메뉴 건너뛰기




Volumn 43, Issue 5, 2008, Pages 435-442

Advance of several types of important marine antitumor drugs

Author keywords

Antitumor drug; Marine natural product; Progress

Indexed keywords

1,3 DIOXOLANE DERIVATIVE; ANTINEOPLASTIC AGENT; BIOLOGICAL PRODUCT; BRYOSTATIN; BRYOSTATIN 1; DEPSIPEPTIDE; DIDEMNINS; DISULFIDE; DOLASTATIN 10; DRUG DERIVATIVE; ETHER DERIVATIVE; HALICHONDRIN B; PSAMMAPLIN A; TETRAHYDROISOQUINOLINE DERIVATIVE; TRABECTEDIN; TYROSINE;

EID: 47249109404     PISSN: 05134870     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (8)

References (50)
  • 1
    • 33746555648 scopus 로고    scopus 로고
    • Bryostatin-1; pharmacology and therapeutic potential as a CNS drug [J]
    • Sun MK, Alkon DL. Bryostatin-1; pharmacology and therapeutic potential as a CNS drug [J]. CNS Drug Rev, 2006,12:1-8.
    • (2006) CNS Drug Rev , vol.12 , pp. 1-8
    • Sun, M.K.1    Alkon, D.L.2
  • 2
    • 16244401633 scopus 로고    scopus 로고
    • Dual effects of bryostatin-1 on spatial memory and depression [J]
    • Sun MK, Alkon DL. Dual effects of bryostatin-1 on spatial memory and depression [J]. Eur J Pharmacol, 2005,512:43-51.
    • (2005) Eur J Pharmacol , vol.512 , pp. 43-51
    • Sun, M.K.1    Alkon, D.L.2
  • 3
    • 0346096818 scopus 로고    scopus 로고
    • Bryostatin-1: A novel PKC inhibitor in clinical development [J]
    • Kortmansky J , Schwartz GK. Bryostatin-1: a novel PKC inhibitor in clinical development [J]. Cancer Invest, 2003,21:924-936.
    • (2003) Cancer Invest , vol.21 , pp. 924-936
    • Kortmansky, J.1    Schwartz, G.K.2
  • 4
    • 34250732910 scopus 로고    scopus 로고
    • Synergistic effect of AS101 and bryostatin-1 on myeloid leukemia cell differentiation in vitro and in an animal model [J]
    • Hayun M, Okun E, Hayun R, et al. Synergistic effect of AS101 and bryostatin-1 on myeloid leukemia cell differentiation in vitro and in an animal model [J]. Leukemia, 2007,21:1504-1513.
    • (2007) Leukemia , vol.21 , pp. 1504-1513
    • Hayun, M.1    Okun, E.2    Hayun, R.3
  • 5
    • 33746912263 scopus 로고    scopus 로고
    • Differential effect of bryostatin 1 and phorbol 12-myristate 13-acetate on HOP-92 cell proliferation is mediated by down-regulation of protein kinase Cdelta [J]
    • Choi SH, Hyman T, Blumberg PM. Differential effect of bryostatin 1 and phorbol 12-myristate 13-acetate on HOP-92 cell proliferation is mediated by down-regulation of protein kinase Cdelta [J]. Cancer Res, 2006, 66: 7261-7269.
    • (2006) Cancer Res , vol.66 , pp. 7261-7269
    • Choi, S.H.1    Hyman, T.2    Blumberg, P.M.3
  • 6
    • 0035702714 scopus 로고    scopus 로고
    • Mitogen-activated protein kinase is required for bryostatin 1-induced differentiation of the human acute lymphoblastic leukemia cell line Reh [J]
    • Wall NR, Mohammad RM, Al-Katib AM. Mitogen-activated protein kinase is required for bryostatin 1-induced differentiation of the human acute lymphoblastic leukemia cell line Reh [J]. Cell Growth Differ, 2001, 12:641 -647.
    • (2001) Cell Growth Differ , vol.12 , pp. 641-647
    • Wall, N.R.1    Mohammad, R.M.2    Al-Katib, A.M.3
  • 7
    • 85009914876 scopus 로고    scopus 로고
    • Primary acute myeloid leukaemia blasts resistant to cytokine-induced differentiation to dendritic-like leukaemia cells can be forced to differentiate by the addition of bryostatin-1 [J]
    • Roddie PH, Horton Y, Turner ML. Primary acute myeloid leukaemia blasts resistant to cytokine-induced differentiation to dendritic-like leukaemia cells can be forced to differentiate by the addition of bryostatin-1 [J]. Leukemia, 2002,16:84-93.
