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Volumn 12, Issue 6, 2012, Pages 704-709

Is there a future for prenyltransferase inhibitors in cancer therapy?

Author keywords

[No Author keywords available]

Indexed keywords

3 BENZYL 7 CYANO 2,3,4,5 TETRAHYDRO 1 (1H IMIDAZOL 4 YLMETHYL) 4 (2 THIENYLSULFONYL) 1H 1,4 BENZODIAZEPINE; ANTINEOPLASTIC AGENT; BORTEZOMIB; CAPECITABINE; CARBOPLATIN; CYTARABINE; DOCETAXEL; ETOPOSIDE; GEMCITABINE; GERANYLGERANYL TRANSFERASE INHIBITOR; GGTI 2418; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; IDARUBICIN; K RAS PROTEIN; L 778123; LONAFARNIB; MAMMALIAN TARGET OF RAPAMYCIN INHIBITOR; N RAS PROTEIN; PACLITAXEL; PRENYLTRANSFERASE INHIBITOR; RAS PROTEIN; SORAFENIB; TAMOXIFEN; TEMOZOLOMIDE; TIPIFARNIB; TRANSFERASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 84870505131     PISSN: 14714892     EISSN: 14714973     Source Type: Journal    
DOI: 10.1016/j.coph.2012.06.013     Document Type: Review
Times cited : (26)

References (39)
  • 1
    • 17444408968 scopus 로고    scopus 로고
    • Protein farnesylation: Implications for normal physiology, malignant transformation, and cancer therapy
    • S.M. Sebti Protein farnesylation: implications for normal physiology, malignant transformation, and cancer therapy Cancer Cell 7 2005 297 300
    • (2005) Cancer Cell , vol.7 , pp. 297-300
    • Sebti, S.M.1
  • 2
    • 51949096166 scopus 로고    scopus 로고
    • Structures of RabGGTase-substrate/product complexes provide insights into the evolution of protein prenylation
    • Z. Guo, Y.W. Wu, D. Das, C. Delon, J. Cramer, S. Yu, S. Thuns, N. Lupilova, H. Waldmann, and L. Brunsveld Structures of RabGGTase-substrate/ product complexes provide insights into the evolution of protein prenylation EMBO J 27 2008 2444 2456
    • (2008) EMBO J , vol.27 , pp. 2444-2456
    • Guo, Z.1    Wu, Y.W.2    Das, D.3    Delon, C.4    Cramer, J.5    Yu, S.6    Thuns, S.7    Lupilova, N.8    Waldmann, H.9    Brunsveld, L.10
  • 3
    • 0030968859 scopus 로고    scopus 로고
    • Direct demonstration of geranylgeranylation and farnesylation of Ki-Ras in vivo
    • C.A. Rowell, J.J. Kowalczyk, M.D. Lewis, and A.M. Garcia Direct demonstration of geranylgeranylation and farnesylation of Ki-Ras in vivo J Biol Chem 272 1997 14093 14097
    • (1997) J Biol Chem , vol.272 , pp. 14093-14097
    • Rowell, C.A.1    Kowalczyk, J.J.2    Lewis, M.D.3    Garcia, A.M.4
  • 5
    • 0030952552 scopus 로고    scopus 로고
    • Inhibition of the prenylation of K-Ras, but not H- or N-Ras, is highly resistant to CAAX peptidomimetics and requires both a farnesyltransferase and a geranylgeranyltransferase i inhibitor in human tumor cell lines
    • E.C. Lerner, T.T. Zhang, D.B. Knowles, Y. Qian, A.D. Hamilton, and S.M. Sebti Inhibition of the prenylation of K-Ras, but not H- or N-Ras, is highly resistant to CAAX peptidomimetics and requires both a farnesyltransferase and a geranylgeranyltransferase I inhibitor in human tumor cell lines Oncogene 15 1997 1283 1288
    • (1997) Oncogene , vol.15 , pp. 1283-1288
    • Lerner, E.C.1    Zhang, T.T.2    Knowles, D.B.3    Qian, Y.4    Hamilton, A.D.5    Sebti, S.M.6
  • 6
    • 0032546264 scopus 로고    scopus 로고
    • Both farnesyltransferase and geranylgeranyltransferase i inhibitors are required for inhibition of oncogenic K-Ras prenylation but each alone is sufficient to suppress human tumor growth in nude mouse xenografts
