Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2115085 | Cancer Letters | 2008 | 6 Pages |
Abstract
The pro-apoptotic Fhit tumor suppressor protein binds and hydrolyses diadenosine triphosphate (Ap3A) and diadenosine tetraphosphate (Ap4A) in vitro. We have measured the level of both these nucleotides in Fhit-positive HEK293 cells exposed to various apoptosis inducers. Cold shock, anti-Fas, cadmium ions and etoposide all increased the basal level of Ap4A of 0.500 pmol/106 cells by about 50%. However, the corresponding increases in Ap3A from a basal 0.079 pmol/106 cells correlated closely with the degree of apoptosis produced, up to a maximum of 0.510 pmol/106 cells with etoposide. These results support the view that Ap3A is the in vivo Fhit ligand and that an inhibition of Fhit activity is a key element in Fhit-mediated apoptosis.
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Authors
David I. Fisher, Alexander G. McLennan,