메뉴 건너뛰기




Volumn 45, Issue 2, 2014, Pages 558-566

Daurinol, a catalytic inhibitor of topoisomerase IIα, suppresses SNU-840 ovarian cancer cell proliferation through cell cycle arrest in S phase

Author keywords

ATP binding pocket; Daurinol; Ovarian cancer; Secondary leukemia; Topoisomerase II inhibitor

Indexed keywords

ADENOSINE TRIPHOSPHATE; ANTINEOPLASTIC AGENT; CAMPTOTHECIN; CYCLIN A; CYCLIN E; DAURINOL; DNA TOPOISOMERASE; DNA TOPOISOMERASE (ATP HYDROLYSING) A; ETOPOSIDE; GYRASE INHIBITOR; LIGNAN; TRANSCRIPTION FACTOR E2F1; UNCLASSIFIED DRUG; 1,3 BENZODIOXOLE DERIVATIVE; DNA BINDING PROTEIN; DNA TOPOISOMERASE (ATP HYDROLYSING); DNA TOPOISOMERASE II ALPHA; NAPHTHALENE DERIVATIVE; TUMOR ANTIGEN;

EID: 84902583141     PISSN: 10196439     EISSN: 17912423     Source Type: Journal    
DOI: 10.3892/ijo.2014.2442     Document Type: Article
Times cited : (27)

