G1 PHASE ARREST BY THE PHOSPHATIDYLINOSITOL 3-KINASE INHIBITOR LY-294002 IS CORRELATED TO UP-REGULATION OF P27KIP1 AND INHIBITION OF G1 CDKS IN CHOROIDAL MELANOMA-CELLS
F. Casagrande et al., G1 PHASE ARREST BY THE PHOSPHATIDYLINOSITOL 3-KINASE INHIBITOR LY-294002 IS CORRELATED TO UP-REGULATION OF P27KIP1 AND INHIBITION OF G1 CDKS IN CHOROIDAL MELANOMA-CELLS, FEBS letters, 422(3), 1998, pp. 385-390
We have investigated the effect of the flavonoid derivative LY 294002,
a potent and selective phosphatidylinositol 3-kinase inhibitor, on ce
ll cycle progression in human choroidal melanoma cells. We demonstrate
that LY 294002 induces a specific G1 block in asynchronously growing
cells leading to an almost complete inhibition of cell proliferation a
fter three days of treatment, When melanoma cells are released from a
nocodazole-induced G2/M block, LY 294002 is shown to delay and greatly
restrain the G1/S transition, The inhibitor is able to exert its acti
on as long as it is added during the G1 progression and before the cel
ls enter in S phase, We report that the LY 294002-induced G1 arrest is
closely correlated to inhibition of CDK4 and CDK2 activities leading
to the impairment of pRb phosphorylation which normally occurs during
G1 progression. While the inhibition of CDK4 may be attributed at leas
t in part to the decline in CDK4 protein level, CDK2 activity reductio
n is rather due to the up-regulation of the CDK inhibitor p27(Kip1) an
d to its increased association to CDK2. (C) 1998 Federation of Europea
n Biochemical Societies.