메뉴 건너뛰기




Volumn 12, Issue 3, 2003, Pages 413-421

Farnesyl transferase inhibitors in the treatment of breast cancer

Author keywords

Breast; Cancer; Farnesyl transferase; Inhibitors

Indexed keywords

3 BENZYL 7 CYANO 2,3,4,5 TETRAHYDRO 1 (1H IMIDAZOL 4 YLMETHYL) 4 (2 THIENYLSULFONYL) 1H 1,4 BENZODIAZEPINE; ALKYLATING AGENT; ANASTROZOLE; ANTHRACYCLINE; ANTIESTROGEN; ANTIMETABOLITE; AROMATASE INHIBITOR; CARBON; CYCLOPHOSPHAMIDE; CYTOTOXIC AGENT; DOCETAXEL; DOXORUBICIN; ESTROGEN RECEPTOR; FLUOROURACIL; GEMCITABINE; L 778123; LETROZOLE; LONAFARNIB; ONCOPROTEIN; PLACEBO; PRENYLAMINE; PROTEIN FARNESYLTRANSFERASE; PROTEIN FARNESYLTRANSFERASE INHIBITOR; RAS PROTEIN; RECEPTOR BLOCKING AGENT; TAMOXIFEN; TAXANE DERIVATIVE; TIPIFARNIB; TRASTUZUMAB; UNINDEXED DRUG;

EID: 0037340739     PISSN: 13543784     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543784.12.3.413     Document Type: Review
Times cited : (38)

References (56)
  • 1
    • 0037036949 scopus 로고    scopus 로고
    • New drugs for breast cancer
    • SMITH IE: New drugs for breast cancer. Lancet (2002) 360:790-792.
    • (2002) Lancet , vol.360 , pp. 790-792
    • Smith, I.E.1
  • 2
    • 37049183697 scopus 로고
    • Human breast cancer: Correlation with relapse and survival with amplification of the HER-2/neu oncogene
    • SLAMON DJ, CLARK GM, WONG SG, LEVIN WJ, ULLRICH A, MCGUIRE WL: Human breast cancer: correlation with relapse and survival with amplification of the HER-2/neu oncogene. Science (1987) 235:177-182.
    • (1987) Science , vol.235 , pp. 177-182
    • Slamon, D.J.1    Clark, G.M.2    Wong, S.G.3    Levin, W.J.4    Ullrich, A.5    McGuire, W.L.6
  • 3
    • 0035869407 scopus 로고    scopus 로고
    • Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2
    • SLAMON DJ, LEYLAND-JONES B, SHAK S et al.: Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. N. Engl. J. Med. (2001) 344:783-792.
    • (2001) N. Engl. J. Med. , vol.344 , pp. 783-792
    • Slamon, D.J.1    Leyland-Jones, B.2    Shak, S.3
  • 4
    • 0035810147 scopus 로고    scopus 로고
    • Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia
    • DRUKER BJ, TALPAZ M, RESTA DJ et al.: Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. N. Engl. J. Med. (2001) 344:1031-1037.
    • (2001) N. Engl. J. Med. , vol.344 , pp. 1031-1037
    • Druker, B.J.1    Talpaz, M.2    Resta, D.J.3
  • 5
    • 0035810148 scopus 로고    scopus 로고
    • Effect of the tyrosine kinase inhibitor STI571 in a patient with a metastatic gastrointestinal stromal tumor
    • JOENSUU H, ROBERTS PJ, SARLOMO-RIKALA M et al.: Effect of the tyrosine kinase inhibitor STI571 in a patient with a metastatic gastrointestinal stromal tumor. N. Engl. J. Med. (2001) 344:1052-1056.
    • (2001) N. Engl. J. Med. , vol.344 , pp. 1052-1056
    • Joensuu, H.1    Roberts, P.J.2    Sarlomo-Rikala, M.3
  • 7
    • 0024376173 scopus 로고
    • Pas oncogenes in human cancer: A review
    • BOS JL: Pas oncogenes in human cancer: A review. Cancer Res. (1989) 49:4682-4689.
