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Volumn 70, Issue 10, 2010, Pages 3996-4004

Disulfiram treatment facilitates phosphoinositide 3-kinase inhibition in human breast cancer cells in vitro and in vivo

Author keywords

[No Author keywords available]

Indexed keywords

2 MORPHOLINO 8 PHENYLCHROMONE; BENZYLOXYCARBONYLLEUCYLLEUCYLLEUCINAL; BETA ACTIN; COPPER; DISULFIRAM; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE; PHOSPHATIDYLINOSITOL 3 KINASE; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE; PROTEIN BAX; PROTEIN KINASE B; S6 KINASE; UBIQUITIN;

EID: 77952829803     PISSN: 00085472     EISSN: 15387445     Source Type: Journal    
DOI: 10.1158/0008-5472.CAN-09-3752     Document Type: Article
Times cited : (88)

References (50)
  • 1
    • 28844448182 scopus 로고    scopus 로고
    • Oncogenic PI3K deregulates transcription and translation
    • DOI 10.1038/nrc1753
    • Bader AG, Kang S, Zhao L, Vogt PK. Oncogenic PI3K deregulates transcription and translation. Nat Rev Cancer 2005;5:921-929 (Pubitemid 41766781)
    • (2005) Nature Reviews Cancer , vol.5 , Issue.12 , pp. 921-929
    • Bader, A.G.1    Kang, S.2    Zhao, L.3    Vogt, P.K.4
  • 2
    • 0037205048 scopus 로고    scopus 로고
    • The phosphoinositide 3-kinase pathway
    • Cantley LC. The phosphoinositide 3-kinase pathway. Science 2002; 296:1655-1657
    • (2002) Science , vol.296 , pp. 1655-1657
    • Cantley, L.C.1
  • 3
    • 0036632368 scopus 로고    scopus 로고
    • The phosphatidylinositol 3-kinase-AKT pathway in human cancer
    • Vivanco I, Sawyers CL. The phosphatidylinositol 3-Kinase AKT pathway in human cancer. Nat Rev Cancer 2002;2:489-501. (Pubitemid 37328931)
    • (2002) Nature Reviews Cancer , vol.2 , Issue.7 , pp. 489-501
    • Vivanco, I.1    Sawyers, C.L.2
  • 5
    • 0034713390 scopus 로고    scopus 로고
    • PIK3CA as an oncogene in cervical cancer
    • Ma YY, Wei SJ, Lin YC, et al. PIK3CA as an oncogene in cervical cancer. Oncogene 2000;19:2739-2744
    • (2000) Oncogene , vol.19 , pp. 2739-2744
    • Ma, Y.Y.1    Wei, S.J.2    Lin, Y.C.3
  • 6
    • 0033119702 scopus 로고    scopus 로고
    • Expression analysis of genes at 3q26-q27 involved in frequent amplification in squamous cell lung carcinoma
    • DOI 10.1016/S0959-8049(98)00419-5, PII S0959804998004195
    • Racz A, Brass N, Heckel D, Pahl S, Remberger K, Meese E. Expression analysis of genes at 3q26-q27 involved in frequent amplification in squamous cell lung carcinoma. Eur J Cancer 1999; 35:641-646 (Pubitemid 29192975)
    • (1999) European Journal of Cancer , vol.35 , Issue.4 , pp. 641-646
    • Racz, A.1    Brass, N.2    Heckel, D.3    Pahl, S.4    Remberger, K.5    Meese, E.6
  • 13
    • 27544515272 scopus 로고    scopus 로고
    • Somatic mutation and gain of copy number of PIK3CA in human breast cancer
    • Wu G, Xing M, Mambo E, et al. Somatic mutation and gain of copy number of PIK3CA in human breast cancer. Breast Cancer Res 2005; 7:R609-16.
