Comparison of α-1-acid glycoprotein isoforms from healthy and cancer patients by capillary IEF

被引:16
作者
Lacunza, Izaskun [1 ]
Kremmer, Tibor [2 ]
Diez-Masa, Jose Carlos [1 ]
Sanz, Jesus [1 ]
de Frutos, Mercedes [1 ]
机构
[1] CSIC, Inst Organ Chem, E-28006 Madrid, Spain
[2] Hungarian Acad Sci, Chem Res Ctr, Budapest, Hungary
关键词
alpha-1-acid glycoprotein; CIEF; glycoprotein; orosomucoid; tumor marker;
D O I
10.1002/elps.200600700
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
alpha-1-Acid glycoprotein (AGP) is a glycoprotein that presents different forms in the same individual, depending on the amino acid sequence and/or on the carbohydrate distribution of each form. Changes in these two types of heterogeneities are related to pathophysiological states. The aim of this work is to study the possibility of comparing AGP samples in terms of their CIEF profiles, what would facilitate in a future to perform studies about the role of AGP as a disease marker. In the present study, the CIEF profiles of AGP samples purified from sera of healthy donors and of ovary cancer and lymphoma patients are qualitatively and quantitatively compared. To make possible the comparison of those electrophoretical profiles, reliable assignment of AGP peaks is necessary. A computer program developed in our laboratory is used to select the migration parameters that make possible an accurate assignment of AGP peaks. Percentages of correct assignment of AGP peaks using the migration time of each peak relative to the migration time of an internal standard dose to 95% are achieved. After peak assignment, a different distribution of the area percentage of AGP forms is observed when comparing samples from diseased and healthy individuals, the most acidic AGP forms being present in a higher proportion in the samples from cancer patients. Although the number of samples studied is too low to get any clinical significance from these results, this work provides a way to study the role of AGP as a biomarker.
引用
收藏
页码:4447 / 4451
页数:5
相关论文
共 19 条
[1]
Expression of the genetic variants of human alpha-1-acid glycoprotein in cancer [J].
Duché, JC ;
Urien, S ;
Simon, N ;
Malaurie, E ;
Monnet, I ;
Barré, J .
CLINICAL BIOCHEMISTRY, 2000, 33 (03) :197-202
[2]
Alpha-1-acid glycoprotein [J].
Fournier, T ;
Medjoubi-N, N ;
Porquet, D .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 2000, 1482 (1-2) :157-171
[3]
DEVELOPMENT OF LARGE-SCALE FRACTIONATION METHODS .4. SIMPLE METHOD FOR LARGE-SCALE PREPARATION OF ALPHA1-ACID GLYCOPROTEIN [J].
HAO, YL ;
WICKERHA.M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1973, 322 (01) :99-108
[4]
α1-acid glycoprotein fucosylation as a marker of carcinoma progression and prognosis [J].
Hashimoto, S ;
Asao, T ;
Takahashi, J ;
Yagihashi, Y ;
Nishimura, T ;
Saniabadi, AR ;
Poland, DCW ;
van Dijk, W ;
Kuwano, H ;
Kochibe, N ;
Yazawa, S .
CANCER, 2004, 101 (12) :2825-2836
[5]
MICROHETEROGENEITY OF ALPHA-1 ACID GLYCOPROTEIN IN RHEUMATOID-ARTHRITIS - DEPENDENT ON DISEASE DURATION [J].
HRYCAJ, P ;
SOBIESKA, M ;
MACKIEWICZ, S ;
MULLER, W .
ANNALS OF THE RHEUMATIC DISEASES, 1993, 52 (02) :138-141
[6]
Iijima S, 2000, ELECTROPHORESIS, V21, P753, DOI 10.1002/(SICI)1522-2683(20000301)21:4<753::AID-ELPS753>3.3.CO
[7]
2-P
[8]
HIGH-RESOLUTION SEPARATION OF RECOMBINANT HUMAN INTERFERON-GAMMA GLYCOFORMS BY MICELLAR ELECTROKINETIC CAPILLARY CHROMATOGRAPHY [J].
JAMES, DC ;
FREEDMAN, RB ;
HOARE, M ;
JENKINS, N .
ANALYTICAL BIOCHEMISTRY, 1994, 222 (02) :315-322
[9]
Liquid chromatographic human serum acid and mass spectrometric analysis of alpha-1-glycoprotein [J].
Kremmer, T ;
Szöllösi, É ;
Boldizsár, M ;
Vincze, B ;
Ludányi, K ;
Imre, T ;
Schlosser, G ;
Vékey, K .
BIOMEDICAL CHROMATOGRAPHY, 2004, 18 (05) :323-329
[10]
Selection of migration parameters for a highly reliable assignment of bands of isoforms of erythropoietin separated by capillary electrophoresis [J].
Lacunza, I ;
Lara-Quintanar, P ;
Moya, G ;
Sanz, J ;
Diez-Masa, JC ;
de Frutos, M .
ELECTROPHORESIS, 2004, 25 (10-11) :1569-1579