    • J. Sun, Y. Qian, A.D. Hamilton, and S.M. Sebti Both farnesyltransferase and geranylgeranyltransferase I inhibitors are required for inhibition of oncogenic K-Ras prenylation but each alone is sufficient to suppress human tumor growth in nude mouse xenografts Oncogene 16 1998 1467 1473
    • (1998) Oncogene , vol.16 , pp. 1467-1473
    • Sun, J.1    Qian, Y.2    Hamilton, A.D.3    Sebti, S.M.4
  • 9
    • 24744465206 scopus 로고    scopus 로고
    • The farnesyl transferase inhibitor (FTI) SCH66336 (lonafarnib) inhibits Rheb farnesylation and mTOR signaling. Role in FTI enhancement of taxane and tamoxifen anti-tumor activity
    • A.D. Basso, A. Mirza, G. Liu, B.J. Long, W.R. Bishop, and P. Kirschmeier The farnesyl transferase inhibitor (FTI) SCH66336 (lonafarnib) inhibits Rheb farnesylation and mTOR signaling. Role in FTI enhancement of taxane and tamoxifen anti-tumor activity J Biol Chem 280 2005 31101 31108
    • (2005) J Biol Chem , vol.280 , pp. 31101-31108
    • Basso, A.D.1    Mirza, A.2    Liu, G.3    Long, B.J.4    Bishop, W.R.5    Kirschmeier, P.6
  • 10
    • 0041356888 scopus 로고    scopus 로고
    • Rheb binds tuberous sclerosis complex 2 (TSC2) and promotes S6 kinase activation in a rapamycin- and farnesylation-dependent manner
    • A.F. Castro, J.F. Rebhun, G.J. Clark, and L.A. Quilliam Rheb binds tuberous sclerosis complex 2 (TSC2) and promotes S6 kinase activation in a rapamycin- and farnesylation-dependent manner J Biol Chem 278 2003 32493 32496
    • (2003) J Biol Chem , vol.278 , pp. 32493-32496
    • Castro, A.F.1    Rebhun, J.F.2    Clark, G.J.3    Quilliam, L.A.4
  • 12
    • 80054866000 scopus 로고    scopus 로고
    • Targeting protein prenylation for cancer therapy
    • N. Berndt, A.D. Hamilton, and S.M. Sebti Targeting protein prenylation for cancer therapy Nat Rev Cancer 11 2011 775 791
    • (2011) Nat Rev Cancer , vol.11 , pp. 775-791
    • Berndt, N.1    Hamilton, A.D.2    Sebti, S.M.3
  • 14
    • 80051932974 scopus 로고    scopus 로고
    • Farnesyl transferase expression determines clinical response to the docetaxel-lonafarnib combination in patients with advanced malignancies
    • J. Kauh, C. Chanel-Vos, D. Escuin, M.P. Fanucchi, R.D. Harvey, N. Saba, D.M. Shin, A. Gal, L. Pan, and M. Kutner Farnesyl transferase expression determines clinical response to the docetaxel-lonafarnib combination in patients with advanced malignancies Cancer 117 2011 4049 4059
    • (2011) Cancer , vol.117 , pp. 4049-4059
    • Kauh, J.1    Chanel-Vos, C.2    Escuin, D.3    Fanucchi, M.P.4    Harvey, R.D.5    Saba, N.6    Shin, D.M.7    Gal, A.8    Pan, L.9    Kutner, M.10
  • 17
    • 84862907863 scopus 로고    scopus 로고
    • Multi-institutional phase 2 clinical and pharmacogenomic trial of tipifarnib plus etoposide for elderly adults with newly diagnosed acute myelogenous leukemia
    • J.E. Karp, T.I. Vener, M. Raponi, E.K. Ritchie, B.D. Smith, S.D. Gore, L.E. Morris, E.J. Feldman, J.M. Greer, and S. Malek Multi-institutional phase 2 clinical and pharmacogenomic trial of tipifarnib plus etoposide for elderly adults with newly diagnosed acute myelogenous leukemia Blood 119 2012 55 63
    • (2012) Blood , vol.119 , pp. 55-63
    • Karp, J.E.1    Vener, T.I.2    Raponi, M.3    Ritchie, E.K.4    Smith, B.D.5    Gore, S.D.6    Morris, L.E.7    Feldman, E.J.8    Greer, J.M.9    Malek, S.10
  • 19
    • 79955505050 scopus 로고    scopus 로고
