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Volumn 9, Issue 2, 2011, Pages 146-150

Reversal of P-glycoprotein-Mediated Multidrug Resistance in Human Leukemia Cell Line K562/A02 by Archangelicin

Author keywords

Archangelicin; K562 A02 cells; Multidrug resistance; P glycoprotein

Indexed keywords

3 (4,5 DIMETHYL 2 THIAZOLYL) 2,5 DIPHENYLTETRAZOLIUM BROMIDE; ARCHANGELICIN; DOXORUBICIN; GLYCOPROTEIN P; MESSENGER RNA; PLANT EXTRACT; RHODAMINE 123; UNCLASSIFIED DRUG;

EID: 79956296911     PISSN: 20956975     EISSN: 18755364     Source Type: Journal    
DOI: 10.3724/SP.J.1009.2011.00146     Document Type: Article
Times cited : (2)

References (14)
  • 1
    • 33846903601 scopus 로고    scopus 로고
    • New 1, 3-dioxolane and 1, 3-dioxane derivatives as effective modulators to overcome multidrug resistance [J]
    • Schmidt M, Ungvari J, Glode J, et al. New 1, 3-dioxolane and 1, 3-dioxane derivatives as effective modulators to overcome multidrug resistance [J]. Bioorg Med Chem 2007, 15(6):2283-2297.
    • (2007) Bioorg Med Chem , vol.15 , Issue.6 , pp. 2283-2297
    • Schmidt, M.1    Ungvari, J.2    Glode, J.3
  • 2
    • 65649084180 scopus 로고    scopus 로고
    • Nilotinib (AMN107, Tasigna (R)) reverses multidrug resistance by inhibiting the activity of the ABCB1/Pgp and ABCG2/BCRP/MXR transporters [J]
    • Tiwari AK, Sodani K, Wang SR, et al. Nilotinib (AMN107, Tasigna (R)) reverses multidrug resistance by inhibiting the activity of the ABCB1/Pgp and ABCG2/BCRP/MXR transporters [J]. Biochem Pharmacol 2009, 78(2):153-161.
    • (2009) Biochem Pharmacol , vol.78 , Issue.2 , pp. 153-161
    • Tiwari, A.K.1    Sodani, K.2    Wang, S.R.3
  • 3
    • 26444570296 scopus 로고    scopus 로고
    • Reversal of p-glycoprotein mediated multidrug resistance in K562 cell line by a novel synthetic calmodulin inhibitor, E6 [J]
    • Zhu HJ, Wang JS, Guo QL, et al. Reversal of p-glycoprotein mediated multidrug resistance in K562 cell line by a novel synthetic calmodulin inhibitor, E6 [J]. Biol Pharm Bull 2005, 28(10):1974-1978.
    • (2005) Biol Pharm Bull , vol.28 , Issue.10 , pp. 1974-1978
    • Zhu, H.J.1    Wang, J.S.2    Guo, Q.L.3
  • 4
    • 0036224915 scopus 로고    scopus 로고
    • Inhibitors of multidrug resistance to antitumor agents (MDR) [J]
    • Avendano C, Menendez JC Inhibitors of multidrug resistance to antitumor agents (MDR) [J]. Curr Med Chem 2002, 9(2):159-193.
    • (2002) Curr Med Chem , vol.9 , Issue.2 , pp. 159-193
    • Avendano, C.1    Menendez, J.C.2
  • 5
    • 26444530671 scopus 로고    scopus 로고
    • Major contribution of the multidrug transporter P-glycoprotein to reduced susceptibility of poly (ADP-ribose) polymerase-1 knock-out cells to doxorubicin action [J]
    • Wesierska-Gadek J Major contribution of the multidrug transporter P-glycoprotein to reduced susceptibility of poly (ADP-ribose) polymerase-1 knock-out cells to doxorubicin action [J]. J Cell Biochem 2005, 95(5):1012-1028.
    • (2005) J Cell Biochem , vol.95 , Issue.5 , pp. 1012-1028
    • Wesierska-Gadek, J.1
  • 6
    • 58349102840 scopus 로고    scopus 로고
    • Cancer multidrug resistance (MDR): A major impediment to effective chemotherapy [J]
    • Ullah MF Cancer multidrug resistance (MDR): A major impediment to effective chemotherapy [J]. Asian Pac J Cancer Prevent 2008, 9(1):1-6.
    • (2008) Asian Pac J Cancer Prevent , vol.9 , Issue.1 , pp. 1-6
    • Ullah, M.F.1
  • 7
    • 67650095567 scopus 로고    scopus 로고
    • Synthesis and multidrug resistance reversal activity of dihydroptychantol A and its novel derivatives [J]
