메뉴 건너뛰기




Volumn 62, Issue 2, 2010, Pages 333-342

Modulation of P-glycoprotein activity by the substituted quinoxalinone compound QA3 in adriamycin-resistant K562/A02 cells

Author keywords

3 dimethyl 1H quinoxalin 2 ones QA3; Apoptosis; ATP; ATPase; Caspases; Compound of the substituted 1; Multidrug resistance (MDR); P glycoprotein (P gp); PKC

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATE; CASPASE 3; CASPASE 9; DOXORUBICIN; FLUORESCEIN ISOTHIOCYANATE; GLYCOPROTEIN P; GLYCOPROTEIN P INHIBITOR; LIPOCORTIN 5; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE; PROCASPASE 3; PROCASPASE 9; PROTEIN KINASE C; QUINOXALINONE COMPOUND QA3; UNCLASSIFIED DRUG; CASPASE; MULTIDRUG RESISTANCE PROTEIN; QUINOXALINE DERIVATIVE;

EID: 77953328108     PISSN: 22995684     EISSN: 22995684     Source Type: Journal    
DOI: 10.1016/S1734-1140(10)70273-5     Document Type: Article
Times cited : (10)

References (45)
  • 1
    • 0346732289 scopus 로고    scopus 로고
    • Transition state analysis of the coupling of drug transport to ATP hydrolysis by P-glycoprotein
    • Al-Shawi MK, Polar MK, Omote H, Figler RA: Transition state analysis of the coupling of drug transport to ATP hydrolysis by P-glycoprotein. J Biol Chem, 2003, 278, 52629-52640.
    • (2003) J Biol Chem , vol.278 , pp. 52629-52640
    • Al-Shawi, M.K.1    Polar, M.K.2    Omote, H.3    Figler, R.A.4
  • 2
    • 0036224915 scopus 로고    scopus 로고
    • Inhibitors of multidrug resistance to antitumor agents (MDR)
    • Avendano C, Menendez JC: Inhibitors of multidrug resistance to antitumor agents (MDR). Curr Med Chem, 2002, 9, 159-193.
    • (2002) Curr Med Chem , vol.9 , pp. 159-193
    • Avendano, C.1    Menendez, J.C.2
  • 3
    • 20544465654 scopus 로고    scopus 로고
    • Multidrugresistant cancer cells contain two populations of Pglycoprotein with differently stimulated P-gp ATPase activities: Evidence from atomic force microscopy and biochemical analysis
    • Barakat S, Gayet L, Dayan G, Labialle S, Lazar A, Oleinikov V, Coleman AW, Baggetto LG: Multidrugresistant cancer cells contain two populations of Pglycoprotein with differently stimulated P-gp ATPase activities: evidence from atomic force microscopy and biochemical analysis. Biochem J, 2005, 388, 563-571.
    • (2005) Biochem J , vol.388 , pp. 563-571
    • Barakat, S.1    Gayet, L.2    Dayan, G.3    Labialle, S.4    Lazar, A.5    Oleinikov, V.6    Coleman, A.W.7    Baggetto, L.G.8
  • 5
    • 17644405457 scopus 로고    scopus 로고
    • Isolated rafts from adriamycin-resistant P388 cells contain functional ATPases and provide an easy test system for P-glycoprotein-related activities
    • Bucher K, Besse CA, Kamau SW, Wunderli-Allenspach H, Krämer SD: Isolated rafts from adriamycin-resistant P388 cells contain functional ATPases and provide an easy test system for P-glycoprotein-related activities. Pharm Res, 2005, 22, 449-57.
