메뉴 건너뛰기




Volumn 450, Issue 4, 2014, Pages 1650-1655

5-(2-Carboxyethenyl) isatin derivative induces G2/M cell cycle arrest and apoptosis in human leukemia K562 cells

Author keywords

Apoptosis; Cell cycle; Isatin derivatives

Indexed keywords

APOPTOSIS; CELL CYCLE; ISATIN DERIVATIVES;

EID: 84906086116     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2014.07.053     Document Type: Article
Times cited : (15)

References (26)
  • 1
    • 1942488330 scopus 로고    scopus 로고
    • Anticonvulsant activity of schiff bases of isatin derivatives
    • M. Verma, S.N. Pandeya, and K.N. Singh et al. Anticonvulsant activity of schiff bases of isatin derivatives Acta Pharm. 54 2004 49 56
    • (2004) Acta Pharm. , vol.54 , pp. 49-56
    • Verma, M.1    Pandeya, S.N.2    Singh, K.N.3
  • 2
    • 84879360881 scopus 로고    scopus 로고
    • Biochemical and pharmacological characterization of isatin and its derivatives: From structure to activity
    • P. Pakravan, S. Kashanian, and M.M. Khodaei et al. Biochemical and pharmacological characterization of isatin and its derivatives: from structure to activity Pharmacol. Rep. 65 2013 313 335
    • (2013) Pharmacol. Rep. , vol.65 , pp. 313-335
    • Pakravan, P.1    Kashanian, S.2    Khodaei, M.M.3
  • 3
    • 67649804836 scopus 로고    scopus 로고
    • Cytotoxic and anticancer activities of isatin and its derivatives: A comprehensive review from 2000-2008
    • K.L. Vine, L. Matesic, and J.M. Locke et al. Cytotoxic and anticancer activities of isatin and its derivatives: a comprehensive review from 2000-2008 Anticancer Agents Med. Chem. 9 2009 397 414
    • (2009) Anticancer Agents Med. Chem. , vol.9 , pp. 397-414
    • Vine, K.L.1    Matesic, L.2    Locke, J.M.3
  • 4
    • 79952159100 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of some isatin derivatives for antimicrobial properties
    • K.C. Chaluvaraju, and Zaranappa Synthesis and biological evaluation of some isatin derivatives for antimicrobial properties Res. J. Pharm. Biol. Chem. Sci. 2 2011 541 546
    • (2011) Res. J. Pharm. Biol. Chem. Sci. , vol.2 , pp. 541-546
    • Chaluvaraju, K.C.1    Zaranappa2
  • 5
    • 0035159356 scopus 로고    scopus 로고
    • Synthesis and pharmacological activities of hydrazones, schiff and mannich bases of isatin derivatives
    • K.S. Seshaiah, and R. Atmakuru Synthesis and pharmacological activities of hydrazones, schiff and mannich bases of isatin derivatives Biol. Pharm. Bull. 24 2001 1149 1152
    • (2001) Biol. Pharm. Bull. , vol.24 , pp. 1149-1152
    • Seshaiah, K.S.1    Atmakuru, R.2
  • 6
    • 0034675333 scopus 로고    scopus 로고
    • The endogenous oxindoles 5-hydroxyoxindole and isatin are antiproliferative and proapoptotic
    • A. Cane, M.C. Tournaire, and D. Barritault et al. The endogenous oxindoles 5-hydroxyoxindole and isatin are antiproliferative and proapoptotic Biochem. Biophys. Res. Commun. 276 2000 379 384
    • (2000) Biochem. Biophys. Res. Commun. , vol.276 , pp. 379-384
    • Cane, A.1    Tournaire, M.C.2    Barritault, D.3
  • 7
    • 33845324541 scopus 로고    scopus 로고
    • In vitro cytotoxicity evaluation of some substituted isatin derivatives
    • K.L. Vine, J.M. Locke, and M. Ranson et al. In vitro cytotoxicity evaluation of some substituted isatin derivatives Bioorg. Med. Chem. 15 2007 931 938
    • (2007) Bioorg. Med. Chem. , vol.15 , pp. 931-938
    • Vine, K.L.1    Locke, J.M.2    Ranson, M.3
