Glycosylation and its implications in breast cancer

被引:69
|
作者
Scott, Danielle A. [1 ,2 ]
Drake, Richard R. [1 ,2 ]
机构
[1] Med Univ South Carolina, Dept Cell & Mol Pharmacol & Expt Therapeut, 173 Ashley Ave,Basic Sci Bldg 358, Charleston, SC 29425 USA
[2] Med Univ South Carolina, Prote Ctr, 173 Ashley Ave,Basic Sci Bldg 358, Charleston, SC 29425 USA
基金
美国国家卫生研究院;
关键词
Biomarkers; breast cancer; glycan; glycosylation; mass spectrometry; MASS-SPECTROMETRY; LEWIS-X; ALTERED GLYCOSYLATION; MONOCLONAL-ANTIBODIES; INCREASED EXPRESSION; TUMOR PROGRESSION; SOMATIC MUTATIONS; IMMUNOREACTIVE T; O-GLYCOSYLATION; GENE-EXPRESSION;
D O I
10.1080/14789450.2019.1645604
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: For decades, the role of glycans and glycoproteins in the progression of breast cancer and other cancers have been evaluated. Through extensive studies focused on elucidating the biological functions of glycosylation, researchers have been able to implicate alterations in these functions to tumor formation and metastasis. Areas covered: In this review, we summarize how changes in glycosylation are associated with tumorigenesis, with emphasis on breast cancers. An overview of the changes in N-linked and O-linked glycans associated with breast cancer tumors and biofluids are described. Recent advances in glycomics are emphasized in the context of continuing to decipher the glycosylation changes associated with breast cancer progression. Expert opinion: While changes in glycosylation have been studied in breast cancer for many years, the clinical relevance of these studies has been limited. This reflects the inherent biological and clinical heterogeneity of breast cancers. Glycomics analysis lags behind the advances in genomics and proteomics, but new approaches are emerging. A summary of known glycosylation changes associated with breast cancer is necessary to implement new findings in the context of clinical outcomes and therapeutic strategies. A better understanding of the dynamics of tumor and immune glycosylation is critical to improving emerging immunotherapeutic treatments.
引用
收藏
页码:665 / 680
页数:16
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