    • (2005) Pharm Res , vol.22 , pp. 449-457
    • Bucher, K.1    Besse, C.A.2    Kamau, S.W.3    Wunderli-Allenspach, H.4    Krämer, S.D.5
  • 6
    • 65249129816 scopus 로고    scopus 로고
    • L1EPO, a novel podophyllotoxin derivative overcomes P-glycoprotein-mediated multidrug resistance in K562/A02 cell line
    • Chen H, Wang J, Zhang J, Wang Y, Cao B, Bai S, Yu PF, Bi W, Xie W: L1EPO, a novel podophyllotoxin derivative overcomes P-glycoprotein-mediated multidrug resistance in K562/A02 cell line. Biol Pharm Bull, 2009, 32, 609-613.
    • (2009) Biol Pharm Bull , vol.32 , pp. 609-613
    • Chen, H.1    Wang, J.2    Zhang, J.3    Wang, Y.4    Cao, B.5    Bai, S.6    Yu, P.F.7    Bi, W.8    Xie, W.9
  • 8
    • 41649087983 scopus 로고    scopus 로고
    • Methoxylation of 3',4'-aromatic side chains improves P-glycoprotein inhibitory and multidrug resistance reversal activities of 7,8-pyranocoumarin against cancer cells
    • Fong WF, Shen XL, Globisch C, Wiese M, Chen GY, Zhu GY, Yu ZL Tse AK, Hu YJ: Methoxylation of 3',4'-aromatic side chains improves P-glycoprotein inhibitory and multidrug resistance reversal activities of 7,8-pyranocoumarin against cancer cells. Bioorg Med Chem, 2008, 16, 3694-3703.
    • (2008) Bioorg Med Chem , vol.16 , pp. 3694-3703
    • Fong, W.F.1    Shen, X.L.2    Globisch, C.3    Wiese, M.4    Chen, G.Y.5    Zhu, G.Y.6    Yu, Z.L.7    Tse, A.K.8    Hu, Y.J.9
  • 9
    • 56949101068 scopus 로고    scopus 로고
    • PI3K/Akt inhibition modulates multidrug resistance and activates NF-kB in murine lymphoma cell lines
    • García MG, Alaniz LD, Cordo Russo RI, Alvarez E, Hajos SE: PI3K/Akt inhibition modulates multidrug resistance and activates NF-kB in murine lymphoma cell lines. Leukemia Res, 2009, 33, 288-296.
    • (2009) Leukemia Res , vol.33 , pp. 288-296
    • García, M.G.1    Alaniz, L.D.2    Cordo Russo, R.I.3    Alvarez, E.4    Hajos, S.E.5
  • 10
    • 4744358624 scopus 로고    scopus 로고
    • The ATP switch model for ABC transporters
    • Higgins CF, Linton KJ: The ATP switch model for ABC transporters. Nat Struct Mol Biol, 2004, 10, 918-926.
    • (2004) Nat Struct Mol Biol , vol.10 , pp. 918-926
    • Higgins, C.F.1    Linton, K.J.2
  • 11
    • 51849149141 scopus 로고    scopus 로고
    • Reversal of P-glycoproteinmediated multidrug resistance of cancer cells by five schizandrins isolated from the chinese herb fructus schizandrae
    • Huang M, Jin J, Sun H, Liu GT: Reversal of P-glycoproteinmediated multidrug resistance of cancer cells by five schizandrins isolated from the Chinese herb Fructus Schizandrae. Cancer Chemother Pharmacol, 2008, 62, 1015-1026.
    • (2008) Cancer Chemother Pharmacol , vol.62 , pp. 1015-1026
    • Huang, M.1    Jin, J.2    Sun, H.3    Liu, G.T.4
  • 12
    • 0033779479 scopus 로고    scopus 로고
    • Selective modulation of P-glycoprotein's ATPase and anion efflux regulation activities with PKC a and PKC e in Sf9 cells
    • Idriss H, Urquidi V, Basavappa S: Selective modulation of P-glycoprotein's ATPase and anion efflux regulation activities with PKC a and PKC e in Sf9 cells. Cancer Chemother Pharmacol, 2000, 46, 287-292.
