메뉴 건너뛰기




Volumn 345, Issue 1-2, 2010, Pages 13-21

SMT-A07, a 3-(Indol-2-yl) indazole derivative, induces apoptosis of leukemia cells in vitro

Author keywords

Apoptosis; Caspases; Leukemia; SMT A07

Indexed keywords

ANTINEOPLASTIC AGENT; INDAZOLE DERIVATIVE; N [2 (1H INDAZOL 3 YL) 1H PYRROLO[3,2 B] PYRIDIN 5 YL] 4 CHLORO N METHYLBENZAMIDE; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE; PROCASPASE 3; PROCASPASE 8; PROTEIN BID; SMT A07; UNCLASSIFIED DRUG;

EID: 78449314063     PISSN: 03008177     EISSN: 15734919     Source Type: Journal    
DOI: 10.1007/s11010-010-0554-y     Document Type: Article
Times cited : (54)

References (29)
  • 1
    • 2642532810 scopus 로고    scopus 로고
    • Emerging treatments in acute myeloid leukaemia
    • 1:CAS:528:DC%2BD2cXkt1Ggt7o%3D 10.1517/14728214.9.1.55 15155136
    • J Kell, et al. 2004 Emerging treatments in acute myeloid leukaemia Expert Opin Emerg Drugs 9 55 71 1:CAS:528:DC%2BD2cXkt1Ggt7o%3D 10.1517/14728214.9.1.55 15155136
    • (2004) Expert Opin Emerg Drugs , vol.9 , pp. 55-71
    • Kell, J.1
  • 2
    • 61549135160 scopus 로고    scopus 로고
    • Emerging treatment strategies for acute myeloid leukemia (AML) in the elderly
    • 1:CAS:528:DC%2BD1MXivVWhsr8%3D 10.1016/j.ctrv.2008.09.001 18951721
    • A Kuendgen U Germing 2009 Emerging treatment strategies for acute myeloid leukemia (AML) in the elderly Cancer Treat Rev 35 97 120 1:CAS:528: DC%2BD1MXivVWhsr8%3D 10.1016/j.ctrv.2008.09.001 18951721
    • (2009) Cancer Treat Rev , vol.35 , pp. 97-120
    • Kuendgen, A.1    Germing, U.2
  • 3
    • 33750020532 scopus 로고    scopus 로고
    • The incidence and outcome of myeloid malignancies in 2112 adult patients in southeast England
    • 17018393
    • KJ Phekoo MA Richards H Moller SA Schey 2006 The incidence and outcome of myeloid malignancies in 2112 adult patients in southeast England Haematologica 91 1400 1404 17018393
    • (2006) Haematologica , vol.91 , pp. 1400-1404
    • Phekoo, K.J.1    Richards, M.A.2    Moller, H.3    Schey, S.A.4
  • 4
    • 0014347896 scopus 로고
    • Arabinosyl cytosine: A useful agent in the treatment of acute leukemia in adults
    • 1:STN:280:DyaF1M%2FhtFKnsg%3D%3D 4879053
    • RR Ellison JF Holland M Weil, et al. 1968 Arabinosyl cytosine: a useful agent in the treatment of acute leukemia in adults Blood 32 507 523 1:STN:280:DyaF1M%2FhtFKnsg%3D%3D 4879053
    • (1968) Blood , vol.32 , pp. 507-523
    • Ellison, R.R.1    Holland, J.F.2    Weil, M.3
  • 5
    • 0014675775 scopus 로고
    • Daunorubicin in the treatment of acute myelocytic leukaemia
    • 1:STN:280:DyaF1M7gvV2mtg%3D%3D 10.1016/S0140-6736(69)91296-3 4179349
    • M Boiron M Weil C Jacquillat, et al. 1969 Daunorubicin in the treatment of acute myelocytic leukaemia Lancet 1 330 333 1:STN:280:DyaF1M7gvV2mtg%3D%3D 10.1016/S0140-6736(69)91296-3 4179349
    • (1969) Lancet , vol.1 , pp. 330-333
    • Boiron, M.1    Weil, M.2    Jacquillat, C.3
  • 6
    • 73249135797 scopus 로고    scopus 로고
    • Molecular prognostic markers for adult acute myeloid leukemia with normal cytogenetics
    • 10.1186/1756-8722-2-23 19490647
