Literature DB >> 22932794

Interphase Chromosome Flow-FISH.

Keyvan Keyvanfar1, Jason Weed, Prashanth Swamy, Sachiko Kajigaya, Rodrigo T Calado, Neal S Young.   

Abstract

A 2-day method using flow cytometry and FISH for interphase cells was developed to detect monosomy 7 cells in myelodysplastic syndrome patients. The method, Interphase Chromosome Flow-FISH (IC Flow-FISH), involves fixation of leukocytes from blood, membrane permeabilization, hybridization of cellular DNA with peptide nucleic acid probes with cells intact, and analysis by flow cytometry. Hundreds to thousands of monosomy 7 cells were consistently detected from 10-20 mL of blood in patients with monosomy 7. Proportions of monosomy 7 cells detected in IC Flow-FISH were compared with results from conventional cytogenetics; identification of monosomy 7 populations was verified with FACS; and patient and donor cells were mixed to test for sensitivity. IC Flow-FISH allows for detecting monosomy 7 without requiring bone marrow procurement or the necessity of metaphase spreads, and wider applications to other chromosomal abnormalities are in development.

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Year:  2012        PMID: 22932794      PMCID: PMC3471523          DOI: 10.1182/blood-2012-05-434266

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  19 in total

1.  Nuclear flow FISH: isolation of cell nuclei improves the determination of telomere lengths.

Authors:  Matthias Wieser; Guido Stadler; Ernst Böhm; Nicole Borth; Hermann Katinger; Johannes Grillari; Regina Voglauer
Journal:  Exp Gerontol       Date:  2005-11-28       Impact factor: 4.032

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Journal:  Nat Biotechnol       Date:  1998-08       Impact factor: 54.908

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Authors:  Armand B Glassman; Kimberly J Hayes
Journal:  Cancer Genet Cytogenet       Date:  2005-04-01

4.  International scoring system for evaluating prognosis in myelodysplastic syndromes.

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Journal:  Blood       Date:  1997-03-15       Impact factor: 22.113

5.  Clonal analysis of myelodysplastic syndrome: monosomy 7 is expressed in the myeloid lineage, but not in the lymphoid lineage as detected by fluorescent in situ hybridization.

Authors:  W R Gerritsen; J Donohue; J Bauman; S C Jhanwar; N A Kernan; H Castro-Malaspina; R J O'Reilly; J H Bourhis
Journal:  Blood       Date:  1992-07-01       Impact factor: 22.113

6.  Hidden monosomy 7 in acute myeloid leukemia and myelodysplastic syndrome detected by interphase fluorescence in situ hybridization.

Authors:  M Arif; K Tanaka; C Damodaran; H Asou; T Kyo; H Dohy; N Kamada
Journal:  Leuk Res       Date:  1996-09       Impact factor: 3.156

7.  Quantum dots thermal stability improves simultaneous phenotype-specific telomere length measurement by FISH-flow cytometry.

Authors:  Veena Kapoor; Fran T Hakim; Najibah Rehman; Ronald E Gress; William G Telford
Journal:  J Immunol Methods       Date:  2009-03-05       Impact factor: 2.303

8.  The importance of diagnostic cytogenetics on outcome in AML: analysis of 1,612 patients entered into the MRC AML 10 trial. The Medical Research Council Adult and Children's Leukaemia Working Parties.

Authors:  D Grimwade; H Walker; F Oliver; K Wheatley; C Harrison; G Harrison; J Rees; I Hann; R Stevens; A Burnett; A Goldstone
Journal:  Blood       Date:  1998-10-01       Impact factor: 22.113

9.  Chromosome specific DNA hybridization in suspension for flow cytometric detection of chimerism in bone marrow transplantation and leukemia.

Authors:  G J Arkesteijn; S L Erpelinck; A C Martens; A Hagenbeek
Journal:  Cytometry       Date:  1995-04-01

10.  Telomere fluorescence measurements in granulocytes and T lymphocyte subsets point to a high turnover of hematopoietic stem cells and memory T cells in early childhood.

Authors:  N Rufer; T H Brümmendorf; S Kolvraa; C Bischoff; K Christensen; L Wadsworth; M Schulzer; P M Lansdorp
Journal:  J Exp Med       Date:  1999-07-19       Impact factor: 14.307

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