    • (2002) Leukemia , vol.16 , pp. 84-93
    • Roddie, P.H.1    Horton, Y.2    Turner, M.L.3
  • 8
    • 1242316960 scopus 로고    scopus 로고
    • 1alpha, 25-Dihydroxyvitamin D3 and bryostatin-1 synergize to induce monocytic differentiation of NB4 acute promyelocytic leukemia cells by modulating cell cycle progression [J]
    • Clark CS, Konyer JE, Meckling KA. 1alpha, 25-Dihydroxyvitamin D3 and bryostatin-1 synergize to induce monocytic differentiation of NB4 acute promyelocytic leukemia cells by modulating cell cycle progression [J]. Exp Cell Res, 2004,294:301-311.
    • (2004) Exp Cell Res , vol.294 , pp. 301-311
    • Clark, C.S.1    Konyer, J.E.2    Meckling, K.A.3
  • 9
    • 0036225876 scopus 로고    scopus 로고
    • Bryostatin 1 increases 1-beta-D- arabinofuranosylcytosine-induced cytochrome c release and apoptosis in human leukemia cells ectopically expressing Bcl-x(L) [J]
    • Wang Z, Wang S, Dai Y, et al. Bryostatin 1 increases 1-beta-D- arabinofuranosylcytosine-induced cytochrome c release and apoptosis in human leukemia cells ectopically expressing Bcl-x(L) [J]. J Pharmacol Exp Ther, 2002, 301:568-577.
    • (2002) J Pharmacol Exp Ther , vol.301 , pp. 568-577
    • Wang, Z.1    Wang, S.2    Dai, Y.3
  • 10
    • 25144434873 scopus 로고    scopus 로고
    • Enhancement of cisplatin sensitivity of cisplatin-resistant human cervical carcinoma cells by bryostatin 1 [J]
    • Mohanty S, Huang J, Basu A. Enhancement of cisplatin sensitivity of cisplatin-resistant human cervical carcinoma cells by bryostatin 1 [J]. Clin Cancer Res, 2005, 1: 6730 - 6737.
    • (2005) Clin Cancer Res , vol.1 , pp. 6730-6737
    • Mohanty, S.1    Huang, J.2    Basu, A.3
  • 11
    • 33746901998 scopus 로고    scopus 로고
    • The antineoplastic agent bryostatin-1 differentially regulates IFN-gamma receptor subunits in monocytic cells; transcriptional and posttranscriptional control of IFN-gamma R2 [J]
    • Garcia CS, Curiel RE, Mwatibo JM, et al. The antineoplastic agent bryostatin-1 differentially regulates IFN-gamma receptor subunits in monocytic cells; transcriptional and posttranscriptional control of IFN-gamma R2 [J]. J Immunol, 2006,177:2707-2716
    • (2006) J Immunol , vol.177 , pp. 2707-2716
    • Garcia, C.S.1    Curiel, R.E.2    Mwatibo, J.M.3
  • 12
    • 1842582465 scopus 로고    scopus 로고
    • Phase II trial of the combination of bryostatin-1 and cisplatin in advanced or recurrent carcinoma of the cervix; a New York Gynecologic Oncology Group study [J]
    • Nezhat F, Wadler S, Muggia F, et al. Phase II trial of the combination of bryostatin-1 and cisplatin in advanced or recurrent carcinoma of the cervix; a New York Gynecologic Oncology Group study [J]. Gynecol Oncol, 2004,93:144-148.
    • (2004) Gynecol Oncol , vol.93 , pp. 144-148
    • Nezhat, F.1    Wadler, S.2    Muggia, F.3
  • 13
    • 20144371613 scopus 로고    scopus 로고
    • Bryostatin-1 in combination with calcium ionophore promotes the maturation of human umbilical cord-blood monocyte-derived dendritic cells capable of activating neonatal alloreactive T cells [J]
    • Do Y, Mainali E, Nagarkatti PS, et al. Bryostatin-1 in combination with calcium ionophore promotes the maturation of human umbilical cord-blood monocyte-derived dendritic cells capable of activating neonatal alloreactive T cells [J]. Cell Immunol, 2004, 231:8-13.
