메뉴 건너뛰기




Volumn 35, Issue 6, 2016, Pages 3659-3668

Osthole shows the potential to overcome P-glycoprotein-mediated multidrug resistance in human myelogenous leukemia K562/ADM cells by inhibiting the PI3K/Akt signaling pathway

Author keywords

Chronic myeloid leukemia; Multidrug resistance; P glycoprotein; Phosphoinositide 3 kinase

Indexed keywords

DOXORUBICIN; MESSENGER RNA; MULTIDRUG RESISTANCE PROTEIN; MULTIDRUG RESISTANCE PROTEIN 1; OSTHOLE; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN KINASE B; RHODAMINE 123; ABCB1 PROTEIN, HUMAN; ANTINEOPLASTIC AGENT; COUMARIN DERIVATIVE;

EID: 84964862002     PISSN: 1021335X     EISSN: 17912431     Source Type: Journal    
DOI: 10.3892/or.2016.4730     Document Type: Article
Times cited : (51)

References (42)
  • 2
    • 84947921308 scopus 로고    scopus 로고
    • Discovery of 2- Acylaminothiophene-3- carboxamides as multitarget inhibitors for BCR-ABL kinase and microtubules
    • Cao R, Wang Y and Huang N: Discovery of 2- Acylaminothiophene-3- carboxamides as multitarget inhibitors for BCR-ABL kinase and microtubules. J Chem Inf Model 55: 2435-2442, 2015.
    • (2015) J Chem Inf Model , vol.55 , pp. 2435-2442
    • Cao, R.1    Wang, Y.2    Huang, N.3
  • 5
    • 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 and Zhao XY: Berbamine exhibits potent antitumor effects on imatinib-resistant CML cells in vitro and in vivo. Acta Pharmacol Sin 30: 451-457, 2009.
    • (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
  • 7
    • 79960875859 scopus 로고    scopus 로고
    • P-glycoprotein and survivin simultaneously regulate vincristine-induced apoptosis in chronic myeloid leukemia cells
    • Souza PS, Vasconcelos FC, De Souza Reis FR, Nestal De Moraes G and Maia RC: P-glycoprotein and survivin simultaneously regulate vincristine-induced apoptosis in chronic myeloid leukemia cells. Int J Oncol 39: 925-933, 2011.
    • (2011) Int J Oncol , vol.39 , pp. 925-933
    • Souza, P.S.1    Vasconcelos, F.C.2    De Souza Reis, F.R.3    De Nestal, M.G.4    Maia, R.C.5
  • 9
    • 52649177063 scopus 로고    scopus 로고
    • Multidrug resistance gene (MDR1) polymorphisms are associated with major molecular responses to standard-dose imatinib in chronic myeloid leukemia
    • Dulucq S, Bouchet S, Turcq B, Lippert E, Etienne G, Reiffers J, Molimard M, Krajinovic M and Mahon FX: Multidrug resistance gene (MDR1) polymorphisms are associated with major molecular responses to standard-dose imatinib in chronic myeloid leukemia. Blood 112: 2024-2027, 2008.
    • (2008) Blood , vol.112 , pp. 2024-2027
    • Dulucq, S.1    Bouchet, S.2    Turcq, B.3    Lippert, E.4    Etienne, G.5    Reiffers, J.6    Molimard, M.7    Krajinovic, M.8    Mahon, F.X.9
  • 10
    • 67749122122 scopus 로고    scopus 로고
    • Targeting PI3K signalling in cancer: Opportunities, challenges and limitations
    • Engelman JA: Targeting PI3K signalling in cancer: Opportunities, challenges and limitations. Nat Rev Cancer 9: 550-562, 2009.
    • (2009) Nat Rev Cancer , vol.9 , pp. 550-562
    • Engelman, J.A.1
  • 11
    • 33644822656 scopus 로고    scopus 로고
    • Thrombin induces expression of FGF-2 via activation of PI3K-Akt-Fra-1 signaling axis leading to DNA synthesis and motility in vascular smooth muscle cells
    • Cao H, Dronadula N and Rao GN: Thrombin induces expression of FGF-2 via activation of PI3K-Akt-Fra-1 signaling axis leading to DNA synthesis and motility in vascular smooth muscle cells. Am J Physiol Cell Physiol 290: C172-C182, 2006.
