Open AccessA study of death by anoikis in cultured epithelial cells
Author(s) -
Bretland A. J.,
Lawry J.,
Sharrard R. M.
Publication year - 2001
Publication title -
cell proliferation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.647
H-Index - 74
eISSN - 1365-2184
pISSN - 0960-7722
DOI - 10.1046/j.1365-2184.2001.00198.x
Subject(s) - anoikis , microbiology and biotechnology , hacat , biology , programmed cell death , kinase , phosphatidylinositol , apoptosis , focal adhesion , cell culture , chemistry , signal transduction , biochemistry , genetics
. Background : Epithelial cells are critically dependent upon cell‐matrix and cell‐cell adhesion for growth and survival. Anoikis is programmed cell death caused by disruption of cell‐substrate adhesion in normal epithelial cells. Methods : We studied the induction of anoikis in vitro in two cell lines; HaCaT and SW742. PI3K, JAK2 and PKC are key elements in signalling pathways regulating cell survival, and using specific inhibitors we also examined their potential role in the induction of anoikis. Results : When prevented from adhesion by culture on polyHEMA, HaCaT cells underwent apoptosis selectively from the proliferating population; surviving cells underwent cell cycle arrest. In SW742 cells anoikis also occurred, but was balanced by increased cycling. The effects of specific kinase inhibitors indicated that both Janus kinase 2 and protein kinase C partially protect HaCaT cells from anoikis through inducing cell cycle arrest of surviving nonadherent cells; inhibition of Phosphatidylinositol 3‐kinase did not induce cycling in HaCaTs prevented from adhesion but did stimulate anoikis. SW742 cells showed markedly different responses: Janus kinase 2 inhibition activated apoptosis directly, Phosphatidylinositol 3‐kinase inhibition stimulated both cell cycling and apoptosis, while protein kinase C inhibition stimulated cycling but inhibited apoptosis. Conclusions : Susceptibility to cell death in adhesion‐prevented epithelial cells may thus be regulated by signalling pathways involving Phosphatidylinositol 3‐kinase, Janus kinase 2 and protein kinase C. The ability of epithelial tumour cells to invade and metastasize may therefore result from disruption of these pathways.