Objectives: We have investigated the AAG and its genetic variants concentra
tions in plasma samples of 61 patients suffering from different types of ca
ncers.
Design and methods: The patients were shared out in three groups, breast, l
ung, and ovary cancers groups. AAG concentration was measured by an immunon
ephelometric method and the phenotype was determined, after desialylation o
f plasma by analytical isoelectric focusing. Detection of AAG variants was
made by immunoblotting and their proportions were determined by laser densi
tometry analysis. A population of 74 healthy individuals served as controls
.
Results: The plasma concentrations of AAG in the breast and lung cancer gro
ups were 2.5 times increased, while in the ovary cancer group, the concentr
ations were 1.6 times increased. AAG concentrations in the cancer populatio
n ranged between 0.45 and 2.85 g/L (mean value 1.12 +/- 0.51 g/L). The prop
ortions of the ORM1 and ORM2 variants were similar to those in the healthy
population. In breast and lung cancer groups, the relative concentrations o
f genetic variants were increased more than 2.5 fold, whereas a 1.6-fold in
crease was observed in the ovary cancer group.
Conclusions: These results show that AAG plasma concentrations are increase
d in these types of cancers and that changes in the expression of the genet
ic variants of AAG could also occur according to the type of cancer. Copyri
ght (C) 2000 The Canadian Society of Clinical Chemists.