Author
Listed:
- Wei Guo
(Department of Molecular and Medical Pharmacology,)
- Joseph L. Lasky
(Department of Pediatric Hematology/Oncology,)
- Chun-Ju Chang
(Department of Molecular and Medical Pharmacology,)
- Sherly Mosessian
(Department of Molecular and Medical Pharmacology,)
- Xiaoman Lewis
(Department of Molecular and Medical Pharmacology,)
- Yun Xiao
(University of Colorado Cancer Center, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA)
- Jennifer E. Yeh
(Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA)
- James Y. Chen
(Department of Molecular and Medical Pharmacology,)
- M. Luisa Iruela-Arispe
(and)
- Marileila Varella-Garcia
(University of Colorado Cancer Center, University of Colorado Health Sciences Center, Denver, Colorado 80262, USA)
- Hong Wu
(Department of Molecular and Medical Pharmacology,
Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, Cellular and Developmental Biology, University of California, Los Angeles, Los Angeles, California 90095, USA)
Abstract
Cancer model: Pten deletion mimics acute T lymphoblastic leukaemia A new leukaemia model has been established in mice by deleting the Pten tumour suppressor gene in fetal liver haematopoietic stem cells. The mice develop a myeloproliferative disorder that can lead to acute T lymphoblastic leukaemia. Progression of the condition is driven by leukaemia stem cells that require beta-catenin and incorporate a translocation that leads to overexpression of the c-myc oncogene, similar to findings in human acute T lymphoblastic leukaemia. The study illustrates how multiple genetic alterations can dictate hyperproliferative disorders and the progression to cancer.
Suggested Citation
Wei Guo & Joseph L. Lasky & Chun-Ju Chang & Sherly Mosessian & Xiaoman Lewis & Yun Xiao & Jennifer E. Yeh & James Y. Chen & M. Luisa Iruela-Arispe & Marileila Varella-Garcia & Hong Wu, 2008.
"Multi-genetic events collaboratively contribute to Pten-null leukaemia stem-cell formation,"
Nature, Nature, vol. 453(7194), pages 529-533, May.
Handle:
RePEc:nat:nature:v:453:y:2008:i:7194:d:10.1038_nature06933
DOI: 10.1038/nature06933
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