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Volumn 8, Issue 7, 2009, Pages 2067-2075

Inhibition of S-adenosylmethionine decarboxylase by inhibitor SAM486A connects polyamine metabolism with p53-Mdm2-Akt/protein kinase B regulation and apoptosis in neuroblastoma

Author keywords

[No Author keywords available]

Indexed keywords

4 AMIDINO 1 INDANONE 2' AMIDINOHYDRAZONE; ADENOSYLMETHIONINE DECARBOXYLASE; ADENOSYLMETHIONINE DECARBOXYLASE INHIBITOR; DECARBOXYLASE INHIBITOR; PROTEIN KINASE B; PROTEIN MDM2; PROTEIN P53; SAM 486A; UNCLASSIFIED DRUG;

EID: 67651183766     PISSN: 15357163     EISSN: None     Source Type: Journal    
DOI: 10.1158/1535-7163.MCT-08-1217     Document Type: Article
Times cited : (27)

References (26)
  • 2
    • 0037342691 scopus 로고    scopus 로고
    • Phase III randomized study of postradiotherapy chemotherapy with combination α-difluoromethylornithine- PCV versus PCV for anaplastic gliomas
    • Levin VA, Hess KR, Choucair A, et al. Phase III randomized study of postradiotherapy chemotherapy with combination α-difluoromethylornithine- PCV versus PCV for anaplastic gliomas. Clin Cancer Res 2003;9: 981-90.
    • (2003) Clin Cancer Res , vol.9 , pp. 981-990
    • Levin, V.A.1    Hess, K.R.2    Choucair, A.3
  • 3
    • 0033755187 scopus 로고    scopus 로고
    • Phase III randomized study of postradiotherapy chemotherapy with α-difluoromethylornithine-procarbazine, N-(2-chloroethyl)-N′-cyclohexyl-N-nitrosurea, vincristine (DFMO-PCV) versus PCV for glioblastoma multiforme
    • Levin VA, Uhm JH, Jaeckle KA, et al. Phase III randomized study of postradiotherapy chemotherapy with α-difluoromethylornithine-procarbazine, N-(2-chloroethyl)-N′-cyclohexyl-N-nitrosurea, vincristine (DFMO-PCV) versus PCV for glioblastoma multiforme. Clin Cancer Res 2000;6:3878-84.
    • (2000) Clin Cancer Res , vol.6 , pp. 3878-3884
    • Levin, V.A.1    Uhm, J.H.2    Jaeckle, K.A.3
  • 4
    • 0026671825 scopus 로고
    • Ornithine decarboxylase as an enzyme target for therapy
    • McCann PP, Pegg AE. Ornithine decarboxylase as an enzyme target for therapy. Pharmacol Ther 1992;54:195-215.
    • (1992) Pharmacol Ther , vol.54 , pp. 195-215
    • McCann, P.P.1    Pegg, A.E.2
  • 5
    • 0345535621 scopus 로고    scopus 로고
    • Development of difluoromethylornithine (DFMO) as a chemoprevention agent
    • Meyskens FL, Jr., Gerner EW. Development of difluoromethylornithine (DFMO) as a chemoprevention agent. Clin Cancer Res 1999;5:945-51.
    • (1999) Clin Cancer Res , vol.5 , pp. 945-951
    • Meyskens Jr., F.L.1    Gerner, E.W.2
  • 6
    • 0034650470 scopus 로고    scopus 로고
    • α-Difluoromethylornithine induces apoptosis as well as anti-angiogenesis in the inhibition of tumor growth and metastasis in a human gastric cancer model
    • Takahashi Y, Mai M, Nishioka K. α-Difluoromethylornithine induces apoptosis as well as anti-angiogenesis in the inhibition of tumor growth and metastasis in a human gastric cancer model. Int J Cancer 2000;85:243-7.
    • (2000) Int J Cancer , vol.85 , pp. 243-247
    • Takahashi, Y.1    Mai, M.2    Nishioka, K.3
  • 7
    • 0026775528 scopus 로고
