LMO2 at 25 years: a paradigm of chromosomal translocation proteins

Journal article : Review

LMO2 was first discovered through proximity to frequently occurring chromosomal translocations in T cell acute lymphoblastic leukaemia (T-ALL). Subsequent studies on its role in tumours and in normal settings have highlighted LMO2 as an archetypical chromosomal translocation oncogene, activated by association with antigen receptor gene loci and a paradigm for translocation gene activation in T-ALL. The normal function of LMO2 in haematopoietic cell fate and angiogenesis suggests it is a master gene regulator exerting a dysfunctional control on differentiation following chromosomal translocations. Its importance in T cell neoplasia has been further emphasized by the recurrent findings of interstitial deletions of chromosome 11 near LMO2 and of LMO2 as a target of retroviral insertion gene activation during gene therapy trials for X chromosome-linked severe combined immuno-deficiency syndrome, both types of event leading to similar T cell leukaemia. The discovery of LMO2 in some B cell neoplasias and in some epithelial cancers suggests a more ubiquitous function as an oncogenic protein, and that the current development of novel inhibitors will be of great value in future cancer treatment. Further, the role of LMO2 in angiogenesis and in haematopoietic stem cells (HSCs) bodes well for targeting LMO2 in angiogenic disorders and in generating autologous induced HSCs for application in various clinical indications.

Authors: Chambers, J; Rabbitts, TH

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: The Royal Society
• Journal: Open Biology
• Volume: 5
• Issue: 6
• Article number: 150062
• Publication date: 2015-01-01
• Acceptance date: 2015-05-29
• DOI: 10.1098/rsob.150062
• EISSN: 2046-2441
• Language: English
• Keywords: leukaemia; angiogenesis; haematopoiesis; chromosomal translocations; LMO2; X chromosome-linked severe combined immuno-deficiency syndrome
• Subtype: Review