    • (2004) Cell Immunol , vol.231 , pp. 8-13
    • Do, Y.1    Mainali, E.2    Nagarkatti, P.S.3
  • 14
    • 0035992301 scopus 로고    scopus 로고
    • Phase I trial and correlative laboratory studies of bryostatin 1 (NSC 339555) and high-dose 1-β-D-arabinofuranosylcytosine in patients with refractory acute leukemia [J]
    • Cragg LH, Andreeff M, Feldman E, et al. Phase I trial and correlative laboratory studies of bryostatin 1 (NSC 339555) and high-dose 1-β-D-arabinofuranosylcytosine in patients with refractory acute leukemia [J]. Clin Cancer Res, 2002,8:2123-2133.
    • (2002) Clin Cancer Res , vol.8 , pp. 2123-2133
    • Cragg, L.H.1    Andreeff, M.2    Feldman, E.3
  • 15
    • 0345459958 scopus 로고    scopus 로고
    • Phase I study of prolonged infusion bryostatin-1 in patients with advanced malignancies [J]
    • Marshall JL, Bangalore N, El-Ashry D, et al. Phase I study of prolonged infusion bryostatin-1 in patients with advanced malignancies [J]. Cancer Biol Ther, 2002,1: 409-416.
    • (2002) Cancer Biol Ther , vol.1 , pp. 409-416
    • Marshall, J.L.1    Bangalore, N.2    El-Ashry, D.3
  • 16
    • 0036954116 scopus 로고    scopus 로고
    • Phase I study of bryostatin-1 and fludarabine in patients with chronic lymphocytic leukemia and indolent non-Hodgkin's lymphoma [J]
    • Roberts JD, Smith MR, Feldman EJ, et al. Phase I study of bryostatin-1 and fludarabine in patients with chronic lymphocytic leukemia and indolent non-Hodgkin's lymphoma [J]. Clin Lymphoma, 2002,3:184-188.
    • (2002) Clin Lymphoma , vol.3 , pp. 184-188
    • Roberts, J.D.1    Smith, M.R.2    Feldman, E.J.3
  • 17
    • 33750313170 scopus 로고    scopus 로고
    • Phase I study of bryostatin 1 and fludarabine in patients with chronic lymphocytic leukemia and indolent (non-Hodgkin's) lymphoma [J]
    • Roberts JD, Smith MR, Feldman EJ, et al. Phase I study of bryostatin 1 and fludarabine in patients with chronic lymphocytic leukemia and indolent (non-Hodgkin's) lymphoma [J]. Clin Cancer Res, 2006,12:5809-5816.
    • (2006) Clin Cancer Res , vol.12 , pp. 5809-5816
    • Roberts, J.D.1    Smith, M.R.2    Feldman, E.J.3
  • 18
    • 33646501280 scopus 로고    scopus 로고
    • A multi-center phase II study of sequential paclitaxel and bryostatin-1 ( NSC 339555) in patients with untreated, advanced gastric or gastroesophageal junction adenocarcinoma [J]
    • Ajani JA, Jiang Y, Faust J, et al. A multi-center phase II study of sequential paclitaxel and bryostatin-1 ( NSC 339555) in patients with untreated, advanced gastric or gastroesophageal junction adenocarcinoma [J]. Invest New Drugs, 2006,24:353-357.
    • (2006) Invest New Drugs , vol.24 , pp. 353-357
    • Ajani, J.A.1    Jiang, Y.2    Faust, J.3
  • 19
    • 33845777994 scopus 로고    scopus 로고
    • Phase I study of bryostatin 1 and gemcitabine [J]
    • El-Rayes BF, Gadgeel S, Shields AF, et al. Phase I study of bryostatin 1 and gemcitabine [J]. Clin Cancer Res, 2006,12:7059-7062.
    • (2006) Clin Cancer Res , vol.12 , pp. 7059-7062
    • El-Rayes, B.F.1    Gadgeel, S.2    Shields, A.F.3
  • 20
    • 0035136529 scopus 로고    scopus 로고
    • Ecteinascidin 743 induces protein-linked DNA breaks in human colon carcinoma HCT116 cells and is cytotoxic independently of topoisomerase I expression [J]
    • Takebayashi Y, Goldwasser F, Urasaki Y, et al. Ecteinascidin 743 induces protein-linked DNA breaks in human colon carcinoma HCT116 cells and is cytotoxic independently of topoisomerase I expression [J]. Clin Cancer Res, 2001,7:185-191.