    • TK Gregory D Wald Y Chen JM Vermaat Y Xiong W Tse 2009 Molecular prognostic markers for adult acute myeloid leukemia with normal cytogenetics J Hematol Oncol 2 23 10.1186/1756-8722-2-23 19490647
    • (2009) J Hematol Oncol , vol.2 , pp. 23
    • Gregory, T.K.1    Wald, D.2    Chen, Y.3    Vermaat, J.M.4    Xiong, Y.5    Tse, W.6
  • 7
    • 33847789058 scopus 로고    scopus 로고
    • Synthesis of furopyrazole analogs of 1-benzyl-3-(5-hydroxymethyl-2-furyl) indazole (YC-1) as novel anti-leukemia agents
    • 1:CAS:528:DC%2BD2sXmtVeitQ%3D%3D 10.1016/j.bmc.2006.12.001 17189698
    • LC Chou LJ Huang JS Yang FY Lee CM Teng SC Kuo 2007 Synthesis of furopyrazole analogs of 1-benzyl-3-(5-hydroxymethyl-2-furyl)indazole (YC-1) as novel anti-leukemia agents Bioorg Med Chem 15 1732 1740 1:CAS:528: DC%2BD2sXmtVeitQ%3D%3D 10.1016/j.bmc.2006.12.001 17189698
    • (2007) Bioorg Med Chem , vol.15 , pp. 1732-1740
    • Chou, L.C.1    Huang, L.J.2    Yang, J.S.3    Lee, F.Y.4    Teng, C.M.5    Kuo, S.C.6
  • 8
    • 35349005731 scopus 로고    scopus 로고
    • Synthesis and evaluation of novel 17-indazole androstene derivatives designed as CYP17 inhibitors
    • 1:CAS:528:DC%2BD2sXht1ams7zP 10.1016/j.steroids.2007.08.004 17884122
    • VM Moreira TS Vasaitis VC Njar JA Salvador 2007 Synthesis and evaluation of novel 17-indazole androstene derivatives designed as CYP17 inhibitors Steroids 72 939 948 1:CAS:528:DC%2BD2sXht1ams7zP 10.1016/j.steroids.2007.08.004 17884122
    • (2007) Steroids , vol.72 , pp. 939-948
    • Moreira, V.M.1    Vasaitis, T.S.2    Njar, V.C.3    Salvador, J.A.4
  • 9
    • 34347219022 scopus 로고    scopus 로고
    • Syntheses of potent, selective, and orally bioavailable indazole-pyridine series of protein kinase B/Akt inhibitors with reduced hypotension
    • 1:CAS:528:DC%2BD2sXlslGgsrs%3D 10.1021/jm0701019 17523610
    • GD Zhu VB Gandhi J Gong S Thomas, et al. 2007 Syntheses of potent, selective, and orally bioavailable indazole-pyridine series of protein kinase B/Akt inhibitors with reduced hypotension J Med Chem 50 2990 3003 1:CAS:528:DC%2BD2sXlslGgsrs%3D 10.1021/jm0701019 17523610
    • (2007) J Med Chem , vol.50 , pp. 2990-3003
    • Zhu, G.D.1    Gandhi, V.B.2    Gong, J.3    Thomas, S.4
  • 10
    • 33750529730 scopus 로고    scopus 로고
    • 3-(Indol-2-yl) indazoles as Chek1 kinase inhibitors: Optimization of potency and selectivity via substitution at C6
    • 1:CAS:528:DC%2BD28XhtF2jsrbO 10.1016/j.bmcl.2006.08.118 16978863
    • ME Fraley JT Steen EJ Brnardic, et al. 2006 3-(Indol-2-yl) indazoles as Chek1 kinase inhibitors: optimization of potency and selectivity via substitution at C6 Bioorg Med Chem Lett 16 6049 6053 1:CAS:528: DC%2BD28XhtF2jsrbO 10.1016/j.bmcl.2006.08.118 16978863
    • (2006) Bioorg Med Chem Lett , vol.16 , pp. 6049-6053
    • Fraley, M.E.1    Steen, J.T.2    Brnardic, E.J.3
  • 11
    • 33845868779 scopus 로고    scopus 로고
    • MZ3 induces apoptosis in human leukemia cells
    • 1:CAS:528:DC%2BD28XhtlCksb%2FF 10.1007/s00280-006-0294-6 16900371
    • L Fang Q He Y Hu B Yang 2007 MZ3 induces apoptosis in human leukemia cells Cancer Chemother Pharmacol 59 397 405 1:CAS:528:DC%2BD28XhtlCksb%2FF 10.1007/s00280-006-0294-6 16900371
