Related Experiment Video
Updated: Jul 14, 2026

Profiling of Permethylated Mucin O-glycans Using Matrix-assisted Laser Desorption/Ionization Time-of-flight Mass Spectrometry
Published on: June 20, 2025
Expression of cancer-associated simple mucin-type O-glycosylated antigens in parasites
1Departamento de Inmunobiología, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay. eosinaga@fmed.edu.uy
Abstract:
Simple mucin-type O-glycan structures, such as Tn, TF, sialyl-Tn and Tk antigens, are among of the most specific human cancer-associated structures. These antigens are involved in several types of receptor-ligand interactions, and they are potential targets for immunotherapy. In the last few years several simple mucin-type O-glycan antigens were identified in different species belonging to the main two helminth parasite phyla, and sialyl-Tn bearing glycoproteins were detected in Trypanosoma cruzi. These results are of interest to understand new aspects in parasite glycoimmunology and may help identify new biological characteristics of parasites as well of the host-parasite relationship. Considering that different groups reported a negative correlation between certain parasite infections and cancer development, we could hypothesize that simple mucin-type O-glycosylated antigens obtained from parasites could be good potential targets for cancer immunotherapy.
Insights
Simple mucin-type O-glycans are cancer-associated structures and potential immunotherapy targets. Parasite-derived O-glycans may offer novel strategies for cancer immunotherapy development.
Area of Science:
- Glycoscience
- Immunology
- Parasitology
Background:
- Simple mucin-type O-glycans (Tn, TF, sialyl-Tn, Tk) are specific human cancer-associated structures.
- These glycans mediate receptor-ligand interactions, making them potential targets for cancer immunotherapy.
Purpose of the Study:
- To explore the presence of simple mucin-type O-glycan antigens in helminth parasites.
- To investigate the potential of parasite-derived O-glycans as targets for cancer immunotherapy.
Main Methods:
- Identification of simple mucin-type O-glycan antigens in helminth parasite species.
- Detection of sialyl-Tn bearing glycoproteins in Trypanosoma cruzi.
- Review of existing literature on parasite infections and cancer development.
Main Results:
- Several simple mucin-type O-glycan antigens were identified across different helminth parasite species.
- Sialyl-Tn bearing glycoproteins were detected in Trypanosoma cruzi.
- A negative correlation between certain parasite infections and cancer development has been reported.
Conclusions:
- Parasite-derived simple mucin-type O-glycans represent a novel area in parasite glycoimmunology.
- These parasite-associated glycans hold potential as candidates for developing new cancer immunotherapies.
Related Concept Videos
Proteoglycans
Amebiasis

