Literature DB >> 9418856

A farnesyltransferase inhibitor induces tumor regression in transgenic mice harboring multiple oncogenic mutations by mediating alterations in both cell cycle control and apoptosis.

R E Barrington1, M A Subler, E Rands, C A Omer, P J Miller, J E Hundley, S K Koester, D A Troyer, D J Bearss, M W Conner, J B Gibbs, K Hamilton, K S Koblan, S D Mosser, T J O'Neill, M D Schaber, E T Senderak, J J Windle, A Oliff, N E Kohl.   

Abstract

The farnesyltransferase inhibitor L-744,832 selectively blocks the transformed phenotype of cultured cells expressing a mutated H-ras gene and induces dramatic regression of mammary and salivary carcinomas in mouse mammary tumor virus (MMTV)-v-Ha-ras transgenic mice. To better understand how the farnesyltransferase inhibitors might be used in the treatment of human tumors, we have further explored the mechanisms by which L-744,832 induces tumor regression in a variety of transgenic mouse tumor models. We assessed whether L-744,832 induces apoptosis or alterations in cell cycle distribution and found that the tumor regression in MMTV-v-Ha-ras mice could be attributed entirely to elevation of apoptosis levels. In contrast, treatment with doxorubicin, which induces apoptosis in many tumor types, had a minimal effect on apoptosis in these tumors and resulted in a less dramatic tumor response. To determine whether functional p53 is required for L-744,832-induced apoptosis and the resultant tumor regression, MMTV-v-Ha-ras mice were interbred with p53(-/-) mice. Tumors in ras/p53(-/-) mice treated with L-744,832 regressed as efficiently as MMTV-v-Ha-ras tumors, although this response was found to be mediated by both the induction of apoptosis and an increase in G1 with a corresponding decrease in the S-phase fraction. MMTV-v-Ha-ras mice were also interbred with MMTV-c-myc mice to determine whether ras/myc tumors, which possess high levels of spontaneous apoptosis, have the potential to regress through a further increase in apoptosis levels. The ras/myc tumors were found to respond nearly as efficiently to L-744,832 treatment as the MMTV-v-Ha-ras tumors, although no induction of apoptosis was observed. Rather, the tumor regression in the ras/myc mice was found to be mediated by a large reduction in the S-phase fraction. In contrast, treatment of transgenic mice harboring an activated MMTV-c-neu gene did not result in tumor regression. These results demonstrate that a farnesyltransferase inhibitor can induce regression of v-Ha-ras-bearing tumors by multiple mechanisms, including the activation of a suppressed apoptotic pathway, which is largely p53 independent, or by cell cycle alterations, depending upon the presence of various other oncogenic genetic alterations.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9418856      PMCID: PMC121456          DOI: 10.1128/MCB.18.1.85

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  53 in total

Review 1.  The potential of farnesyltransferase inhibitors as cancer chemotherapeutics.

Authors:  J B Gibbs; A Oliff
Journal:  Annu Rev Pharmacol Toxicol       Date:  1997       Impact factor: 13.820

2.  Differential regulation of cell cycle characteristics and apoptosis in MMTV-myc and MMTV-ras mouse mammary tumors.

Authors:  J E Hundley; S K Koester; D A Troyer; S G Hilsenbeck; R E Barrington; J J Windle
Journal:  Cancer Res       Date:  1997-02-15       Impact factor: 12.701

3.  E2F-1 cooperates with topoisomerase II inhibition and DNA damage to selectively augment p53-independent apoptosis.

Authors:  J Nip; D K Strom; B E Fee; G Zambetti; J L Cleveland; S W Hiebert
Journal:  Mol Cell Biol       Date:  1997-03       Impact factor: 4.272

4.  Farnesyl transferase inhibitors induce apoptosis of Ras-transformed cells denied substratum attachment.

Authors:  P F Lebowitz; D Sakamuro; G C Prendergast
Journal:  Cancer Res       Date:  1997-02-15       Impact factor: 12.701

5.  Isoprenoid addition to Ras protein is the critical modification for its membrane association and transforming activity.

