JAK2 and genomic instability in the myeloproliferative neoplasms: A case of the chicken or the egg?

被引:17
作者
Scott, Linda M. [1 ,2 ,3 ]
Rebel, Vivienne I. [1 ,2 ,4 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Greehey Childrens Canc Res Inst, San Antonio, TX 78229 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Canc Therapy & Res Ctr, San Antonio, TX 78229 USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, San Antonio, TX 78229 USA
[4] Univ Texas Hlth Sci Ctr San Antonio, Dept Cellular & Struct Biol, San Antonio, TX 78229 USA
关键词
METHYLTRANSFERASE GENE EZH2; CHRONIC MYELOID-LEUKEMIA; TYROSINE KINASE JAK2; POLYCYTHEMIA-VERA; HEMATOPOIETIC STEM; V617F MUTATION; EXON-12; MUTATIONS; DNA-DAMAGE; BCR-ABL; ESSENTIAL THROMBOCYTHEMIA;
D O I
10.1002/ajh.23243
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The myeloproliferative neoplasms (MPNs) are a particularly useful model for studying mutation accumulation in neoplastic cells, and the mechanisms underlying their acquisition. This review summarizes our current understanding of the molecular defects present in patients with an MPN, and the effects of mutations targeting Janus kinase 2 (JAK2)-mediated intracellular signaling on DNA damage and on the elimination of mutation-bearing cells by programmed cell death. Moreover, we discuss findings that suggest that the acquisition of disease-initiating mutations in hematopoietic stem cells of some MPN patients may be the consequence of an inherent genomic instability that was not previously appreciated. Am. J. Hematol. 2012. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:1028 / 1036
页数:9
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