    • (2000) Cancer Chemother Pharmacol , vol.46 , pp. 287-292
    • Idriss, H.1    Urquidi, V.2    Basavappa, S.3
  • 13
    • 66149139241 scopus 로고    scopus 로고
    • Opening of the ADP-bound active site in the ABC transporter ATPase dimer: Evidence for a constant contact, alternating sites model for the catalytic cycle
    • Jones PM, George AM: Opening of the ADP-bound active site in the ABC transporter ATPase dimer: evidence for a constant contact, alternating sites model for the catalytic cycle. Proteins, 2009, 75, 387-396.
    • (2009) Proteins , vol.75 , pp. 387-396
    • Jones, P.M.1    George, A.M.2
  • 14
    • 0035865923 scopus 로고    scopus 로고
    • Structure-activity studies of substituted quinoxalinones as multiple-rugresistance antagonists
    • Lawrence DS, Copper JE, Smith CD: Structure-activity studies of substituted quinoxalinones as multiple-rugresistance antagonists. J Med Chem, 2001, 44, 594-601.
    • (2001) J Med Chem , vol.44 , pp. 594-601
    • Lawrence, D.S.1    Copper, J.E.2    Smith, C.D.3
  • 15
    • 0842348985 scopus 로고    scopus 로고
    • Development of a syngeneic in vivo tumor model and its use in evaluating a novel P-glycoprotein modulator, PGP-4008
    • Lee BD, French KJ, Zhuang Y, Smith CD: Development of a syngeneic in vivo tumor model and its use in evaluating a novel P-glycoprotein modulator, PGP-4008. Oncol Res, 2003, 14, 49-60.
    • (2003) Oncol Res , vol.14 , pp. 49-60
    • Lee, B.D.1    French, K.J.2    Zhuang, Y.3    Smith, C.D.4
  • 16
    • 1542268189 scopus 로고    scopus 로고
    • Synthesis and evaluation of dihydropyrroloquinolines that selectively antagonize P-glycoprotein
    • Lee BD, Li Z, French KJ, Zhuang Y, Xia Z, Smith CD: Synthesis and evaluation of dihydropyrroloquinolines that selectively antagonize P-glycoprotein. J Med Chem, 2004, 47, 1413-1422.
    • (2004) J Med Chem , vol.47 , pp. 1413-1422
    • Lee, B.D.1    Li, Z.2    French, K.J.3    Zhuang, Y.4    Xia, Z.5    Smith, C.D.6
  • 17
    • 58149185271 scopus 로고    scopus 로고
    • Reversal of p-glycoprotein-mediated multidrug resistance by macrocyclic bisbibenzyl derivatives in adriamycin-resistant human myelogenous leukemia (K562/A02) cells
    • Li X, Sun B, Zhu CJ, Yuan HQ, Shi YQ, Gao J, Li SJ, Lou HX: Reversal of p-glycoprotein-mediated multidrug resistance by macrocyclic bisbibenzyl derivatives in adriamycin-resistant human myelogenous leukemia (K562/A02) cells. Toxicol In Vitro, 2009, 23, 29-36.
    • (2009) Toxicol in Vitro , vol.23 , pp. 29-36
    • Li, X.1    Sun, B.2    Zhu, C.J.3    Yuan, H.Q.4    Shi, Y.Q.5    Gao, J.6    Li, S.J.7    Lou, H.X.8
  • 18
    • 33646887025 scopus 로고    scopus 로고
    • Synthesis of substituted 1,3-dimethyl-1H-quinoxalin-2-ones from aniline derivatives
    • Li X, Wang D, Wu J, Xu W: Synthesis of substituted 1,3-dimethyl-1H-quinoxalin-2-ones from aniline derivatives. Heterocycles, 2005, 65, 2741-2751.
