Gene expression profile, pathways, and transcriptional system regulation in indolent systemic mastocytosis

被引:17
作者
Niedoszytko, M. [1 ,2 ]
Elberink, J. N. G. Oude [2 ]
Bruinenberg, M. [3 ]
Nedoszytko, B. [4 ]
de Monchy, J. G. R. [2 ]
Meerman, G. J. Te [3 ]
Weersma, R. K. [5 ]
Mulder, A. B. [6 ]
Jassem, E. [1 ]
van Doormaal, J. J. [2 ]
机构
[1] Med Univ Gdansk, Dept Allergol, PL-80952 Gdansk, Poland
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Allergol, Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands
[4] Med Univ Gdansk, Dept Dermatol, PL-80952 Gdansk, Poland
[5] Univ Groningen, Univ Med Ctr Groningen, Dept Gastroenterol & Hepatol, Groningen, Netherlands
[6] Univ Groningen, Univ Med Ctr Groningen, Dept Lab Med, Groningen, Netherlands
关键词
gene expression; gene profiling; mastocytosis; KIT MUTATION; C-KIT; PROTEIN; PROLIFERATION; DISORDERS; LEUKEMIA; FAMILY; BREAST; CANCER; CELLS;
D O I
10.1111/j.1398-9995.2010.02477.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
P>Background: Mastocytosis is an uncommon disease resulting from proliferation of abnormal mast cells infiltrating skin, bone marrow, liver, and other tissues. The aim of this study was to find differences in gene expression in peripheral blood cells of patients with indolent systemic mastocytosis compared to healthy controls. The second aim was to define a specific gene expression profile in patients with mastocytosis. Methods: Twenty-two patients with indolent systemic mastocytosis and 43 healthy controls were studied. Whole genome gene expression analysis was performed on RNA samples isolated from the peripheral blood. For amplification and labelling of the RNA, the Illumina TotalPrep 96 RNA Amplification Kit was used. Human HT-12_V3_expression arrays were processed. Data analysis was performed using GeneSpring, Genecodis, and Transcriptional System Regulators. Results: Comparison of gene expression between patients and controls revealed a significant difference (P < 0.05 corrected for multiple testing) and the fold change difference > 2 in gene expression in 2303 of the 48.794 analysed transcripts. Functional annotation indicated that the main pathways in which the differently expressed genes were involved are ubiquitin-mediated proteolysis, MAPK signalling pathway, pathways in cancer, and Jak-STAT signalling. The expression distributions for both groups did not overlap at all, indicating that many genes are highly differentially expressed in both groups. Conclusion: We were able to find abnormalities in gene expression in peripheral blood cells of patients with indolent systemic mastocytosis and to construct a gene expression profile which may be useful in clinical practice to predict the presence of mastocytosis and in further research of novel drugs.
引用
收藏
页码:229 / 237
页数:9
相关论文
共 35 条
[1]   Interaction of AF4 wild-type and AF4. MLL fusion protein with SIAH proteins: indication for t(4;11) pathobiology? [J].
Bursen, A ;
Moritz, S ;
Gaussmann, A ;
Moritz, S ;
Dingermann, T ;
Marschalek, R .
ONCOGENE, 2004, 23 (37) :6237-6249
[2]   TRIP-Br2 promotes oncogenesis in nude mice and is frequently overexpressed in multiple human tumors [J].
Cheong, Jit Kong ;
Gunaratnam, Lakshman ;
Zang, Zhi Jiang ;
Yang, Christopher M. ;
Sun, Xiaoming ;
Nasr, Susan L. ;
Sim, Khe Guan ;
Peh, Bee Keow ;
Rashid, Suhaimi Bin Abdul ;
Bonventre, Joseph V. ;
Salto-Tellez, Manuel ;
Hsu, Stephen I. .
JOURNAL OF TRANSLATIONAL MEDICINE, 2009, 7
[3]  
Crijns APG, 2009, PLOS MED, V6, P181, DOI 10.1371/journal.pmed.1000024
[4]   Gene expression analysis in mastocytosis reveals a highly consistent profile with candidate molecular markers [J].
D'ambrosio, C ;
Akin, C ;
Wu, YL ;
Magnusson, MK ;
Metcalfe, DD .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2003, 112 (06) :1162-1170
[5]   Association of the Q576R polymorphism in the interleukin-4 receptor α chain with indolent mastocytosis limited to the skin [J].
Daley, T ;
Metcalfe, DD ;
Akin, C .
BLOOD, 2001, 98 (03) :880-882
[6]   A New Perspective on Transcriptional System Regulation (TSR): Towards TSR Profiling [J].
Fehrmann, Rudolf S. N. ;
de Jonge, Hendrik J. M. ;
ter Elst, Arja ;
de Vries, Andre ;
Crijns, Anne G. P. ;
Weidenaar, Alida C. ;
Gerbens, Frans ;
de Jong, Steven ;
van der Zee, Ate G. J. ;
de Vries, Elisabeth G. E. ;
Kamps, Willem A. ;
Hofstra, Robert M. W. ;
Meerman, Gerard J. te ;
de Bont, Eveline S. J. M. .
PLOS ONE, 2008, 3 (02)
[7]   KIT mutation in mast cells and other bone marrow hematopoietic cell lineages in systemic mast cell disorders:: a prospective study of the Spanish Network on Mastocytosis (REMA) in a series of 113 patients [J].
Garcia-Montero, Andres C. ;
Jara-Acevedo, Maria ;
Teodosio, Cristina ;
Luz Sanchez, Maria ;
Nunez, Rosa ;
Prados, Aranzazu ;
Aldanondo, Isabel ;
Sanchez, Laura ;
Dominguez, Mercedes ;
Botana, Luis M. ;
Sanchez-Jimenez, Francisca ;
Sotlar, Karl ;
Almeida, Julia ;
Escribano, Luis ;
Orfao, Alberto .
BLOOD, 2006, 108 (07) :2366-2372
[8]   Involvement of Rab27 in antigen-induced histamine release from rat basophilic leukemia 2H3 cells [J].
Goishi, K ;
Mizuno, K ;
Nakanishi, H ;
Sasaki, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 324 (01) :294-301
[9]   ATM mediates constitutive NF-κB activation in high-risk myelodysplastic syndrome and acute myeloid leukemia [J].
Grosjean-Raillard, J. ;
Tailler, M. ;
Ades, L. ;
Perfettini, J-L ;
Fabre, C. ;
Braun, T. ;
De Botton, S. ;
Fenaux, P. ;
Kroemer, G. .
ONCOGENE, 2009, 28 (08) :1099-1109
[10]   Role of human sphingosine-1-phosphate phosphatase 1 in the regulation of intra- and extracellular sphingosine-1-phosphate levels and cell viability [J].
Johnson, KR ;
Johnson, KY ;
Becker, KP ;
Bielawski, J ;
Mao, CG ;
Obeid, LM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (36) :34541-34547