    • (2006) Am J Physiol Cell Physiol , vol.290 , pp. C172-C182
    • Cao, H.1    Dronadula, N.2    Rao, G.N.3
  • 12
    • 84887242051 scopus 로고    scopus 로고
    • New insights into Notch1 regulation of the PI3K-AKT-mTOR1 signaling axis: Targeted therapy of γ-secretase inhibitor resistant T-cell acute lymphoblastic leukemia
    • Hales EC, Taub JW and Matherly LH: New insights into Notch1 regulation of the PI3K-AKT-mTOR1 signaling axis: Targeted therapy of γ-secretase inhibitor resistant T-cell acute lymphoblastic leukemia. Cell Signal 26: 149-161, 2014.
    • (2014) Cell Signal , vol.26 , pp. 149-161
    • Hales, E.C.1    Taub, J.W.2    Matherly, L.H.3
  • 13
    • 33846316306 scopus 로고    scopus 로고
    • Quantitative analysis of Akt phosphorylation and activity in response to EGF and insulin treatment
    • Kumar N, Afeyan R, Sheppard S, Harms B and Lauffenburger DA: Quantitative analysis of Akt phosphorylation and activity in response to EGF and insulin treatment. Biochem Biophys Res Commun 354: 14-20, 2007.
    • (2007) Biochem Biophys Res Commun , vol.354 , pp. 14-20
    • Kumar, N.1    Afeyan, R.2    Sheppard, S.3    Harms, B.4    Lauffenburger, D.A.5
  • 15
    • 56949101068 scopus 로고    scopus 로고
    • PI3K/Akt inhibition modulates multidrug resistance and activates NF-kappaB in murine lymphoma cell lines
    • García MG, Alaniz LD, Cordo Russo RI, Alvarez E and Hajos SE: PI3K/Akt inhibition modulates multidrug resistance and activates NF-kappaB in murine lymphoma cell lines. Leuk Res 33: 288-296, 2009.
    • (2009) Leuk Res , vol.33 , pp. 288-296
    • García, M.G.1    Alaniz, L.D.2    Cordo, R.R.I.3    Alvarez, E.4    Hajos, S.E.5
  • 16
    • 45149121372 scopus 로고    scopus 로고
    • The novel Akt inhibitor, perifosine, induces caspase-dependent apoptosis and downregulates P-glycoprotein expression in multidrug-resistant human T- Acute leukemia cells by a JNK-dependent mechanism
    • Chiarini F, Del Sole M, Mongiorgi S, Gaboardi GC, Cappellini A, Mantovani I, Follo MY, McCubrey JA and Martelli AM: The novel Akt inhibitor, perifosine, induces caspase-dependent apoptosis and downregulates P-glycoprotein expression in multidrug-resistant human T- Acute leukemia cells by a JNK-dependent mechanism. Leukemia 22: 1106-1116, 2008.
    • (2008) Leukemia , vol.22 , pp. 1106-1116
    • Chiarini, F.1    Del Sole, M.2    Mongiorgi, S.3    Gaboardi, G.C.4    Cappellini, A.5    Mantovani, I.6    Follo, M.Y.7    McCubrey, J.A.8    Martelli, A.M.9
  • 17
    • 84879682726 scopus 로고    scopus 로고
    • Inhibition of the PI3K/Akt pathway increases the chemosensitivity of gastric cancer to vincristine
    • Xie X, Tang B, Zhou J, Gao Q and Zhang P: Inhibition of the PI3K/Akt pathway increases the chemosensitivity of gastric cancer to vincristine. Oncol Rep 30: 773-782, 2013.
    • (2013) Oncol Rep , vol.30 , pp. 773-782
    • Xie, X.1    Tang, B.2    Zhou, J.3    Gao, Q.4    Zhang, P.5
  • 18
    • 84889593263 scopus 로고    scopus 로고
    • FUT family mediates the multidrug resistance of human hepatocellular carcinoma via the PI3K/Akt signaling pathway
    • Cheng L, Luo S, Jin C, Ma H, Zhou H and Jia L: FUT family mediates the multidrug resistance of human hepatocellular carcinoma via the PI3K/Akt signaling pathway. Cell Death Dis 4: E923, 2013.
