Literature DB >> 16411093

Exclusion/confirmation of ataxia-telangiectasia via cell-cycle testing.

Tilman Heinrich1, Carolin Prowald, Richard Friedl, Benni Gottwald, Reinhard Kalb, Kornelia Neveling, Sabine Herterich, Holger Hoehn, Detlev Schindler.   

Abstract

Ataxia telangiectasia (AT) is an autosomal recessive multisystem disorder with increased radiosensitivity and cancer susceptibility. The responsible gene (ATM) consists of 66 exons and a coding region of 9171 bp which precludes direct sequencing as a screening assay for confirmation or exclusion of the clinical suspicion of AT. Peripheral blood mononuclear cells of 330 patients referred for the exclusion of AT were exposed to ionizing radiation (IR) and incubated for 72 h in the presence of phytohemagglutinin. Using bivariate BrdU-Hoechst/ethidium bromide flowcytometry, the following cell cycle parameters were ascertained: (1) proportion of non-proliferating (G0,G1) cells as a measure of mitogen response, (2) proportion of first-cycle G2-phase cells relative to the growth fraction (G2/GF) as a measure of radiosensitivity. Of the cases tested, 94.2% could be unequivocally assigned either to the AT-negative or the AT-positive group of patients. Of the AT-positive cases, 11 were confirmed by ATM mutation analysis. Nineteen cases presented with non-conclusive results, mostly due to poor mitogen response; however, a combination of cell-cycle data with serum AFP concentrations led to the exclusion of AT in all but two of the uncertain cases. Substitution of ionizing radiation by the radiomimetic bleomycin was additionally tested in a small series of patients. We conclude that cell-cycle testing complemented by serum AFP measurements fulfills the criteria as a rapid and economical screening procedure for the differential diagnosis of juvenile ataxias.

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Year:  2006        PMID: 16411093     DOI: 10.1007/s00431-005-0037-4

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  45 in total

1.  Radiosensitivity of ataxia-telangiectasia, X-linked agammaglobulinemia, and related syndromes using a modified colony survival assay.

Authors:  Y K Huo; Z Wang; J H Hong; L Chessa; W H McBride; S L Perlman; R A Gatti
Journal:  Cancer Res       Date:  1994-05-15       Impact factor: 12.701

2.  Interstitial lung disease in patients with ataxia-telangiectasia.

Authors:  Scott A Schroeder; Michael Swift; Claudio Sandoval; Claire Langston
Journal:  Pediatr Pulmonol       Date:  2005-06

3.  Genotype-phenotype relationships in ataxia-telangiectasia and variants.

Authors:  S Gilad; L Chessa; R Khosravi; P Russell; Y Galanty; M Piane; R A Gatti; T J Jorgensen; Y Shiloh; A Bar-Shira
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

4.  Defective anti-polysaccharide antibody response in patients with ataxia-telangiectasia.

Authors:  Ozden Sanal; Filiz Ozbaş-Gerçeker; Leman Yel; Fügen Ersoy; Ilhan Tezcan; A Izzet Berkel; Ayşe Metin; Richard A Gatti
Journal:  Turk J Pediatr       Date:  2004 Jul-Sep       Impact factor: 0.552

5.  Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.

Authors:  D Moshous; I Callebaut; R de Chasseval; B Corneo; M Cavazzana-Calvo; F Le Deist; I Tezcan; O Sanal; Y Bertrand; N Philippe; A Fischer; J P de Villartay
Journal:  Cell       Date:  2001-04-20       Impact factor: 41.582

6.  Immunoassay to measure ataxia-telangiectasia mutated protein in cellular lysates.

Authors:  Anthony W Butch; Helen H Chun; Shareef A Nahas; Richard A Gatti
Journal:  Clin Chem       Date:  2004-10-14       Impact factor: 8.327

Review 7.  Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaks.

Authors:  Martin Digweed; Karl Sperling
Journal:  DNA Repair (Amst)       Date:  2004 Aug-Sep

Review 8.  Ataxia-telangiectasia-like disorder (ATLD)-its clinical presentation and molecular basis.

Authors:  A M R Taylor; A Groom; P J Byrd
Journal:  DNA Repair (Amst)       Date:  2004 Aug-Sep

9.  Independent mutational events are rare in the ATM gene: haplotype prescreening enhances mutation detection rate.

Authors:  Midori Mitui; Catarina Campbell; Gabriela Coutinho; Xia Sun; Chih-Hung Lai; Yvonne Thorstenson; Sergi Castellvi-Bel; Luis Fernandez; Eugenia Monros; Beatriz Tavares Costa Carvalho; Oscar Porras; Gumersindo Fontan; Richard A Gatti
Journal:  Hum Mutat       Date:  2003-07       Impact factor: 4.878

10.  Early diagnosis of ataxia-telangiectasia using radiosensitivity testing.

Authors:  Xia Sun; Sara G Becker-Catania; Helen H Chun; Mee Jeong Hwang; Yong Huo; Zhijun Wang; Midori Mitui; Ozden Sanal; Luciana Chessa; Barbara Crandall; Richard A Gatti
Journal:  J Pediatr       Date:  2002-06       Impact factor: 4.406

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  2 in total

1.  Characterisation of ATM mutations in Slavic Ataxia telangiectasia patients.

Authors:  Jana Soukupova; Petr Pohlreich; Eva Seemanova
Journal:  Neuromolecular Med       Date:  2011-08-11       Impact factor: 3.843

2.  Cancer in Children With Fanconi Anemia and Ataxia-Telangiectasia-A Nationwide Register-Based Cohort Study in Germany.

Authors:  Christina M Dutzmann; Claudia Spix; Isabell Popp; Melanie Kaiser; Friederike Erdmann; Miriam Erlacher; Thilo Dörk; Detlev Schindler; Reinhard Kalb; Christian P Kratz
Journal:  J Clin Oncol       Date:  2021-10-01       Impact factor: 44.544

  2 in total

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