Cellular FLIPL plays a survival role and regulates morphogenesis in breast epithelial cells

Citations of this article
Mendeley users who have this article in their library.


Strong evidences support the inhibitory activity of cellular FLICE-inhibitory protein (FLIP) in the apoptotic signalling by death receptors in tumor cells. However, little is known about the role of FLIP in the regulation of apoptosis in non-transformed cells. In this report, we demonstrate that FLIPL plays an important role as a survival protein in non-transformed breast epithelial cells. Silencing of FLIPL by siRNA methodology enhances TRAIL-R2 expression and activates a caspase-dependent cell death process in breast epithelial cells. This cell death requires the expression of TRAIL, TRAIL-R2, FADD and procaspase-8 proteins. A mitochondria-operated apoptotic pathway is partially required for FLIPL siRNA-induced apoptosis. Interestingly, FLIPL silencing markedly abrogates formation of acinus-like structures in a three-dimensional basement membrane culture model (3D) of the human mammary MCF-10A cell line through a caspase-8 dependent process. Furthermore, over-expression of FLIPL in MCF-10A cells delayed lumen formation in 3D cultures. Our results highlight the central role of FLIP in maintaining breast epithelial cell viability and suggest that the mechanisms regulating FLIP levels should be finely controlled to prevent unwanted cell demise. © 2010 Elsevier B.V.

Author supplied keywords




Yerbes, R., Palacios, C., Reginato, M. J., & López-Rivas, A. (2011). Cellular FLIPL plays a survival role and regulates morphogenesis in breast epithelial cells. Biochimica et Biophysica Acta - Molecular Cell Research, 1813(1), 168–178. https://doi.org/10.1016/j.bbamcr.2010.10.003

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free