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Volumn 45, Issue 9, 2010, Pages 1109-1115

Cinnamaldehyde ofloxacin-3-ylhydrazone induces apoptosis of human hepatocarcinoma SMMC-7721 cells

Author keywords

Apoptosis; Mitochondrial membrane potential; Quinolone derivative; Topoisomerase II

Indexed keywords

CASPASE 3; CASPASE 8; CASPASE 9; CINNAMALDEHYDE OFLOXACIN 3 YLHYDRAZONE; DNA TOPOISOMERASE (ATP HYDROLYSING); FQ 16; N (3 PHENYLALLYLIDENE) 6 FLUORO 1,8 (2,1 PROPOXY) 7 (4 METHYLPIPERAZIN 1 YL)QUINOLIN 4(1H) ONE 3 CARBONYLHYDRAZINE; PROTEIN BAX; PROTEIN BCL 2; PROTEIN P53; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 78349231350     PISSN: 05134870     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (14)

References (25)
  • 1
    • 0001534829 scopus 로고
    • Mechanism of action of nalidixic acid: Purification of Escherichia coli na1A gene product and its relationship to DNA gyrase and a novel nicking-closing enzyme
    • J
    • Sugino A, Peebles CL, Kreuzer KN, et al. Mechanism of action of nalidixic acid: purification of Escherichia coli na1A gene product and its relationship to DNA gyrase and a novel nicking-closing enzyme [J]. Proc Natl Acad Sci USA, 1977, 74: 4767-4771.
    • (1977) Proc Natl Acad Sci USA , vol.74 , pp. 4767-4771
    • Sugino, A.1    Peebles, C.L.2    Kreuzer, K.N.3
  • 2
    • 34249302775 scopus 로고    scopus 로고
    • Functionalized N-(2-oxyiminoethyl) piperazinyl quinolones as new cytotoxic agents
    • J
    • Rajabalian S, Foroumadi A, Shafiee A, et al. Functionalized N-(2-oxyiminoethyl) piperazinyl quinolones as new cytotoxic agents [J]. J Pharm Pharm Sci, 2007, 10: 153-158.
    • (2007) J Pharm Pharm Sci , vol.10 , pp. 153-158
    • Rajabalian, S.1    Foroumadi, A.2    Shafiee, A.3
  • 3
    • 70349638919 scopus 로고    scopus 로고
    • Structure-activity relationship and molecular mechanisms of ethyl 2-amino-4-(2-ethoxy-2-oxoethyl)-6-phenyl-4H-chromene-3-carboxylate (sha14-1) and its analogues
    • J
    • Das SG, Doshi JM, Tian D, et al. Structure-activity relationship and molecular mechanisms of ethyl 2-amino-4-(2-ethoxy-2-oxoethyl)-6-phenyl-4H- chromene-3-carboxylate (sha14-1) and its analogues [J]. J Med Chem, 2009, 52: 5937-5949.
    • (2009) J Med Chem , vol.52 , pp. 5937-5949
    • Das, S.G.1    Doshi, J.M.2    Tian, D.3
  • 4
    • 14744292724 scopus 로고    scopus 로고
    • An advance of study in antitumor quinolone drugs
    • J
    • Wang XT, Zhang JB, Lei YJ. An advance of study in antitumor quinolone drugs [J]. Chin Pharm J, 2004, 39: 890-894.
    • (2004) Chin Pharm J , vol.39 , pp. 890-894
    • Wang, X.T.1    Zhang, J.B.2    Lei, Y.J.3
  • 5
    • 56649109508 scopus 로고    scopus 로고
    • Synthesis and antitumor activity of C3 heterocyclic-substituted fluoroquinolone derivatives (I): Ciprofloxacin aminothiodiazole Schiff-bases
    • J
    • Hu GQ, Wu XK, Wang X, et al. Synthesis and antitumor activity of C3 heterocyclic-substituted fluoroquinolone derivatives (I): ciprofloxacin aminothiodiazole Schiff-bases [J]. Acta Pharm Sin, 2008, 43: 1112-1115.