    • (2001) Clin Cancer Res , vol.7 , pp. 185-191
    • Takebayashi, Y.1    Goldwasser, F.2    Urasaki, Y.3
  • 21
    • 33846438202 scopus 로고    scopus 로고
    • Extreme sensitivity to Yondelis (Trabectedin, ET-743) in low passaged sarcoma cell lines correlates with mutated p53 [J]
    • Moneo V, Serelde BG, Fominaya J, et al. Extreme sensitivity to Yondelis (Trabectedin, ET-743) in low passaged sarcoma cell lines correlates with mutated p53 [J]. J Cell Biochem, 2007,100:339-348.
    • (2007) J Cell Biochem , vol.100 , pp. 339-348
    • Moneo, V.1    Serelde, B.G.2    Fominaya, J.3
  • 22
    • 0037096739 scopus 로고    scopus 로고
    • Ecteinascidin-743 inhibits activated but not constitutive transcription [J]
    • Friedman D, Hu Z, Kolb EA, et al. Ecteinascidin-743 inhibits activated but not constitutive transcription [J]. Cancer Res, 2002,62:3377-3381.
    • (2002) Cancer Res , vol.62 , pp. 3377-3381
    • Friedman, D.1    Hu, Z.2    Kolb, E.A.3
  • 23
    • 0037074625 scopus 로고    scopus 로고
    • A3. (ET743) -DNA complex that both resembles an RNA-DNA hybrid and mimicks zinc finger-induced DNA structural distortions [J]
    • Marco E, García-Nieto R, Mendieta J, et al. A3. (ET743) -DNA complex that both resembles an RNA-DNA hybrid and mimicks zinc finger-induced DNA structural distortions [J]. J Med Chem, 2002,45:871-880.
    • (2002) J Med Chem , vol.45 , pp. 871-880
    • Marco, E.1    García-Nieto, R.2    Mendieta, J.3
  • 24
    • 0034813203 scopus 로고    scopus 로고
    • Sensitivity of soft tissue sarcoma cell lines to chemotherapeutic agents: Identification of ecteinascidin-743 as a potent cytotoxic agent [J]
    • Li WW, Takahashi N, Jhanwar S, et al. Sensitivity of soft tissue sarcoma cell lines to chemotherapeutic agents: identification of ecteinascidin-743 as a potent cytotoxic agent [J]. Clin Cancer Res, 2001,7:2908-2911.
    • (2001) Clin Cancer Res , vol.7 , pp. 2908-2911
    • Li, W.W.1    Takahashi, N.2    Jhanwar, S.3
  • 25
    • 31444456167 scopus 로고    scopus 로고
    • ET-743: A novel agent with activity in soft tissue sarcomas [J]
    • Fayette J, Coquard IR, Alberti L, et al. ET-743: a novel agent with activity in soft tissue sarcomas [J]. Oncologist, 2005,10:827-832.
    • (2005) Oncologist , vol.10 , pp. 827-832
    • Fayette, J.1    Coquard, I.R.2    Alberti, L.3
  • 26
    • 0036895987 scopus 로고    scopus 로고
    • Scotlandi K, Perdichizzi S, Manara MC, et al. Effectiveness of ecteinascidin-743 against drug-sensitive and -resistant bone tumor cells [J]. Clin Cancer Res, 2002,8.-3893-3903.
    • Scotlandi K, Perdichizzi S, Manara MC, et al. Effectiveness of ecteinascidin-743 against drug-sensitive and -resistant bone tumor cells [J]. Clin Cancer Res, 2002,8.-3893-3903.
  • 28
    • 0038380364 scopus 로고    scopus 로고
    • Overcoming multidrug drug resistance in P-glycoprotein/MDR1-overexpressing cell lines by ecteinascidin 743 [J]
    • Kanzaki A, Takebayashi Y, Ren XQ, et al. Overcoming multidrug drug resistance in P-glycoprotein/MDR1-overexpressing cell lines by ecteinascidin 743 [J]. Mol Cancer Ther, 2002,1:1327 - 1334.