    • New S-adenosylmethionine decarboxylase inhibitors with potent antitumor activity
    • Regenass U, Caravatti G, Mett H, et al. New S-adenosylmethionine decarboxylase inhibitors with potent antitumor activity. Cancer Res 1992;52:4712-8.
    • (1992) Cancer Res , vol.52 , pp. 4712-4718
    • Regenass, U.1    Caravatti, G.2    Mett, H.3
  • 8
    • 0028361273 scopus 로고
    • CGP 48664, a new S-adenosylmethionine decarboxylase inhibitor with broad spectrum antiproliferative and antitumor activity
    • Regenass U, Mett H, Stanek J, Mueller M, Kramer D, Porter CW. CGP 48664, a new S-adenosylmethionine decarboxylase inhibitor with broad spectrum antiproliferative and antitumor activity. Cancer Res 1994;54:3210-7.
    • (1994) Cancer Res , vol.54 , pp. 3210-3217
    • Regenass, U.1    Mett, H.2    Stanek, J.3    Mueller, M.4    Kramer, D.5    Porter, C.W.6
  • 9
    • 0027324170 scopus 로고
    • 4-Amidinoindan-1-one 2′-amidinohydrazone: A new potent and selective inhibitor of S-adenosylmethionine decarboxylase
    • Stanek J, Caravatti G, Frei J, et al. 4-Amidinoindan-1-one 2′-amidinohydrazone: a new potent and selective inhibitor of S-adenosylmethionine decarboxylase. J Med Chem 1993;36:2168-71.
    • (1993) J Med Chem , vol.36 , pp. 2168-2171
    • Stanek, J.1    Caravatti, G.2    Frei, J.3
  • 10
    • 0031045715 scopus 로고    scopus 로고
    • CGP 48664, a potent and specific S-adenosylmethionine decarboxylase inhibitor: Effects on regulation and stability of the enzyme
    • Svensson F, Mett H, Persson L. CGP 48664, a potent and specific S-adenosylmethionine decarboxylase inhibitor: effects on regulation and stability of the enzyme. Biochem J 1997;322:297-302.
    • (1997) Biochem J , vol.322 , pp. 297-302
    • Svensson, F.1    Mett, H.2    Persson, L.3
  • 11
    • 0030904094 scopus 로고    scopus 로고
    • 4-Amidinoindan-1-one 2′-amidinohydrazone (CGP 48664A) exerts in vitro growth inhibitory effects that are not only related to S-adenosylmethionine decarboxylase (SAMdc) inhibition
    • Dorhout B, Odink MF, de Hoog E, Kingma AW, van der Veer E, Muskiet FA. 4-Amidinoindan-1-one 2′-amidinohydrazone (CGP 48664A) exerts in vitro growth inhibitory effects that are not only related to S-adenosylmethionine decarboxylase (SAMdc) inhibition. Biochim Biophys Acta 1997;1335:144-52.
    • (1997) Biochim Biophys Acta , vol.1335 , pp. 144-152
    • Dorhout, B.1    Odink, M.F.2    de Hoog, E.3    Kingma, A.W.4    van der Veer, E.5    Muskiet, F.A.6
  • 12
    • 0029127116 scopus 로고
    • In vivo effects of 4-amidinoindan-1-one 2′-amidinohydrazone (CGP 48664A) and α-difluoromethylornithine (DFMO) on L1210 growth, cell-cycle phase distribution and polyamine contents
    • Dorhout B, te Velde RJ, Ferwerda H, Kingma AW, de Hoog E, Muskiet FA. In vivo effects of 4-amidinoindan-1-one 2′-amidinohydrazone (CGP 48664A) and α-difluoromethylornithine (DFMO) on L1210 growth, cell-cycle phase distribution and polyamine contents. Int J Cancer 1995;62:738-42.
    • (1995) Int J Cancer , vol.62 , pp. 738-742
    • Dorhout, B.1    te Velde, R.J.2    Ferwerda, H.3    Kingma, A.W.4    de Hoog, E.5    Muskiet, F.A.6
  • 13
    • 0141633535 scopus 로고    scopus 로고
