MSI2 protein expression predicts unfavorable outcome in acute myeloid leukemia

被引:88
作者
Byers, Richard J. [1 ,2 ,3 ]
Currie, Treeve [4 ]
Tholouli, Eleni [3 ,5 ]
Rodig, Scott J. [4 ]
Kutok, Jeffery L. [4 ]
机构
[1] Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Royal Infirm, Dept Histopathol, Manchester M13 9WL, Lancs, England
[2] Univ Manchester, Sch Canc & Enabling Sci, Fac Med & Human Sci, Manchester, Lancs, England
[3] Manchester Acad Hlth Sci Ctr, Manchester, Lancs, England
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Pathol, Boston, MA 02115 USA
[5] Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Royal Infirm, Dept Hematol, Manchester M13 9WL, Lancs, England
关键词
RNA-BINDING PROTEIN; HEMATOPOIETIC STEM-CELL; GENE-EXPRESSION; MARKER EXPRESSION; MESSENGER-RNA; MUSASHI; CANCER; FATE; NUMB; CLASSIFICATION;
D O I
10.1182/blood-2011-04-346767
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
MSI2 is highly expressed in human myeloid leukemia (AML) cell lines, and high expression of MSI2 mRNA is associated with decreased survival in AML, suggesting its use as a new prognostic marker. To test this, we measured MSI2 protein level by immunohistochemistry in 120 AML patients. Most cases (70%) showed some nuclear or cytoplasmic positivity, but the percentage of positive cells was low in most cases. Despite this, MSI2 protein expression was negatively associated with outcome, particularly for patients with good cytogenetic subgroup. For practical diagnostic purposes, the strongest significance of association was seen in cases with > 1% of cells showing strong MSI2 staining, these having a very poor outcome (P < .0001). Multivariate analysis with cytogenetic category, age, white cell count, and French-American-British subtype demonstrated that nuclear MSI2 levels were independently predictive of outcome (P = .0497). These results confirm the association of MSI2 expression with outcome in AML at the protein level and demonstrate the utility of MSI2 protein as a clinical prognostic biomarker. In addition, although positive at some level in most cases, its prognostic power derived from few positive cells, supporting its role in control of normal hematopoietic stem cell function and highlighting its role in disease progression. (Blood. 2011; 118(10): 2857-2867)
引用
收藏
页码:2857 / 2867
页数:11
相关论文
共 35 条
[1]  
Barbouti A, 2003, CANCER RES, V63, P1202
[2]   Use of gene-expression profiling to identify prognostic subclasses in adult acute myeloid leukemia [J].
Bullinger, L ;
Döhner, K ;
Bair, E ;
Fröhling, S ;
Schlenk, RF ;
Tibshirani, R ;
Döhner, H ;
Pollack, JR .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (16) :1605-1616
[3]   High levels of Notch signaling down-regulate Numb and Numblike [J].
Chapman, Gavin ;
Liu, Lining ;
Sahlgren, Cecilia ;
Dahlqvist, Camilla ;
Lenclahl, Urban .
JOURNAL OF CELL BIOLOGY, 2006, 175 (04) :535-540
[4]   Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European LeukemiaNet [J].
Doehner, Hartmut ;
Estey, Elihu H. ;
Amadori, Sergio ;
Appelbaum, Frederick R. ;
Buechner, Thomas ;
Burnett, Alan K. ;
Dombret, Herve ;
Fenaux, Pierre ;
Grimwade, David ;
Larson, Richard A. ;
Lo-Coco, Francesco ;
Naoe, Tomoki ;
Niederwieser, Dietger ;
Ossenkoppele, Gert J. ;
Sanz, Miguel A. ;
Sierra, Jorge ;
Tallman, Martin S. ;
Loewenberg, Bob ;
Bloomfield, Clara D. .
BLOOD, 2010, 115 (03) :453-474
[5]   Quantitative HOX expression in chromosomally defined subsets of acute myelogenous leukemia [J].
Drabkin, H ;
Parsy, C ;
Ferguson, K ;
Guilhot, F ;
Lacotte, L ;
Roy, L ;
Zeng, C ;
Baron, A ;
Hunger, SP ;
Varella-Garcia, M ;
Gemmill, R ;
Brizard, F ;
Brizard, A ;
Roche, J .
LEUKEMIA, 2002, 16 (02) :186-195
[6]   Association of a Leukemic Stem Cell Gene Expression Signature With Clinical Outcomes in Acute Myeloid Leukemia [J].
Gentles, Andrew J. ;
Plevritis, Sylvia K. ;
Majeti, Ravindra ;
Alizadeh, Ash A. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2010, 304 (24) :2706-2715
[7]   Molecular classification of cancer: Class discovery and class prediction by gene expression monitoring [J].
Golub, TR ;
Slonim, DK ;
Tamayo, P ;
Huard, C ;
Gaasenbeek, M ;
Mesirov, JP ;
Coller, H ;
Loh, ML ;
Downing, JR ;
Caligiuri, MA ;
Bloomfield, CD ;
Lander, ES .
SCIENCE, 1999, 286 (5439) :531-537
[8]   Notch 1 activation in the molecular pathogenesis of T-cell acute lymphoblastic leukaemia [J].
Grabher, C ;
von Boehmer, H ;
Look, AT .
NATURE REVIEWS CANCER, 2006, 6 (05) :347-359
[9]   The importance of diagnostic cytogenetics on outcome in AML: Analysis of 1,612 patients entered into the MRC AML 10 trial [J].
Grimwade, D ;
Walker, H ;
Oliver, F ;
Wheatley, K ;
Harrison, C ;
Harrison, G ;
Rees, J ;
Hann, I ;
Stevens, R ;
Burnett, A ;
Goldstone, A .
BLOOD, 1998, 92 (07) :2322-2333
[10]   Multi-genetic events collaboratively contribute to Pten-null leukaemia stem-cell formation [J].
Guo, Wei ;
Lasky, Joseph L. ;
Chang, Chun-Ju ;
Mosessian, Sherly ;
Lewis, Xiaoman ;
Xiao, Yun ;
Yeh, Jennifer E. ;
Chen, James Y. ;
Iruela-Arispe, M. Luisa ;
Varella-Garcia, Marileila ;
Wu, Hong .
NATURE, 2008, 453 (7194) :529-U7