    • (2002) Mol Cancer Ther , vol.1 , pp. 1327-1334
    • Kanzaki, A.1    Takebayashi, Y.2    Ren, X.Q.3
  • 29
    • 33748033029 scopus 로고    scopus 로고
    • ET-743: A novel agent with activity in soft-tissue sarcomas [J]
    • Fayette J, Coquard IR, Alberti L, et al. ET-743: a novel agent with activity in soft-tissue sarcomas [J]. Curr Opin Oncol, 2006,18:347-353.
    • (2006) Curr Opin Oncol , vol.18 , pp. 347-353
    • Fayette, J.1    Coquard, I.R.2    Alberti, L.3
  • 30
    • 33745259879 scopus 로고    scopus 로고
    • A phase II study of Yondelis (trabectedin, ET-743) as a 24-h continuous intravenous infusion in pretreated advanced breast cancer [J]
    • Zelek L, Yovine A, Brain E, et al. A phase II study of Yondelis (trabectedin, ET-743) as a 24-h continuous intravenous infusion in pretreated advanced breast cancer [J]. Br J Cancer, 2006,94:1610-1614.
    • (2006) Br J Cancer , vol.94 , pp. 1610-1614
    • Zelek, L.1    Yovine, A.2    Brain, E.3
  • 31
    • 0037384048 scopus 로고    scopus 로고
    • A phase II trial of dolastatin-10 in recurrent platinum-sensitive ovarian carcinoma: A Gynecologic Oncology Group study [J]
    • Hoffman M, Blessing J, Lentz S. A phase II trial of dolastatin-10 in recurrent platinum-sensitive ovarian carcinoma: a Gynecologic Oncology Group study [J]. Gynecol Oncol, 2003,89:95-98.
    • (2003) Gynecol Oncol , vol.89 , pp. 95-98
    • Hoffman, M.1    Blessing, J.2    Lentz, S.3
  • 32
    • 0141892724 scopus 로고    scopus 로고
    • Antitumor activity of TZT-1027 (soblidotin) against vascular endothelial growth factor-secreting human lung cancer in vivo [J]
    • Natsume T, Watanabe J, Koh Y, et al. Antitumor activity of TZT-1027 (soblidotin) against vascular endothelial growth factor-secreting human lung cancer in vivo [J]. Cancer Sci, 2003,94:826-833.
    • (2003) Cancer Sci , vol.94 , pp. 826-833
    • Natsume, T.1    Watanabe, J.2    Koh, Y.3
  • 33
    • 0141447346 scopus 로고    scopus 로고
    • Dolastatin 15 binds in the Vinca domain of tubulin as demonstrated by hummel-dreyer chromatography [J]
    • Cruz-Monserrate Z, Mullaney J, Harran P, et al. Dolastatin 15 binds in the Vinca domain of tubulin as demonstrated by hummel-dreyer chromatography [J]. Eur J Biochem, 2003,270:3822-3828.
    • (2003) Eur J Biochem , vol.270 , pp. 3822-3828
    • Cruz-Monserrate, Z.1    Mullaney, J.2    Harran, P.3
  • 34
    • 34248592567 scopus 로고    scopus 로고
    • Mechanism of action of the microtubule-targeted antimitotic depsipeptide tasidotin (formerly ILX651) and its major metabolite tasidotin C-carboxylate [J]
    • Ray A, Okouneva T, Manna T, et al. Mechanism of action of the microtubule-targeted antimitotic depsipeptide tasidotin (formerly ILX651) and its major metabolite tasidotin C-carboxylate [J]. Cancer Res, 2007, 67:3767-3776.
    • (2007) Cancer Res , vol.67 , pp. 3767-3776
    • Ray, A.1    Okouneva, T.2    Manna, T.3
  • 35
    • 4344650390 scopus 로고    scopus 로고
    • Marine natural products and related compounds in clinical and advanced preclinical trials [J]
    • Newman DJ, Cragg GM. Marine natural products and related compounds in clinical and advanced preclinical trials [J]. J Nat Prod, 2004,67:1216-1238.
    • (2004) J Nat Prod , vol.67 , pp. 1216-1238
    • Newman, D.J.1    Cragg, G.M.2
  • 36
    • 0030515609 scopus 로고    scopus 로고
    • Compounds produced from potential tunicate-blue-green algal symbiosis [J]
    • Sings HL, Rinehart KL. Compounds produced from potential tunicate-blue-green algal symbiosis [J]. J Ind Microbiol Biotechnol, 1996,17:385-396.
