Literature DB >> 20113834

Three-way translocation involving MLL, MLLT1, and a novel third partner, NRXN1, in a patient with acute lymphoblastic leukemia and t(2;19;11) (p12;p13.3;q23).

Sang-Guk Lee1, Tae Sung Park, Sung Chul Won, Jaewoo Song, Kyung-A Lee, Jong Rak Choi, Rolf Marschalek, Claus Meyer.   

Abstract

Translocations involving mixed lineage leukemia (MLL) gene at 11q23 are associated with de novo acute leukemia as well as therapy-related acute leukemia. More than 100 different translocations involving MLL have been described in acute leukemia, with more than 60 translocation partner genes characterized on the molecular level. In addition to various simple translocations affecting MLL, there are also complex forms involving three or more chromosomes. Here, we describe a novel three-way translocation of t(2;19;11)(p12;p13.3;q23) in a patient with acute lymphoblastic leukemia (ALL). In this translocation, the distal 19p13.3 joins the proximal 11q23 on der(11), whereas the distal 11q23 is translocated to 2p12. Three-way translocations involving 11q23 are often difficult to detect with cytogenetic means alone. In the present case, however, the chromosomes involved in the three-way translocation were readily identifiable by GTG banding. The MLL-MLLT1 fusion products from the derivative chromosome 11 were detected by reverse transcriptase-polymerase chain reaction (RT-PCR), and two splicing variant forms were confirmed by cloning and sequencing. Furthermore, the novel third partner gene, NRXN1, was detected by systematic breakpoint analysis using long-distance inverse-PCR methods (LDI-PCR). The apparent three-way translocation thus identified is noteworthy because few studies have reported complex rearrangements involving 11q23 and 19p13.3 in acute leukemias. Copyright (c) 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20113834     DOI: 10.1016/j.cancergencyto.2009.10.009

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


  5 in total

1.  Diagnostic usefulness of genomic breakpoint analysis of various gene rearrangements in acute leukemias: a perspective of long distance- or long distance inverse-PCR-based approaches.

Authors:  John Jeongseok Yang; Rolf Marschalek; Claus Meyer; Tae Sung Park
Journal:  Ann Lab Med       Date:  2012-06-20       Impact factor: 3.464

2.  Evaluation of Cytogenetic Abnormalities in Patients with Acute Lymphoblastic Leukemia.

Authors:  Pavan Reddy; Ramesh Shankar; Teena Koshy; Venkatraman Radhakrishnan; Prasanth Ganesan; P K Jayachandran; Manikandan Dhanushkodi; Nikita Mehra; S Krupashankar; P Manasa; R P Nagare; R Swaminathan; Krishnarathinam Kannan; T G Sagar; T S Ganesan
Journal:  Indian J Hematol Blood Transfus       Date:  2019-04-17       Impact factor: 0.900

3.  Increased Risk of Acute Myelogenous Leukemia After Early Onset but Not Late-Onset Colorectal Cancer.

Authors:  Steven Lehrer; Peter H Rheinstein
Journal:  Am J Clin Oncol       Date:  2020-04       Impact factor: 2.787

4.  Simultaneous involvement of 11q23 translocation resulting in chimeric MLL-AFF1 and a second translocation [t (9;21) (p13; p11.2)] in an infant acute lymphoblastic leukemia patient at relapse: A case report.

Authors:  Guangming Liu; Xianglan Lu; Young Mi Kim; Xianfu Wang; Shibo Li; Yuanyuan Liu
Journal:  Medicine (Baltimore)       Date:  2018-05       Impact factor: 1.889

5.  Identification of Key Genes and Pathways Associated with RUNX1 Mutations in Acute Myeloid Leukemia Using Bioinformatics Analysis.

Authors:  Fangxiao Zhu; Rui Huang; Jing Li; Xiwen Liao; Yumei Huang; Yongrong Lai
Journal:  Med Sci Monit       Date:  2018-10-05
  5 in total

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