    • (2005) Heterocycles , vol.65 , pp. 2741-2751
    • Li, X.1    Wang, D.2    Wu, J.3    Xu, W.4
  • 19
    • 34548081194 scopus 로고    scopus 로고
    • Cyclin-dependent kinase inhibitor, flavopiridol, induces apoptosis and inhibits tumor growth in drug-resistant osteosarcoma and Ewing's family tumor cells
    • Li Y, Tanaka K, Li X, Okada T, Nakamura T, Takasaki M, Yamamoto S, Oda Y, Tsuneyoshi M, Iwamoto Y: Cyclin-dependent kinase inhibitor, flavopiridol, induces apoptosis and inhibits tumor growth in drug-resistant osteosarcoma and Ewing's family tumor cells. Int J Cancer, 2007, 121, 1212-1218.
    • (2007) Int J Cancer , vol.121 , pp. 1212-1218
    • Li, Y.1    Tanaka, K.2    Li, X.3    Okada, T.4    Nakamura, T.5    Takasaki, M.6    Yamamoto, S.7    Oda, Y.8    Tsuneyoshi, M.9    Iwamoto, Y.10
  • 20
    • 34247123807 scopus 로고    scopus 로고
    • Structure and function of ABC transporters
    • Linton KJ: Structure and function of ABC transporters. Physiology (Bethesda), 2007, 22, 122-130.
    • (2007) Physiology (Bethesda) , vol.22 , pp. 122-130
    • Linton, K.J.1
  • 21
    • 33846688359 scopus 로고    scopus 로고
    • Structure and function of ABC transporters: The ATP switch provides flexible control
    • Linton KJ, Higgins C: Structure and function of ABC transporters: the ATP switch provides flexible control. Pflugers Arch, 2007, 453, 555-567.
    • (2007) Pflugers Arch , vol.453 , pp. 555-567
    • Linton, K.J.1    Higgins, C.2
  • 22
    • 34547911075 scopus 로고    scopus 로고
    • Nucleotide binding, ATP hydrolysis, and mutation of the catalytic carboxylates of human P-glycoprotein cause distinct conformational changes in the transmembrane segments
    • Loo TW, Bartlett MC, Clarke DM: Nucleotide binding, ATP hydrolysis, and mutation of the catalytic carboxylates of human P-glycoprotein cause distinct conformational changes in the transmembrane segments. Biochemistry, 2007, 46, 9328-9336.
    • (2007) Biochemistry , vol.46 , pp. 9328-9336
    • Loo, T.W.1    Bartlett, M.C.2    Clarke, D.M.3
  • 23
    • 0037400577 scopus 로고    scopus 로고
    • Multidrug resistance modulators PSC 833 and CsA show differential capacity to induce apoptosis in lymphoid leukemia cell lines independently of their MDR phenotype
    • Lopes EC, Garcia M, Benavides F, Shen J, Conti CJ, Alvarez E, Hajos SE: Multidrug resistance modulators PSC 833 and CsA show differential capacity to induce apoptosis in lymphoid leukemia cell lines independently of their MDR phenotype. Leukemia Res, 2003, 27, 413-423.
    • (2003) Leukemia Res , vol.27 , pp. 413-423
    • Lopes, E.C.1    Garcia, M.2    Benavides, F.3    Shen, J.4    Conti, C.J.5    Alvarez, E.6    Hajos, S.E.7
  • 24
    • 57149098598 scopus 로고    scopus 로고
    • Evidence that resistance to nilotinib may be due to BCR-ABL, Pgp, or Src kinase overexpression
    • Mahon FX, Hayette S, Lagarde V, Belloc F, Turcq B, Nicolini F, Belanger C et al.: Evidence that resistance to nilotinib may be due to BCR-ABL, Pgp, or Src kinase overexpression. Cancer Res, 2008, 68, 9809-9816.
    • (2008) Cancer Res , vol.68 , pp. 9809-9816
    • Mahon, F.X.1    Hayette, S.2    Lagarde, V.3    Belloc, F.4    Turcq, B.5    Nicolini, F.6    Belanger, C.7
  • 25
    • 33646354397 scopus 로고    scopus 로고
    • Caspase-dependent cleavage of 170-kDa P-glycoprotein during apoptosis of human T-lymphoblastoid CEM cells
    • Mantovani I, Cappellini A, Tazzari PL, Papa V, Cocco L, Martelli AM: Caspase-dependent cleavage of 170-kDa P-glycoprotein during apoptosis of human T-lymphoblastoid CEM cells. J Cell Physiol, 2006, 207, 836-844.