    • Thirty years of polyamine-related approaches to cancer therapy. Retrospect and prospect. Part 1. Selective enzyme inhibitors
    • Seiler N. Thirty years of polyamine-related approaches to cancer therapy. Retrospect and prospect. Part 1. Selective enzyme inhibitors. Curr Drug Targets 2003;4:537-64.
    • (2003) Curr Drug Targets , vol.4 , pp. 537-564
    • Seiler, N.1
  • 14
    • 17444446928 scopus 로고    scopus 로고
    • European Organization for Research and Treatment of Cancer Early Clinical Studies Group. Phase I and pharmacological study of weekly administration of the polyamine synthesis inhibitor SAM 486A (CGP 48 664) in patients with solid tumors
    • Eskens FA, Greim GA, van Zuylen C, et al, European Organization for Research and Treatment of Cancer Early Clinical Studies Group. Phase I and pharmacological study of weekly administration of the polyamine synthesis inhibitor SAM 486A (CGP 48 664) in patients with solid tumors. Clin Cancer Res 2000;6:1736-43.
    • (2000) Clin Cancer Res , vol.6 , pp. 1736-1743
    • Eskens, F.A.1    Greim, G.A.2    van Zuylen, C.3
  • 15
    • 12144288924 scopus 로고    scopus 로고
    • Clinical efficacy, tolerability, and safety of SAM486A, a novel polyamine biosynthesis inhibitor, in patients with relapsed or refractory non-Hodgkin's lymphoma: Results from a phase II multicenter study
    • Pless M, Belhadj K, Menssen HD, et al. Clinical efficacy, tolerability, and safety of SAM486A, a novel polyamine biosynthesis inhibitor, in patients with relapsed or refractory non-Hodgkin's lymphoma: results from a phase II multicenter study. Clin Cancer Res 2004;10:1299-305.
    • (2004) Clin Cancer Res , vol.10 , pp. 1299-1305
    • Pless, M.1    Belhadj, K.2    Menssen, H.D.3
  • 16
    • 55549132996 scopus 로고    scopus 로고
    • Difluoromethylornithine plus sulindac for the prevention of sporadic colorectal adenomas: A randomized placebo-controlled, double-blind trial
    • Meyskens FL, Jr., McLaren CE, Pelot D, et al. Difluoromethylornithine plus sulindac for the prevention of sporadic colorectal adenomas: a randomized placebo-controlled, double-blind trial. Cancer Prev Res 2008;1:32-8.
    • (2008) Cancer Prev Res , vol.1 , pp. 32-38
    • Meyskens Jr., F.L.1    McLaren, C.E.2    Pelot, D.3
  • 17
    • 0037366067 scopus 로고    scopus 로고
    • Neuroblastoma: Biological insights into a clinical enigma
    • Brodeur GM. Neuroblastoma: biological insights into a clinical enigma. Nat Rev Cancer 2003;3:203-16.
    • (2003) Nat Rev Cancer , vol.3 , pp. 203-216
    • Brodeur, G.M.1
  • 18
    • 0029868075 scopus 로고    scopus 로고
    • The p53 signal transduction pathway is intact in human neuroblastoma despite cytoplasmic localization
    • Goldman SC, Chen CY, Lansing TJ, Gilmer TM, Kastan MB. The p53 signal transduction pathway is intact in human neuroblastoma despite cytoplasmic localization. Am J Pathol 1996;148:1381-5.
    • (1996) Am J Pathol , vol.148 , pp. 1381-1385
    • Goldman, S.C.1    Chen, C.Y.2    Lansing, T.J.3    Gilmer, T.M.4    Kastan, M.B.5
  • 19
    • 0028224658 scopus 로고
    • Low frequency of the p53 gene mutations in neuroblastoma
