期刊论文详细信息
Proteome Science
Plasma proteome changes associated with refractory cytopenia with multilineage dysplasia
Jan E Dyr1  Jaroslav Čermák1  Jiří Suttnar1  Zuzana Reicheltová1  Pavel Májek1 
[1] Department of Biochemistry, Institute of Hematology and Blood Transfusion, Prague, Czech Republic
关键词: proteome;    dysplasia;    refractory cytopenia;    myelodysplastic syndrome;   
Others  :  820192
DOI  :  10.1186/1477-5956-9-64
 received in 2011-05-23, accepted in 2011-10-05,  发布年份 2011
PDF
【 摘 要 】

Background

Refractory cytopenia with multilineage dysplasia (RCMD) is a subgroup of myelodysplastic syndrome (MDS), which belongs to oncohematological diseases, occurring particularly in elderly patients, and represents a heterogeneous group of bone marrow diseases. The goal of this study was to look for plasma proteins that changed quantitatively or qualitatively in RCMD patients.

Results

A total of 46 plasma samples were depleted, proteins were separated by 2D SDS-PAGE (pI 4-7), and proteomes were compared using Progenesis SameSpots statistical software. Proteins were identified by nanoLC-MS/MS. Sixty-one unique, significantly (p < 0.05, ANOVA) different spots were found; proteins in 59 spots were successfully identified and corresponded to 57 different proteins. Protein fragmentation was observed in several proteins: complement C4-A, complement C4-B, inter-alpha-trypsin inhibitor heavy chain H4, and endorepellin.

Conclusions

This study describes proteins, which change quantitatively or qualitatively in RCMD patients, and represents the first report on significant alterations in C4-A and C4-B complement proteins and ITIH4 fragments in patients with MDS-RCMD.

【 授权许可】

   
2011 Májek et al; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20140712031223700.pdf 2347KB PDF download
Figure 3. 31KB Image download
Figure 2. 31KB Image download
Figure 1. 41KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