    • (1989) Cancer Res. , vol.49 , pp. 4682-4689
    • Bos, J.L.1
  • 8
    • 0024406286 scopus 로고
    • All ras proteins are polyisoprenylated but only some are palmitoylated
    • HANCOCK JF, MAGEE AI, CHILDS JE, MARSHALL CJ: All ras proteins are polyisoprenylated but only some are palmitoylated. Cell (1989) 57:1167-1177.
    • (1989) Cell , vol.57 , pp. 1167-1177
    • Hancock, J.F.1    Magee, A.I.2    Childs, J.E.3    Marshall, C.J.4
  • 9
    • 0029150669 scopus 로고
    • Inhibition of farnesyltransferase induces regression of mammary and salivary carcinomas in ras transgenic mice
    • KOHL NE, OMER CA, CONNER MW et al.: Inhibition of farnesyltransferase induces regression of mammary and salivary carcinomas in ras transgenic mice. Nat. Medicine (1995) 1:792-797.
    • (1995) Nat. Medicine , vol.1 , pp. 792-797
    • Kohl, N.E.1    Omer, C.A.2    Conner, M.W.3
  • 10
    • 0029002907 scopus 로고
    • Aberrant function of the Ras signal transduction pathway in human breast cancer
    • CLARK GJ, DER CJ: Aberrant function of the Ras signal transduction pathway in human breast cancer. Breast Cancer Res. Treat. (1995) 35:133-144.
    • (1995) Breast Cancer Res. Treat. , vol.35 , pp. 133-144
    • Clark, G.J.1    Der, C.J.2
  • 11
    • 0032900619 scopus 로고    scopus 로고
    • Treatment with farnesyl-protein transferase inhibitor induces regression of mammary tumors in transforming growth factor (TGF) alpha and TGF alpha/neu transgenic mice by inhibition of mitogenic activity and induction of apoptosis
    • NORGAARD P, LAW B, JOSEPH H et al.: Treatment with farnesyl-protein transferase inhibitor induces regression of mammary tumors in transforming growth factor (TGF) alpha and TGF alpha/neu transgenic mice by inhibition of mitogenic activity and induction of apoptosis. Clin. Cancer Res. (1999) 5:35-42.
    • (1999) Clin. Cancer Res. , vol.5 , pp. 35-42
    • Norgaard, P.1    Law, B.2    Joseph, H.3
  • 12
    • 0028835253 scopus 로고
    • A peptidomimetic inhibitor of farnesyl protein transferase blocks the anchorage-dependent and -independent growth of human tumor cell lines
    • SEPP-LORENZINO L, MA Z, RANDS E, KOHL NE, GIBBS JB, ROSEN NA: A peptidomimetic inhibitor of farnesyl protein transferase blocks the anchorage-dependent and -independent growth of human tumor cell lines. Cancer Res. (1995) 55:5301-5309.
    • (1995) Cancer Res. , vol.55 , pp. 5301-5309
    • Sepp-Lorenzino, L.1    Ma, Z.2    Rands, E.3    Kohl, N.E.4    Gibbs, J.B.5    Rosen, N.A.6
  • 13
    • 0035132538 scopus 로고    scopus 로고
    • Characterization of the antitumor effects of the selective farnesyl protein transferase inhibitor R115777 in vivo and in vitro
    • END DW, SMETS G, TODD A et al.: Characterization of the antitumor effects of the selective farnesyl protein transferase inhibitor R115777 in vivo and in vitro. Cancer Res. (2001) 61:131-137.
    • (2001) Cancer Res. , vol.61 , pp. 131-137
    • End, D.W.1    Smets, G.2    Todd, A.3
  • 14
    • 0030749458 scopus 로고    scopus 로고
    • Farnesyltransferase inhibitors and cancer treatment: Targeting simply ras?
    • 1333
    • COX AD, DER CJ: Farnesyltransferase inhibitors and cancer treatment: targeting simply ras? Biochim. Biophys. Acta (1997) 1333:F51-F71.
