4.3 Article

Acquired PTPN11 mutations occur rarely in adult patients with myelodysplastic syndromes and chronic myelomonocytic leukemia

Journal

LEUKEMIA RESEARCH
Volume 29, Issue 4, Pages 459-462

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.leukres.2004.10.001

Keywords

SHP-2; PTPN11; RAS signaling; MDS; CMML

Funding

  1. Telethon [GGP04172] Funding Source: Medline

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Myelodysplastic syndromes (MIDS) are comprised of a heterogeneous group of stem cell disorders characterized by ineffective hematopoiesis and susceptibility to transform to acute myeloid leukemia. The molecular pathways underlying disease initiation and evolution are still largely unknown. We recently demonstrated that acquired mutations in PTPN11 are a major event in JMML and occur with variable prevalence in children with other hematologic malignancies, including MDS. Here, we investigated contribution of PTPN11 mutations to adult MDS and CMML pathogenesis. Our results indicate that PTPN11 lesions might play a role in adult MDS/CMML pathogenesis but do not represent a major molecular event. (c) 2004 Elsevier Ltd. All rights reserved.

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