    • Phase i accelerated dose-escalating safety and pharmacokinetic (PK) study of GGTI-2418, a novel geranylgeranyltransferase i inhibitor in patients with refractory solid tumors
    • P.J. O'Dwyer, M. Gallagher, B. Nguyen, M.J. Waddell, and E.G. Chiorean Phase I accelerated dose-escalating safety and pharmacokinetic (PK) study of GGTI-2418, a novel geranylgeranyltransferase I inhibitor in patients with refractory solid tumors Ann Oncol 21 2010 ii42
    • (2010) Ann Oncol , vol.21 , pp. 42
    • O'Dwyer, P.J.1    Gallagher, M.2    Nguyen, B.3    Waddell, M.J.4    Chiorean, E.G.5
  • 20
    • 79952360375 scopus 로고    scopus 로고
    • Isoprenoid biosynthetic pathway inhibition disrupts monoclonal protein secretion and induces the unfolded protein response pathway in multiple myeloma cells
    • S.A. Holstein, and R.J. Hohl Isoprenoid biosynthetic pathway inhibition disrupts monoclonal protein secretion and induces the unfolded protein response pathway in multiple myeloma cells Leuk Res 35 2011 551 559
    • (2011) Leuk Res , vol.35 , pp. 551-559
    • Holstein, S.A.1    Hohl, R.J.2
  • 21
    • 79958858286 scopus 로고    scopus 로고
    • Procathepsin L secretion, which triggers tumour progression, is regulated by Rab4a in human melanoma cells
    • A. Barbarin, and R. Frade Procathepsin L secretion, which triggers tumour progression, is regulated by Rab4a in human melanoma cells Biochem J 437 2011 97 107
    • (2011) Biochem J , vol.437 , pp. 97-107
    • Barbarin, A.1    Frade, R.2
  • 26
    • 81255144864 scopus 로고    scopus 로고
    • The isoprenoid biosynthetic pathway and statins
    • C.A. Hrycyna, M.O. Bergo, F. Tamanoi, Elsevier
    • S.A. Holstein The isoprenoid biosynthetic pathway and statins C.A. Hrycyna, M.O. Bergo, F. Tamanoi, The Enzymes 2011 Elsevier 279 299
    • (2011) The Enzymes , pp. 279-299
    • Holstein, S.A.1
  • 27
    • 81255177932 scopus 로고    scopus 로고
    • Inhibition of farnesyl and geranylgeranyl diphosphate synthases
    • C.A. Hrycyna, M.O. Bergo, F. Tamanoi, Elsevier
    • S.A. Holstein, and R.J. Hohl Inhibition of farnesyl and geranylgeranyl diphosphate synthases C.A. Hrycyna, M.O. Bergo, F. Tamanoi, The Enzymes 2011 Elsevier 301 319
    • (2011) The Enzymes , pp. 301-319
    • Holstein, S.A.1    Hohl, R.J.2
  • 28
    • 81355135331 scopus 로고    scopus 로고
    • Geranylgeranyl diphosphate synthase: An emerging therapeutic target
    • A.J. Wiemer, D.F. Wiemer, and R.J. Hohl Geranylgeranyl diphosphate synthase: an emerging therapeutic target Clin Pharmacol Ther 90 2011 804 812
    • (2011) Clin Pharmacol Ther , vol.90 , pp. 804-812
    • Wiemer, A.J.1    Wiemer, D.F.2    Hohl, R.J.3
  • 29
    • 78650091355 scopus 로고    scopus 로고
    • Phase 1 trial and pharmacokinetic study of the farnesyl transferase inhibitor tipifarnib in children and adolescents with refractory leukemias: A report from the Children's Oncology Group
    • B.C. Widemann, R.J. Arceci, N. Jayaprakash, E. Fox, P. Zannikos, W. Goodspeed, A. Goodwin, J.J. Wright, S.M. Blaney, and P.C. Adamson Phase 1 trial and pharmacokinetic study of the farnesyl transferase inhibitor tipifarnib in children and adolescents with refractory leukemias: a report from the Children's Oncology Group Pediatr Blood Cancer 56 2011 226 233
    • (2011) Pediatr Blood Cancer , vol.56 , pp. 226-233
    • Widemann, B.C.1    Arceci, R.J.2    Jayaprakash, N.3    Fox, E.4    Zannikos, P.5    Goodspeed, W.6    Goodwin, A.7    Wright, J.J.8    Blaney, S.M.9    Adamson, P.C.10
  • 30