    • (1997) Biochim. Biophys. Acta
    • Cox, A.D.1    Der, C.J.2
  • 15
    • 0034730625 scopus 로고    scopus 로고
    • Farnesyl transferase inhibitors block the farnesylation of CENP-E and CENP-F and alter the association of CENP-E with the microtubules
    • ASHAR HR, JAMES L, GRAY K et al.: Farnesyl transferase inhibitors block the farnesylation of CENP-E and CENP-F and alter the association of CENP-E with the microtubules. J. Biol. Chem. (2000) 275:30451-30457.
    • (2000) J. Biol. Chem. , vol.275 , pp. 30451-30457
    • Ashar, H.R.1    James, L.2    Gray, K.3
  • 16
    • 0030968859 scopus 로고    scopus 로고
    • Direct demonstration of geranylgeranylation and farnesylation of ki-ras in vivo
    • ROWELL CA, KOWALCZYK JJ, LEWIS MD, GARCIA AM: Direct demonstration of geranylgeranylation and farnesylation of ki-ras in vivo. J. Biol. Chem. (1997) 272:14093-14097.
    • (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
  • 17
    • 0030923192 scopus 로고    scopus 로고
    • K- and N-ras are geranylgeranylated in cells treated with farnesyl protein transferase inhibitors
    • WHYTE DB, KIRSCHMEIER P, HOCKENBERRY TNJ et al.: K- and N-ras are geranylgeranylated in cells treated with farnesyl protein transferase inhibitors. J. Biol. Chem. (1997) 272:14459-14464.
    • (1997) J. Biol. Chem. , vol.272 , pp. 14459-14464
    • Whyte, D.B.1    Kirschmeier, P.2    Hockenberry, T.N.J.3
  • 18
    • 0035523359 scopus 로고    scopus 로고
    • Actin' up: RhoB in cancer and apoptosis
    • PRENDERGAST GC: Actin' up: RhoB in cancer and apoptosis. Nat. Rev. Cancer (2001) 1:162-168.
    • (2001) Nat. Rev. Cancer , vol.1 , pp. 162-168
    • Prendergast, G.C.1
  • 19
    • 0033016719 scopus 로고    scopus 로고
    • Cell growth inhibition by farnesyltransferase inhibitors is mediated by gain of geranylgeranylated RhoB
    • DU W, LEBOWITZ PF, PRENDERGAST GC: Cell growth inhibition by farnesyltransferase inhibitors is mediated by gain of geranylgeranylated RhoB. Mol. Cell. Biol. (1999) 19:1831-1840.
    • (1999) Mol. Cell. Biol. , vol.19 , pp. 1831-1840
    • Du, W.1    Lebowitz, P.F.2    Prendergast, G.C.3
  • 20
    • 0030916369 scopus 로고    scopus 로고
    • Farnesyltransferase inhibitors alter the prenylation and growth-stimulating function of Rho B
    • LEBOWITZ PF, CASEY PJ, PRENDERGAST GC, THISSEN JA: Farnesyltransferase inhibitors alter the prenylation and growth-stimulating function of Rho B. J. Biol. Chem. (1997) 272:15591-15594.
    • (1997) J. Biol. Chem. , vol.272 , pp. 15591-15594
    • Lebowitz, P.F.1    Casey, P.J.2    Prendergast, G.C.3    Thissen, J.A.4
  • 21
    • 0036599583 scopus 로고    scopus 로고
    • Reversion of RhoC GTPase-induced inflammatory breast cancer phenotype by treatment with a farnesyl transferase inhibitor
    • VAN GOLEN KL, BAO L, DIVITO MM, PRENDERGAST GC, MERAJVER SD: Reversion of RhoC GTPase-induced inflammatory breast cancer phenotype by treatment with a farnesyl transferase inhibitor. Mol. Cancer Ther. (2002) 1:575-583.
    • (2002) Mol. Cancer Ther. , vol.1 , pp. 575-583
    • Van Golen, K.L.1    Bao, L.2    Divito, M.M.3    Prendergast, G.C.4    Merajver, S.D.5
  • 22
    • 0033986790 scopus 로고    scopus 로고
    • The phosphoinositide 3-OH kinase/AKT2 pathway as a critical target for farnesyltransferase inhibitor-induced apoptosis
    • JIANG K, COPPOLA D, CRESPO NC et al.: The phosphoinositide 3-OH kinase/AKT2 pathway as a critical target for farnesyltransferase inhibitor-induced apoptosis. Mol. Cell. Biol. (2000) 20:139-148.