    • (2007) Cancer Chemother Pharmacol , vol.59 , pp. 397-405
    • Fang, L.1    He, Q.2    Hu, Y.3    Yang, B.4
  • 12
    • 33847400139 scopus 로고    scopus 로고
    • R16, a novel amonafide analogue, induces apoptosis and G2-M arrest via poisoning topoisomerase II
    • 1:CAS:528:DC%2BD2sXhvVWku7k%3D 10.1158/1535-7163.MCT-06-0584 17308047
    • H Zhu M Huang F Yang Y Chen ZH Miao XH Qian, et al. 2007 R16, a novel amonafide analogue, induces apoptosis and G2-M arrest via poisoning topoisomerase II Mol Cancer Ther 6 484 495 1:CAS:528:DC%2BD2sXhvVWku7k%3D 10.1158/1535-7163.MCT-06-0584 17308047
    • (2007) Mol Cancer Ther , vol.6 , pp. 484-495
    • Zhu, H.1    Huang, M.2    Yang, F.3    Chen, Y.4    Miao, Z.H.5    Qian, X.H.6
  • 13
    • 17644416399 scopus 로고    scopus 로고
    • Tirapazamine cytotoxicity for neuroblastoma is p53 dependent
    • 1:CAS:528:DC%2BD2MXivFKisb8%3D 10.1158/1078-0432.CCR-04-2382 15814660
    • B Yang CP Reynolds 2005 Tirapazamine cytotoxicity for neuroblastoma is p53 dependent Clin Cancer Res 11 2774 2780 1:CAS:528:DC%2BD2MXivFKisb8%3D 10.1158/1078-0432.CCR-04-2382 15814660
    • (2005) Clin Cancer Res , vol.11 , pp. 2774-2780
    • Yang, B.1    Reynolds, C.P.2
  • 14
    • 53749099768 scopus 로고    scopus 로고
    • CPT21, a novel compound with anti-proliferative effect against gastric cancer cell SGC7901
    • 1:CAS:528:DC%2BD1cXht1amsrrF 10.1007/s10637-008-9120-9
    • B Zhang Y Luo Q Weng Q He W Lu B Yang 2008 CPT21, a novel compound with anti-proliferative effect against gastric cancer cell SGC7901 Investig New Drugs 26 517 524 1:CAS:528:DC%2BD1cXht1amsrrF 10.1007/s10637-008-9120-9
    • (2008) Investig New Drugs , vol.26 , pp. 517-524
    • Zhang, B.1    Luo, Y.2    Weng, Q.3    He, Q.4    Lu, W.5    Yang, B.6
  • 15
    • 0037115761 scopus 로고    scopus 로고
    • Oxidation-triggered c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein (MAP) kinase pathways for apoptosis in human leukaemic cells stimulated by epigallocatechin-3-gallate (EGCG): A distinct pathway from those of chemically induced and receptor-mediated apoptosis
    • 1:CAS:528:DC%2BD38Xptlykt70%3D 10.1042/BJ20020101 12206715
    • K Saeki N Kobayashi Y Inazawa, et al. 2002 Oxidation-triggered c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein (MAP) kinase pathways for apoptosis in human leukaemic cells stimulated by epigallocatechin-3-gallate (EGCG): a distinct pathway from those of chemically induced and receptor-mediated apoptosis Biochem J 368 705 720 1:CAS:528:DC%2BD38Xptlykt70%3D 10.1042/BJ20020101 12206715
    • (2002) Biochem J , vol.368 , pp. 705-720
    • Saeki, K.1    Kobayashi, N.2    Inazawa, Y.3
  • 16
    • 0034765627 scopus 로고    scopus 로고
    • Apoptosis and the response to anticancer therapy
    • 1:CAS:528:DC%2BD3MXos1Oqs7w%3D 10.1097/00001622-200111000-00007 11673685
    • BM Mow AL Blajeski J Chandra SH Kaufmann 2001 Apoptosis and the response to anticancer therapy Curr Opin Oncol 13 453 462 1:CAS:528:DC%2BD3MXos1Oqs7w%3D 10.1097/00001622-200111000-00007 11673685
    • (2001) Curr Opin Oncol , vol.13 , pp. 453-462
    • Mow, B.M.1    Blajeski, A.L.2    Chandra, J.3    Kaufmann, S.H.4
  • 17