    • (2005) Breast Cancer Res , vol.7
    • Wu, G.1    Xing, M.2    Mambo, E.3
  • 14
    • 0346690261 scopus 로고    scopus 로고
    • Combinatorial Efficacy Achieved Through Two-Point Blockade within a Signaling Pathway - A Chemical Genetic Approach
    • Fan QW, Specht KM, Zhang C, Goldenberg DD, Shokat KM, Weiss WA. Combinatorial efficacy achieved through two-point blockade within a signaling pathway-a chemical genetic approach. Cancer Res 2003;63:8930-8938 (Pubitemid 38064073)
    • (2003) Cancer Research , vol.63 , Issue.24 , pp. 8930-8938
    • Fan, Q.-W.1    Specht, K.M.2    Zhang, C.3    Goldenberg, D.D.4    Shokat, K.M.5    Weiss, W.A.6
  • 15
    • 0036168948 scopus 로고    scopus 로고
    • Inhibition of phosphatidylinositol 3′-kinase increases efficacy of paclitaxel in in vitro and in vivo ovarian cancer models
    • Hu L, Hofmann J, Lu Y,Mills GB, Jaffe RB. Inhibition of phosphatidylinositol 3′-kinase increases efficacy of paclitaxel in in vitro and in vivo ovarian cancer models. Cancer Res 2002;62:1087-1092 (Pubitemid 34160292)
    • (2002) Cancer Research , vol.62 , Issue.4 , pp. 1087-1092
    • Hu, L.1    Hofmann, J.2    Lu, Y.3    Mills, G.B.4    Jaffe, R.B.5
  • 16
    • 0037194613 scopus 로고    scopus 로고
    • Phosphatidylinositol-3 kinase inhibitors enhance the anti-leukemia effect of STI571
    • DOI 10.1038/sj.onc.1205724
    • Klejman A, Rushen L, Morrione A, Slupianek A, Skorski T. Phosphatidylinositol-3 kinase inhibitors enhance the anti-leukemia effect of STI571. Oncogene 2002;21:5868-5876 (Pubitemid 35007237)
    • (2002) Oncogene , vol.21 , Issue.38 , pp. 5868-5876
    • Klejman, A.1    Rushen, L.2    Morrione, A.3    Slupianek, A.4    Skorski, T.5
  • 17
    • 43549112362 scopus 로고    scopus 로고
    • Potentiation of antileukemic therapies by the dual PI3K/PDK-1 inhibitor, BAG956: Effects on BCR-ABL- And mutant FLT3-expressing cells
    • Weisberg E, Banerji L, Wright RD, et al. Potentiation of antileukemic therapies by the dual PI3K/PDK-1 inhibitor, BAG956: effects on BCR-ABL- and mutant FLT3-expressing cells. Blood 2008;111: 3723-3734
    • (2008) Blood , vol.111 , pp. 3723-3734
    • Weisberg, E.1    Banerji, L.2    Wright, R.D.3
  • 18
    • 0036240701 scopus 로고    scopus 로고
    • The proteasome: A target novel for cancer chemotherapy
    • DOI 10.1038/sj/leu/2402417
    • Almond JB, Cohen GM. The proteasome: a novel target for cancer chemotherapy. Leukemia 2002;16:433-443 (Pubitemid 34449723)
    • (2002) Leukemia , vol.16 , Issue.4 , pp. 433-443
    • Almond, J.B.1    Cohen, G.M.2
  • 19
    • 0033178142 scopus 로고    scopus 로고
    • Proteasome inhibitors as potential novel anticancer agents
    • DOI 10.1054/drup.1999.0095
    • Dou QP, Li B. Proteasome inhibitors as potential novel anticancer agents. Drug Resist Updat 1999;2:215-223 (Pubitemid 29526245)
    • (1999) Drug Resistance Updates , vol.2 , Issue.4 , pp. 215-223
    • Dou, Q.P.1    Li, B.2
  • 20
    • 0034864799 scopus 로고    scopus 로고
    • Proteasome inhibitors: From research tools to drug candidates
    • Kisselev AF, Goldberg AL. Proteasome inhibitors: from research tools to drug candidates. Chem Biol 2001;8:739-758
    • (2001) Chem Biol , vol.8 , pp. 739-758
    • Kisselev, A.F.1    Goldberg, A.L.2
  • 21
    • 0036181371 scopus 로고    scopus 로고
    • Development of the proteasome inhibitor PS-341
    • Adams J. Development of the proteasome inhibitor PS-341. Oncologist 2002;7:9-16.