    • (2000) Mol. Cell. Biol. , vol.20 , pp. 139-148
    • Jiang, K.1    Coppola, D.2    Crespo, N.C.3
  • 23
    • 0035181479 scopus 로고    scopus 로고
    • Preclinical antitumor activity and pharmacodynamic studies with the farnesyl protein transferase inhibitor R115777 in human breast cancer
    • KELLAND LR, SMITH V, VALENTI M et al.: Preclinical antitumor activity and pharmacodynamic studies with the farnesyl protein transferase inhibitor R115777 in human breast cancer. Clin. Cancer Res. (2001) 7:3544-3550.
    • (2001) Clin. Cancer Res. , vol.7 , pp. 3544-3550
    • Kelland, L.R.1    Smith, V.2    Valenti, M.3
  • 24
    • 18544412314 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of farnesyl protein transferase inhibitor R115777 in advanced cancer
    • ZUJEWSKI J, HORAK ID, BOL CJ, et al.: Phase I and pharmacokinetic study of farnesyl protein transferase inhibitor R115777 in advanced cancer. J. Clin. Oncol. (2000) 18:927-941.
    • (2000) J. Clin. Oncol. , vol.18 , pp. 927-941
    • Zujewski, J.1    Horak, I.D.2    Bol, C.J.3
  • 25
    • 0035383789 scopus 로고    scopus 로고
    • Clinical and biologic activity of the farnesyltransferase inhibitor R115777 in adults with refractory and relapsed acute leukemias: A Phase I clinical-laboratory correlative trial
    • KARP JE, LANCET JE, KAUFMANN SH et al.: Clinical and biologic activity of the farnesyltransferase inhibitor R115777 in adults with refractory and relapsed acute leukemias: a Phase I clinical-laboratory correlative trial. Blood (2001) 97:3361-3369.
    • (2001) Blood , vol.97 , pp. 3361-3369
    • Karp, J.E.1    Lancet, J.E.2    Kaufmann, S.H.3
  • 26
    • 0035064808 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of the orally administered farnesyl transferase inhibitor R115777 in patients with advanced solid tumors
    • PUNT CJ, VAN MAANEN L, BOL CJ, SEIFERT WF, WAGENER DJ: Phase I and pharmacokinetic study of the orally administered farnesyl transferase inhibitor R115777 in patients with advanced solid tumors. Anticancer Drugs (2001) 12:193-197.
    • (2001) Anticancer Drugs , vol.12 , pp. 193-197
    • Punt, C.J.1    Van Maanen, L.2    Bol, C.J.3    Seifert, W.F.4    Wagener, D.J.5
  • 27
    • 0036605562 scopus 로고    scopus 로고
    • Phase I clinical and pharmacologic study of chronic oral administration of the farnesyl protein transferase inhibitor R115777 in advanced cancer
    • CRUL M, DE KLERK G, SWART M et al.: Phase I clinical and pharmacologic study of chronic oral administration of the farnesyl protein transferase inhibitor R115777 in advanced cancer. J. Clin. Oncol. (2002) 20:2726-2735.
    • (2002) J. Clin. Oncol. , vol.20 , pp. 2726-2735
    • Crul, M.1    De Klerk, G.2    Swart, M.3
  • 28
    • 0036656207 scopus 로고    scopus 로고
    • Farnesyltransferase inhibitors and myeloid malignancies: Phase I evidence of Zarnestra activity in high-risk leukemias
    • LANCET JE, ROSENBLATT J, KARP JE: Farnesyltransferase inhibitors and myeloid malignancies: Phase I evidence of Zarnestra activity in high-risk leukemias. Semin. Hematol. (2002) 39:31-35.
