Geranylgeranyltransferase-1 Inhibitors

Norbert Berndt, Andrew D. Hamilton, Saïd M. Sebti

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

The ability of many small G-proteins such as RHO and RAL GTPases to contribute to malignant transformation depends on their lipid posttranslational modification by geranylgeranyltransferase-1 (GGT-1). This, coupled with the observation that conditional deletion of GGT-1 compromises KRAS-driven oncogenesis, further spurred interest in the development of GGT-1 inhibitors (GGTIs) as anticancer agents. In this chapter, we describe the development of GGTIs from structure-based drug design to mechanism of action in cultured cells, to antitumor activity in animal models and finally to a recent human phase I clinical trial with GGTI-2418. Highly potent and selective GGTIs inhibit geranylgeranylation of GTPases such as RHOA, CDC42, and RAC1, proteins critical to the G1/S transition of the cell cycle, and induce G1 arrest. This appears to be mediated by induction of p21Cip1, CDK2 and CDK4 inhibition, and RB hypophosphorylation. GGTIs also inhibit CDK2-mediated phosphorylation of p27Kip1 at Thr187, thereby inducing its nuclear accumulation, and this appears to be required for GGTIs ability to induce tumor cell death. Furthermore, suppression of the levels of phospho-Akt, c-FLIP, and survivin as well as induction of death receptors and TRAIL have all been suggested to contribute to GGTIs' ability to induce apoptosis. Extensive work is ongoing to identify proteins whose inhibition of geranylgeranylation contributes toGGTIs' antitumor activity, and the possible involvement of RHOA, RHOC, CDC42, RAC1, RAC3, RALA, and RALB has been suggested.

Original languageEnglish (US)
Title of host publicationEnzymes
PublisherAcademic Press
Pages129-163
Number of pages35
DOIs
StatePublished - 2011

Publication series

NameEnzymes
Volume30
ISSN (Print)1874-6047

Keywords

  • Anticancer drugs
  • CaaX
  • Drug discovery
  • GGTIs
  • Genetic mouse model
  • Protein prenylation

ASJC Scopus subject areas

  • Biotechnology
  • Biophysics
  • Biochemistry
  • Molecular Biology

Fingerprint Dive into the research topics of 'Geranylgeranyltransferase-1 Inhibitors'. Together they form a unique fingerprint.

  • Cite this

    Berndt, N., Hamilton, A. D., & Sebti, S. M. (2011). Geranylgeranyltransferase-1 Inhibitors. In Enzymes (pp. 129-163). (Enzymes; Vol. 30). Academic Press. https://doi.org/10.1016/B978-0-12-415922-8.00006-9