    • (2008) Acta Pharm Sin , vol.43 , pp. 1112-1115
    • Hu, G.Q.1    Wu, X.K.2    Wang, X.3
  • 6
    • 70349410539 scopus 로고    scopus 로고
    • Discovery of a novel series of quinolone and naphthyridine derivatives as potential topoisomerase I inhibitors by scaffold modification
    • J
    • You QD, Li ZY, Huang CH, et al. Discovery of a novel series of quinolone and naphthyridine derivatives as potential topoisomerase I inhibitors by scaffold modification [J]. J Med Chem, 2009, 52: 5649-5661.
    • (2009) J Med Chem , vol.52 , pp. 5649-5661
    • You, Q.D.1    Li, Z.Y.2    Huang, C.H.3
  • 7
    • 67649950035 scopus 로고    scopus 로고
    • An efficient synthesis and biological study of novel indolyl-1, 3, 4-oxadiazoles as potent anticancer agents
    • J
    • Kumar D, Sundaree S, Johnson EO, et al. An efficient synthesis and biological study of novel indolyl-1, 3, 4-oxadiazoles as potent anticancer agents [J]. Bioorg Med Chem Lett, 2009, 19: 4492-4494.
    • (2009) Bioorg Med Chem Lett , vol.19 , pp. 4492-4494
    • Kumar, D.1    Sundaree, S.2    Johnson, E.O.3
  • 9
    • 0033121315 scopus 로고    scopus 로고
    • Bcl-XI and Bax-alpha-mediated regulation of apoptosis of human neutrophils via caspase-3
    • J
    • Weinmann P, Gaehtgens P, Walzog B. Bcl-XI and Bax-alpha-mediated regulation of apoptosis of human neutrophils via caspase-3 [J]. Blood, 1999, 93: 3106-3115.
    • (1999) Blood , vol.93 , pp. 3106-3115
    • Weinmann, P.1    Gaehtgens, P.2    Walzog, B.3
  • 10
    • 33845458214 scopus 로고    scopus 로고
    • Structure and biological properties of the copper (II) complex with the quinolone antibacterial drug N-propyl-norfloxacin and 2, 2′-bipyridine
    • J
    • Efthimiadou EK, Thomadaki H, Sanakis Y, et al. Structure and biological properties of the copper (II) complex with the quinolone antibacterial drug N-propyl-norfloxacin and 2, 2′-bipyridine [J]. J Inorg Biochem, 2007, 101: 64-73.
    • (2007) J Inorg Biochem , vol.101 , pp. 64-73
    • Efthimiadou, E.K.1    Thomadaki, H.2    Sanakis, Y.3
  • 11
    • 0036581843 scopus 로고    scopus 로고
    • Synthesis, photochemical synthesis and antitumor evaluation of novel derivatives of thieno (3′, 2′: 4, 5) thieno (2, 3-c) quinolones
    • J
    • DoganKoruznjak J, Slade N, Zamola B, et al. Synthesis, photochemical synthesis and antitumor evaluation of novel derivatives of thieno (3′, 2′: 4, 5) thieno (2, 3-c) quinolones [J]. Chem Pharm Bull, 2002, 50: 56-660.
    • (2002) Chem Pharm Bull , vol.50 , pp. 56-660
    • Dogankoruznjak, J.1    Slade, N.2    Zamola, B.3
  • 12
    • 0030045003 scopus 로고    scopus 로고
    • Structure and mechanism of DNA topoisomerase II
    • J
    • Berger JM, Gamblin SJ, Harrison SC, et al. Structure and mechanism of DNA topoisomerase II [J]. Nature, 1996, 379: 225-232.
    • (1996) Nature , vol.379 , pp. 225-232
    • Berger, J.M.1    Gamblin, S.J.2    Harrison, S.C.3
  • 13
    • 0042729669 scopus 로고    scopus 로고
    • Studies on synthesis antibacterial and antitumor activity of (S)-(-)-ofloxacin analogues