    • (2002) Semin. Hematol. , vol.39 , pp. 31-35
    • Lancet, J.E.1    Rosenblatt, J.2    Karp, J.E.3
  • 29
    • 0000990647 scopus 로고    scopus 로고
    • Efficacy and tolerability of two dosing regimens of R115777 (Zarnestra), a farnesyl protein transferase inhibitor, in patients with advanced breast cancer
    • (Abstract)
    • JOHNSTON SRD, HICKISH T, HOUSTON S, ELLIS PA, HOWES AJ, THIBAULT A: Efficacy and tolerability of two dosing regimens of R115777 (Zarnestra), a farnesyl protein transferase inhibitor, in patients with advanced breast cancer. Proc. Am. Soc. Clin. Oncol. (2002) 21:35a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Johnston, S.R.D.1    Hickish, T.2    Houston, S.3    Ellis, P.A.4    Howes, A.J.5    Thibault, A.6
  • 30
    • 0003268466 scopus 로고    scopus 로고
    • Interim results from a Phase II study of R115777 (Zarnestra) in patients with relapsed and refractory acute myelogenous leukemia
    • (Abstract)
    • HAROUSSEAU J-L, STONE R, THOMAS X et al.: Interim results from a Phase II study of R115777 (Zarnestra) in patients with relapsed and refractory acute myelogenous leukemia. Proc. Am. Soc. Clin. Oncol. (2002) 21:265a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Harousseau, J.-L.1    Stone, R.2    Thomas, X.3
  • 31
    • 0012446889 scopus 로고    scopus 로고
    • Efficacy of the farnesyl transferase inhibitor, ZARNESTRATM (R115777), in chronic myeloid leukemia and other other hematological malignancies
    • (E-pub ahead of print)
    • CORTES JE, ALBITAR M, THOMAS D et al.: Efficacy of the farnesyl transferase inhibitor, ZARNESTRATM (R115777), in chronic myeloid leukemia and other other hematological malignancies. Blood (2002) (E-pub ahead of print).
    • (2002) Blood
    • Cortes, J.E.1    Albitar, M.2    Thomas, D.3
  • 32
    • 0003230749 scopus 로고    scopus 로고
    • Phase I/II study of farnesyltransferase inhibitor R115777 (Zarnestra) in patients with myeloproliferative disorders (MPDs): Preliminary results
    • (Abstract)
    • GOTLIB J, DUGAN K, KATAMNENI U et al.: Phase I/II study of farnesyltransferase inhibitor R115777 (Zarnestra) in patients with myeloproliferative disorders (MPDs): preliminary results. Proc. Am. Soc. Clin. Oncol. (2002) 21:4a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Gotlib, J.1    Dugan, K.2    Katamneni, U.3
  • 33
    • 0003258673 scopus 로고    scopus 로고
    • Phase II trial of R115777 (Zarnestra) in patients with recurrent glioma not taking enzyme inducing antiepileptic drugs (EIAED): A North American Brain Tumor Consortium (NABTC) report
    • (Abstract)
    • CLOUGHESY TF, KUHN J, WEN P et al.: Phase II trial of R115777 (Zarnestra) in patients with recurrent glioma not taking enzyme inducing antiepileptic drugs (EIAED): a North American Brain Tumor Consortium (NABTC) report. Proc. Am. Soc. Clin. Oncol. (2002) 21:80a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Cloughesy, T.F.1    Kuhn, J.2    Wen, P.3
  • 34
    • 0001120711 scopus 로고    scopus 로고
    • Phase II study of the farnesyl transferase inhibitor (FTI) R115777 (Zarnestra) in patients with relapsed small cell lung cancer (SCLC)
    • (Abstract)
    • HEYMACH JV, DE PORRE PM, DEVORE RF et al.: Phase II study of the farnesyl transferase inhibitor (FTI) R115777 (Zarnestra) in patients with relapsed small cell lung cancer (SCLC). Proc. Am. Soc. Clin. Oncol. (2002) 21:139a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Heymach, J.V.1    Deporre, P.M.2    Devore, R.F.3
  • 35
    • 0003230747 scopus 로고    scopus 로고
    • A Phase II study of the farnesyltransferase inhibitor R115777 in patients with advanced non-small cell lung cancer
    • (Abstract)
    • ADJEI AA, MAUER A, MARKS R et al.: A Phase II study of the farnesyltransferase inhibitor R115777 in patients with advanced non-small cell lung cancer. Proc. Am. Soc. Clin. Oncol. (2002) 21:290a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Adjei, A.A.1    Mauer, A.2    Marks, R.3