    • Hosoi G, Hara J, Okamura T, et al. Low frequency of the p53 gene mutations in neuroblastoma. Cancer 1994;73:3087-93.
    • (1994) Cancer , vol.73 , pp. 3087-3093
    • Hosoi, G.1    Hara, J.2    Okamura, T.3
  • 20
    • 24644520814 scopus 로고    scopus 로고
    • 1 cell cycle arrest in MYCN-amplified human neuroblastoma cells
    • 1 cell cycle arrest in MYCN-amplified human neuroblastoma cells. Oncogene 2005;24:5606-18.
    • (2005) Oncogene , vol.24 , pp. 5606-5618
    • Wallick, C.J.1    Gamper, I.2    Thorne, M.3
  • 21
    • 14144250455 scopus 로고    scopus 로고
    • The p53 regulatory gene MDM2 is a direct transcriptional target of MYCN in neuroblastoma
    • Slack A, Chen Z, Tonelli R, et al. The p53 regulatory gene MDM2 is a direct transcriptional target of MYCN in neuroblastoma. Proc Natl Acad Sci U S A 2005;102:731-6.
    • (2005) Proc Natl Acad Sci U S A , vol.102 , pp. 731-736
    • Slack, A.1    Chen, Z.2    Tonelli, R.3
  • 22
    • 57149097471 scopus 로고    scopus 로고
    • Ornithine decarboxylase inhibition by α-difluoromethylornithine activates opposing signaling pathways via phosphorylation of both Akt/protein kinase B and p27Kip1 in neuroblastoma
    • Koomoa DL, Yco LP, Borsics T, Wallick CJ, Bachmann AS. Ornithine decarboxylase inhibition by α-difluoromethylornithine activates opposing signaling pathways via phosphorylation of both Akt/protein kinase B and p27Kip1 in neuroblastoma. Cancer Res 2008;68:9825-31.
    • (2008) Cancer Res , vol.68 , pp. 9825-9831
    • Koomoa, D.L.1    Yco, L.P.2    Borsics, T.3    Wallick, C.J.4    Bachmann, A.S.5
  • 23
    • 43049170219 scopus 로고    scopus 로고
    • Benzo(a)pyrene increases phosphorylation of p53 at serine 392 in relation to p53 induction and cell death in MCF-7 cells
    • Tampio M, Loikkanen J, Myllynen P, Mertanen A, Vahakangas KH. Benzo(a)pyrene increases phosphorylation of p53 at serine 392 in relation to p53 induction and cell death in MCF-7 cells. Toxicol Lett 2008;178:152-9.
    • (2008) Toxicol Lett , vol.178 , pp. 152-159
    • Tampio, M.1    Loikkanen, J.2    Myllynen, P.3    Mertanen, A.4    Vahakangas, K.H.5
  • 24
    • 59749090405 scopus 로고    scopus 로고
    • Role of polyamines in p53-dependent apoptosis of intestinal epithelial cells
    • Bhattacharya S, Ray RM, Johnson LR. Role of polyamines in p53-dependent apoptosis of intestinal epithelial cells. Cell Signal 2009;21:509-22.
    • (2009) Cell Signal , vol.21 , pp. 509-522
    • Bhattacharya, S.1    Ray, R.M.2    Johnson, L.R.3
  • 25
    • 0030777230 scopus 로고    scopus 로고
    • The mdm2 proto-oncogene
    • Haines DS. The mdm2 proto-oncogene. Leuk Lymphoma 1997;26:227-38.
    • (1997) Leuk Lymphoma , vol.26 , pp. 227-238
    • Haines, D.S.1
  • 26
    • 0030957746 scopus 로고    scopus 로고
    • Identification of the MDM2 oncoprotein as a substrate for CPP32-like apoptotic proteases
    • Erhardt P, Tomaselli KJ, Cooper GM. Identification of the MDM2 oncoprotein as a substrate for CPP32-like apoptotic proteases. J Biol Chem 1997;272:15049-52.
    • (1997) J Biol Chem , vol.272 , pp. 15049-15052
    • Erhardt, P.1    Tomaselli, K.J.2    Cooper, G.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.