Exploring Glycan Markers for Immunotyping and Precision-targeting of Breast Circulating Tumor Cells.

Journal Article (Clinical Trial;Journal Article)

BACKGROUND AND AIMS: Recognition of abnormal glycosylation in virtually every cancer type has raised great interest in exploration of the tumor glycome for biomarker discovery. Identifying glycan markers of circulating tumor cells (CTCs) represents a new development in tumor biomarker discovery. The aim of this study was to establish an experimental approach to enable rapid screening of CTCs for glycan marker identification and characterization. METHODS: We applied carbohydrate microarrays and a high-speed fiber-optic array scanning technology (FAST scan) to explore potential glycan markers of breast CTCs (bCTCs) and targeting antibodies. An anti-tumor monoclonal antibody, HAE3-C1 (C1), was identified as a key immunological probe in this study. RESULTS: In our carbohydrate microarray analysis, C1 was found to be highly specific for an O-glycan cryptic epitope, gp(C1). Using FAST-scan technology, we established a procedure to quantify expression levels of gp(C1) in tumor cells. In blood samples from five stage IV metastatic breast cancer patients, the gp(C1) positive CTCs were detected in all subjects; ∼40% of bCTCs were strongly gp(C1) positive. Interestingly, CTCs from a triple-negative breast cancer patient with multiple sites of metastasis were predominantly gp(C1) positive (92.5%, 37/40 CTCs). CONCLUSIONS: Together we present here a practical approach to examine rare cell expression of glycan markers. Using this approach, we identified an O-core glyco-determinant gp(C1) as a potential immunological target of bCTCs. Given its bCTC-expression profile, this target warrants an extended investigation in a larger cohort of breast cancer patients.

Full Text

Duke Authors

Cited Authors

  • Wang, D; Liu, X; Hsieh, B; Bruce, R; Somlo, G; Huang, J; Sambucetti, L

Published Date

  • November 2015

Published In

Volume / Issue

  • 46 / 8

Start / End Page

  • 642 - 650

PubMed ID

  • 26657044

Pubmed Central ID

  • PMC4729604

Electronic International Standard Serial Number (EISSN)

  • 1873-5487

Digital Object Identifier (DOI)

  • 10.1016/j.arcmed.2015.11.007

Language

  • eng

Conference Location

  • United States