    • (1996) J Ind Microbiol Biotechnol , vol.17 , pp. 385-396
    • Sings, H.L.1    Rinehart, K.L.2
  • 37
    • 0041733458 scopus 로고    scopus 로고
    • Effect of aplidin in acute lymphoblastic leukaemia cells [J]
    • Erba E, Serafini M , Gaipa G, et al. Effect of aplidin in acute lymphoblastic leukaemia cells [J]. Br J Cancer, 2003,89:763-773.
    • (2003) Br J Cancer , vol.89 , pp. 763-773
    • Erba, E.1    Serafini, M.2    Gaipa, G.3
  • 38
    • 0037265805 scopus 로고    scopus 로고
    • Aplidine, a new anticancer agent of marine origin, inhibits vascular endothelial growth factor (VEGF) secretion and blocks VEGF-VEGFR-1 (flt-1) autocrine loop in human leukemia cells MOLT-4 [J]
    • Broggini M, Marchini SV, Galliera E, et al. Aplidine, a new anticancer agent of marine origin, inhibits vascular endothelial growth factor (VEGF) secretion and blocks VEGF-VEGFR-1 (flt-1) autocrine loop in human leukemia cells MOLT-4 [J]. Leukemia, 2003,17:52-59.
    • (2003) Leukemia , vol.17 , pp. 52-59
    • Broggini, M.1    Marchini, S.V.2    Galliera, E.3
  • 39
    • 47249141130 scopus 로고    scopus 로고
    • Jimeno J, Faircloth G, Fernandez Souse-Faro JM, et al. New marine derived anticancer therapeutics; a journey from the sea to clinical trials [J]. Marine Drugs, 2004, 2.14-29.
    • Jimeno J, Faircloth G, Fernandez Souse-Faro JM, et al. New marine derived anticancer therapeutics; a journey from the sea to clinical trials [J]. Marine Drugs, 2004, 2.14-29.
  • 40
    • 0344082608 scopus 로고    scopus 로고
    • Amador ML, Jimeno J, Paz-Ares L, et al. Progress in the development and acquisition of anticancer agents from marine sources [J]. Ann Oncol, 2003,14-1607-1615.
    • Amador ML, Jimeno J, Paz-Ares L, et al. Progress in the development and acquisition of anticancer agents from marine sources [J]. Ann Oncol, 2003,14-1607-1615.
  • 41
    • 33748745549 scopus 로고    scopus 로고
    • Phase I study of aplidine in a dailyx5 one-hour infusion every 3 weeks in patients with solid tumors refractory to standard therapy. A National Cancer Institute of Canada Clinical Trials Group study; NCIC CTG IND 115 [J]
    • Maroun JA, Belanger K, Seymour L, et al. Phase I study of aplidine in a dailyx5 one-hour infusion every 3 weeks in patients with solid tumors refractory to standard therapy. A National Cancer Institute of Canada Clinical Trials Group study; NCIC CTG IND 115 [J]. Ann Oncol, 2006,17:1371-1378.
    • (2006) Ann Oncol , vol.17 , pp. 1371-1378
    • Maroun, J.A.1    Belanger, K.2    Seymour, L.3
  • 42
    • 0038627550 scopus 로고    scopus 로고
    • Psammaplins from the sponge Pseudoceratina purpurea: Inhibition of both histone deacetylase and DNA methyltransferase [J]
    • Pifia IC, Gautschi JT, Wang GY, et al. Psammaplins from the sponge Pseudoceratina purpurea: inhibition of both histone deacetylase and DNA methyltransferase [J]. J Org Chem, 2003,68:3866-3873.
    • (2003) J Org Chem , vol.68 , pp. 3866-3873
    • Pifia, I.C.1    Gautschi, J.T.2    Wang, G.Y.3
  • 43
    • 0346094302 scopus 로고    scopus 로고
    • Psammaplin A, a marine natural product, inhibits aminopeptidase N and suppresses angiogenesis in vitro [J]
    • Shim JS, Lee HS, Shin J, et al. Psammaplin A, a marine natural product, inhibits aminopeptidase N and suppresses angiogenesis in vitro [J]. Cancer Lett, 2004, 203:163-169.
