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Inhibition of protein farnesylation enhances the chemotherapeutic efficacy of the novel geranylgeranyltransferase inhibitor BAL9611 in human colon cancer cells
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  • Published: 29 May 2001

Inhibition of protein farnesylation enhances the chemotherapeutic efficacy of the novel geranylgeranyltransferase inhibitor BAL9611 in human colon cancer cells

  • A Di Paolo1,
  • R Danesi1,
  • S Caputo1,
  • M Macchia2,
  • M Lastella1,
  • U Boggi3,
  • F Mosca3,
  • A Marchetti4 &
  • …
  • M Del Tacca1 

British Journal of Cancer volume 84, pages 1535–1543 (2001)Cite this article

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Abstract

Proteins belonging to the ras superfamily are involved in cell proliferation of normal and neoplastic tissues. To be biologically active, they require post-translational isoprenylation by farnesyl-transferase and geranylgeranyl-transferase. Enzyme inhibition by drugs may thus represent a promising approach to the treatment of cancer. Therefore, the combined effect of BAL9611, a novel inhibitor of geranylgeranylation, and manumycin, a farnesyl-transferase inhibitor, was evaluated on the SW620 human colon cancer cell line which harbours a mutated K-ras gene. BAL9611 and manumycin dose-dependently inhibited SW620 cell growth with 50% inhibitory concentration (IC50) of 0.47 ± 0.03 and 5.24 ± 1.41 μM (mean ± SE), respectively. The isobologram analysis performed at the IC50 level revealed that the combined treatment was highly synergistic with respect to cell growth inhibition. BAL9611 and manumycin were able to inhibit the geranylgeranylation of p21rhoA and farnesylation of p21ras; both drugs inhibited p42ERK2/MAPK phosphorylation, but their combination was more effective than either drug alone. Moreover, the enhanced inhibition of cell growth in vitro by the BAL9611-manumycin combination was also observed in vivo in CD nu/nu female mice xenografted with SW620 tumours. Finally, both drugs were able to induce cell death by apoptosis in vitro and in vivo, as demonstrated by perinuclear chromatin condensation, cytoplasm budding and nuclear fragmentation, and interoligonucleosomal DNA digestion. In conclusion, the inhibition of protein farnesylation enhances the chemotherapeutic effect of BAL9611 in vitro and in vivo in a synergistic fashion, as a result of the impairment of post-translational isoprenylation of proteins and phosphorylation of p42ERK2/MAPK, whose activation is associated with post-translational geranylgeranylation and farnesylation of p21rhoA and p21ras. © 2001 Cancer Research Campaign http://www.bjcancer.com

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

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Authors and Affiliations

  1. Division of Pharmacology and Chemotherapy,

    A Di Paolo, R Danesi, S Caputo, M Lastella & M Del Tacca

  2. Department of Pharmaceutical Sciences, University of Pisa,

    M Macchia

  3. Division of General Surgery and Transplants, Department of Oncology, Transplants and Advanced Technologies in Medicine,

    U Boggi & F Mosca

  4. University of Chieti, Italy,

    A Marchetti

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From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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Paolo, A., Danesi, R., Caputo, S. et al. Inhibition of protein farnesylation enhances the chemotherapeutic efficacy of the novel geranylgeranyltransferase inhibitor BAL9611 in human colon cancer cells. Br J Cancer 84, 1535–1543 (2001). https://doi.org/10.1054/bjoc.2001.1820

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  • Received: 31 July 2000

  • Revised: 23 February 2001

  • Accepted: 26 February 2001

  • Published: 29 May 2001

  • Issue date: 01 June 2001

  • DOI: https://doi.org/10.1054/bjoc.2001.1820

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Keywords

  • isoprenylation
  • colon cancer
  • ras superfamily
  • isoprenyl transferases
  • inhibitors
  • cytotoxicity

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