메뉴 건너뛰기




Volumn 69, Issue 8, 2009, Pages 851-860

Oleanane triterpenoid CDDO-Me inhibits growth and induces apoptosis in prostate cancer cells by independently targeting pro-survival Akt and mTOR

Author keywords

Akt; Apoptosis; CDDO Me; mTOR; Prostate cancer; Xenograft

Indexed keywords

ANTINEOPLASTIC AGENT; CYCLIN D1; CYCLOOXYGENASE 2; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; INITIATION FACTOR 4E; INITIATION FACTOR 4E BINDING PROTEIN 1; MAMMALIAN TARGET OF RAPAMYCIN; METHYL-2-CYANO 3,12 DIOXOOLEANA 1,9(11) DIEN 28 OATE; NUCLEAR PROTEIN; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN BAD; PROTEIN KINASE B; RAPAMYCIN; TRANSCRIPTION FACTOR FKHRL1; TRITERPENOID; UNCLASSIFIED DRUG; VASCULOTROPIN; DRUG DERIVATIVE; METHYL 2 CYANO 3,12 DIOXOOLEAN 1,9 DIEN 28 OATE; METHYL 2-CYANO-3,12-DIOXOOLEAN-1,9-DIEN-28-OATE; OLEANOLIC ACID; PROTEIN KINASE; TRITERPENE;

EID: 65549127616     PISSN: 02704137     EISSN: 10970045     Source Type: Journal    
DOI: 10.1002/pros.20937     Document Type: Article
Times cited : (61)

References (41)
  • 1
    • 0030939099 scopus 로고    scopus 로고
    • Hormonal therapy in the management of prostate cancer: From Higgins to the present
    • Garnick MB. Hormonal therapy in the management of prostate cancer: From Higgins to the present. Urology 1997;49:5-15.
    • (1997) Urology , vol.49 , pp. 5-15
    • Garnick, M.B.1
  • 2
    • 0030455892 scopus 로고    scopus 로고
    • Long-term control of prostate cancer with radiation
    • Hanks GE. Long-term control of prostate cancer with radiation. Urol Clin North Am 1996;23:605-616.
    • (1996) Urol Clin North Am , vol.23 , pp. 605-616
    • Hanks, G.E.1
  • 6
    • 0023732557 scopus 로고
    • Inhibition of the tumor-promoting action of 12-O-tetradecanoylphorbol-13- acetate by some oleanane-type triterpenoid compounds
    • Nishino H, Nishino A, Takayasu J, Hasegawa T, Iwashima A, Hirabayashi K, Iwata S, Shibata S. Inhibition of the tumorpromoting action of 12-O-tetradecanoylphorbol-13-accetate by some oleanane-type triterpenoid compounds. Cancer Res 1988;48:5210-5215. (Pubitemid 18220623)
    • (1988) Cancer Research , vol.48 , Issue.18 , pp. 5210-5215
    • Nishino, H.1    Nishino, A.2    Takayasu, J.3    Hasegawa, T.4    Iwashima, A.5    Hirabayashi, K.6    Iwata, S.7    Shibata, S.8
  • 7
    • 0034119806 scopus 로고    scopus 로고
    • Anti-allergic and anti-inflammatory triterpenes from the herb of Prunella vulgaris
    • DOI 10.1055/s-2000-8531
    • Ryu SY, Oak MH, Yoon SK, Cho DI, Yoo GS, Kim TS, Kim KM. Anti-allergic and anti-inflammatory triterpenes from the herb of Prunella vulgaris. Planta Med 2000;66:358-360. (Pubitemid 30346302)
    • (2000) Planta Medica , vol.66 , Issue.4 , pp. 358-360
    • Ryu, S.Y.1    Oak, M.-H.2    Yoon, S.-K.3    Cho, D.-I.4    Yoo, G.-S.5    Kim, T.-S.6    Kim, K.-M.7
  • 8
    • 0032491276 scopus 로고    scopus 로고
    • Design and synthesis of 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid, a novel and highly active inhibitor of nitric oxide production in mouse macrophages
    • DOI 10.1016/S0960-894X(98)00479-X, PII S0960894X9800479X
    • Honda T, Rounds BV, Gribble GW, Suh N, Wang Y, Sporn MB. Design and synthesis of 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid, a novel and highly active inhibitor of nitric oxide production in mouse macrophages. Biorg Med Chem Lett 1998;8:2711-2714. (Pubitemid 28496657)
    • (1998) Bioorganic and Medicinal Chemistry Letters , vol.8 , Issue.19 , pp. 2711-2714
    • Honda, T.1    Rounds, B.V.2    Gribble, G.W.3    Suh, N.4    Wang, Y.5    Sporn, M.B.6
  • 10
    • 0033590265 scopus 로고    scopus 로고
    • Novel synthetic oleanane triterpenoids: A series of highly active inhibitors of nitric oxide production in mouse macrophages
    • Honda T, Rounds BV, Bore L, Favaloro FG, Gibble GW, Suh N, Wang Y, Sporn MB. Novel synthetic oleanane triterpenoids: A series of highly active inhibitors of nitric oxide production in mouse macrophages. Bioorg Chem Lett 1999;9:3429-3434.
