ARLTS1, potential candidate gene in familial aggregation of hematological malignancies.

Abstract:

INTRODUCTION:Genetic predisposition to familial hematological malignancies was previously described through several epidemiological analyses, but the genetic basis remains unclear. The tumor-suppressor ARLTS1 gene was previously described in sporadic hematological malignancies and familial cancer context. METHODS:In this study, we sequence the ARLTS1 gene in 100 patients belonging to 88 independent Tunisian and French families. RESULTS:After gene sequencing, we report 8 genetic variations, most of which were previously reported in several cancer forms. The most common variants were W149X and C148R and were previously associated to B-cell chronic lymphocytic leukemia and to high-risk of familial breast cancer. CONCLUSIONS:These results emphasize the fact that ARLTS1 gene mutations can be considered as a potential predisposing factor in familial hematological malignancies and other several cancer forms.

journal_name

Bull Cancer

journal_title

Bulletin du cancer

authors

Hamadou WS,Besbes S,Mani R,Bourdon V,Ben Youssef Y,Achour B,Regaieg H,Eisinger F,Mari V,Gesta P,Dreyfus H,Bonadona V,Dugast C,Zattara H,Faivre L,Noguchi T,Khélif A,Sobol H,Soua Z

doi

10.1016/j.bulcan.2016.10.016

subject

Has Abstract

pub_date

2017-02-01 00:00:00

pages

123-127

issue

2

eissn

0007-4551

issn

1769-6917

pii

S0007-4551(16)30283-1

journal_volume

104

pub_type

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