    • 84863990603 scopus 로고    scopus 로고
    • A phase II trial of capecitabine in combination with the farnesyltransferase inhibitor tipifarnib in patients with anthracycline-treated and taxane-resistant metastatic breast cancer: An Eastern Cooperative Oncology Group Study (E1103)
    • [Epub ahead of print]
    • T. Li, M. Guo, W.J. Gradishar, J.A. Sparano, E.A. Perez, M. Wang, and G.W. Sledge A phase II trial of capecitabine in combination with the farnesyltransferase inhibitor tipifarnib in patients with anthracycline-treated and taxane-resistant metastatic breast cancer: an Eastern Cooperative Oncology Group Study (E1103) Breast Cancer Res Treat 2012 [Epub ahead of print]
    • (2012) Breast Cancer Res Treat
    • Li, T.1    Guo, M.2    Gradishar, W.J.3    Sparano, J.A.4    Perez, E.A.5    Wang, M.6    Sledge, G.W.7
  • 31
    • 79952263744 scopus 로고    scopus 로고
    • A phase i clinical-pharmacodynamic study of the farnesyltransferase inhibitor tipifarnib in combination with the proteasome inhibitor bortezomib in advanced acute leukemias
    • J.E. Lancet, V.H. Duong, E.F. Winton, R.K. Stuart, M. Burton, S. Zhang, C. Cubitt, M.A. Blaskovich, J.J. Wright, and S. Sebti A phase I clinical-pharmacodynamic study of the farnesyltransferase inhibitor tipifarnib in combination with the proteasome inhibitor bortezomib in advanced acute leukemias Clin Cancer Res 17 2011 1140 1146
    • (2011) Clin Cancer Res , vol.17 , pp. 1140-1146
    • Lancet, J.E.1    Duong, V.H.2    Winton, E.F.3    Stuart, R.K.4    Burton, M.5    Zhang, S.6    Cubitt, C.7    Blaskovich, M.A.8    Wright, J.J.9    Sebti, S.10
  • 32
    • 79952398715 scopus 로고    scopus 로고
    • A phase 1-2 study of a farnesyltransferase inhibitor, tipifarnib, combined with idarubicin and cytarabine for patients with newly diagnosed acute myeloid leukemia and high-risk myelodysplastic syndrome
    • E. Jabbour, H. Kantarjian, F. Ravandi, G. Garcia-Manero, Z. Estrov, S. Verstovsek, S. O'Brien, S. Faderl, D.A. Thomas, and J.J. Wright A phase 1-2 study of a farnesyltransferase inhibitor, tipifarnib, combined with idarubicin and cytarabine for patients with newly diagnosed acute myeloid leukemia and high-risk myelodysplastic syndrome Cancer 117 2011 1236 1244
    • (2011) Cancer , vol.117 , pp. 1236-1244
    • Jabbour, E.1    Kantarjian, H.2    Ravandi, F.3    Garcia-Manero, G.4    Estrov, Z.5    Verstovsek, S.6    O'Brien, S.7    Faderl, S.8    Thomas, D.A.9    Wright, J.J.10
  • 33
    • 79953904634 scopus 로고    scopus 로고
    • Inhibition of the Ras/Raf/MEK/ERK and RET kinase pathways with the combination of the multikinase inhibitor sorafenib and the farnesyltransferase inhibitor tipifarnib in medullary and differentiated thyroid malignancies
    • D.S. Hong, M.E. Cabanillas, J. Wheler, A. Naing, A.M. Tsimberidou, L. Ye, S.G. Waguespack, M. Hernandez, A.K. El Naggar, and S. Bidyasar Inhibition of the Ras/Raf/MEK/ERK and RET kinase pathways with the combination of the multikinase inhibitor sorafenib and the farnesyltransferase inhibitor tipifarnib in medullary and differentiated thyroid malignancies J Clin Endocrinol Metab 96 2011 997 1005
    • (2011) J Clin Endocrinol Metab , vol.96 , pp. 997-1005
    • Hong, D.S.1    Cabanillas, M.E.2    Wheler, J.3    Naing, A.4    Tsimberidou, A.M.5    Ye, L.6    Waguespack, S.G.7    Hernandez, M.8    El Naggar, A.K.9    Bidyasar, S.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.