When cells proliferate in a confined environment, they build up a growth-induced compressive stress as a necessary condition for cell proliferation. This is the case of tree roots growing into the ground, solid tumors growing in the body of an organ, or even microbes proliferating inside a biofilm. This pressure can be tremendous: roots break concrete for instance. Cell proliferation is impacted by this self-inflicted compressive stress: it decreases. The understanding of this decrease is fundamental for at least two aspects. First, as it seems to be occurring for all cells of the living and understanding it will shed light on how cells proliferate and regulate their size and mass. Second, understanding the molecular aspects of it can help us fight cancer, accounting for this mechanical stress to control cell proliferation, in combination to other treatments. Our project thus aims to study why cells stop proliferating under confinement. To do so, we engineer cages to trap cells and study them, from bacteria to cancer cells. We study in particular how cells produce proteins, and how this production is impacted by mechanical pressure. At the end of the project, we should be able to understand the salient regulation of protein production, with the hope to control it, and offer novel strategies in our battle against cancer.