Journal article
Lethal giant larvae 1 tumour suppressor activity is not conserved in models of mammalian T and B cell leukaemia
ED Hawkins, J Oliaro, KM Ramsbottom, SB Ting, F Sacirbegovic, M Harvey, T Kinwell, J Ghysdael, RW Johnstone, PO Humbert, SM Russell
Plos One | Published : 2014
Abstract
In epithelial and stem cells, lethal giant larvae (Lgl) is a potent tumour suppressor, a regulator of Notch signalling, and a mediator of cell fate via asymmetric cell division. Recent evidence suggests that the function of Lgl is conserved in mammalian haematopoietic stem cells and implies a contribution to haematological malignancies. To date, direct measurement of the effect of Lgl expression on malignancies of the haematopoietic lineage has not been tested. In Lgl1-/- mice, we analysed the development of haematopoietic malignancies either alone, or in the presence of common oncogenic lesions. We show that in the absence of Lgl1, production of mature white blood cell lineages and long-ter..
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Funding Acknowledgements
The work was funded by the Australian National Health and Medical Research Council (NHRMC, project grants and fellowships to EDH, JO, SMR, POH, RWJ, SBT), the Human Frontiers Science Program, the Australian Research Council (ARC, fellowship to SMR) and the Australian Cancer Research Foundation (ACRF, ACRF Cell Biology Program). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.