    • (1999) Bioorg Chem Lett , vol.9 , pp. 3429-3434
    • Honda, T.1    Rounds, B.V.2    Bore, L.3    Favaloro, F.G.4    Gibble, G.W.5    Suh, N.6    Wang, Y.7    Sporn, M.B.8
  • 11
    • 34547621658 scopus 로고    scopus 로고
    • Synthetic triterpenoids inhibit growth and induce apoptosis in human glioblastoma and neuroblastoma cells through inhibition of prosurvival Akt, NF-κB and Notch1 signaling
    • DOI 10.1007/s11060-007-9364-9
    • Gao X, Deeb D, Jiang H, Liu Y, Dulchavsky S, Gautam S. Synthetic triterpenoids inhibit growth and induce apoptosis in human glioblastoma and neuroblastoma cells through inhibition of prosurvival Akt, NF-κB and Notch1 signaling. J Neurooncol 2007;84:147-157. (Pubitemid 47202123)
    • (2007) Journal of Neuro-Oncology , vol.84 , Issue.2 , pp. 147-157
    • Gao, X.1    Deeb, D.2    Jiang, H.3    Liu, Y.4    Dulchavsky, S.A.5    Gautam, S.C.6
  • 13
    • 33645693409 scopus 로고    scopus 로고
    • A synthetic triterpenoid, CDDO-Me, inhibits IkappaBalpha kinase and enhances apoptosis induced by TNF and chemotherapeutic agents through down-regulation of expression of nuclear factor kappaB-regulated gene products in human leukemic cells
    • Shishodia S, Sethi G, Konopleva M, Andreeff M, Aggarwal BB. A synthetic triterpenoid, CDDO-Me, inhibits IkappaBalpha kinase and enhances apoptosis induced by TNF and chemotherapeutic agents through down-regulation of expression of nuclear factor kappaB-regulated gene products in human leukemic cells. Clin Cancer Res 2006;12:1828-1838.
    • (2006) Clin Cancer Res , vol.12 , pp. 1828-1838
    • Shishodia, S.1    Sethi, G.2    Konopleva, M.3    Andreeff, M.4    Aggarwal, B.B.5
  • 14
    • 0141815939 scopus 로고    scopus 로고
    • The novel triterpenoid CDDO and its derivatives induce apoptosis by disruption of intracellular redox balance
    • Ikeda T, Sporn M, Honda T, Gribble GW, Kufe D. The novel triterpenoid CDDO and its derivatives induce apoptosis by disruption of intracellular redox balance. Cancer Res 2003;63:5551-5558. (Pubitemid 37139877)
    • (2003) Cancer Research , vol.63 , Issue.17 , pp. 5551-5558
    • Ikeda, T.1    Sporn, M.2    Honda, T.3    Gribble, G.W.4    Kufe, D.5
  • 16
    • 0035037586 scopus 로고    scopus 로고
    • The novel triterpenoid CDDO induces apoptosis and differentiation of human osteosarcoma cells by a caspase-8 dependent mechanism
    • Ito Y, Pandey P, Sporn MB, Datta R, Kharbanda S, Kufe D. The novel triterpenoid CDDO induces apoptosis and differentiation of human osteosarcoma cells by a caspase-8 dependent mechanism. Mol Pharmacol 2001;59:1094-1099. (Pubitemid 32381589)
    • (2001) Molecular Pharmacology , vol.59 , Issue.5 , pp. 1094-1099
    • Ito, Y.1    Pandey, P.2    Sporn, M.B.3    Datta, R.4    Kharbanda, S.5    Kufe, D.6
  • 17
    • 23744501131 scopus 로고    scopus 로고
    • The novel triterpenoid CDDO-Me suppresses MAPK pathways and promotes p38 activation in acute myeloid leukemia cells
    • Konopleva M, Contractor R, Kurinna SM, Chen W, Andreeff M, Ruvolo PP. The novel triterpenoid CDDO-Me suppresses MAPK pathways and promotes p38 activation in acute myeloid leukemia cells. Leukemia 2005;19:1350-1354.