  • 36
    • 0001120709 scopus 로고    scopus 로고
    • A Phase II study of the farnesyl transferase inhibitor R115777 in pancreatic cancer
    • A southwest oncology group (SWOG) study (Abstract)
    • MACDONALD JS, CHANSKY K, WHITEHEAD R, WADE J, GIGUERE J, ABBRUZZESE JL: A Phase II study of the farnesyl transferase inhibitor R115777 in pancreatic cancer. A southwest oncology group (SWOG) study. Proc. Am. Soc. Clin. Oncol. (2002) 21:138a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • MacDonald, J.S.1    Chansky, K.2    Whitehead, R.3    Wade, J.4    Giguere, J.5    Abbruzzese, J.L.6
  • 37
    • 0001674319 scopus 로고    scopus 로고
    • Randomized double-blind placebo-controlled trial of the farnesyltransferase inhibitor R115777 (Zarnestra) in advanced refractory colorectal cancer
    • (Abstract)
    • CUNNINGHAM D, DE GRAMONT A, SCHEITHAUER W et al.: Randomized double-blind placebo-controlled trial of the farnesyltransferase inhibitor R115777 (Zarnestra) in advanced refractory colorectal cancer. Proc. Am. Soc. Clin. Oncol. (2002) 21:126a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Cunningham, D.1    De Gramont, A.2    Scheithauer, W.3
  • 38
    • 0000324578 scopus 로고    scopus 로고
    • Phase III trial comparing gemcitabine + R115777 (Zarnestra) versus gemcitabine + placebo in advanced pancreatic cancer (PC)
    • (Abstract)
    • VAN CUTSEM E, KARASEK P, OETTLE H et al.: Phase III trial comparing gemcitabine + R115777 (Zarnestra) versus gemcitabine + placebo in advanced pancreatic cancer (PC). Proc. Am. Soc. Clin. Oncol. (2002) 21:130a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Van Cutsem, E.1    Karasek, P.2    Oettle, H.3
  • 39
    • 14344254868 scopus 로고    scopus 로고
    • Antitumor activity of SCH66336, an orally bioavailable tricyclic inhibitor of farnesyl protein transferase, in human tumor xenograft models and wap-ras transgenic mice
    • LIU M, BRYANT MS, CHEN J, LEE S et al.: Antitumor activity of SCH66336, an orally bioavailable tricyclic inhibitor of farnesyl protein transferase, in human tumor xenograft models and wap-ras transgenic mice. Cancer Res. (1998) 58:4947-4956.
    • (1998) Cancer Res. , vol.58 , pp. 4947-4956
    • Liu, M.1    Bryant, M.S.2    Chen, J.3    Lee, S.4
  • 40
    • 0034071688 scopus 로고    scopus 로고
    • A Phase I trial of the farnesyl transferase inhibitor SCH66336: Evidence for biological and clinical activity
    • ADJEI AA, ERLICHMAN C, DAVIS JN et al.: A Phase I trial of the farnesyl transferase inhibitor SCH66336: evidence for biological and clinical activity. Cancer Res. (2000) 60:1871-1877.
    • (2000) Cancer Res. , vol.60 , pp. 1871-1877
    • Adjei, A.A.1    Erlichman, C.2    Davis, J.N.3
  • 41
    • 0035865305 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of the oral farnesyl transferase inhibitor SCH 66336 given twice daily to patients with advanced solid tumors
    • ESKENS FA, AWADA A, CUTLER DL et al.: Phase I and pharmacokinetic study of the oral farnesyl transferase inhibitor SCH 66336 given twice daily to patients with advanced solid tumors. J. Clin. Oncol. (2001) 19:1167-1175.
    • (2001) J. Clin. Oncol. , vol.19 , pp. 1167-1175
    • Eskens, F.A.1    Awada, A.2    Cutler, D.L.3
  • 42
    • 0035990832 scopus 로고    scopus 로고
    • A Phase II trial of farnesyl protein transferase inhibitor SCH 66336, given by twice-daily oral administration, in patients with metastatic colorectal cancer refractory to 5-fluorouracil and irinotecan
    • SHARMA S, KEMENY N, KELSEN DP et al.: A Phase II trial of farnesyl protein transferase inhibitor SCH 66336, given by twice-daily oral administration, in patients with metastatic colorectal cancer refractory to 5-fluorouracil and irinotecan. Ann. Oncol. (2002) 13:1067-1071.