    • J
    • Yang YS, Ji RY, Chen KX, et al. Studies on synthesis antibacterial and antitumor activity of (S)-(-)-ofloxacin analogues [J]. Acta Pharm Sin, 1999, 34: 119-124.
    • (1999) Acta Pharm Sin , vol.34 , pp. 119-124
    • Yang, Y.S.1    Ji, R.Y.2    Chen, K.X.3
  • 14
    • 0033168775 scopus 로고    scopus 로고
    • Quinolone antibiotics: A potential adjunct to intravesical chemotherapy for bladder cancer
    • DOI 10.1016/S0090-4295(99)00064-3, PII S0090429599000643
    • Kamat AM, De Haven JI, Lamm DL. A potential adjunct to intravesical chemotherapy for bladder cancer [J]. Urology, 1999, 54: 56-61. (Pubitemid 29323333)
    • (1999) Urology , vol.54 , Issue.1 , pp. 56-61
    • Kamat, A.M.1    Dehaven, J.I.2    Lamm, D.L.3
  • 15
    • 0026333913 scopus 로고
    • Effects of quinolone derivatives on eukaryotic topoisomerase II. A novel mechanism for enhancement of enzyme-mediated DNA cleavage
    • J
    • Robinson MJ, Martin BA, Gootz TD, et al. Effects of quinolone derivatives on eukaryotic topoisomerase II. A novel mechanism for enhancement of enzyme-mediated DNA cleavage [J]. J Biol Chem, 1991, 266: 14585-14592.
    • (1991) J Biol Chem , vol.266 , pp. 14585-14592
    • Robinson, M.J.1    Martin, B.A.2    Gootz, T.D.3
  • 16
    • 0026628327 scopus 로고
    • Cytotoxicity of quinolones toward eukaryotic cells. Identification of topoisomerase II as the primary cellular target for the quinolone CP-115, 953 in yeast
    • J
    • Elsea SH, Osheroff N, Nitiss JL. Cytotoxicity of quinolones toward eukaryotic cells. Identification of topoisomerase II as the primary cellular target for the quinolone CP-115, 953 in yeast [J]. J Biol Chem, 1992, 267: 13150-13153.
    • (1992) J Biol Chem , vol.267 , pp. 13150-13153
    • Elsea, S.H.1    Osheroff, N.2    Nitiss, J.L.3
  • 17
    • 27844582219 scopus 로고    scopus 로고
    • Synthesis and in-vitro cytotoxicity evaluation of gatifloxacin Mannich bases
    • J
    • Yogeeswari P, Sriram D, Kavya R, et al. Synthesis and in-vitro cytotoxicity evaluation of gatifloxacin Mannich bases [J]. Biomed Pharmacother, 2005, 59: 501-510.
    • (2005) Biomed Pharmacother , vol.59 , pp. 501-510
    • Yogeeswari, P.1    Sriram, D.2    Kavya, R.3
  • 18
    • 69049100261 scopus 로고    scopus 로고
    • 2D-QSAR studies on antitumor quinolones with the modification on site C-3
    • J
    • Lin KJ, You QD, Liu ZH. 2D-QSAR studies on antitumor quinolones with the modification on site C-3 [J]. Chin J Med Chem, 2003, 13: 316-319.
    • (2003) Chin J Med Chem , vol.13 , pp. 316-319
    • Lin, K.J.1    You, Q.D.2    Liu, Z.H.3
  • 19
    • 0034647434 scopus 로고    scopus 로고
    • Increased sensitivity to quinolone antibacterials can be engineered in human topoisomerase II alpha by selective mutagenesis
    • J
    • Hammonds TR, Foster SR, Maxwell A. Increased sensitivity to quinolone antibacterials can be engineered in human topoisomerase II alpha by selective mutagenesis [J]. J Mol Biol, 2000, 300: 481-491.
    • (2000) J Mol Biol , vol.300 , pp. 481-491