【 参考文献 】
  • [1]Vardiman JW, Harris NL, Brunning RD: The World Health Organization (WHO) classification of the myeloid neoplasms. Blood 2002, 100:2292-2302.
  • [2]Vasikova A, Belickova M, Budinska E, Cermak J: A distinct expression of various gene subsets in CD34+ cells from patients with early and advanced myelodysplastic syndrome. Leuk Res 2010, 34:1566-1572.
  • [3]Votavova H, Grmanova M, Dostalova Merkerova M, Belickova M, Vasikova A, Neuwirtova R, Cermak J: Differential expression of microRNAs in CD34+ cells of 5q- syndrome. J Hematol Oncol 2011, 4:1. BioMed Central Full Text
  • [4]Vasikova A, Budinska E, Belickova M, Cermak J, Bruchova H: Differential gene expression of bone marrow CD34+ cells in early and advanced myelodysplastic syndrome. Neoplasma 2009, 56:335-342.
  • [5]Kracmarova A, Cermak J, Brdicka R, Bruchova H: High expression of ERCC1, FLT1, NME4 and PCNA associated with poor prognosis and advanced stages in myelodysplastic syndrome. Leuk Lymphoma 2008, 49:1297-1305.
  • [6]Dostalova Merkerova M, Krejcik Z, Votavova H, Belickova M, Vasikova A, Cermak J: Distinctive microRNA expression profiles in CD34+ bone marrow cells from patients with myelodysplastic syndrome. Eur J Hum Genet 2011, 19:313-319.
  • [7]Aivado M, Spentzos D, Germing U, Alterovitz G, Meng XY, Grall F, Giagounidis AA, Klement G, Steidl U, Otu HH, Czibere A, Prall WC, Iking-Konert C, Shayne M, Ramoni MF, Gattermann N, Haas R, Mitsiades CS, Fung ET, Libermann TA: Serum proteome profiling detects myelodysplastic syndromes and identifies CXC chemokine ligands 4 and 7 as markers for advanced disease. Proc Natl Acad Sci USA 2007, 104:1307-1312.
  • [8]Májek P, Reicheltová Z, Suttnar J, Malý M, Oravec M, Pečánková K, Dyr JE: Plasma proteome changes in cardiovascular disease patients: novel isoforms of apolipoprotein A1. J Transl Med 2011, 9:84. BioMed Central Full Text
  • [9]Chen C, Bowen DT, Giagounidis AA, Schlegelberger B, Haase S, Wright EG: Identification of disease- and therapy-associated proteome changes in the sera of patients with myelodysplastic syndromes and del(5q). Leukemia 2010, 24:1875-1884.
  • [10]Ma W, Kantarjian H, Bekele B, Donahue AC, Zhang X, Zhang ZJ, O'Brien S, Estey E, Estrov Z, Cortes J, Keating M, Giles F, Albitar M: Proteasome enzymatic activities in plasma as risk stratification of patients with acute myeloid leukemia and advanced-stage myelodysplastic syndrome. Clin Cancer Res 2009, 15:3820-3826.
  • [11]Májek P, Reicheltová Z, Stikarová J, Suttnar J, Sobotková A, Dyr JE: Proteome changes in platelets activated by arachidonic acid, collagen, and thrombin. Proteome Sci 2010, 8:56.
  • [12]Riedel T, Suttnar J, Brynda E, Houska M, Medved L, Dyr JE: Fibrinopeptides A and B release in the process of surface fibrin formation. Blood 2011, 117:1700-1706.
  • [13]Chang JW, Kang UB, Kim DH, Yi JK, Lee JW, Noh DY, Lee C, Yu MH: Identification of circulating endorepellin LG3 fragment: Potential use as a serological biomarker for breast cancer. Proteomics Clin Appl 2008, 2:23-32.
  • [14]Markiewski MM, DeAngelis RA, Benencia F, Ricklin-Lichtsteiner SK, Koutoulaki A, Gerard C, Coukos G, Lambris JD: Modulation of the antitumor immune response by complement. Nat Immunol 2008, 9:1225-1235.
  • [15]Coussens LM, Werb Z: Inflammation and cancer. Nature 2002, 420:860-867.
  • [16]Torrealba JR, Samaniego M, Pascual J, Becker Y, Pirsch J, Sollinger H, Odorico J: C4d-positive interacinar capillaries correlates with donor-specific antibody-mediated rejection in pancreas allografts. Transplantation 2008, 86:1849-1856.
  • [17]David-Neto E, Prado E, Beutel A, Ventura CG, Siqueira SA, Hung J, Lemos FB, de Souza NA, Nahas WC, Ianhez LE, David DR: C4d-positive chronic rejection: a frequent entity with a poor outcome. Transplantation 2007, 84:1391-1398.
  • [18]Nickeleit V, Mihatsch MJ: Kidney transplants, antibodies and rejection: is C4d a magic marker? Nephrol Dial Transplant 2003, 18:2232-2239.
  • [19]Gorter A, Meri S: Immune evasion of tumor cells using membrane-bound complement regulatory proteins. Immunol Today 1999, 20:576-582.
  • [20]Moretti S, Lanza F, Spisani S, Latorraca A, Rigolin GM, Giuliani AL, Castoldi GL, Traniello S: Neutrophils from patients with myelodysplastic syndromes: relationship between impairment of granular contents, complement receptors, functional activities and disease status. Leuk Lymphoma 1994, 13:471-477.
  • [21]Abdullah-Soheimi SS, Lim BK, Hashim OH, Shuib AS: Patients with ovarian carcinoma excrete different altered levels of urine CD59, kininogen-1 and fragments of inter-alpha-trypsin inhibitor heavy chain H4 and albumin. Proteome Sci 2010, 8:58. BioMed Central Full Text
  • [22]Villanueva J, Shaffer DR, Philip J, Chaparro CA, Erdjument-Bromage H, Olshen AB, Fleisher M, Lilja H, Brogi E, Boyd J, Sanchez-Carbayo M, Holland EC, Cordon-Cardo C, Scher HI, Tempst P: Differential exoprotease activities confer tumor-specific serum peptidome patterns. J Clin Invest 2006, 116:271-284.
  • [23]Fung ET, Yip TT, Lomas L, Wang Z, Yip C, Meng XY, Lin S, Zhang F, Zhang Z, Chan DW, Weinberger SR: Classification of cancer types by measuring variants of host response proteins using SELDI serum assays. Int J Cancer 2005, 115:783-789.
  • [24]Zhang Z, Bast RC Jr, Yu Y, Li J, Sokoll LJ, Rai AJ, Rosenzweig JM, Cameron B, Wang YY, Meng XY, Berchuck A, Van Haaften-Day C, Hacker NF, de Bruijn HW, van der Zee AG, Jacobs IJ, Fung ET, Chan DW: Three biomarkers identified from serum proteomic analysis for the detection of early stage ovarian cancer. Cancer Res 2004, 64:5882-5890.
  • [25]Mohamed E, Abdul-Rahman PS, Doustjalali SR, Chen Y, Lim BK, Omar SZ, Bustam AZ, Singh VA, Mohd-Taib NA, Yip CH, Hashim OH: Lectin-based electrophoretic analysis of the expression of the 35 kDa inter-alpha-trypsin inhibitor heavy chain H4 fragment in sera of patients with five different malignancies. Electrophoresis 2008, 29:2645-2650.
  • [26]Bix G, Castello R, Burrows M, Zoeller JJ, Weech M, Iozzo RA, Cardi C, Thakur ML, Barker CA, Camphausen K, Iozzo RV: Endorepellin in vivo: targeting the tumor vasculature and retarding cancer growth and metabolism. J Natl Cancer Inst 2006, 98:1634-1646.
  • [27]Bix G, Fu J, Gonzalez EM, Macro L, Barker A, Campbell S, Zutter MM, Santoro SA, Kim JK, Höök M, Reed CC, Iozzo RV: Endorepellin causes endothelial cell disassembly of actin cytoskeleton and focal adhesions through alpha2beta1 integrin. J Cell Biol 2004, 166:97-109.
  • [28]Gonzalez EM, Reed CC, Bix G, Fu J, Zhang Y, Gopalakrishnan B, Greenspan DS, Iozzo RV: BMP-1/Tolloid-like metalloproteases process endorepellin, the angiostatic C-terminal fragment of perlecan. J Biol Chem 2005, 280:7080-7087.
  • [29]Vuadens F, Benay C, Crettaz D, Gallot D, Sapin V, Schneider P, Bienvenut WV, Lémery D, Quadroni M, Dastugue B, Tissot JD: Identification of biologic markers of the premature rupture of fetal membranes: proteomic approach. Proteomics 2003, 3:1521-1525.
  • [30]Oda O, Shinzato T, Ohbayashi K, Takai I, Kunimatsu M, Maeda K, Yamanaka N: Purification and characterization of perlecan fragment in urine of end-stage renal failure patients. Clin Chim Acta 1996, 255:119-132.
  • [31]Ignjatovic V, Lai C, Summerhayes R, Mathesius U, Tawfilis S, Perugini MA, Monagle P: Age-related differences in plasma proteins: how plasma proteins change from neonates to adults. PLoS One 2011, 6:e17213.
  文献评价指标  
  下载次数:14次 浏览次数:3次