    • (2006) J Cell Physiol , vol.207 , pp. 836-844
    • Mantovani, I.1    Cappellini, A.2    Tazzari, P.L.3    Papa, V.4    Cocco, L.5    Martelli, A.M.6
  • 26
    • 35848939204 scopus 로고    scopus 로고
    • Cobalamin potentiates vinblastine cytotoxicity through downregulation of mdr-1 gene expression in HepG2 cells
    • Marguerite V, Beri-Dexheimer M, Ortiou S, Guéant JL, Merten M: Cobalamin potentiates vinblastine cytotoxicity through downregulation of mdr-1 gene expression in HepG2 cells. Cell Physiol Biochem, 2007, 20, 967-976.
    • (2007) Cell Physiol Biochem , vol.20 , pp. 967-976
    • Marguerite, V.1    Beri-Dexheimer, M.2    Ortiou, S.3    Guéant, J.L.4    Merten, M.5
  • 27
    • 35349014682 scopus 로고    scopus 로고
    • How integration of positive and negative regulatory signals by a STAND signaling protein depends on ATP hydrolysis
    • Marquenet E, Richet E: How integration of positive and negative regulatory signals by a STAND signaling protein depends on ATP hydrolysis. Mol Cell, 2007, 28, 187-199.
    • (2007) Mol Cell , vol.28 , pp. 187-199
    • Marquenet, E.1    Richet, E.2
  • 29
    • 33646455879 scopus 로고    scopus 로고
    • The glycine residues G551 and G1349 within the ATP-binding cassette signature motifs play critical roles in the activation and inhibition of cystic fibrosis transmembrane conductance regulator channels by phloxine
    • Melin P, Norez C, Callebaut I, Becq F: The glycine residues G551 and G1349 within the ATP-binding cassette signature motifs play critical roles in the activation and inhibition of cystic fibrosis transmembrane conductance regulator channels by phloxine. J Membr Biol, 2005, 208, 203-212.
    • (2005) J Membr Biol , vol.208 , pp. 203-212
    • Melin, P.1    Norez, C.2    Callebaut, I.3    Becq, F.4
  • 30
    • 0035863315 scopus 로고    scopus 로고
    • In vitro and in vivo reversal of P-glycoprotein-mediated multidrug resistance by a novel potent modulator, XR9576
    • Mistry P, Stewart AJ, Dangerfield W, Okiji S, Liddle C, Bootle D, Plumb JA et al.: In vitro and in vivo reversal of P-glycoprotein-mediated multidrug resistance by a novel potent modulator, XR9576. Cancer Res, 2001, 61, 749-758.
    • (2001) Cancer Res , vol.61 , pp. 749-758
    • Mistry, P.1    Stewart, A.J.2    Dangerfield, W.3    Okiji, S.4    Liddle, C.5    Bootle, D.6    Plumb, J.A.7
  • 31
    • 0035695214 scopus 로고    scopus 로고
    • Prospects for targeting protein kinase C isozymes in the therapy of drug-resistant cancer - an evolving story
    • O'Brian CA, Ward NE, Stewart JR, Chu F: Prospects for targeting protein kinase C isozymes in the therapy of drug-resistant cancer - an evolving story. Cancer Metastasis Rev, 2001, 20, 95-100.
    • (2001) Cancer Metastasis Rev , vol.20 , pp. 95-100
    • O'Brian, C.A.1    Ward, N.E.2    Stewart, J.R.3    Chu, F.4
  • 32
    • 34347374838 scopus 로고    scopus 로고
    • Comparison of five methods for determination of total plasma protein concentration
    • Okutucu B, Dincer A, Habib O, Zihnioglu F: Comparison of five methods for determination of total plasma protein concentration. J Biochem Biophys Methods, 2007, 70, 709-711.
