Phospho-STAT5 expression pattern with the MPL W515L mutation is similar to that seen in chronic myetoproliferative disorders with JAK2 V617F

被引:10
作者
Gibson, Sarah E. [1 ]
Schade, Andrew E. [1 ]
Szpurka, Hadrian [2 ]
Bak, Beata [2 ]
Maciejewski, Jaroslaw P. [2 ]
Hsi, Eric D. [1 ]
机构
[1] Cleveland Clin, Dept Clin Pathol, Cleveland, OH 44195 USA
[2] Cleveland Clin, Taussig Canc Ctr, Expt Hematol & Hematopoiesis Sect, Cleveland, OH 44195 USA
关键词
phospho-STAT5; MPL W515L; chronic myeloproliferative disorders;
D O I
10.1016/j.humpath.2007.10.034
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Abnormal nuclear megakaryocytic staining for phospho-STAT5 (pSTAT5) correlates with JAK2 V617F mutational status in non-chronic myelogenous leukemia chronic myeloproliferative disorders. However, a proportion of wild-type JAK2 non-chronic myelogenous leukemia chronic myeloproliferative disorders cases also demonstrate this abnormal pSTAT5 expression pattern. We report a patient with a JAK2 V617F-negative myeloproliferative/myelodysplastic syndrome who had abnormal megakaryocytic pSTAT5 expression and a MPL W515L mutation. The patient was a 71-year-old man with anemia and thrombocythemia on laboratory examination. His peripheral blood smear demonstrated occasional dysplastic neutrophils. Bone marrow biopsy revealed hypercellular marrow with features consistent with myeloproliferative/myelodysplastic syndrome. Immunohistochemistry for pSTAT5 showed abnormal nuclear megakaryocyte positivity. Cytogenetic analysis revealed a normal karyotype, fluorescence in situ hybridization for BCR-ABL was negative, and JAK2 genotyping demonstrated wild-type JAK2. However, MPL genotyping showed a MPL W515L mutation. Abnormal nuclear megakaryocytic staining for pSTAT5 expression, previously associated with the JAK2 V617F mutation, is also associated with MPL W515L, likely reflecting activation of the JAK-STAT signaling pathway. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1111 / 1114
页数:4
相关论文
共 11 条
[1]   Bone marrow phospho-STAT5 expression in non-CML chronic myeloproliferative disorders correlates with JAK2 V617F mutation and provides evidence of in vivo JAK2 activation [J].
Aboudola, Samer ;
Murugesan, Guruanthan ;
Szpurka, Hadrian ;
Ramsingh, Giri ;
Zhao, Xiaoxian ;
Prescott, Nichole ;
Tubbs, Raymond R. ;
Maciejewski, Jaroslaw P. ;
Hsi, Eric D. .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2007, 31 (02) :233-239
[2]   Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders [J].
Baxter, EJ ;
Scott, LM ;
Campbell, PJ ;
East, C ;
Fourouclas, N ;
Swanton, S ;
Vassiliou, GS ;
Bench, AJ ;
Boyd, EM ;
Curtin, N ;
Scott, MA ;
Erber, WN ;
Green, AR .
LANCET, 2005, 365 (9464) :1054-1061
[3]   In vitro interaction between STAT5 and JAK2;: dependence upon phosphorylation status of STAT5 and JAK2 [J].
Flores-Morales, A ;
Pircher, TJ ;
Silvennoinen, O ;
Gustafsson, JÅ ;
Sanchez-Gomez, M ;
Norstedt, G ;
Haldosén, LA ;
Wood, TJJ .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1998, 138 (1-2) :1-10
[4]   Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders [J].
Jones, AV ;
Kreil, S ;
Zoi, K ;
Waghorn, K ;
Curtis, C ;
Zhang, LY ;
Score, J ;
Seear, R ;
Chase, AJ ;
Grand, FH ;
White, H ;
Zoi, C ;
Loukopoulos, D ;
Terpos, E ;
Vervessou, EC ;
Schultheis, B ;
Emig, M ;
Ernst, T ;
Lengfelder, E ;
Hehlmann, R ;
Hochhaus, A ;
Oscier, D ;
Silver, RT ;
Reiter, A ;
Cross, NCP .
BLOOD, 2005, 106 (06) :2162-2168
[5]   Expression of a homodimeric type I cytokine receptor is required for JAK2V617F-mediated transformation [J].
Lu, XH ;
Levine, R ;
Tong, W ;
Wernig, G ;
Pikman, Y ;
Zarnegar, S ;
Gilliland, DG ;
Lodish, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (52) :18962-18967
[6]   Identification of the JAK2 V617F mutation in chronic myeloproliferative disorders using FRET probes and melting curve analysis [J].
Murugesan, G ;
Aboudola, S ;
Szpurka, H ;
Verbic, MA ;
Maciejewski, JP ;
Tubbs, RR ;
Hsi, ED .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2006, 125 (04) :625-633
[7]   MPL515 mutations in myeloproliferative and other myeloid disorders:: a study of 1182 patients [J].
Pardanani, Animesh D. ;
Levine, Ross L. ;
Lasho, Terra ;
Pikman, Yana ;
Mesa, Ruben A. ;
Wadleigh, Martha ;
Steensma, David P. ;
Elliott, Michelle A. ;
Wolanskyj, Alexandra R. ;
Hogan, William J. ;
McClure, Rebecca F. ;
Litzow, Mark R. ;
Gilliland, D. Gary ;
Tefferi, Ayalew .
BLOOD, 2006, 108 (10) :3472-3476
[8]   MPLW515L is anovel somatic activating mutation in myelofibrosis with myeloid metaplasia [J].
Pikman, Yana ;
Lee, Benjamin H. ;
Mercher, Thomas ;
McDowell, Elizabeth ;
Ebert, Benjamin L. ;
Gozo, Maricel ;
Cuker, Adam ;
Wernig, Gerlinde ;
Moore, Sandra ;
Galinsky, Ilene ;
DeAngelo, Daniel J. ;
Clark, Jennifer J. ;
Lee, Stephanie J. ;
Golub, Todd R. ;
Wadleigh, Martha ;
Gilliland, D. Gary ;
Levine, Ross L. .
PLOS MEDICINE, 2006, 3 (07) :1140-1151
[9]   JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis [J].
Scott, Linda M. ;
Tong, Wei ;
Levine, Ross L. ;
Scott, Mike A. ;
Beer, Philip A. ;
Stratton, Michael R. ;
Futreal, P. Andrew ;
Erber, Wendy N. ;
McMullin, Mary Frances ;
Harrison, Claire N. ;
Warren, Alan J. ;
Gilliland, D. Gary ;
Lodish, Harvey F. ;
Green, Anthony R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (05) :459-468
[10]   Erythropoietin can induce the expression of Bcl-xL through Stat5 in erythropoietin-dependent progenitor cell lines [J].
Silva, M ;
Benito, A ;
Sanz, C ;
Prosper, F ;
Ekhterae, D ;
Nuñez, G ;
Fernandez-Luna, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (32) :22165-22169