Literature DB >> 18929536

Geranylgeranyl transferase type II inhibition prevents myeloma bone disease.

Michelle A Lawson1, Les Coulton1, Frank H Ebetino2, Karin Vanderkerken3, Peter I Croucher4.   

Abstract

Geranylgeranyl transferase II (GGTase II) is an enzyme that plays a key role in the isoprenylation of proteins. 3-PEHPC, a novel GGTase II inhibitor, blocks bone resorption and induces myeloma cell apoptosis in vitro. Its effect on bone resorption and tumor growth in vivo is unknown. We investigated the effect of 3-PEHPC on tumor burden and bone disease in the 5T2MM model of multiple myeloma in vivo. 3-PEHPC significantly reduced osteoclast numbers and osteoclast surface. 3-PEHPC prevented the bone loss and the development of osteolytic bone lesions induced by 5T2MM myeloma cells. Treatment with 3-PEHPC also significantly reduced myeloma burden in bone. The magnitude of response was similar to that seen with the bisphosphonate, risedronate. These data show that targeting GGTase II with 3-PEHPC can prevent osteolytic bone disease and reduce tumor burden in vivo, and represents a novel approach to treating tumors that grow in bone.

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Year:  2008        PMID: 18929536     DOI: 10.1016/j.bbrc.2008.09.157

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  9 in total

1.  In Vivo Evaluation of Isoprenoid Triazole Bisphosphonate Inhibitors of Geranylgeranyl Diphosphate Synthase: Impact of Olefin Stereochemistry on Toxicity and Biodistribution.

Authors:  Staci L Haney; Yashpal S Chhonker; Michelle L Varney; Geoffrey Talmon; Lynette M Smith; Daryl J Murry; Sarah A Holstein
Journal:  J Pharmacol Exp Ther       Date:  2019-08-16       Impact factor: 4.030

Review 2.  Role of Rab GTPases in membrane traffic and cell physiology.

Authors:  Alex H Hutagalung; Peter J Novick
Journal:  Physiol Rev       Date:  2011-01       Impact factor: 37.312

3.  Isoprenoid biosynthetic pathway inhibition disrupts monoclonal protein secretion and induces the unfolded protein response pathway in multiple myeloma cells.

Authors:  Sarah A Holstein; Raymond J Hohl
Journal:  Leuk Res       Date:  2010-09-09       Impact factor: 3.156

4.  Differential activities of thalidomide and isoprenoid biosynthetic pathway inhibitors in multiple myeloma cells.

Authors:  Sarah A Holstein; Huaxiang Tong; Raymond J Hohl
Journal:  Leuk Res       Date:  2009-07-30       Impact factor: 3.156

5.  Structure of the disordered C terminus of Rab7 GTPase induced by binding to the Rab geranylgeranyl transferase catalytic complex reveals the mechanism of Rab prenylation.

Authors:  Yao-Wen Wu; Roger S Goody; Ruben Abagyan; Kirill Alexandrov
Journal:  J Biol Chem       Date:  2009-02-24       Impact factor: 5.157

6.  In vivo evaluation of combination therapy targeting the isoprenoid biosynthetic pathway.

Authors:  Staci L Haney; Michelle L Varney; Yashpal Chhonker; Geoffrey Talmon; Lynette M Smith; Daryl J Murry; Sarah A Holstein
Journal:  Pharmacol Res       Date:  2021-03-03       Impact factor: 7.658

Review 7.  Bisphosphonates as antimyeloma drugs.

Authors:  N D Modi; S Lentzsch
Journal:  Leukemia       Date:  2011-10-18       Impact factor: 11.528

Review 8.  Novel functions for Rab GTPases in multiple aspects of tumour progression.

Authors:  Chiara Recchi; Miguel C Seabra
Journal:  Biochem Soc Trans       Date:  2012-12-01       Impact factor: 5.407

9.  HRES-1/Rab4-mediated depletion of Drp1 impairs mitochondrial homeostasis and represents a target for treatment in SLE.

Authors:  Tiffany N Caza; David R Fernandez; Gergely Talaber; Zachary Oaks; Mark Haas; Michael P Madaio; Zhi-Wei Lai; Gabriella Miklossy; Ram R Singh; Dmitriy M Chudakov; Walter Malorni; Frank Middleton; Katalin Banki; Andras Perl
Journal:  Ann Rheum Dis       Date:  2013-07-29       Impact factor: 19.103

  9 in total

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