    • (2007) J Biochem Biophys Methods , vol.70 , pp. 709-711
    • Okutucu, B.1    Dincer, A.2    Habib, O.3    Zihnioglu, F.4
  • 33
    • 33745658614 scopus 로고    scopus 로고
    • P-glycoprotein enhances TRAIL-triggered apoptosis in multidrug resistant cancer cells by interacting with the death receptor DR5
    • Park SJ, Wu CH, Choi MR, Najafi F, Emami A, Safa AR: P-glycoprotein enhances TRAIL-triggered apoptosis in multidrug resistant cancer cells by interacting with the death receptor DR5. Biochem Pharmacol, 2006, 72, 293-307.
    • (2006) Biochem Pharmacol , vol.72 , pp. 293-307
    • Park, S.J.1    Wu, C.H.2    Choi, M.R.3    Najafi, F.4    Emami, A.5    Safa, A.R.6
  • 34
    • 0036018927 scopus 로고    scopus 로고
    • Multidrug resistance phenotype mediated by the P-glycoprotein-like transporter in Leishmania: A search for reversal agents
    • Pérez-Victoria JM, Di Pietro A, Barron D, Ravelo AG, Castanys S, Gamarro F: Multidrug resistance phenotype mediated by the P-glycoprotein-like transporter in Leishmania: a search for reversal agents. Curr Drug Targets, 2002, 3, 311-333.
    • (2002) Curr Drug Targets , vol.3 , pp. 311-333
    • Pérez-Victoria, J.M.1    Di Pietro, A.2    Barron, D.3    Ravelo, A.G.4    Castanys, S.5    Gamarro, F.6
  • 36
    • 57049161490 scopus 로고    scopus 로고
    • High-throughput screening platform for anticancer therapeutic drug cytotoxicity
    • Sekhon BK, Roubin RH, Tan A, Chan WK, Sze DM: High-throughput screening platform for anticancer therapeutic drug cytotoxicity. Assay Drug Dev Technol, 2008, 6, 711-721.
    • (2008) Assay Drug Dev Technol , vol.6 , pp. 711-721
    • Sekhon, B.K.1    Roubin, R.H.2    Tan, A.3    Chan, W.K.4    Sze, D.M.5
  • 37
    • 37349069575 scopus 로고    scopus 로고
    • Quantitation of doxorubicin uptake, efflux, and modulation of multidrug resistance (MDR) in MDR human cancer cells
    • Shen F, Chu S, Bence AK, Bailey B, Xue X, Erickson PA, Montrose MH et al.: Quantitation of doxorubicin uptake, efflux, and modulation of multidrug resistance (MDR) in MDR human cancer cells. J Pharmacol Exp Ther, 2008, 324, 95-102.
    • (2008) J Pharmacol Exp Ther , vol.324 , pp. 95-102
    • Shen, F.1    Chu, S.2    Bence, A.K.3    Bailey, B.4    Xue, X.5    Erickson, P.A.6    Montrose, M.H.7
  • 38
    • 41149176382 scopus 로고    scopus 로고
    • Reversal effect of a macrocyclic bisbibenzyl plagiochin E on multidrug resistance in adriamycin-resistant K562/A02 cells
    • Shi YQ, Qu XJ, Liao YX, Xie CF, Cheng YN, Li S, Lou HX: Reversal effect of a macrocyclic bisbibenzyl plagiochin E on multidrug resistance in adriamycin-resistant K562/A02 cells. Eur J Pharmacol, 2008, 584, 66-71.