Authors:  K Kato; A D Cox; M M Hisaka; S M Graham; J E Buss; C J Der
Journal:  Proc Natl Acad Sci U S A       Date:  1992-07-15       Impact factor: 11.205

6.  Increased tumor proliferation and genomic instability without decreased apoptosis in MMTV-ras mice deficient in p53.

Authors:  J E Hundley; S K Koester; D A Troyer; S G Hilsenbeck; M A Subler; J J Windle
Journal:  Mol Cell Biol       Date:  1997-02       Impact factor: 4.272

Review 7.  The p53 tumour suppressor gene: a mediator of a G1 growth arrest and of apoptosis.

Authors:  E Yonish-Rouach
Journal:  Experientia       Date:  1996-10-31

8.  p53 status and the efficacy of cancer therapy in vivo.

Authors:  S W Lowe; S Bodis; A McClatchey; L Remington; H E Ruley; D E Fisher; D E Housman; T Jacks
Journal:  Science       Date:  1994-11-04       Impact factor: 47.728

9.  Mutation and cancer: statistical study of retinoblastoma.

Authors:  A G Knudson
Journal:  Proc Natl Acad Sci U S A       Date:  1971-04       Impact factor: 11.205

10.  Apoptotic death of tumor cells correlates with chemosensitivity, independent of p53 or bcl-2.

Authors:  G S Wu; W S El-Deiry
Journal:  Clin Cancer Res       Date:  1996-04       Impact factor: 12.531

View more
  25 in total

1.  K-Ras-independent effects of the farnesyl transferase inhibitor L-744,832 on cyclin B1/Cdc2 kinase activity, G2/M cell cycle progression and apoptosis in human pancreatic ductal adenocarcinoma cells.

Authors:  S Y Song; I M Meszoely; R J Coffey; J A Pietenpol; S D Leach
Journal:  Neoplasia       Date:  2000 May-Jun       Impact factor: 5.715

Review 2.  Unraveling the mechanism of the farnesyltransferase enzyme.

Authors:  Sérgio Filipe Sousa; Pedro Alexandrino Fernandes; Maria João Ramos
Journal:  J Biol Inorg Chem       Date:  2004-12-21       Impact factor: 3.358

3.  Farnesyltransferase inhibitors inhibit T-cell cytokine production at the posttranscriptional level.

Authors:  Reinhard E Marks; Allen W Ho; Christian Robbel; Todd Kuna; Seth Berk; Thomas F Gajewski
Journal:  Blood       Date:  2007-06-01       Impact factor: 22.113

4.  Farnesyltransferase inhibitors induce cytochrome c release and caspase 3 activation preferentially in transformed cells.

Authors:  N Suzuki; J Urano; F Tamanoi
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-22       Impact factor: 11.205

Review 5.  Establishing a link between oncogenes and tumor angiogenesis.

Authors:  R S Kerbel; A Viloria-Petit; F Okada; J Rak
Journal:  Mol Med       Date:  1998-05       Impact factor: 6.354

6.  Farnesyltransferase inhibitors induce dramatic morphological changes of KNRK cells that are blocked by microtubule interfering agents.

Authors:  N Suzuki; K Del Villar; F Tamanoi
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-01       Impact factor: 11.205

Review 7.  Mitogenic signaling and the relationship to cell cycle regulation in astrocytomas.

Authors:  A Besson; V W Yong
Journal:  J Neurooncol       Date:  2001-02       Impact factor: 4.130

Review 8.  Farnesyltransferase inhibitors: potential role in the treatment of cancer.

Authors:  A D Cox
Journal:  Drugs       Date:  2001       Impact factor: 9.546

9.  Caution! Analyze transcripts from conditional knockout alleles.

Authors:  Shao H Yang; Martin O Bergo; Emily Farber; Xin Qiao; Loren G Fong; Stephen G Young
Journal:  Transgenic Res       Date:  2008-12-18       Impact factor: 2.788

10.  Inhibitors of cellular signalling are cytotoxic or block the budded-to-hyphal transition in the pathogenic yeast Candida albicans.

Authors:  Kurt A Toenjes; Benjamin C Stark; Krista M Brooks; Douglas I Johnson
Journal:  J Med Microbiol       Date:  2009-06       Impact factor: 2.472

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.