# Investigating the utilization mechanism and kinetics of sialic acid mimetics in mammalian cell lines

**Authors:** Eline A. Visser, Daniël L. A. H. Hornikx, Moritz Rahm, Özden Öztürk, Venetia Psomiadou, Matteo Calzari, Celine Mennen, Sam J. Moons, Martin Jaeger, Dirk J. Lefeber, Christian Büll, Thomas J. Boltje

PMC · DOI: 10.1039/d5cb00193e · 2025-10-29

## TL;DR

This paper investigates how sialic acid mimetics are used and processed in mammalian cells, revealing differences in their metabolism and identifying a key bottleneck in their utilization.

## Contribution

The study identifies esterase activity as a critical factor limiting the effectiveness of sialic acid mimetics in certain cell lines.

## Key findings

- Differences in SAM metabolism determine their potency in various mammalian cell lines.
- A murine macrophage cell line was found to be insensitive to SAMs due to esterase activity.
- The study provides insights for improving the design and application of SAMs in mammalian systems.

## Abstract

Sialic acid mimetics (SAMs) are chemically modified derivatives of sialic acids that can act as metabolic inhibitors or as sugar donors for sialyltransferases. This makes SAMs highly useful research tools to study and manipulate the biosynthesis of sialic acid-carrying glycans (sialoglycans). Moreover, SAMs that inhibit aberrant sialylation in cancer cells are emerging as potential therapeutics. Despite the wide use of SAMs, many aspects regarding their cellular uptake and metabolic fate are unknown. Here, we investigated the metabolic fate of an inhibitory SAM (P-SiaFNEtoc) and an incorporative SAM (P-SiaNPoc) in various mammalian cell lines. Using kinetic experiments and read-outs based on sialic acid-binding lectins, click chemistry, and nucleotide sugar analysis, we monitored the key steps of cellular SAM utilization. We found differences in the metabolism of SAMs that determine their potency in different mammalian cell lines. By identifying a murine macrophage cell line that is insensitive to SAMs, we have identified esterase activity as a bottleneck for the cellular utilization of SAMs. This study contributes to the understanding of the mechanisms underlying SAMs utilization in mammalian cell lines and provide relevant considerations for the future chemical design of SAMs and their application in mammalian systems.

Sialic acid mimetics (SAMs) are chemically modified sialic acid derivatives that can act as metabolic inhibitors or as sugar donors for sialyltransferases.

## Full-text entities

- **Diseases:** cancer (MESH:D009369)
- **Chemicals:** P-SiaFNEtoc (-), Sialic acid (MESH:D019158), sialic acids (MESH:D012794), glycans (MESH:D011134), sugar (MESH:D000073893)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12580913/full.md

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Source: https://tomesphere.com/paper/PMC12580913