Literature DB >> 15120908

Acquired Robertsonian translocations are not rare events in acute leukemia and lymphoma.

Jeanna Welborn1.   

Abstract

Robertsonian translocations are the most common constitutional structural abnormalities but are rarely reported as acquired aberrations in hematologic malignancies. The nonhomologous acrocentric rearrangements are designated as Robertsonian translocations, whereas the homologous acrocentric rearrangements are referred to as isochromosomes. Robertsonian rearrangements have the highest mutation rates of structural chromosome rearrangements based on surveys of newborns and spontaneous abortions. It would be expected that Robertsonian recombinations would be more common than suggested by the literature. A survey of the cytogenetics database from a single institution found 17 patients with acquired Robertsonian rearrangement and hematologic malignancies. This is combined with data from the literature for a total of 237 patients. All of the possible types of Robertsonian rearrangements have been reported in hematologic malignancies, with the i(13q), i(14q), and i(21q) accounting for nearly 60%. Complex karyotypic changes are seen in the majority of cases, corresponding with disease evolution. These karyotypes consistently show loss of chromosomes 5 and/or 7 in the myelocytic disorders, nonacrocentric isochromosomes, and centromeric breakage and reunion. However, nearly 25% of the acquired rearrangements were found as the sole abnormality or in addition to an established cytogenetic aberration. Most of these were the i(14q) with the myelodysplasia subtypes refractory anemia and chronic myelomonocytic leukemia.

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Year:  2004        PMID: 15120908     DOI: 10.1016/j.cancergencyto.2003.09.019

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  9 in total

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Journal:  Bone Marrow Transplant       Date:  2015-07-20       Impact factor: 5.483

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3.  c-Myc-dependent formation of Robertsonian translocation chromosomes in mouse cells.

Authors:  Amanda Guffei; Zelda Lichtensztejn; Amanda Gonçalves Dos Santos Silva; Sherif F Louis; Andrea Caporali; Sabine Mai
Journal:  Neoplasia       Date:  2007-07       Impact factor: 5.715

4.  Telomere-centromere-driven genomic instability contributes to karyotype evolution in a mouse model of melanoma.

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Journal:  Int J Mol Sci       Date:  2021-04-21       Impact factor: 5.923

6.  Recurrent isochromosome 21 and multiple abnormalities in a patient suspected of having acute myeloid leukemia with eosinophilic differentiation -- a rare case from South India.

Authors:  Sangeetha Vijay; Santhi Sarojam; Sureshkumar Raveendran; Vani Syamala; Sreeja Leelakumari; Geetha Narayanan; Sreedharan Hariharan
Journal:  Chin J Cancer       Date:  2011-12-16

7.  Trisomy 14 as a sole chromosome abnormality is associated with older age, a heterogenous group of myeloid neoplasms with dysplasia, and a wide spectrum of disease progression.

Authors:  Wei Cui; Carlos E Bueso-Ramos; C Cameron Yin; Jianlan Sun; Su Chen; Ramya Muddasani; Gary Lu
Journal:  J Biomed Biotechnol       Date:  2011-01-20

8.  Mortality and Cancer Incidence in Carriers of Balanced Robertsonian Translocations: A National Cohort Study.

Authors:  Minouk J Schoemaker; Michael E Jones; Craig D Higgins; Alan F Wright; Anthony J Swerdlow
Journal:  Am J Epidemiol       Date:  2019-03-01       Impact factor: 4.897

9.  Chromosomal disruption and rearrangements during murine sarcoma development converge to stable karyotypic formation kept by telomerase overexpression.

Authors:  Robson José de Oliveira-Júnior; Carlos Ueira-Vieira; Angela Aparecida Servino Sena; Carolina Fernandes Reis; José Roberto Mineo; Luiz Ricardo Goulart; Sandra Morelli
Journal:  J Biomed Sci       Date:  2016-02-03       Impact factor: 8.410

  9 in total

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