    • (2013) Cell Death Dis , vol.4 , pp. e923
    • Cheng, L.1    Luo, S.2    Jin, C.3    Ma, H.4    Zhou, H.5    Jia, L.6
  • 19
    • 84897092972 scopus 로고    scopus 로고
    • Tamoxifen reduces P-gp-mediated multidrug resistance via inhibiting the PI3K/Akt signaling pathway in ER-negative human gastric cancer cells
    • Mao Z, Zhou J, Luan J, Sheng W, Shen X and Dong X: Tamoxifen reduces P-gp-mediated multidrug resistance via inhibiting the PI3K/Akt signaling pathway in ER-negative human gastric cancer cells. Biomed Pharmacother 68: 179-183, 2014.
    • (2014) Biomed Pharmacother , vol.68 , pp. 179-183
    • Mao, Z.1    Zhou, J.2    Luan, J.3    Sheng, W.4    Shen, X.5    Dong, X.6
  • 20
    • 33847225602 scopus 로고    scopus 로고
    • Multidrug resistance- Associated protein 1 expression is under the control of the phosphoinositide 3 kinase/Akt signal transduction network in human acute myelogenous leukemia blasts
    • Tazzari PL, Cappellini A, Ricci F, Evangelisti C, Papa V, Grafone T, Martinelli G, Conte R, Cocco L, McCubrey JA, et al: Multidrug resistance- Associated protein 1 expression is under the control of the phosphoinositide 3 kinase/Akt signal transduction network in human acute myelogenous leukemia blasts. Leukemia 21: 427-438, 2007.
    • (2007) Leukemia , vol.21 , pp. 427-438
    • Tazzari, P.L.1    Cappellini, A.2    Ricci, F.3    Evangelisti, C.4    Papa, V.5    Grafone, T.6    Martinelli, G.7    Conte, R.8    Cocco, L.9    McCubrey, J.A.10
  • 21
    • 84896735052 scopus 로고    scopus 로고
    • Anti-cancer activity of an osthole derivative, NBM-T-BMX-OS01: Targeting vascular endothelial growth factor receptor signaling and angiogenesis
    • Yang HY, Hsu YF, Chiu PT, Ho SJ, Wang CH, Chi CC, Huang YH, Lee CF, Li YS, Ou G, et al: Anti-cancer activity of an osthole derivative, NBM-T-BMX-OS01: Targeting vascular endothelial growth factor receptor signaling and angiogenesis. PLoS One 8: E81592, 2013.
    • (2013) PLoS One , vol.8 , pp. e81592
    • Yang, H.Y.1    Hsu, Y.F.2    Chiu, P.T.3    Ho, S.J.4    Wang, C.H.5    Chi, C.C.6    Huang, Y.H.7    Lee, C.F.8    Li, Y.S.9    Ou, G.10
  • 22
    • 84892563180 scopus 로고    scopus 로고
    • Osthole reverses beta- Amyloid peptide cytotoxicity on neural cells by enhancing cyclic AMP response element-binding protein phosphorylation
    • Hu Y, Wen Q, Liang W, Kang T, Ren L, Zhang N, Zhao D, Sun D and Yang J: Osthole reverses beta- Amyloid peptide cytotoxicity on neural cells by enhancing cyclic AMP response element-binding protein phosphorylation. Biol Pharm Bull 36: 1950-1958, 2013.
    • (2013) Biol Pharm Bull , vol.36 , pp. 1950-1958
    • Hu, Y.1    Wen, Q.2    Liang, W.3    Kang, T.4    Ren, L.5    Zhang, N.6    Zhao, D.7    Sun, D.8    Yang, J.9
  • 23
    • 33947581715 scopus 로고    scopus 로고
    • Antitumor effects of osthol from Cnidium monnieri: An in vitro and in vivo study
    • Chou SY, Hsu CS, Wang KT, Wang MC and Wang CC: Antitumor effects of osthol from Cnidium monnieri: An in vitro and in vivo study. Phytother Res 21: 226-230, 2007.