  • 8
    • 84861542974 scopus 로고    scopus 로고
    • Schiff bases of indoline-2,3-dione (isatin) with potential antiproliferative activity
    • T. Aboul-Fadl, A.A. Radwan, and M.I. Attia et al. Schiff bases of indoline-2,3-dione (isatin) with potential antiproliferative activity Chem. Cent. J. 30 2012 49 59
    • (2012) Chem. Cent. J. , vol.30 , pp. 49-59
    • Aboul-Fadl, T.1    Radwan, A.A.2    Attia, M.I.3
  • 9
    • 75849132121 scopus 로고    scopus 로고
    • QSAR study of isatin analogues as in vitro anti-cancer agents
    • R. Sabet, M. Mohammadpour, and A. Sadeghi et al. QSAR study of isatin analogues as in vitro anti-cancer agents Eur. J. Med. Chem. 45 2010 1113 1118
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 1113-1118
    • Sabet, R.1    Mohammadpour, M.2    Sadeghi, A.3
  • 10
    • 33644833910 scopus 로고    scopus 로고
    • Activity of SU11248, a multitargeted inhibitor of vascular endothelial growth factor receptor and platelet-derived growth factor receptor, in patients with metastatic renal cell carcinoma
    • R.J. Motzer, M.D. Michaelson, and B.G. Redman et al. Activity of SU11248, a multitargeted inhibitor of vascular endothelial growth factor receptor and platelet-derived growth factor receptor, in patients with metastatic renal cell carcinoma J. Clin. Oncol. 24 2006 16 24
    • (2006) J. Clin. Oncol. , vol.24 , pp. 16-24
    • Motzer, R.J.1    Michaelson, M.D.2    Redman, B.G.3
  • 11
    • 33646432734 scopus 로고    scopus 로고
    • Efficacy of the kinase inhibitor SU11248 against gastrointestinal stromal tumor mutants refractory to imatinib mesylate
    • H. Prenen, J. Cools, and N. Mentens et al. Efficacy of the kinase inhibitor SU11248 against gastrointestinal stromal tumor mutants refractory to imatinib mesylate Clin. Cancer Res. 12 2006 2622 2627
    • (2006) Clin. Cancer Res. , vol.12 , pp. 2622-2627
    • Prenen, H.1    Cools, J.2    Mentens, N.3
  • 12
    • 34547593361 scopus 로고    scopus 로고
    • Isatin sulfonamide analogs containing a Michael addition acceptor: A new class of caspase-3/7 inhibitors
    • W. Chu, J. Rothfuss, and A. d'Avignon et al. Isatin sulfonamide analogs containing a Michael addition acceptor: a new class of caspase-3/7 inhibitors J. Med. Chem. 50 2007 3751 3755
    • (2007) J. Med. Chem. , vol.50 , pp. 3751-3755
    • Chu, W.1    Rothfuss, J.2    D'Avignon, A.3
  • 13
    • 28144443339 scopus 로고    scopus 로고
    • N-benzylisatin sulfonamide analogues as potent caspase-3 inhibitors: Synthesis, in vitro activity, and molecular modeling studies
    • W. Chu, J. Zhang, and C. Zeng et al. N-benzylisatin sulfonamide analogues as potent caspase-3 inhibitors: synthesis, in vitro activity, and molecular modeling studies J. Med. Chem. 48 2005 7637 7647
    • (2005) J. Med. Chem. , vol.48 , pp. 7637-7647
    • Chu, W.1    Zhang, J.2    Zeng, C.3
  • 14
    • 69549129599 scopus 로고    scopus 로고
    • Docking and 3D-QSAR studies on isatin sulfonamide analogues as caspase-3 inhibitors
    • Q. Wang, R.H. Mach, and D.E. Reichert Docking and 3D-QSAR studies on isatin sulfonamide analogues as caspase-3 inhibitors J. Chem. Inf. Model. 49 2009 1963 1973
    • (2009) J. Chem. Inf. Model. , vol.49 , pp. 1963-1973
    • Wang, Q.1    Mach, R.H.2    Reichert, D.E.3
  • 15
    • 34547915994 scopus 로고    scopus 로고
    • Genes regulating the sensitivity of solid tumor cell lines to cytotoxic agents: A literature review
