Abstract

Aberrant O-glycans expressed at the surface of cancer cells consist of membrane-tethered glycoproteins (T and Tn antigens) and glycolipids (Lewis a, Lewis x and Forssman antigens). All of these O-glycans have been identified as glyco-markers of interest for the diagnosis and the prognosis of cancer diseases. These epitopes are specifically detected using T/Tn-specific lectins isolated from various plants such as jacalin from Artocarpus integrifola, and fungi such as the Agaricus bisporus lectin. These lectins accommodate T/Tn antigens at the monosaccharide-binding site; residues located in the surrounding extended binding-site of the lectins often participate in the binding of more extended epitopes. Depending on the shape and size of the extended carbohydrate-binding site, their fine sugar-binding specificity towards complex O-glycans readily differs from one lectin to another, resulting in a great diversity in their sugar-recognition capacity. T/Tn-specific lectins have been extensively used for the histochemical detection of cancer cells in biopsies and for the follow up of the cancer progression and evolution. T/Tn-specific lectins also induce a caspase-dependent apoptosis in cancer cells, often associated with a more or less severe inhibition of proliferation. Moreover, they provide another potential source of molecules adapted to the building of photosensitizer-conjugates allowing a specific targeting to cancer cells, for the photodynamic treatment of tumors.

Highlights

  • The malignant transformation is accompanied by profound alterations in both the N- and O-glycosylation processes in healthy cells [1,2,3]

  • Plant and fungal lectins displaying a T/Tn-specificity have been widely used as relevant probes for the histochemical detection of aberrant O-glycan glycomarkers expressed at the surface of malignant cells

  • With the aid of the fast-developing glycan- and lectin-microarray technologies, our increasing knowledge on the fine carbohydrate-binding specificity of plant and fungal lectins has revealed the extreme versatility of the lectin tool to recognize discrete/subtle differences in the expression of altered glycans by cancer cells

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Summary

Introduction

The malignant transformation is accompanied by profound alterations in both the N- and O-glycosylation processes in healthy cells [1,2,3]. Mucin, a heavily O-GalNAc glycosylated protein, is overexpressed and subsequently secreted by cancer cells, essentially at the last stages of the malignant progression [13,14]. All of these aberrant O-glycans may serve as potential targets to improve the diagnosis and the treatment of tumors, provided the molecular probes are available for their specific recognition [15,16,17]. We present an updated review on the potential use of plant and fungal lectins as probes for both the diagnosis, the prognosis, and the treatment of cancer

Altered O-Glycan Patterns Expressed by Cancer Cells
Findings
Conclusions

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