    • (2002) Ann. Oncol. , vol.13 , pp. 1067-1071
    • Sharma, S.1    Kemeny, N.2    Kelsen, D.P.3
  • 43
    • 0000409316 scopus 로고    scopus 로고
    • Phase I study of continuous oral lonafarnib plus weekly paclitaxel for advanced cancer
    • (Abstract)
    • LIPTON A, READY N, BUKOWSKI RM et al.: Phase I study of continuous oral lonafarnib plus weekly paclitaxel for advanced cancer. Proc. Am. Soc. Clin. Oncol. (2002) 21:92a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Lipton, A.1    Ready, N.2    Bukowski, R.M.3
  • 44
    • 0003282149 scopus 로고    scopus 로고
    • A Phase I pharmacokinetic (PK) and biological study of the farnesyl transferase inhibitor (FTI) sarasar (lonafarnib, SCH66336), cisplatin(C) and gemcitabine (G) in patients (pts) with advanced solid tumors
    • (Abstract)
    • PIERSON AS, HOLDEN SN, BASCHE M et al.: A Phase I pharmacokinetic (PK) and biological study of the farnesyl transferase inhibitor (FTI) sarasar (lonafarnib, SCH66336), cisplatin(C) and gemcitabine (G) in patients (pts) with advanced solid tumors. Proc. Am. Soc. Clin. Oncol. (2002) 21:92a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Pierson, A.S.1    Holden, S.N.2    Basche, M.3
  • 45
    • 0033214457 scopus 로고    scopus 로고
    • Antitumor efficacy of a novel class of non-thiol-containing peptidomimetic inhibitors of Farnesyltransferase and Geranylgeranyltransferase I: Combination therapy with the cytotoxic agents cisplatin, taxol and gemcitabine
    • SUN J, BLASKOVICH MA, KNOWLES D et al.: Antitumor efficacy of a novel class of non-thiol-containing peptidomimetic inhibitors of Farnesyltransferase and Geranylgeranyltransferase I: Combination therapy with the cytotoxic agents cisplatin, taxol and gemcitabine. Cancer Res. (1999) 59:4919-4926.
    • (1999) Cancer Res. , vol.59 , pp. 4919-4926
    • Sun, J.1    Blaskovich, M.A.2    Knowles, D.3
  • 46
    • 0033729718 scopus 로고    scopus 로고
    • The farnesyl protein transferase inhibitor SCH66336 synergizes with taxanes in vitro and enhances their antitumor activity in vivo
    • SHI B, YAREMKO B, HAJIAN G et al.: The farnesyl protein transferase inhibitor SCH66336 synergizes with taxanes in vitro and enhances their antitumor activity in vivo. Cancer Chemother. Pharmacol. (2000) 46:387-393.
    • (2000) Cancer Chemother. Pharmacol. , vol.46 , pp. 387-393
    • Shi, B.1    Yaremko, B.2    Hajian, G.3
  • 47
    • 0035886842 scopus 로고    scopus 로고
    • Preclinical antitumor activity of BMS-214662, a highly apoptotic and novel farnesyltransferase inhibitor
    • ROSE WC, LEE FYF, FAIRCHILD CR et al.: Preclinical antitumor activity of BMS-214662, a highly apoptotic and novel farnesyltransferase inhibitor. Cancer Res. (2001) 61:7507-7517.