    • (2007) Phytother Res , vol.21 , pp. 226-230
    • Chou, S.Y.1    Hsu, C.S.2    Wang, K.T.3    Wang, M.C.4    Wang, C.C.5
  • 25
    • 84899500214 scopus 로고    scopus 로고
    • N-Hydroxycinnamide derivatives of osthole inhibit cell migration and invasion by suppressing Smad2 and Akt pathways in human colorectal adenocarcinoma cells
    • Liu LY, Huang WJ, Ho FM, Lin RJ, Lin SY, Suk FM and Liang YC: N-Hydroxycinnamide derivatives of osthole inhibit cell migration and invasion by suppressing Smad2 and Akt pathways in human colorectal adenocarcinoma cells. Chem Biol Interact 217: 1-8, 2014.
    • (2014) Chem Biol Interact , vol.217 , pp. 1-8
    • Liu, L.Y.1    Huang, W.J.2    Ho, F.M.3    Lin, R.J.4    Lin, S.Y.5    Suk, F.M.6    Liang, Y.C.7
  • 26
    • 84896487334 scopus 로고    scopus 로고
    • Osthole suppresses the migratory ability of human glioblastoma multiforme cells via inhibition of focal adhesion kinase-mediated matrix metalloproteinase-13 expression
    • Tsai CF, Yeh WL, Chen JH, Lin C, Huang SS and Lu DY: Osthole suppresses the migratory ability of human glioblastoma multiforme cells via inhibition of focal adhesion kinase-mediated matrix metalloproteinase-13 expression. Int J Mol Sci 15: 3889-3903, 2014.
    • (2014) Int J Mol Sci , vol.15 , pp. 3889-3903
    • Tsai, C.F.1    Yeh, W.L.2    Chen, J.H.3    Lin, C.4    Huang, S.S.5    Lu, D.Y.6
  • 27
    • 84866463562 scopus 로고    scopus 로고
    • Osthole suppresses migration and invasion of A549 human lung cancer cells through inhibition of matrix metalloproteinase-2 and matrix metallopeptidase-9 in vitro
    • Xu XM, Zhang Y, Qu D, Feng XW, Chen Y and Zhao L: Osthole suppresses migration and invasion of A549 human lung cancer cells through inhibition of matrix metalloproteinase-2 and matrix metallopeptidase-9 in vitro. Mol Med Rep 6: 1018-1022, 2012.
    • (2012) Mol Med Rep , vol.6 , pp. 1018-1022
    • Xu, X.M.1    Zhang, Y.2    Qu, D.3    Feng, X.W.4    Chen, Y.5    Zhao, L.6
  • 28
    • 84876725466 scopus 로고    scopus 로고
    • Combination treatment with platycodin D and osthole inhibits cell proliferation and invasion in mammary carcinoma cell lines
    • Ye Y, Han X, Guo B, Sun Z and Liu S: Combination treatment with platycodin D and osthole inhibits cell proliferation and invasion in mammary carcinoma cell lines. Environ Toxicol Pharmacol 36: 115-124, 2013.
    • (2013) Environ Toxicol Pharmacol , vol.36 , pp. 115-124
    • Ye, Y.1    Han, X.2    Guo, B.3    Sun, Z.4    Liu, S.5
  • 29
    • 84861475028 scopus 로고    scopus 로고
    • Growth inhibition and apoptosis induced by osthole, a natural coumarin, in hepatocellular carcinoma
    • Zhang L, Jiang G, Yao F, He Y, Liang G, Zhang Y, Hu B, Wu Y, Li Y and Liu H: Growth inhibition and apoptosis induced by osthole, a natural coumarin, in hepatocellular carcinoma. PLoS One 7: E37865, 2012.