    • (2005) Leukemia , vol.19 , pp. 1350-1354
    • Konopleva, M.1    Contractor, R.2    Kurinna, S.M.3    Chen, W.4    Andreeff, M.5    Ruvolo, P.P.6
  • 19
    • 22344451742 scopus 로고    scopus 로고
    • 2-Cyano-3,12-dioxoolean-1,9-dien-28-oic acid and related compounds inhibit growth of colon cancer cells through peroxisome proliferator-activated receptor γ-dependent and -independent pathways
    • DOI 10.1124/mol.105.011437
    • Chintharlapalli S, Papineni S, Konopleva M, Andreef M, Samudio I, Safe S. 2-Cyano-3,12-dioxoolean-1,9-dien-28-oic acid and related compounds inhibit growth of colon cancer cells through peroxisome proliferator-activated receptor gamma-dependent and -independent pathways. Mol Pharmacol 2005;68:119-128. (Pubitemid 41002950)
    • (2005) Molecular Pharmacology , vol.68 , Issue.1 , pp. 119-128
    • Chintharlapalli, S.1    Papineni, S.2    Konopleva, M.3    Andreef, M.4    Samudio, I.5    Safe, S.6
  • 21
    • 34249337388 scopus 로고    scopus 로고
    • The novel triterpenoid C-28 methyl ester of 2-cyano-3, 12-dioxoolen-1, 9-dien-28-oic acid inhibits metastatic murine breast tumor growth through inactivation of STAT3 signaling
    • DOI 10.1158/0008-5472.CAN-06-3629
    • Xiaoyang L, Konopleva M, Zeng Z, Ruvolo V, Stephens LC, Schober W, McQueen T, Dietrich M, Madden TL, Andreeff M. The novel triterpenoid C-28 methyl ester of 2-cyano-3, 12-dioxoolen-1, 9-dien-28-oic acid inhibits metastatic murine breast tumor growth through inactivation of STAT3 signaling. Cancer Res 2007;67:4210-4218. (Pubitemid 46815067)
    • (2007) Cancer Research , vol.67 , Issue.9 , pp. 4210-4218
    • Ling, X.1    Konopleva, M.2    Zeng, Z.3    Ruvolo, V.4    Stephens, L.C.5    Schober, W.6    McQueen, T.7    Dietrich, M.8    Madden, T.L.9    Andreeff, M.10
  • 23
    • 35349001174 scopus 로고    scopus 로고
    • CDDO-Me induces apoptosis and inhibits Akt, mTOR and NF-κB signaling proteins in prostate cancer cells
    • Deeb D, Gao X, Dulchavsky SA, Gautam SC. CDDO-Me induces apoptosis and inhibits Akt, mTOR and NF-κB in prostate cancer cells. Anticancer Res 2007;27:3035-3044. (Pubitemid 47607524)
    • (2007) Anticancer Research , vol.27 , Issue.5 A , pp. 3035-3044
    • Deeb, D.1    Gao, X.2    Dulchavsky, S.A.3    Gautam, S.C.4
  • 24
    • 0034234924 scopus 로고    scopus 로고
    • A direct linkage between the phosphoinositide 3-kinase-AKT signaling pathway and the mammalian target of rapamycin in mitogen-stimulated and transformed cells
    • Sekulic A, Hudson CC, Homme JL, Yin P, Otterness DM, Karnitz LM, Abraham RT. A direct linkage between the phosphoinositide 3-kinase-AKT signaling pathway and the mammalian target of rapamycin in mitogen-stimulated and transformed cells. Cancer Res 2000;60:3504-3513. (Pubitemid 30482170)
    • (2000) Cancer Research , vol.60 , Issue.13 , pp. 3504-3513
    • Sekulic, A.1    Hudson, C.C.2    Homme, J.L.3    Yin, P.4    Otterness, D.M.5    Karnitz, L.M.6    Abraham, R.T.7
  • 25
    • 4043171462 scopus 로고    scopus 로고
    • Upstream and downstream of mTOR
    • DOI 10.1101/gad.1212704
    • Hay N, Sonenberg N. Upstream and downstream of mTOR. Gene Dev 2006;18:1926-1945. (Pubitemid 39071573)
    • (2004) Genes and Development , vol.18 , Issue.16 , pp. 1926-1945
    • Hay, N.1    Sonenberg, N.2
  • 26
    • 0028329172 scopus 로고
    • Apoptosis: Its significance in cancer and cancer therapy
    • Kerr JF, Winterford CM, Harmon BV. Apoptosis. Its significance in cancer and cancer therapy. Cancer 1994;73:2013-2026. (Pubitemid 24107952)
    • (1994) Cancer , vol.73 , Issue.8 , pp. 2013-2026
    • Kerr, J.F.R.1    Winterford, C.M.2    Harmon, B.V.3
  • 27
    • 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
  • 28
    • 0034719680 scopus 로고    scopus 로고
    • The transcription factor NF-κB: Control of oncogenesis and cancer therapy resistance
    • Mayo MW, Baldwin AS. The transcription factor NF-κB: Control of oncogenesis and cancer therapy resistance. Biochim Biophys Acta 2000;1470:M55-M62.