    • (2004) Cancer Lett , vol.203 , pp. 163-169
    • Shim, J.S.1    Lee, H.S.2    Shin, J.3
  • 44
    • 0141953928 scopus 로고    scopus 로고
    • The discovery of NVP-LAQ824; from concept to clinic [J]
    • Remiszewski SW. The discovery of NVP-LAQ824; from concept to clinic [J]. Curr Med Chem, 2003,10:2393-2402.
    • (2003) Curr Med Chem , vol.10 , pp. 2393-2402
    • Remiszewski, S.W.1
  • 45
    • 0026069885 scopus 로고
    • Halichondrin B and homohalichondrin B, marine natural products binding in the Vinca domain of tubulin. Discovery of tubulin-based mechanism of action by analysis of differential cytotoxicity data [J]
    • Bai RL, Paull KD, Herald CL, et al. Halichondrin B and homohalichondrin B, marine natural products binding in the Vinca domain of tubulin. Discovery of tubulin-based mechanism of action by analysis of differential cytotoxicity data [J]. J Biol Chem, 1991,266:15882-15889.
    • (1991) J Biol Chem , vol.266 , pp. 15882-15889
    • Bai, R.L.1    Paull, K.D.2    Herald, C.L.3
  • 46
    • 2142818569 scopus 로고    scopus 로고
    • A quantitative evaluation of the effects of inhibitors of tubulin assembly on polymerization induced by discodermolide, epothilone B, and paclitaxel [J]
    • Dabydeen D, Florence G, Paterson I, et al. A quantitative evaluation of the effects of inhibitors of tubulin assembly on polymerization induced by discodermolide, epothilone B, and paclitaxel [J]. Cancer Chemother Pharmacol, 2004,53:397-403.
    • (2004) Cancer Chemother Pharmacol , vol.53 , pp. 397-403
    • Dabydeen, D.1    Florence, G.2    Paterson, I.3
  • 47
    • 33751102419 scopus 로고    scopus 로고
    • Comparison of the activities of the truncated halichondrin B analog NSC 707389 (E7389) with those of the parent compound and a proposed binding site on tubulin [J]
    • Dabydeen DA, Burnett JC, Bai R, et al. Comparison of the activities of the truncated halichondrin B analog NSC 707389 (E7389) with those of the parent compound and a proposed binding site on tubulin [J]. Mol Pharmacol, 2006,70:1866-1875.
    • (2006) Mol Pharmacol , vol.70 , pp. 1866-1875
    • Dabydeen, D.A.1    Burnett, J.C.2    Bai, R.3
  • 48
    • 42549160421 scopus 로고    scopus 로고
    • Anthracenedione derivative 1403P-3 induces apoptosis in KB and KBv200 cells via reactive oxygen species-independent mitochondrial pathway and death receptor pathway [J]
    • Zhang JY, Wu HY, Xia XK, et al. Anthracenedione derivative 1403P-3 induces apoptosis in KB and KBv200 cells via reactive oxygen species-independent mitochondrial pathway and death receptor pathway [J]. Cancer Biol Ther. 2007,6:1413-1421.
    • (2007) Cancer Biol Ther , vol.6 , pp. 1413-1421
    • Zhang, J.Y.1    Wu, H.Y.2    Xia, X.K.3
  • 49
    • 35549004397 scopus 로고    scopus 로고
    • Structural and biological properties of vermistatin and two new vermistatin derivatives isolated from the marine-mangrove endophytic fungus guignardia sp. No 4382 [J]
    • Xia XK, Huang HR, She ZG, et al. Structural and biological properties of vermistatin and two new vermistatin derivatives isolated from the marine-mangrove endophytic fungus guignardia sp. No 4382 [J]. Helv Chim Acta, 2007,90:1925-1931.
    • (2007) Helv Chim Acta , vol.90 , pp. 1925-1931
    • Xia, X.K.1    Huang, H.R.2    She, Z.G.3
  • 50
    • 34547815196 scopus 로고    scopus 로고
    • Sipholenol A, a marine-derived sipholane triterpene, potently reverses P-glycoprotein (ABCB1) -mediated multidrug resistance in cancer cells [J]
    • Shi Z, Jain S, Kim IW, et al. Sipholenol A, a marine-derived sipholane triterpene, potently reverses P-glycoprotein (ABCB1) -mediated multidrug resistance in cancer cells [J]. Cancer Sci. 2007,98:1373-1380.
    • (2007) Cancer Sci , vol.98 , pp. 1373-1380
    • Shi, Z.1    Jain, S.2    Kim, I.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.