    • (2012) PLoS One , vol.7 , pp. e37865
    • Zhang, L.1    Jiang, G.2    Yao, F.3    He, Y.4    Liang, G.5    Zhang, Y.6    Hu, B.7    Wu, Y.8    Li, Y.9    Liu, H.10
  • 30
    • 84855208681 scopus 로고    scopus 로고
    • Oroxylin A reverses multi-drug resistance of human hepatoma BEL7402/5-FU cells via downregulation of P-glycoprotein expression by inhibiting NF-κB signaling pathway
    • Yang HY, Zhao L, Yang Z, Zhao Q, Qiang L, Ha J, Li ZY, You QD and Guo QL: Oroxylin A reverses multi-drug resistance of human hepatoma BEL7402/5-FU cells via downregulation of P-glycoprotein expression by inhibiting NF-κB signaling pathway. Mol Carcinog 51: 185-195, 2012.
    • (2012) Mol Carcinog , vol.51 , pp. 185-195
    • Yang, H.Y.1    Zhao, L.2    Yang, Z.3    Zhao, Q.4    Qiang, L.5    Ha, J.6    Li, Z.Y.7    You, Q.D.8    Guo, Q.L.9
  • 31
    • 84908353712 scopus 로고    scopus 로고
    • Wogonin reverses multi-drug resistance of human myelogenous leukemia K562/A02 cells via downregulation of MRP1 expression by inhibiting Nrf2/ARE signaling pathway
    • Xu X, Zhang Y, Li W, Miao H, Zhang H, Zhou Y, Li Z, You Q, Zhao L and Guo Q: Wogonin reverses multi-drug resistance of human myelogenous leukemia K562/A02 cells via downregulation of MRP1 expression by inhibiting Nrf2/ARE signaling pathway. Biochem Pharmacol 92: 220-234, 2014.
    • (2014) Biochem Pharmacol , vol.92 , pp. 220-234
    • Xu, X.1    Zhang, Y.2    Li, W.3    Miao, H.4    Zhang, H.5    Zhou, Y.6    Li, Z.7    You, Q.8    Zhao, L.9    Guo, Q.10
  • 32
    • 33750702508 scopus 로고    scopus 로고
    • LY294, 002, a specific inhibitor of PI3K/Akt kinase pathway, antagonizes P-glycoprotein-mediated multidrug resistance
    • Barancík M, Bohácová V, Sedlák J, Sulová Z and Breier A: LY294, 002, a specific inhibitor of PI3K/Akt kinase pathway, antagonizes P-glycoprotein-mediated multidrug resistance. Eur J Pharm Sci 29: 426-434, 2006.
    • (2006) Eur J Pharm Sci , vol.29 , pp. 426-434
    • Barancík, M.1    Bohácová, V.2    Sedlák, J.3    Sulová, Z.4    Breier, A.5
  • 33
    • 84866885402 scopus 로고    scopus 로고
    • The PI3K/Akt/mTOR signaling pathway mediates insulin-like growth factor 1-induced E-cadherin down-regulation and cell proliferation in ovarian cancer cells
    • Lau MT and Leung PC: The PI3K/Akt/mTOR signaling pathway mediates insulin-like growth factor 1-induced E-cadherin down-regulation and cell proliferation in ovarian cancer cells. Cancer Lett 326: 191-198, 2012.
    • (2012) Cancer Lett , vol.326 , pp. 191-198
    • Lau, M.T.1    Leung, P.C.2
  • 34
    • 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 and 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 23: 29-36, 2009.
    • (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
  • 35
    • 84869094020 scopus 로고    scopus 로고
    • Reversal of P-gp and MRP1-mediated multidrug resistance by H6, a gypenoside aglycon from gynostemma pentaphyllum, in vincristine-resistant human oral cancer (KB/VCR) cells
    • Zhu H, Liu Z, Tang L, Liu J, Zhou M, Xie F, Wang Z, Wang Y, Shen S, Hu L, et al: Reversal of P-gp and MRP1-mediated multidrug resistance by H6, a gypenoside aglycon from Gynostemma pentaphyllum, in vincristine-resistant human oral cancer (KB/VCR) cells. Eur J Pharmacol 696: 43-53, 2012.