    • (2000) Biochim Biophys Acta , vol.1470
    • Mayo, M.W.1    Baldwin, A.S.2
  • 29
    • 27844445642 scopus 로고    scopus 로고
    • Perturbations of the AKT signaling pathway in human cancer
    • DOI 10.1038/sj.onc.1209085, PII 1209085
    • Altomare DA, Testa JR. Perturbations of the Akt signaling pathway in human cancer. Oncogene 2005;24:7455-7464. (Pubitemid 41637985)
    • (2005) Oncogene , vol.24 , Issue.50 , pp. 7455-7464
    • Altomare, D.A.1    Testa, J.R.2
  • 30
    • 0036546501 scopus 로고    scopus 로고
    • NF-κB in cancer. From innocent bystander to major culprit
    • Karin M, Cao Y, Greten FR, Li Z-W. NF-κB in cancer. From innocent bystander to major culprit. Nat Rev Cancer 2002;2:301-310.
    • (2002) Nat Rev Cancer , vol.2 , pp. 301-310
    • Karin, M.1    Cao, Y.2    Greten, F.R.3    Li, Z.-W.4
  • 31
    • 2342559981 scopus 로고    scopus 로고
    • The TOR pathway: A target for cancer therapy
    • Bjornsti MA, Houghton PJ. The TOR pathway; a target for cancer therapy. Nat Rev Cancer 2004;4:335-348. (Pubitemid 38579480)
    • (2004) Nature Reviews Cancer , vol.4 , Issue.5 , pp. 335-348
    • Bjornsti, M.-A.1    Houghton, P.J.2
  • 32
    • 0030702123 scopus 로고    scopus 로고
    • Akt phosphorylation of BAD couples survival signals to the cell- Intrinsic death machinery
    • DOI 10.1016/S0092-8674(00)80405-5
    • Datta SR, Dudek H, Tao X, Masters S, Fu H, Gotoh Y, Greenberg ME. Akt phosphorylation of Bad couples survival signals to the cell-intrinsic death machinery. Cell 1997;91:231-241. (Pubitemid 27456390)
    • (1997) Cell , vol.91 , Issue.2 , pp. 231-241
    • Datta, S.R.1    Dudek, H.2    Xu, T.3    Masters, S.4    Haian, F.5    Gotoh, Y.6    Greenberg, M.E.7
  • 34
    • 0345732640 scopus 로고    scopus 로고
    • MTOR Controls Cell Cycle Progression through Its Cell Growth Effectors S6K1 and 4E-BP1/Eukaryotic Translation Initiation Factor 4E
    • DOI 10.1128/MCB.24.1.200-216.2004
    • Fingar DC, Richardson CJ, Tee AR, Cheatham L, Tsou C, Blenis J. mTOR controls cell cycle progression through its cell growth effectors S6K1 and 4E-BP1/eukaryotic translation initiation factor 4E. Mol Cell Biol 2004;24:200-216. (Pubitemid 38010048)
    • (2004) Molecular and Cellular Biology , vol.24 , Issue.1 , pp. 200-216
    • Fingar, D.C.1    Richardson, C.J.2    Tee, A.R.3    Cheatham, L.4    Tsou, C.5    Blenis, J.6
  • 35
    • 33750858427 scopus 로고    scopus 로고
    • Rapamycin inhibits cell motility by suppression of mTOR-mediated S6K1 and 4E-BP1 pathway
    • Liu L, Li F, Cardelli JA, Martin KA, Blenis J, Huang S. Rapamycin inhibits cell motility by suppression of mTOR-mediated S6K1 and 4E-BP1 pathway. Oncogene 2006;25:7029-7040.
