ELEVATED LEVELS OF ABNORMALLY-FUCOSYLATED HAPTOGLOBINS IN CANCER SERA

被引:89
作者
THOMPSON, S [1 ]
TURNER, GA [1 ]
机构
[1] MED SCH NEWCASTLE UPON TYNE,DEPT CLIN BIOCHEM,NEWCASTLE TYNE NE2 4HH,ENGLAND
关键词
D O I
10.1038/bjc.1987.249
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer sera have higher levels of serum protein-bound fucose than sera from healthy individuals. In an attempt to identify the cause of this increase, fucoproteins were extracted from the sera of cancer patients and healthy individuals using a fucose-specific lectin (lotus tetragonolobus) coupled to Sepharose, and were analysed by polyacrylamide gel electrophoresis and silver staining. Of the several consistent changes observed for the cancer sera, the most striking was a large increase in a component of 40–45 Kdaltons. The expression of this component in the cancer sera was related to the elevation in serum fucose levels. Two dimensional (2D) electrophoretic analysis of lectin extracts showed that this component had a similar isoelectric point to the fi chains of haptoglobin. Its identity as haptoglobin was confirmed using Western blotting and an anti-haptoglobin antibody. Fucosylated haptoglobins (FHp) were also isolated from some rheumatoid arthritis sera, but there was no correlation between serum fucose levels and the FHp expression. The FHp in cancer sera was of higher molecular weight than that found in rheumatoid sera. Serial specimens from two ovarian cancer patients undergoing chemotherapy had elevated FHp associated with increased amounts of tumour. To the best of our knowledge this is the first time a molecule of this type has been reported in cancer sera and because of its uniqueness it deserves further investigation as a potential cancer marker. © 1987 The Macmillan Press Ltd.
引用
收藏
页码:605 / 610
页数:6
相关论文
共 15 条
[1]   A RAPID, SENSITIVE METHOD FOR DETECTION OF ALKALINE-PHOSPHATASE CONJUGATED ANTI-ANTIBODY ON WESTERN BLOTS [J].
BLAKE, MS ;
JOHNSTON, KH ;
RUSSELLJONES, GJ ;
GOTSCHLICH, EC .
ANALYTICAL BIOCHEMISTRY, 1984, 136 (01) :175-179
[2]  
CLAMP JR, 1975, PLASMA PROTEINS, V2, P163
[3]  
DEBRAY H, 1981, EUR J BIOCHEM, V117, P41
[4]  
KOJ A, 1974, STRUCTURE FUNCTION P, V1, P73
[5]  
KORNFELD K, 1981, J BIOL CHEM, V256, P6633
[6]   SILVER STAIN FOR PROTEINS IN POLYACRYLAMIDE GELS - A MODIFIED PROCEDURE WITH ENHANCED UNIFORM SENSITIVITY [J].
MORRISSEY, JH .
ANALYTICAL BIOCHEMISTRY, 1981, 117 (02) :307-310
[7]  
NILSSON ML, 1981, GLYCOCONJUGATES, P275
[8]   IMMUNOCHEMICAL STUDIES ON THE INTERACTION BETWEEN SYNTHETIC GLYCOCONJUGATES AND ALPHA-L-FUCOSYL BINDING LECTINS [J].
PETRYNIAK, J ;
GOLDSTEIN, IJ .
BIOCHEMISTRY, 1986, 25 (10) :2829-2838
[9]   A MONOCLONAL-ANTIBODY WHICH DETECTS A 125 KD GLYCOPROTEIN ON EMBRYONAL CARCINOMA-CELLS AND IS MITOGENIC FOR MURINE SPLEEN-CELLS [J].
STERN, P ;
GILBERT, P ;
STERNBERG, S ;
THOMPSON, S ;
CHADA, K .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 1984, 6 (05) :313-328
[10]  
THOMPSON S, 1987, BRIT J CANCER, V55, P348