Arf6 wins the MVP award

The biosynthetic mevalonate pathway (MVP) produces the building blocks for a wide range of biological molecules, from cholesterol to the long-chain prenyl groups that mediate the membrane association of Ras family GTPases (1). Mutations in the tumor suppressor p53 can up-regulate the MVP, a phenomenon that enhances the invasiveness of certain breast cancer cell lines by an unknown mechanism (2). Hashimoto et al. reveal that the MVP drives cancer cell invasion by promoting the activation of the GTPase Arf6, suggesting that MVP inhibitors may be effective treatments for breast cancer patients whose tumors express high levels of Arf6 signaling components (3). Mutations in p53 up-regulate the MVP in both MDA-MB-231 and MDA-MB-468 breast cancer cell lines, but only MDA-MB-231 cells show an increased tendency to invade their surroundings (2). Hisataka Sabe and colleagues at Hokkaido University Graduate School of Medicine in Sapporo, Japan, noticed that MDA-MB-231 cells overexpress Arf6 and its downstream effector proteins, components of a signaling pathway that enhances cancer cell invasion and metastasis by promoting the cells' transition to a more mesenchy-mal phenotype (4). MDA-MB-468 cells, in contrast, do not overexpress Arf6 signal-ing proteins. " Thus, we hypothesized that mutant p53 and the MVP utilize Arf6 sig-naling to promote invasiveness, " Sabe says. Sabe and colleagues, led by assistant professor Ari Hashimoto, fi rst determined that the cytokine TGFβ1 activates Arf6 signaling and MDA-MB-231 cell invasion through the receptor tyrosine kinase c-Met (3). But silencing mutant p53, or inhibiting the MVP, blocked Arf6 activation and invasion. Knocking down mutant p53 prevented Arf6's recruitment to the plasma membrane, a critical step in the GTPase's activation by receptor tyrosine kinases. Hashimoto et al. found that silencing the enzyme geranylgeranyl transferase II (GGT-II) also inhibited Arf6's plasma membrane recruitment and activation. GGT-II promotes the membrane association of certain GTPases by modifying them with prenyl groups generated by the MVP. " But Arf6 is acylated, not prenylated, so it can't be a direct target of the MVP or GGT-II, " Sabe explains. Instead, the researchers thought, GGT-II might pre-nylate a Rab family GTPase responsible for delivering Arf6 to the plasma membrane. Hashimoto et al. found that knocking down the endo-somal Rab protein Rab11b blocked the plasma membrane recruitment and activation of Arf6. Moreover , MDA-MB-231 cells lacking Rab11b were less invasive in vitro and were no longer able to metastasize when injected into nude mice, suggesting that the MVP enhances Arf6 …