    • (2002) Oncologist , vol.7 , pp. 9-16
    • Adams, J.1
  • 22
    • 33751285781 scopus 로고    scopus 로고
    • Disulfiram, a clinically used anti-alcoholism drug and copper-binding agent, induces apoptotic cell death in breast cancer cultures and xenografts via inhibition of the proteasome activity
    • DOI 10.1158/0008-5472.CAN-06-2126
    • Chen D, Cui QC, Yang H, Dou QP. Disulfiram, a clinically used anti-alcoholism drug and copper-binding agent, induces apoptotic cell death in breast cancer cultures and xenografts via inhibition of the proteasome activity. Cancer Res 2006;66:10425-10433 (Pubitemid 44799763)
    • (2006) Cancer Research , vol.66 , Issue.21 , pp. 10425-10433
    • Chen, D.1    Cui, Q.C.2    Yang, H.3    Dou, Q.P.4
  • 23
    • 0346692671 scopus 로고    scopus 로고
    • Bortezomib (millennium pharmaceuticals)
    • Dou QP, Goldfarb RH. Bortezomib (millennium pharmaceuticals). IDrugs 2002;5:828-834
    • (2002) IDrugs , vol.5 , pp. 828-834
    • Dou, Q.P.1    Goldfarb, R.H.2
  • 24
    • 33751275548 scopus 로고    scopus 로고
    • A novel anticancer gold(III) dithiocarbamate compound inhibits the activity of a purified 20S proteasome and 26S proteasome in human breast cancer cell cultures and xenografts
    • DOI 10.1158/0008-5472.CAN-06-3017
    • Milacic V, Chen D, Ronconi L, Landis-Piwowar KR, Fregona D, Dou QP. A novel anticancer gold(III) dithiocarbamate compound inhibits the activity of a purified 20S proteasome and 26S proteasome in human breast cancer cell cultures and xenografts. Cancer Res 2006;66: 10478-10486 (Pubitemid 44799769)
    • (2006) Cancer Research , vol.66 , Issue.21 , pp. 10478-10486
    • Milacic, V.1    Chen, D.2    Ronconi, L.3    Landis-Piwowar, K.R.4    Fregona, D.5    Dou, Q.P.6
  • 25
    • 53949099847 scopus 로고    scopus 로고
    • Comprehensive analysis of oncogenic effects of PIK3CA mutations in human mammary epithelial cells
    • Zhang H, Liu G, Dziubinski M, Yang Z, Ethier SP, Wu G. Comprehensive analysis of oncogenic effects of PIK3CA mutations in human mammary epithelial cells. Breast Cancer Res Treat 2008;112: 217-227
    • (2008) Breast Cancer Res Treat , vol.112 , pp. 217-227
    • Zhang, H.1    Liu, G.2    Dziubinski, M.3    Yang, Z.4    Ethier, S.P.5    Wu, G.6
  • 26
    • 33847746963 scopus 로고    scopus 로고
    • Clioquinol, a therapeutic agent for alzheimer's disease, has proteasome-inhibitory, androgen receptor-suppressing, apoptosis-inducing, and antitumor activities in human prostate cancer cells and xenografts
    • DOI 10.1158/0008-5472.CAN-06-3546
    • Chen D, Cui QC, Yang H, et al. Clioquinol, a therapeutic agent for Alzheimer's disease, has proteasome-inhibitory, androgen receptor-suppressing, apoptosis-inducing, and antitumor activities in human prostate cancer cells and xenografts. Cancer Res 2007;67: 1636-1644 (Pubitemid 46383389)
    • (2007) Cancer Research , vol.67 , Issue.4 , pp. 1636-1644
    • Chen, D.1    Cui, Q.C.2    Yang, H.3    Barrea, R.A.4    Sarkar, F.H.5    Sheng, S.6    Yan, B.7    Reddy, G.P.V.8    Dou, Q.P.9
  • 27
    • 84901648175 scopus 로고    scopus 로고
    • Clioquinol and pyrrolidine dithiocarbamate complex with copper to form proteasome inhibitors and apoptosis inducers in human breast cancer cells
    • Daniel KG, Chen D, Orlu S, Cui QC, Miller FR, Dou QP. Clioquinol and pyrrolidine dithiocarbamate complex with copper to form proteasome inhibitors and apoptosis inducers in human breast cancer cells. Breast Cancer Res 2005;7:R897-908.
