Serum N‐glycan analysis in breast cancer patients – Relation to tumour biology and clinical outcome. Issue 1 (19th August 2015)

• Record Type: Journal Article
• Authors: Haakensen, Vilde D.; Steinfeld, Israel; Saldova, Radka; Shehni, Akram Asadi; Kifer, Ilona; Naume, Bjørn; Rudd, Pauline M.; Børresen-Dale, Anne-Lise; Yakhini, Zohar
• Is Part Of: Molecular oncology. Volume 10:Issue 1(2016:Jan.)
• Page Start: 59
• Page End: 72
• Publication Date: 2015-08-19
• Subjects: Serum N-glycans -- mRNA -- Gene expression -- Breast cancer -- Integrated data analysis; Cancer -- Molecular aspects -- Periodicals; 616.994005
• DOI: 10.1016/j.molonc.2015.08.002
• Languages: English
• ISSNs: 1574-7891

Abstract

Abstract : Glycosylation and related processes play important roles in cancer development and progression, including metastasis. Several studies have shown that N‐glycans have potential diagnostic value as cancer serum biomarkers. We have explored the significance of the abundance of particular serum N‐glycan structures as important features of breast tumour biology by studying the serum glycome and tumour transcriptome (mRNA and miRNA) of 104 breast cancer patients. Integration of these types of molecular data allows us to study the relationship between serum glycans and transcripts representing functional pathways, such as metabolic pathways or DNA damage response. We identified tri antennary trigalactosylated trisialylated glycans in serum as being associated with lower levels of tumour transcripts involved in focal adhesion and integrin‐mediated cell adhesion. These glycan structures were also linked to poor prognosis in patients with ER negative tumours. High abundance of simple monoantennary glycan structures were associated with increased survival, particularly in the basal‐like subgroup. The presence of circulating tumour cells was found to be significantly associated with several serum glycome structures like bi and triantennary, di‐ and trigalactosylated, di‐ and trisialylated. The link between tumour miRNA expression levels and N‐glycan production is also examined. Highlights: Serum N‐glycan structures reflect biological processes in breast carcinomas. Serum N‐glycan structures are associated with clinical traits. High serum abundance of small N‐glycans is associated with favorable prognosis. Increased branching of serum N‐glycans is associated with poor prognosis.