    • (2001) Cancer Res. , vol.61 , pp. 7507-7517
    • Rose, W.C.1    Lee, F.Y.F.2    Fairchild, C.R.3
  • 48
    • 0003282157 scopus 로고    scopus 로고
    • A Phase I clinical, pharmacokinetic and pharmacodynamic study of the farnesyltransferase inhibitor BMS-214662 given as a 24 hour continuous intravenous infusion once weekly × 3 in patients with advanced solid tumors
    • (Abstract)
    • ZHU AX, SUPKO JG, RYAN DR, CLARK JW, BUTKIEWICZ L, EDER JP: A Phase I clinical, pharmacokinetic and pharmacodynamic study of the farnesyltransferase inhibitor BMS-214662 given as a 24 hour continuous intravenous infusion once weekly × 3 in patients with advanced solid tumors. Proc. Am. Soc. Clin. Oncol. (2002) 21:92a (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Zhu, A.X.1    Supko, J.G.2    Ryan, D.R.3    Clark, J.W.4    Butkiewicz, L.5    Eder, J.P.6
  • 49
    • 0003262222 scopus 로고    scopus 로고
    • A Phase II study of efficacy and tolerability of the farnesyl-protein transferase inhibitor L-778,123 as first-line therapy in patients with advanced non-small cell lung cancer (NSCLC)
    • (Abstract)
    • EVANS TL, FIDIAS P, SKARIN A et al.: A Phase II study of efficacy and tolerability of the farnesyl-protein transferase inhibitor L-778,123 as first-line therapy in patients with advanced non-small cell lung cancer (NSCLC). Proc. Am. Soc. Clin. Oncol. (2002) 21:13b (Abstract).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Evans, T.L.1    Fidias, P.2    Skarin, A.3
  • 50
    • 0036097103 scopus 로고    scopus 로고
    • A Phase I trial of the farnesyltransferase inhibitor L-778,123 and radiotherapy for locally advanced lung and head and neck cancer
    • HAHN SM, BERNHARD EJ, REGINA W et al.: A Phase I trial of the farnesyltransferase inhibitor L-778,123 and radiotherapy for locally advanced lung and head and neck cancer. Clin. Cancer Res. (2002) 8:1065-1072.
    • (2002) Clin. Cancer Res. , vol.8 , pp. 1065-1072
    • Hahn, S.M.1    Bernhard, E.J.2    Regina, W.3
  • 52
    • 0035678051 scopus 로고    scopus 로고
    • A Phase I and pharmacological study of the farnesyl protein transferase inhibitor L-778,123 in patients with solid malignancies
    • BRITTEN CD, ROWINSKY EK, SOIGNET S et al.: A Phase I and pharmacological study of the farnesyl protein transferase inhibitor L-778,123 in patients with solid malignancies. Clin. Cancer Res. (2001) 7:3894-3903.
    • (2001) Clin. Cancer Res. , vol.7 , pp. 3894-3903
    • Britten, C.D.1    Rowinsky, E.K.2    Soignet, S.3
  • 53
    • 0035991542 scopus 로고    scopus 로고
    • The use of molecular markers in farnesyltransferase inhibitor (FTI) therapy of breast cancer
    • MOASSER MM, ROSEN N: The use of molecular markers in farnesyltransferase inhibitor (FTI) therapy of breast cancer. Breast Cancer Res. Treat. (2002) 73:135-144.
    • (2002) Breast Cancer Res. Treat. , vol.73 , pp. 135-144
    • Moasser, M.M.1    Rosen, N.2
  • 55
    • 0036284741 scopus 로고    scopus 로고
    • Establishment and characterization of acquired resistance to the farnesyl protein transferase inhibitor R115777 in a human colon cancer cell line
    • SMITH V, ROWLANDS MG, BARRIE E, WORKMAN P, KELLAND LR: Establishment and characterization of acquired resistance to the farnesyl protein transferase inhibitor R115777 in a human colon cancer cell line. Clin. Cancer Res. (2002) 8:2002-2009.
    • (2002) Clin. Cancer Res. , vol.8 , pp. 2002-2009
    • Smith, V.1    Rowlands, M.G.2    Barrie, E.3    Workman, P.4    Kelland, L.R.5
  • 56
    • 0029954843 scopus 로고    scopus 로고
    • P-glycoprotein - A mediator of multidrug resistance in tumour cells
    • GERMANN UA: P-glycoprotein - a mediator of multidrug resistance in tumour cells. Eur. J. Cancer (1996) 32A:927-944.
    • (1996) Eur. J. Cancer , vol.32 A , pp. 927-944
    • Germann, U.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.