    • (2005) Breast Cancer Res , vol.7
    • Daniel, K.G.1    Chen, D.2    Orlu, S.3    Cui, Q.C.4    Miller, F.R.5    Dou, Q.P.6
  • 28
    • 67649371133 scopus 로고    scopus 로고
    • The use of copper-lowering therapy with tetrathiomolyb-date in medicine
    • Brewer GJ. The use of copper-lowering therapy with tetrathiomolyb-date in medicine. Expert Opin Investig Drugs 2009;18:89-97.
    • (2009) Expert Opin Investig Drugs , vol.18 , pp. 89-97
    • Brewer, G.J.1
  • 29
    • 34548083741 scopus 로고    scopus 로고
    • Phase II trial of copper depletion with tetrathiomolybdate as an antiangiogenesis strategy in patients with hormone-refractory prostate cancer
    • Henry NL, Dunn R, Merjaver S, et al. Phase II trial of copper depletion with tetrathiomolybdate as an antiangiogenesis strategy in patients with hormone-refractory prostate cancer. Oncology 2006;71: 168-175
    • (2006) Oncology , vol.71 , pp. 168-175
    • Henry, N.L.1    Dunn, R.2    Merjaver, S.3
  • 30
    • 0033551070 scopus 로고    scopus 로고
    • New insights into tumor suppression: PTEN suppresses tumor formation by restraining the phosphoinositide 3-kinase/AKT pathway
    • Cantley LC, Neel BG. New insights into tumor suppression: PTEN suppresses tumor formation by restraining the phosphoinositide 3-kinase/AKT pathway. Proc Natl Acad Sci U S A 1999;96:4240-4245
    • (1999) Proc Natl Acad Sci U S a , vol.96 , pp. 4240-4245
    • Cantley, L.C.1    Neel, B.G.2
  • 31
    • 69949170092 scopus 로고    scopus 로고
    • Activation of the PI3K pathway in cancer through inhibition of PTEN by exchange factor P-REX2a
    • Fine B, Hodakoski C, Koujak S, et al. Activation of the PI3K pathway in cancer through inhibition of PTEN by exchange factor P-REX2a. Science 2009;325:1261-1265
    • (2009) Science , vol.325 , pp. 1261-1265
    • Fine, B.1    Hodakoski, C.2    Koujak, S.3
  • 32
    • 1342342989 scopus 로고    scopus 로고
    • Human cancer, PTEN and the PI-3 kinase pathway
    • Parsons R. Human cancer, PTEN and the PI-3 kinase pathway. Semin Cell Dev Biol 2004;15:171-176
    • (2004) Semin Cell Dev Biol , vol.15 , pp. 171-176
    • Parsons, R.1
  • 33
    • 42449107999 scopus 로고    scopus 로고
    • Suppression of PTEN function increases breast cancer chemotherapeutic drug resistance while conferring sensitivity to mTOR inhibitors
    • Steelman LS, Navolanic PM, Sokolosky ML, et al. Suppression of PTEN function increases breast cancer chemotherapeutic drug resistance while conferring sensitivity to mTOR inhibitors. Oncogene 2008;27:4086-4095
    • (2008) Oncogene , vol.27 , pp. 4086-4095
    • Steelman, L.S.1    Navolanic, P.M.2    Sokolosky, M.L.3
  • 34
    • 0018817726 scopus 로고
    • The zinc and copper content of blood leucocytes and plasma from patients with benign and malignant prostates
    • Habib FK, Dembinski TC, Stitch SR. The zinc and copper content of blood leucocytes and plasma from patients with benign and malignant prostates. Clin Chim Acta 1980;104:329-335
    • (1980) Clin Chim Acta , vol.104 , pp. 329-335
    • Habib, F.K.1    Dembinski, T.C.2    Stitch, S.R.3
  • 36
    • 0021720704 scopus 로고
    • Comparison between concentrations of trace elements in normal and neoplastic human breast tissue
    • Rizk SL, Sky-Peck HH. Comparison between concentrations of trace elements in normal and neoplastic human breast tissue. Cancer Res 1984;44:5390-5394
    • (1984) Cancer Res , vol.44 , pp. 5390-5394
    • Rizk, S.L.1    Sky-Peck, H.H.2