    • 0034641932 scopus 로고    scopus 로고
    • From bench to clinic with apoptosis-based therapeutic agents
    • 1:CAS:528:DC%2BD3cXnsFWrtr8%3D 10.1038/35037747 11048733
    • DW Nicholson 2000 From bench to clinic with apoptosis-based therapeutic agents Nature 407 810 816 1:CAS:528:DC%2BD3cXnsFWrtr8%3D 10.1038/35037747 11048733
    • (2000) Nature , vol.407 , pp. 810-816
    • Nicholson, D.W.1
  • 18
    • 62549108186 scopus 로고    scopus 로고
    • Inhibitor of apoptosis proteins in hematological malignancies
    • 1:CAS:528:DC%2BD1MXivVKhu7o%3D 10.1038/leu.2008.329 19039324
    • S Fulda, et al. 2009 Inhibitor of apoptosis proteins in hematological malignancies Leukemia 23 467 476 1:CAS:528:DC%2BD1MXivVKhu7o%3D 10.1038/leu.2008.329 19039324
    • (2009) Leukemia , vol.23 , pp. 467-476
    • Fulda, S.1
  • 19
    • 0037868272 scopus 로고    scopus 로고
    • Apoptosis induced by topoisomerase inhibitors
    • 1:CAS:528:DC%2BD3sXks1Giu7g%3D 10.2174/1568011033482378 12769773
    • O Sordet QA Khan KW Kohn Y Pommier 2003 Apoptosis induced by topoisomerase inhibitors Curr Med Chem Anticancer Agents 3 271 290 1:CAS:528:DC%2BD3sXks1Giu7g%3D 10.2174/1568011033482378 12769773
    • (2003) Curr Med Chem Anticancer Agents , vol.3 , pp. 271-290
    • Sordet, O.1    Khan, Q.A.2    Kohn, K.W.3    Pommier, Y.4
  • 20
    • 0034708169 scopus 로고    scopus 로고
    • Differential role of caspase-8 and Bid activation during radiation- and CD95-induced apoptosis
    • 1:CAS:528:DC%2BD3cXitFeqtLk%3D 10.1038/sj.onc.1203401 10713706
    • C Belka J Rudner S Wesselborg A Stepczynska P Marini 2000 Differential role of caspase-8 and Bid activation during radiation- and CD95-induced apoptosis Oncogene 19 1181 1190 1:CAS:528:DC%2BD3cXitFeqtLk%3D 10.1038/sj.onc.1203401 10713706
    • (2000) Oncogene , vol.19 , pp. 1181-1190
    • Belka, C.1    Rudner, J.2    Wesselborg, S.3    Stepczynska, A.4    Marini, P.5
  • 21
    • 49849090421 scopus 로고    scopus 로고
    • Emodin azide methyl anthraquinone derivative triggers mitochondrial-dependent cell apoptosis involving in caspase-8-mediated Bid cleavage
    • 1:CAS:528:DC%2BD1cXnsVSkur0%3D 10.1158/1535-7163.MCT-07-2362 18566240
    • Y Yan X Su Y Liang J Zhang C Shi Y Lu 2008 Emodin azide methyl anthraquinone derivative triggers mitochondrial-dependent cell apoptosis involving in caspase-8-mediated Bid cleavage Mol Cancer Ther 7 1688 1697 1:CAS:528:DC%2BD1cXnsVSkur0%3D 10.1158/1535-7163.MCT-07-2362 18566240
    • (2008) Mol Cancer Ther , vol.7 , pp. 1688-1697
    • Yan, Y.1    Su, X.2    Liang, Y.3    Zhang, J.4    Shi, C.5    Lu, Y.6
  • 22
    • 15144345497 scopus 로고    scopus 로고
    • Pro-caspase-3 is a major physiologic target of caspase-8
    • 1:CAS:528:DyaK1cXntVShtr0%3D 10.1074/jbc.273.42.27084 9765224
    • HR Stennicke JM Jürgensmeier H Shin, et al. 1998 Pro-caspase-3 is a major physiologic target of caspase-8 J Biol Chem 273 27084 27090 1:CAS:528:DyaK1cXntVShtr0%3D 10.1074/jbc.273.42.27084 9765224
    • (1998) J Biol Chem , vol.273 , pp. 27084-27090
    • Stennicke, H.R.1    Jürgensmeier, J.M.2    Shin, H.3
  • 23
    • 0033647484 scopus 로고    scopus 로고
    • Caspase-8 in apoptosis: The beginning of "the end"?
