4.7 Article

Budesonide Analogues Preserve Stem Cell Pluripotency and Delay 3D Gastruloid Development

Journal

PHARMACEUTICS
Volume 15, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/pharmaceutics15071897

Keywords

drug toxicity; budesonide analogues; stem cells; pluripotency exit; 3D gastruloids

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Small molecules that can modulate or stabilize cell-cell interactions are valuable tools for investigating the impact of collective cell behavior on various biological processes. Budesonide, an anti-asthmatic drug, has been shown to be a potent regulator of stem cell pluripotency. In this study, a derivative of budesonide called CHD-030498 was identified as a more effective analogue that can prevent stem cell pluripotency exit in different cell-based models at lower doses compared to budesonide.
Small molecules that can modulate or stabilize cell-cell interactions are valuable tools for investigating the impact of collective cell behavior on various biological processes such as development/morphogenesis, tissue regeneration and cancer progression. Recently, we showed that budesonide, a glucocorticoid widely used as an anti-asthmatic drug, is a potent regulator of stem cell pluripotency. Here we tested the effect of different budesonide derivatives and identified CHD-030498 as a more effective analogue of budesonide. CHD-030498 was able to prevent stem cell pluripotency exit in different cell-based models, including embryonic stem-to-mesenchymal transition, spontaneous differentiation and 3D gastruloid development, and at lower doses compared to budesonide.

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