  • 37
    • 8644263976 scopus 로고    scopus 로고
    • A proteasomal stress response: Pre-treatment with proteasome inhibitors increases proteasome activity and reduces neuronal vulnerability to oxidative injury
    • DOI 10.1111/j.1471-4159.2004.02813.x
    • Lee CS, Tee LY, Warmke T, et al. A proteasomal stress response: pre-treatment with proteasome inhibitors increases proteasome activity and reduces neuronal vulnerability to oxidative injury. J Neurochem 2004;91:996-1006. (Pubitemid 39507376)
    • (2004) Journal of Neurochemistry , vol.91 , Issue.4 , pp. 996-1006
    • Lee, C.-S.1    Tee, L.Y.2    Warmke, T.3    Vinjamoori, A.4    Cai, A.5    Fagan, A.M.6    Snider, B.J.7
  • 38
    • 0037821846 scopus 로고    scopus 로고
    • Inhibition of proteasome activity induces concerted expression of proteasome genes and de novo formation of Mammalian proteasomes
    • Meiners S, Heyken D, Weller A, et al. Inhibition of proteasome activity induces concerted expression of proteasome genes and de novo formation of Mammalian proteasomes. J Biol Chem 2003;278: 21517-21525
    • (2003) J Biol Chem , vol.278 , pp. 21517-21525
    • Meiners, S.1    Heyken, D.2    Weller, A.3
  • 40
    • 57349194139 scopus 로고    scopus 로고
    • Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers
    • Engelman JA, Chen L, Tan X, et al. Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers. Nat Med 2008;14:1351-1356
    • (2008) Nat Med , vol.14 , pp. 1351-1356
    • Engelman, J.A.1    Chen, L.2    Tan, X.3
  • 43
    • 40649096375 scopus 로고    scopus 로고
    • Helical domain and kinase domain mutations in p110α of phosphatidylinositol 3-kinase induce gain of function by different mechanisms
    • DOI 10.1073/pnas.0712169105
    • Zhao L, Vogt PK. Helical domain and kinase domain mutations in p110α of phosphatidylinositol 3-kinase induce gain of function by different mechanisms. Proc Natl Acad Sci U S A 2008;105:2652-2657 (Pubitemid 351520568)
    • (2008) Proceedings of the National Academy of Sciences of the United States of America , vol.105 , Issue.7 , pp. 2652-2657
    • Zhao, L.1    Vogt, P.K.2
  • 46
    • 55649084906 scopus 로고    scopus 로고
    • Phosphoinositide 3-kinase p110β activity: Key role in metabolism and mammary gland cancer but not development
    • Ciraolo E, Iezzi M, Marone R, et al. Phosphoinositide 3-kinase p110β activity: key role in metabolism and mammary gland cancer but not development. Sci Signal 2008;1:ra3.
    • (2008) Sci Signal , vol.1
    • Ciraolo, E.1    Iezzi, M.2    Marone, R.3
  • 47
    • 49649087385 scopus 로고    scopus 로고
    • Essential roles of PI(3)K-p110β in cell growth, metabolism and tumorigenesis
    • Jia S, Liu Z, Zhang S, et al. Essential roles of PI(3)K-p110β in cell growth, metabolism and tumorigenesis. Nature 2008;454:776-779
    • (2008) Nature , vol.454 , pp. 776-779
    • Jia, S.1    Liu, Z.2    Zhang, S.3
  • 48
    • 31944448780 scopus 로고    scopus 로고
    • Oncogenic transformation induced by the p110β, -γ, and -δ isoforms of class I phosphoinositide 3-kinase
    • Kang S, Denley A, Vanhaesebroeck B, Vogt PK. Oncogenic transformation induced by the p110β, -γ, and -δ isoforms of class I phosphoinositide 3-kinase. Proc Natl Acad Sci U S A 2006;103: 1289-1294
    • (2006) Proc Natl Acad Sci U S a , vol.103 , pp. 1289-1294
    • Kang, S.1    Denley, A.2    Vanhaesebroeck, B.3    Vogt, P.K.4


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