Investigation of genetic variants of α-1 acid glycoprotein by ultra-performance liquid chromatography-mass spectrometry

被引:38
作者
Budai, Livia [1 ]
Ozohanics, Oliver [1 ]
Ludanyi, Krisztina [2 ]
Drahos, Laszlo [1 ]
Kremmer, Tibor [1 ]
Krenyacz, Judit [1 ]
Vekey, Karoly [1 ]
机构
[1] Hungarian Acad Sci, Chem Res Ctr, H-1025 Budapest, Hungary
[2] Semmelweis Univ, Dept Pharmaceut, H-1092 Budapest, Hungary
关键词
Alpha-1 acid glycoprotein; Cancer; Genetic variant; Peptide marker; UPLC-MS; HUMAN ALPHA(1)-ACID GLYCOPROTEIN; HUMAN SERUM ACID; SELECTIVE BINDING; ENANTIOSELECTIVE BINDING; BIANTENNARY GLYCANS; PROTEIN; EXPRESSION; GLYCOSYLATION; ALPHA-1-GLYCOPROTEIN; IDENTIFICATION;
D O I
10.1007/s00216-008-2518-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Genetic variants of human plasma alpha-1 acid glycoprotein (AGP) have been studied in cancer, compared with a group of healthy control. AGP has four genetic variants: AGP F1, F2, and S variants correspond to the ORM1 gene whereas AGP A corresponds to the ORM2 gene. The proportion of ORM1 and ORM2 variants were studied in plasma using a novel UPLC-MS method. Plasma total AGP level was 0.5 +/- 0.2 g L-1 and the proportions of the ORM1 and ORM2 variants were 76.3 +/- 8.2% and 23.7 +/- 8.2%, respectively. In cancer plasma AGP levels increased fourfold and the proportion of ORM1 variants increased to 88.7 +/- 6.8%. Changes in the proportion of genetic variants due to cancer were clearly significant, as shown by statistical analysis. Three different cancer types have been studied, lymphoma, melanoma, and ovarian cancer. The results did not show any difference depending on cancer type. The results indicate that, in accordance with prior expectations, the ORM1 variant is predominantly responsible for the acute-phase property of AGP.
引用
收藏
页码:991 / 998
页数:8
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