References (25)
  • 1
    • 84865102002 scopus 로고    scopus 로고
    • Contemporary challenges in the design of topoisomerase II inhibitors for cancer chemotherapy
    • Bailly C: Contemporary challenges in the design of topoisomerase II inhibitors for cancer chemotherapy. Chem Rev 112: 3611-3640, 2012.
    • (2012) Chem Rev , vol.112 , pp. 3611-3640
    • Bailly, C.1
  • 2
    • 84877965129 scopus 로고    scopus 로고
    • Recent advances in the development of catalytic inhibitors of human DNA topo-isomerase IIα as novel anticancer agents
    • Pogorelcnik B, Perdih A and Solmajer T: Recent advances in the development of catalytic inhibitors of human DNA topo-isomerase IIα as novel anticancer agents. Curr Med Chem 20: 694-709, 2013.
    • (2013) Curr Med Chem , vol.20 , pp. 694-709
    • Pogorelcnik, B.1    Perdih, A.2    Solmajer, T.3
  • 3
    • 84863867276 scopus 로고    scopus 로고
    • Secondary leukemia associated with the anti-cancer agent, etoposide, a topoisomerase II inhibitor
    • Ezoe S: Secondary leukemia associated with the anti-cancer agent, etoposide, a topoisomerase II inhibitor. Int J Environ Res Public Health 9: 2444-2453, 2012.
    • (2012) Int J Environ Res Public Health , vol.9 , pp. 2444-2453
    • Ezoe, S.1
  • 4
    • 85008737005 scopus 로고    scopus 로고
    • Topoisomerase IIα, rather than IIβ, is a promising target in development of anti-cancer drugs
    • Chen W, Qiu J and Shen YM: Topoisomerase IIα, rather than IIβ, is a promising target in development of anti-cancer drugs. Drug Discov Ther 6: 230-237, 2012.
    • (2012) Drug Discov Ther , vol.6 , pp. 230-237
    • Chen, W.1    Qiu, J.2    Shen, Y.M.3
  • 5
    • 81355133687 scopus 로고    scopus 로고
    • A novel topoisomerase inhibitor, daurinol, suppresses growth of HCT116 cells with low hematological toxicity compared to etoposide
    • Kang K, Oh SH, Yun JH, et al: A novel topoisomerase inhibitor, daurinol, suppresses growth of HCT116 cells with low hematological toxicity compared to etoposide. Neoplasia 13: 1043-1057, 2011.
    • (2011) Neoplasia , vol.13 , pp. 1043-1057
    • Kang, K.1    Oh, S.H.2    Yun, J.H.3
  • 7
    • 0033697116 scopus 로고    scopus 로고
    • Plants used against cancer - an extension of the work of Jonathan Hartwell
    • Graham JG, Quinn ML, Fabricant DS and Farnsworth NR: Plants used against cancer - an extension of the work of Jonathan Hartwell. J Ethnopharmacol 73: 347-377, 2000.
    • (2000) J Ethnopharmacol , vol.73 , pp. 347-377
    • Graham, J.G.1    Quinn, M.L.2    Fabricant, D.S.3    Farnsworth, N.R.4
  • 8
    • 0032168167 scopus 로고    scopus 로고
    • Etoposide: Four decades of development of a topoisomerase II inhibitor
    • Hande KR: Etoposide: four decades of development of a topoisomerase II inhibitor. Eur J Cancer 34: 1514-1521, 1998.
    • (1998) Eur J Cancer , vol.34 , pp. 1514-1521
    • Hande, K.R.1
  • 9
    • 84892437040 scopus 로고    scopus 로고
    • Regioselective route for arylnaphthalene lactones: Convenient synthesis of taiwanin C, justicidin E, and daurinol
    • Park JE, Lee J, Seo SY and Shin D: Regioselective route for arylnaphthalene lactones: convenient synthesis of taiwanin C, justicidin E, and daurinol. Tetrahedron Lett 55: 818-820, 2014.
    • (2014) Tetrahedron Lett , vol.55 , pp. 818-820
    • Park, J.E.1    Lee, J.2    Seo, S.Y.3    Shin, D.4
  • 10
    • 0018600707 scopus 로고
    • An improved assay for nanomole amounts of inorganic phosphate
    • DOI 10.1016/0003-2697(79)90115-5
    • Lanzetta PA, Alvarez LJ, Reinach PS and Candia OA: An improved assay for nanomole amounts of inorganic phosphate. Anal Biochem 100: 95-97, 1979. (Pubitemid 10157636)
    • (1979) Analytical Biochemistry , vol.100 , Issue.1 , pp. 95-97
    • Lanzetta, P.A.1    Alvarez, L.J.2    Reinach, P.S.3    Candia, O.A.4
  • 11
    • 77958453863 scopus 로고    scopus 로고
    • The three proline residues (P25, P242, and P434) of Agrobacterium CP4 5-enolpyruvylshikimate-3-phosphate synthase are crucial for the enzyme activity
    • Kang K, Jin YM, Jeon H, et al: The three proline residues (P25, P242, and P434) of Agrobacterium CP4 5-enolpyruvylshikimate-3-phosphate synthase are crucial for the enzyme activity. Plant Biotechnol Rep 4: 329-334, 2010.
    • (2010) Plant Biotechnol Rep , vol.4 , pp. 329-334
    • Kang, K.1    Jin, Y.M.2    Jeon, H.3
  • 12
    • 79955601050 scopus 로고    scopus 로고
    • Synthesis, biological evaluation, and molecular docking study of 3-(3′-heteroatom substituted-2′-hydroxy-1′-propyloxy) xanthone analogues as novel topoisomerase IIα catalytic inhibitor
    • Jun KY, Lee EY, Jung MJ, et al: Synthesis, biological evaluation, and molecular docking study of 3-(3′-heteroatom substituted-2′-hydroxy- 1′-propyloxy) xanthone analogues as novel topoisomerase IIα catalytic inhibitor. Eur J Med Chem 46: 1964-1971, 2011.