    • Sun B, Yuan HQ, Xi GM, et al. Synthesis and multidrug resistance reversal activity of dihydroptychantol A and its novel derivatives [J]. Bioorg Med Chem 2009, 17(14):4981-4989.
    • (2009) Bioorg Med Chem , vol.17 , Issue.14 , pp. 4981-4989
    • Sun, B.1    Yuan, H.Q.2    Xi, G.M.3
  • 8
    • 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 [J]
    • Li X, Sun B, Zhu CJ, et al. Reversal of p-glycoprotein-mediated multidrug resistance by macrocyclic bisbibenzyl derivatives in adriamycin-resistant human myelogenous leukemia (K562/A02) cells [J]. Toxicol in Vitro 2009, 23(1):29-36.
    • (2009) Toxicol in Vitro , vol.23 , Issue.1 , pp. 29-36
    • Li, X.1    Sun, B.2    Zhu, C.J.3
  • 9
    • 34447342246 scopus 로고    scopus 로고
    • CJY, an isoflavone, reverses P-glycoprotein-mediated multidrug-resistance in doxorubicin-resistant human myelogenous leukaemia (K562/DOX) cells [J]
    • Ji BS, He L CJY, an isoflavone, reverses P-glycoprotein-mediated multidrug-resistance in doxorubicin-resistant human myelogenous leukaemia (K562/DOX) cells [J]. J Pharm Pharmacol 2007, 59(7):1011-1015.
    • (2007) J Pharm Pharmacol , vol.59 , Issue.7 , pp. 1011-1015
    • Ji, B.S.1    He, L.2
  • 10
    • 33646807161 scopus 로고    scopus 로고
    • Chemosensitizing multiple drug resistance of human carcinoma by Bicyclol involves attenuated p-glycoprotein, GST-P and Bcl-2 [J]
    • Zhu B, Liu GT, Zhao YM, et al. Chemosensitizing multiple drug resistance of human carcinoma by Bicyclol involves attenuated p-glycoprotein, GST-P and Bcl-2 [J]. Cancer Biol Ther 2006, 5(5):536-543.
    • (2006) Cancer Biol Ther , vol.5 , Issue.5 , pp. 536-543
    • Zhu, B.1    Liu, G.T.2    Zhao, Y.M.3
  • 11
    • 23844445265 scopus 로고    scopus 로고
    • Reversal of p-glycoprotein-mediated multidrug resistance by CJX1, an amlodipine derivative, in doxorubicin-resistant human myelogenous leukemia (K562/DOX) cells [J]
    • Ji BS, He L, Liu GQ Reversal of p-glycoprotein-mediated multidrug resistance by CJX1, an amlodipine derivative, in doxorubicin-resistant human myelogenous leukemia (K562/DOX) cells [J]. Life Sci 2005, 77(18):2221-2232.
    • (2005) Life Sci , vol.77 , Issue.18 , pp. 2221-2232
    • Ji, B.S.1    He, L.2    Liu, G.Q.3
  • 12
    • 33847017659 scopus 로고    scopus 로고
    • Reversal of multidrug resistance by 4-chloro-N-(3-((E)-3-(4-hydroxy-3-methoxy-phenyl) acryloyl) phenyl) benzamide through the reversible inhibition of P-glycoprotein [J]
    • Kim YK, Song YJ, Seo DW, et al. Reversal of multidrug resistance by 4-chloro-N-(3-((E)-3-(4-hydroxy-3-methoxy-phenyl) acryloyl) phenyl) benzamide through the reversible inhibition of P-glycoprotein [J]. Biochem Biophys Res Commun 2007, 355(1):136-142.
    • (2007) Biochem Biophys Res Commun , vol.355 , Issue.1 , pp. 136-142
    • Kim, Y.K.1    Song, Y.J.2    Seo, D.W.3
  • 13
    • 33749255173 scopus 로고    scopus 로고
    • Down-regulation of P-glycoprotein expression in MDR breast cancer cell MCF-7/ADR by honokiol [J]
    • Xu D, Lu Q, Hu X Down-regulation of P-glycoprotein expression in MDR breast cancer cell MCF-7/ADR by honokiol [J]. Cancer Lett 2006, 243(2):274-280.
    • (2006) Cancer Lett , vol.243 , Issue.2 , pp. 274-280
    • Xu, D.1    Lu, Q.2    Hu, X.3
  • 14
    • 0037810918 scopus 로고    scopus 로고
    • Reversal of multidrug resistance in cancer cells by pyranocoumarins isolated from Radix Peucedani [J]
    • Wu JY, Fong WF, Zhang JX, et al. Reversal of multidrug resistance in cancer cells by pyranocoumarins isolated from Radix Peucedani [J]. Euro J Pharmacol 2003, 473(1):9-17.
    • (2003) Euro J Pharmacol , vol.473 , Issue.1 , pp. 9-17
    • Wu, J.Y.1    Fong, W.F.2    Zhang, J.X.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.