    • (2006) Oncogene , vol.25 , pp. 7029-7040
    • Liu, L.1    Li, F.2    Cardelli, J.A.3    Martin, K.A.4    Blenis, J.5    Huang, S.6
  • 36
    • 0345269064 scopus 로고    scopus 로고
    • Potentiation of chemotherapeutic agents following antagonism of nuclear factor kappa B in human gliomas
    • DOI 10.1023/A:1022554824129
    • Weaver KD, Yeyeodu S, Cusack JC Jr, Baldwin AS Jr, Ewend MG. Potentiation of chemotherapeutic agents following antagonism of nuclear factor kappa B in human gliomas. J Neurooncol 2003;61:187-196. (Pubitemid 36342295)
    • (2003) Journal of Neuro-Oncology , vol.61 , Issue.3 , pp. 187-196
    • Weaver, K.D.1    Yeyeodu, S.2    Cusack Jr., J.C.3    Baldwin Jr., A.S.4    Ewend, M.G.5
  • 37
    • 1542649570 scopus 로고    scopus 로고
    • Overcoming antiapoptotic responses to promote chemosensitivity in metastatic colorectal cancer to the liver
    • DOI 10.1245/ASO.2003.07.518
    • Cusack JC Jr., Overcoming antiapoptotic responses to promote chemosensitivity in metastatic colorectal cancer to the liver. Ann Surg Oncol 2003;10:852-862. (Pubitemid 40486848)
    • (2003) Annals of Surgical Oncology , vol.10 , Issue.8 , pp. 852-862
    • Cusack Jr., J.C.1
  • 38
    • 18044381192 scopus 로고    scopus 로고
    • Rheb binds and regulates the mTOR kinase
    • DOI 10.1016/j.cub.2005.02.053
    • Long X, Lin Y, Ortiz-Vega S, Yonezawa K, Avruch J. Rheb binds and regulates the mTOR kinase. Curr Biol 2005;15:702-713. (Pubitemid 40599924)
    • (2005) Current Biology , vol.15 , Issue.8 , pp. 702-713
    • Long, X.1    Lin, Y.2    Ortiz-Vega, S.3    Yonezawa, K.4    Avruch, J.5
  • 39
    • 44449161481 scopus 로고    scopus 로고
    • The TSC1-TSC2 complex: A molecular switchboard controlling cell growth
    • Huang J, Manning BD. The TSC1-TSC2 complex: A molecular switchboard controlling cell growth. Biochem J 2008;412:179-190.
    • (2008) Biochem J , vol.412 , pp. 179-190
    • Huang, J.1    Manning, B.D.2
  • 40
    • 34247229225 scopus 로고    scopus 로고
    • Curcumin [1,7-bis(4-hydroxy-3-methoxyphenyl)-1-6-heptadine-3,5-dione; C21H20O6] sensitizes human prostate cancer cells to tumor necrosis factor-related apoptosis-inducing ligand/Apo2L-induced apoptosis by suppressing nuclear factor-kappaB via inhibition of the prosurvival Akt signaling pathway
    • Deeb D, Jiang H, Gao X, Al-Holou S, Danyluk AL, Dulchavsky SA, Gautam SC. Curcumin [1,7-bis(4-hydroxy-3-methoxyphenyl)-1-6-heptadine-3,5-dione; C21H20O6] sensitizes human prostate cancer cells to tumor necrosis factor-related apoptosis-inducing ligand/Apo2L-induced apoptosis by suppressing nuclear factor-kappaB via inhibition of the prosurvival Akt signaling pathway. J Pharmacol Exp Ther 2007;321:616-625.
    • (2007) J Pharmacol Exp Ther , vol.321 , pp. 616-625
    • Deeb, D.1    Jiang, H.2    Gao, X.3    Al-Holou, S.4    Danyluk, A.L.5    Dulchavsky, S.A.6    Gautam, S.C.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.