Exploring the Glycosylation of Serum CA125

被引:68
|
作者
Saldova, Radka [1 ]
Struwe, Weston B. [1 ]
Wynne, Kieran [2 ]
Elia, Giuliano [2 ]
Duffy, Michael J. [3 ,4 ]
Rudd, Pauline M. [1 ]
机构
[1] Natl Inst Bioproc Res & Training, NIBRT GlycoSci Grp, Dublin 4, Ireland
[2] Univ Coll Dublin, Conway Inst, Dublin 4, Ireland
[3] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, UCD Sch Med & Med Sci, Dublin 4, Ireland
[4] St Vincents Univ Hosp, Dept Pathol & Lab Med, Dublin 4, Ireland
来源
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | 2013年 / 14卷 / 08期
基金
爱尔兰科学基金会;
关键词
CA125; N-glycosylation; biomarker; ovarian cancer; PROSTATE-SPECIFIC ANTIGEN; OVARIAN-CANCER ANTIGEN; N-LINKED GLYCANS; NEGATIVE-IONS; PANCREATIC-CANCER; MASS-SPECTROMETRY; O-GLYCANS; FRAGMENTATION; GLYCOPROTEINS; IDENTIFICATION;
D O I
10.3390/ijms140815636
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ovarian cancer is the most lethal gynaecologic cancer affecting women. The most widely used biomarker for ovarian cancer, CA125, lacks sensitivity and specificity. Here, we explored differences in glycosylation of CA125 between serum from patients with ovarian cancer and healthy controls. We found differences between CA125 N-glycans from patient sera compared to controls. These include increases in core-fucosylated bi-antennary monosialylated glycans, as well as decreases in mostly bisecting bi-antennary and non-fucosylated glycans in patients compared to controls. Measurement of the glycosylated state of CA125 may therefore provide a more specific biomarker for patients with ovarian cancer.
引用
收藏
页码:15636 / 15654
页数:19
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