Senescent fibroblasts promote epithelial cell growth and tumorigenesis: A link between cancer and aging

TLDR

Cellular senescence is a growth‑arrested state that suppresses early tumorigenesis and contributes to aging, though its mechanisms remain poorly understood. Senescent fibroblasts stimulate premalignant and malignant epithelial cells to proliferate and form tumors, even when only 10 % of the fibroblast population is senescent, indicating that senescence can promote cancer in aged organisms.

Abstract

Mammalian cells can respond to damage or stress by entering a state of arrested growth and altered function termed cellular senescence. Several lines of evidence suggest that the senescence response suppresses tumorigenesis. Cellular senescence is also thought to contribute to aging, but the mechanism is not well understood. We show that senescent human fibroblasts stimulate premalignant and malignant, but not normal, epithelial cells to proliferate in culture and form tumors in mice. In culture, the growth stimulation was evident when senescent cells comprised only 10% of the fibroblast population and was equally robust whether senescence was induced by replicative exhaustion, oncogenic RAS, p14 ARF , or hydrogen peroxide. Moreover, it was due at least in part to soluble and insoluble factors secreted by senescent cells. In mice, senescent, much more than presenescent, fibroblasts caused premalignant and malignant epithelial cells to form tumors. Our findings suggest that, although cellular senescence suppresses tumorigenesis early in life, it may promote cancer in aged organisms, suggesting it is an example of evolutionary antagonistic pleiotropy.