Journal Article

Mechanism of lovastatin-induced apoptosis in intestinal epithelial cells

Banke Agarwal, Balazs Halmos, Aleksander S. Feoktistov, Petr Protiva, William G. Ramey, Ming Chen, Charalabos Pothoulakis, J.Thomas Lamont and Peter R. Holt

in Carcinogenesis

Volume 23, issue 3, pages 521-528
Published in print March 2002 | ISSN: 0143-3334
Published online March 2002 | e-ISSN: 1460-2180 | DOI: http://dx.doi.org/10.1093/carcin/23.3.521
Mechanism of lovastatin-induced apoptosis in intestinal epithelial cells

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We earlier showed that lovastatin potentiated the chemopreventive effects of sulindac against colon neoplasia in a rodent model and augments apoptosis induced by 5-FU and cisplatin in human colon cancer cells. In the present study, we investigated effects of lovastatin in spontaneously immortalized rat intestinal epithelial cells, IEC-18 and their K-ras transformed clones. Lovastatin induced morphologic changes (cell rounding and detachment) and apoptosis that were not influenced by K-ras mutations, but were prevented by geranylgeranyl-pyrophosphate or by mevalonate. Clostridium difficile toxin B, which directly inactivates rho, induced similar morphologic changes and apoptosis. Cycloheximide prevented these effects of lovastatin, but not C. difficile toxin B. Lovastatin decreased the amounts of membrane bound rhoA and rhoB. Cycloheximide and geranylgeranylpyrophosphate prevented lovastatin induced morphologic changes and apoptosis but did not inhibit lovastatin-induced changes in membrane translocation of rho. Our data suggest that lovastatin induces morphologic changes and apoptosis by inhibiting geranylgeranylation of small GTPases of the rho family and thereby inactivating them. Restoration of membrane translocation of rho is not necessary for preventing lovastatin-induced morphologic changes or apoptosis.

Keywords: CHX, cycloheximide; FPP, farnesylpyrophosphate; GDI, G-protein dissociation inhibitor; GGPP, geranylgeranyl-pyrophosphate.

Journal Article.  5313 words.  Illustrated.

Subjects: Clinical Cytogenetics and Molecular Genetics

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