    • I. Sekine, J.D. Minna, and K. Nishio et al. Genes regulating the sensitivity of solid tumor cell lines to cytotoxic agents: a literature review Jpn. J. Clin. Oncol. 37 2007 329 336
    • (2007) Jpn. J. Clin. Oncol. , vol.37 , pp. 329-336
    • Sekine, I.1    Minna, J.D.2    Nishio, K.3
  • 16
    • 84880264045 scopus 로고    scopus 로고
    • Cdks, cyclins and CKIs: Roles beyond cell cycle regulation
    • S. Lim, and P. Kaldis Cdks, cyclins and CKIs: roles beyond cell cycle regulation Development 140 2013 3079 3093
    • (2013) Development , vol.140 , pp. 3079-3093
    • Lim, S.1    Kaldis, P.2
  • 18
    • 84893435713 scopus 로고    scopus 로고
    • Apoptotic cell: Linkage of inflammation and wound healing
    • Y.S. Wu, and S.N. Chen Apoptotic cell: linkage of inflammation and wound healing Front. Pharmacol. 5 2014 1 6
    • (2014) Front. Pharmacol. , vol.5 , pp. 1-6
    • Wu, Y.S.1    Chen, S.N.2
  • 19
    • 0032575752 scopus 로고    scopus 로고
    • Mitochondria and apoptosis
    • D.R. Green, and J.C. Reed Mitochondria and apoptosis Science 281 1998 1309 1312
    • (1998) Science , vol.281 , pp. 1309-1312
    • Green, D.R.1    Reed, J.C.2
  • 20
    • 84879165160 scopus 로고    scopus 로고
    • Oxidative stress: The mitochondria-dependent and mitochondria-independent pathways of apoptosis
    • K. Sinha, J. Das, and P.B. Pal et al. Oxidative stress: the mitochondria-dependent and mitochondria-independent pathways of apoptosis Arch. Toxicol. 87 2013 1157 1180
    • (2013) Arch. Toxicol. , vol.87 , pp. 1157-1180
    • Sinha, K.1    Das, J.2    Pal, P.B.3
  • 21
    • 0037184877 scopus 로고    scopus 로고
    • Role of mitochondria in toxic cell death
    • J.D. Robertson, and S. Orrenius Role of mitochondria in toxic cell death Toxicology 181-182 2002 491 496
    • (2002) Toxicology , vol.181-182 , pp. 491-496
    • Robertson, J.D.1    Orrenius, S.2
  • 23
    • 84891861316 scopus 로고    scopus 로고
    • Design, synthesis and in vitro cytotoxicity evaluation of 5-(2-carboxyethenyl) isatin derivatives as anticancer agents
    • K. Han, Y. Zhou, and F. Liu et al. Design, synthesis and in vitro cytotoxicity evaluation of 5-(2-carboxyethenyl) isatin derivatives as anticancer agents Bioorg. Med. Chem. Lett. 24 2014 591 594
    • (2014) Bioorg. Med. Chem. Lett. , vol.24 , pp. 591-594
    • Han, K.1    Zhou, Y.2    Liu, F.3
  • 24
    • 0037879052 scopus 로고    scopus 로고
    • The mitochondrial membrane potential (Δψm) in apoptosis; An update
    • J.D. Ly, D.R. Grubb, and A. Lawen The mitochondrial membrane potential (Δψm) in apoptosis; an update Apoptosis 8 2003 115 128
    • (2003) Apoptosis , vol.8 , pp. 115-128
    • Ly, J.D.1    Grubb, D.R.2    Lawen, A.3
  • 25
    • 77951919835 scopus 로고    scopus 로고
    • Bcl-2 family proteins and mitochondrial fission/fusion dynamics
    • A. Autret, and S.J. Martin Bcl-2 family proteins and mitochondrial fission/fusion dynamics Cell Mol. Life Sci. 67 2010 1599 1606
    • (2010) Cell Mol. Life Sci. , vol.67 , pp. 1599-1606
    • Autret, A.1    Martin, S.J.2
  • 26
    • 79960230433 scopus 로고    scopus 로고
    • Mitochondria in apoptosis: Bcl-2 family members and mitochondrial dynamics
    • J.C. Martinou, and R.J. Youle Mitochondria in apoptosis: Bcl-2 family members and mitochondrial dynamics Dev. Cell 21 2011 92 101
    • (2011) Dev. Cell , vol.21 , pp. 92-101
    • Martinou, J.C.1    Youle, R.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.