    • 1:CAS:528:DC%2BD3cXoslWks7c%3D 11185963
    • M Kruidering GI Evan 2000 Caspase-8 in apoptosis: the beginning of "the end"? IUBMB Life 50 85 90 1:CAS:528:DC%2BD3cXoslWks7c%3D 11185963
    • (2000) IUBMB Life , vol.50 , pp. 85-90
    • Kruidering, M.1    Evan, G.I.2
  • 24
    • 33644657517 scopus 로고    scopus 로고
    • Bid, a BH3-only multi-functional molecule, is at the cross road of life and death
    • 1:CAS:528:DC%2BD28XhvF2nurs%3D 10.1016/j.gene.2005.10.038 16446060
    • XM Yin 2006 Bid, a BH3-only multi-functional molecule, is at the cross road of life and death Gene 369 7 19 1:CAS:528:DC%2BD28XhvF2nurs%3D 10.1016/j.gene.2005.10.038 16446060
    • (2006) Gene , vol.369 , pp. 7-19
    • Yin, X.M.1
  • 25
    • 0033525591 scopus 로고    scopus 로고
    • Solution structure of Bid, an intracellular amplifier of apoptotic signaling
    • 1:CAS:528:DyaK1MXitVChsro%3D 10.1016/S0092-8674(00)80572-3 10089877
    • JJ Chou H Li GS Salvesen J Yuan G Wagner 1999 Solution structure of Bid, an intracellular amplifier of apoptotic signaling Cell 96 615 624 1:CAS:528:DyaK1MXitVChsro%3D 10.1016/S0092-8674(00)80572-3 10089877
    • (1999) Cell , vol.96 , pp. 615-624
    • Chou, J.J.1    Li, H.2    Salvesen, G.S.3    Yuan, J.4    Wagner, G.5
  • 26
    • 17844362452 scopus 로고    scopus 로고
    • Bid acts on the permeability transition pore complex to induce apoptosis
    • 1:CAS:528:DC%2BD3MXnsleiug%3D%3D 10.1038/sj.onc.1204030 11175349
    • N Zamzami, et al. 2000 Bid acts on the permeability transition pore complex to induce apoptosis Oncogene 19 6342 6350 1:CAS:528: DC%2BD3MXnsleiug%3D%3D 10.1038/sj.onc.1204030 11175349
    • (2000) Oncogene , vol.19 , pp. 6342-6350
    • Zamzami, N.1
  • 27
    • 0042324618 scopus 로고    scopus 로고
    • Bid activates multiple mitochondrial apoptotic mechanisms in primary hepatocytes after death receptor engagement
    • 1:CAS:528:DC%2BD3sXnvVSiu7s%3D 10.1016/S0016-5085(03)01066-7 12949730
    • Y Zhao WX Ding T Qian S Watkins JJ Lemasters XM Yin 2003 Bid activates multiple mitochondrial apoptotic mechanisms in primary hepatocytes after death receptor engagement Gastroenterology 125 854 867 1:CAS:528:DC%2BD3sXnvVSiu7s%3D 10.1016/S0016-5085(03)01066-7 12949730
    • (2003) Gastroenterology , vol.125 , pp. 854-867
    • Zhao, Y.1    Ding, W.X.2    Qian, T.3    Watkins, S.4    Lemasters, J.J.5    Yin, X.M.6
  • 28
    • 0037016814 scopus 로고    scopus 로고
    • Caspase activation in equine influenza virus induced apoptotic cell death
    • 1:CAS:528:DC%2BD3MXpt1ansrc%3D 10.1016/S0378-1135(01)00468-0 11750143
    • C Lin RE Holland Jr JC Donofrio MH McCoy LR Tudor TM Chambers 2002 Caspase activation in equine influenza virus induced apoptotic cell death Vet Microbiol 84 357 365 1:CAS:528:DC%2BD3MXpt1ansrc%3D 10.1016/S0378-1135(01)00468- 0 11750143
    • (2002) Vet Microbiol , vol.84 , pp. 357-365
    • Lin, C.1    Holland Jr., R.E.2    Donofrio, J.C.3    McCoy, M.H.4    Tudor, L.R.5    Chambers, T.M.6
  • 29
    • 39049092700 scopus 로고    scopus 로고
    • Effect of proteasome inhibitors on proliferation and apoptosis of human cutaneous melanoma-derived cell lines
    • 1:CAS:528:DC%2BD1cXktFelu7s%3D 10.1111/j.1365-2133.2007.08390.x 18205878
    • A Sorolla A Yeramian X Dolcet AM Pérez de Santos D Llobet, et al. 2008 Effect of proteasome inhibitors on proliferation and apoptosis of human cutaneous melanoma-derived cell lines Br J Dermatol 158 496 504 1:CAS:528:DC%2BD1cXktFelu7s%3D 10.1111/j.1365-2133.2007.08390.x 18205878
    • (2008) Br J Dermatol , vol.158 , pp. 496-504
    • Sorolla, A.1    Yeramian, A.2    Dolcet, X.3    Santos De Pérez, A.M.4    Llobet, D.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.