    • (2011) Eur J Med Chem , vol.46 , pp. 1964-1971
    • Jun, K.Y.1    Lee, E.Y.2    Jung, M.J.3
  • 13
    • 0027172883 scopus 로고
    • Effects of topoisomerase II-targeted drugs on enzyme-mediated DNA cleavage and ATP hydrolysis: Evidence for distinct drug interaction domains on topoisomerase II
    • Robinson MJ, Corbett AH and Osheroff N: Effects of topoisomerase II-targeted drugs on enzyme-mediated DNA cleavage and ATP hydrolysis: evidence for distinct drug interaction domains on topoisomerase II. Biochemistry 32: 3638-3643, 1993. (Pubitemid 23126939)
    • (1993) Biochemistry , vol.32 , Issue.14 , pp. 3638-3643
    • Robinson, M.J.1    Corbett, A.H.2    Osheroff, N.3
  • 14
  • 15
    • 79960959134 scopus 로고    scopus 로고
    • Cell and nuclear enlargement of SW480 cells induced by a plant lignan, arctigenin: Evaluation of cellular DNA content using fluorescence microscopy and flow cytometry
    • Kang K, Lee HJ, Yoo JH, et al: Cell and nuclear enlargement of SW480 cells induced by a plant lignan, arctigenin: evaluation of cellular DNA content using fluorescence microscopy and flow cytometry. DNA Cell Biol 30: 623-629, 2011.
    • (2011) DNA Cell Biol , vol.30 , pp. 623-629
    • Kang, K.1    Lee, H.J.2    Yoo, J.H.3
  • 16
    • 77954543287 scopus 로고    scopus 로고
    • Flow cytometric fluorescence pulse width analysis of etoposide-induced nuclear enlargement in HCT116 cells
    • Kang K, Lee SB, Yoo JH and Nho CW: Flow cytometric fluorescence pulse width analysis of etoposide-induced nuclear enlargement in HCT116 cells. Biotechnol Lett 32: 1045-1052, 2010.
    • (2010) Biotechnol Lett , vol.32 , pp. 1045-1052
    • Kang, K.1    Lee, S.B.2    Yoo, J.H.3    Nho, C.W.4
  • 17
    • 0028949206 scopus 로고
    • The mechanisms of DNA topoisomerases
    • Roca J: The mechanisms of DNA topoisomerases. Trends Biochem Sci 20: 156-160, 1995.
    • (1995) Trends Biochem Sci , vol.20 , pp. 156-160
    • Roca, J.1
  • 18
    • 0042346439 scopus 로고    scopus 로고
    • Catalytic topoisomerase II inhibitors in cancer therapy
    • DOI 10.1016/S0163-7258(03)00058-5
    • Larsen AK, Escargueil AE and Skladanowski A: Catalytic topoisomerase II inhibitors in cancer therapy. Pharmacol Ther 99: 167-181, 2003. (Pubitemid 36897748)
    • (2003) Pharmacology and Therapeutics , vol.99 , Issue.2 , pp. 167-181
    • Larsen, A.K.1    Escargueil, A.E.2    Skladanowski, A.3
  • 19
    • 5144223978 scopus 로고    scopus 로고
    • Cell cycle checkpoints and their impact on anticancer therapeutic strategies
    • Eastman A: Cell cycle checkpoints and their impact on anticancer therapeutic strategies. J Cell Biochem 91: 223-231, 2004.
    • (2004) J Cell Biochem , vol.91 , pp. 223-231
    • Eastman, A.1
  • 21
    • 0029049577 scopus 로고
    • Cellular targets for activation by the E2F1 transcription factor include DNA synthesis- and G1/S-regulatory genes
    • DeGregori J, Kowalik T and Nevins JR: Cellular targets for activation by the E2F1 transcription factor include DNA synthesis- and G1/S-regulatory genes. Mol Cell Biol 15: 4215-4224, 1995.
    • (1995) Mol Cell Biol , vol.15 , pp. 4215-4224
    • DeGregori, J.1    Kowalik, T.2    Nevins, J.R.3
  • 22
    • 84855768356 scopus 로고    scopus 로고
    • D11, a novel glycosylated diphyllin derivative, exhibits potent anticancer activity by targeting topoisomerase IIα
    • Gui M, Shi DK, Huang M, et al: D11, a novel glycosylated diphyllin derivative, exhibits potent anticancer activity by targeting topoisomerase IIα. Invest New Drugs 29: 800-810, 2011.
    • (2011) Invest New Drugs , vol.29 , pp. 800-810
    • Gui, M.1    Shi, D.K.2    Huang, M.3
  • 23
    • 84877794094 scopus 로고    scopus 로고
    • Mitochondrial hormesis links low-dose arsenite exposure to lifespan extension
    • Schmeisser S, Schmeisser K, Weimer S, et al: Mitochondrial hormesis links low-dose arsenite exposure to lifespan extension. Aging cell 12: 508-517, 2013.
    • (2013) Aging Cell , vol.12 , pp. 508-517
    • Schmeisser, S.1    Schmeisser, K.2    Weimer, S.3
  • 24
    • 7444254046 scopus 로고    scopus 로고
    • Caenorhabditis elegans as model system for rapid toxicity assessment of pharmaceutical compounds
    • DOI 10.1016/j.vascn.2004.04.002, PII S1056871904000346
    • Dengg M and van Meel JC: Caenorhabditis elegans as model system for rapid toxicity assessment of pharmaceutical compounds. J Pharmacol Toxicol Methods 50: 209-214, 2004. (Pubitemid 39440718)
    • (2004) Journal of Pharmacological and Toxicological Methods , vol.50 , Issue.3 , pp. 209-214
    • Dengg, M.1    Van Meel, J.C.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.