-25

7.  Heterozygous mutations in DNA repair genes and hereditary breast cancer: a question of power.

Authors:  Nathan A Ellis; Kenneth Offit
Journal:  PLoS Genet       Date:  2012-09-27       Impact factor: 5.917

8.  Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles.

Authors:  Ella R Thompson; Maria A Doyle; Georgina L Ryland; Simone M Rowley; David Y H Choong; Richard W Tothill; Heather Thorne; Daniel R Barnes; Jason Li; Jason Ellul; Gayle K Philip; Yoland C Antill; Paul A James; Alison H Trainer; Gillian Mitchell; Ian G Campbell
Journal:  PLoS Genet       Date:  2012-09-27       Impact factor: 5.917

9.  Genetic variation in the NBS1, MRE11, RAD50 and BLM genes and susceptibility to non-Hodgkin lymphoma.

Authors:  Johanna M Schuetz; Amy C MaCarthur; Stephen Leach; Agnes S Lai; Richard P Gallagher; Joseph M Connors; Randy D Gascoyne; John J Spinelli; Angela R Brooks-Wilson
Journal:  BMC Med Genet       Date:  2009-11-16       Impact factor: 2.103

10.  Multimeric BLM is dissociated upon ATP hydrolysis and functions as monomers in resolving DNA structures.

Authors:  Ya-Nan Xu; Nicolas Bazeille; Xiu-Yan Ding; Xi-Ming Lu; Peng-Ye Wang; Elisabeth Bugnard; Virginie Grondin; Shuo-Xing Dou; Xu Guang Xi
Journal:  Nucleic Acids Res       Date:  2012-08-09       Impact factor: 16.971

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