    • Hammonds, T.R.1    Foster, S.R.2    Maxwell, A.3
  • 20
    • 37349019737 scopus 로고    scopus 로고
    • Ofloxacin induces apoptosis in microencapsulated juvenile rabbit chondrocytes by caspase-8-dependent mitochondrial pathway
    • J
    • Sheng Z, Cao X, Peng S, et al. Ofloxacin induces apoptosis in microencapsulated juvenile rabbit chondrocytes by caspase-8-dependent mitochondrial pathway [J]. Toxicol Appl Pharmacol, 2008, 226: 119-127.
    • (2008) Toxicol Appl Pharmacol , vol.226 , pp. 119-127
    • Sheng, Z.1    Cao, X.2    Peng, S.3
  • 21
    • 42549130980 scopus 로고    scopus 로고
    • 2 arrest and apoptosis in TK6 lymphoblastoid cells is not dependent on DNA double-strand break formation
    • Smart DJ, Halicka HD, Traganos F, et al. Ciprofloxacin-induced G2 arrest and apoptosis in TK6 lymphoblastoid cells is not dependent on DNA double-strand break formation [J]. Cancer Biol Ther, 2008, 7: 113-119. (Pubitemid 351590463)
    • (2008) Cancer Biology and Therapy , vol.7 , Issue.1 , pp. 113-119
    • Smart, D.J.1    Halicka, H.D.2    Traganos, F.3    Darzynkiewicz, Z.4    Williams, G.M.5
  • 22
    • 36749050957 scopus 로고    scopus 로고
    • MFTZ-1, an actinomycetes subspecies derived antitumor macrolide, functions as a novel topoisomerase II poison
    • J
    • Xie CY, Zhu H, Lin LP, et al. MFTZ-1, an actinomycetes subspecies derived antitumor macrolide, functions as a novel topoisomerase II poison [J]. Mol Cancer Ther, 2007, 6: 3059-3070.
    • (2007) Mol Cancer Ther , vol.6 , pp. 3059-3070
    • Xie, C.Y.1    Zhu, H.2    Lin, L.P.3
  • 23
    • 34249044753 scopus 로고    scopus 로고
    • Quinolone analogue inhibits tubulin polymerization and induces apoptosis via Cdk1-involved signaling pathways
    • J
    • Chen YC, Lu PH, Pan SL, et al. Quinolone analogue inhibits tubulin polymerization and induces apoptosis via Cdk1-involved signaling pathways [J]. Biochem Pharmacol, 2007, 74: 10-19.
    • (2007) Biochem Pharmacol , vol.74 , pp. 10-19
    • Chen, Y.C.1    Lu, P.H.2    Pan, S.L.3
  • 24
    • 71549161851 scopus 로고    scopus 로고
    • Novel quinolone CHM-1 induces apoptosis and inhibits metastasis in a human osterogenic sarcoma cell line
    • J
    • Hsu SC, Yang JS, Kuo CL, et al. Novel quinolone CHM-1 induces apoptosis and inhibits metastasis in a human osterogenic sarcoma cell line [J]. J Orthop Res, 2009, 27: 1637-1644.
    • (2009) J Orthop Res , vol.27 , pp. 1637-1644
    • Hsu, S.C.1    Yang, J.S.2    Kuo, C.L.3
  • 25
    • 39749168393 scopus 로고    scopus 로고
    • CHM-1, a novel synthetic quinolone with potent and selective antimitotic antitumor activity against human hepatocellular carcinoma in vitro and in vivo
    • J
    • Wang SW, Pan SL, Huang YC, et al. CHM-1, a novel synthetic quinolone with potent and selective antimitotic antitumor activity against human hepatocellular carcinoma in vitro and in vivo [J]. Mol Cancer Ther, 2008, 7: 350-360.
    • (2008) Mol Cancer Ther , vol.7 , pp. 350-360
    • Wang, S.W.1    Pan, S.L.2    Huang, Y.C.3


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