    • (2008) Eur J Pharmacol , vol.584 , pp. 66-71
    • Shi, Y.Q.1    Qu, X.J.2    Liao, Y.X.3    Xie, C.F.4    Cheng, Y.N.5    Li, S.6    Lou, H.X.7
  • 40
    • 0037023705 scopus 로고    scopus 로고
    • Regulation of protein kinase C in Escherichia coli K1 invasion of human brain microvascular endothelial cells
    • Sukumaran SK, Prasadarao NV: Regulation of protein kinase C in Escherichia coli K1 invasion of human brain microvascular endothelial cells. J Biol Chem, 2002, 277, 12253-12262.
    • (2002) J Biol Chem , vol.277 , pp. 12253-12262
    • Sukumaran, S.K.1    Prasadarao, N.V.2
  • 41
    • 61349086677 scopus 로고    scopus 로고
    • Reversal effect of substituted 1,3-dimethyl-1H-quinoxalin-2-ones on multidrug resistance in adriamycin-resistant K562/A02 cells
    • Sun LR, Li X, Cheng YN, Yuan HY, Chen MH, Tang W, Ward SG, Qu XJ: Reversal effect of substituted 1,3-dimethyl-1H-quinoxalin-2-ones on multidrug resistance in adriamycin-resistant K562/A02 cells. Biomed Pharmacother, 2009, 63, 202-208.
    • (2009) Biomed Pharmacother , vol.63 , pp. 202-208
    • Sun, L.R.1    Li, X.2    Cheng, Y.N.3    Yuan, H.Y.4    Chen, M.H.5    Tang, W.6    Ward, S.G.7    Qu, X.J.8
  • 42
    • 0035887454 scopus 로고    scopus 로고
    • The farnesyl protein transferase inhibitor SCH66336 is a potent inhibitor of MDR1 product P-glycoprotein
    • Wang E, Casciano CN, Clement RP, Johnson WW: The farnesyl protein transferase inhibitor SCH66336 is a potent inhibitor of MDR1 product P-glycoprotein. Cancer Res, 2001, 61, 7525-7529.
    • (2001) Cancer Res , vol.61 , pp. 7525-7529
    • Wang, E.1    Casciano, C.N.2    Clement, R.P.3    Johnson, W.W.4
  • 43
    • 65249094734 scopus 로고    scopus 로고
    • Berbamine exhibits potent antitumor effects on imatinib-resistant CML cells in vitro and in vivo
    • Wei YL, Xu L, Liang Y, Xu XH, Zhao XY: Berbamine exhibits potent antitumor effects on imatinib-resistant CML cells in vitro and in vivo. Acta Pharmacol Sin, 2009, 30, 451-457.
    • (2009) Acta Pharmacol Sin , vol.30 , pp. 451-457
    • Wei, Y.L.1    Xu, L.2    Liang, Y.3    Xu, X.H.4    Zhao, X.Y.5
  • 44
    • 0037371275 scopus 로고    scopus 로고
    • Effects of the flavonoids biochanin A, morin, phloretin, and silymarin on P-lycoproteinmediated transport
    • Zhang S, Morris ME: Effects of the flavonoids biochanin A, morin, phloretin, and silymarin on P-lycoproteinmediated transport. J Pharmacol Exp Ther, 2003, 304, 1258-1267.
    • (2003) J Pharmacol Exp Ther , vol.304 , pp. 1258-1267
    • Zhang, S.1    Morris, M.E.2
  • 45
    • 70350568219 scopus 로고    scopus 로고
    • Enediyne lidamycin induces apoptosis in human multiple myeloma cells through activation of p38 mitogen-activated protein kinase and c-Jun NH2-terminal kinase
    • Zhen YZ, Lin YJ, Shang BY, Zhen YS: Enediyne lidamycin induces apoptosis in human multiple myeloma cells through activation of p38 mitogen-activated protein kinase and c-Jun NH2-terminal kinase. Int J Hematol, 2009, 90, 44-51.
    • (2009) Int J Hematol , vol.90 , pp. 44-51
    • Zhen, Y.Z.1    Lin, Y.J.2    Shang, B.Y.3    Zhen, Y.S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.