    • (2012) Eur J Pharmacol , vol.696 , pp. 43-53
    • Zhu, H.1    Liu, Z.2    Tang, L.3    Liu, J.4    Zhou, M.5    Xie, F.6    Wang, Z.7    Wang, Y.8    Shen, S.9    Hu, L.10
  • 36
    • 84906486965 scopus 로고    scopus 로고
    • Effects of HM30181, a P-glycoprotein inhibitor, on the pharmacokinetics and pharmacodynamics of loperamide in healthy volunteers
    • Kim TE, Lee H, Lim KS, Lee S, Yoon SH, Park KM, Han H, Shin SG, Jang IJ, Yu KS, et al: Effects of HM30181, a P-glycoprotein inhibitor, on the pharmacokinetics and pharmacodynamics of loperamide in healthy volunteers. Br J Clin Pharmacol 78: 556-564, 2014.
    • (2014) Br J Clin Pharmacol , vol.78 , pp. 556-564
    • Kim, T.E.1    Lee, H.2    Lim, K.S.3    Lee, S.4    Yoon, S.H.5    Park, K.M.6    Han, H.7    Shin, S.G.8    Jang, I.J.9    Yu, K.S.10
  • 37
    • 84860535245 scopus 로고    scopus 로고
    • Three decades of P-gp inhibitors: Skimming through several generations and scaffolds
    • Palmeira A, Sousa E, Vasconcelos MH and Pinto MM: Three decades of P-gp inhibitors: Skimming through several generations and scaffolds. Curr Med Chem 19: 1946-2025, 2012.
    • (2012) Curr Med Chem , vol.19 , pp. 1946-2025
    • Palmeira, A.1    Sousa, E.2    Vasconcelos, M.H.3    Pinto, M.M.4
  • 38
    • 84902690174 scopus 로고    scopus 로고
    • In vivo imaging of multidrug resistance using a third generation MDR1 inhibitor
    • Sprachman MM, Laughney AM, Kohler RH and Weissleder R: In vivo imaging of multidrug resistance using a third generation MDR1 inhibitor. Bioconjug Chem 25: 1137-1142, 2014.
    • (2014) Bioconjug Chem , vol.25 , pp. 1137-1142
    • Sprachman, M.M.1    Laughney, A.M.2    Kohler, R.H.3    Weissleder, R.4
  • 39
    • 84928109376 scopus 로고    scopus 로고
    • Α-2, 8-Sialyltransferase is involved in the development of multidrug resistance via PI3K/Akt pathway in human chronic myeloid leukemia
    • Zhang X, Dong W, Zhou H, Li H, Wang N, Miao X and Jia L: α-2, 8-Sialyltransferase is involved in the development of multidrug resistance via PI3K/Akt pathway in human chronic myeloid leukemia. IUBMB Life 67: 77-87, 2015.
    • (2015) IUBMB Life , vol.67 , pp. 77-87
    • Zhang, X.1    Dong, W.2    Zhou, H.3    Li, H.4    Wang, N.5    Miao, X.6    Jia, L.7
  • 41
    • 34347383964 scopus 로고    scopus 로고
    • Phospho Akt mediates multidrug resistance of gastric cancer cells through regulation of P-gp, Bcl-2 and Bax
    • Han Z, Hong L, Han Y, Wu K, Han S, Shen H, Li C, Yao L, Qiao T and Fan D: Phospho Akt mediates multidrug resistance of gastric cancer cells through regulation of P-gp, Bcl-2 and Bax. J Exp Clin Cancer Res 26: 261-268, 2007.
    • (2007) J Exp Clin Cancer Res , vol.26 , pp. 261-268
    • Han, Z.1    Hong, L.2    Han, Y.3    Wu, K.4    Han, S.5    Shen, H.6    Li, C.7    Yao, L.8    Qiao, T.9    Fan, D.10
  • 42
    • 84865282157 scopus 로고    scopus 로고
    • Perifosine downregulates MDR1 gene expression and reverses multidrug-resistant phenotype by inhibiting PI3K/Akt/NF-κB signaling pathway in a human breast cancer cell line
    • Lin X, Zhang X, Wang Q, Li J, Zhang P, Zhao M and Li X: Perifosine downregulates MDR1 gene expression and reverses multidrug-resistant phenotype by inhibiting PI3K/Akt/NF-κB signaling pathway in a human breast cancer cell line. Neoplasma 59: 248-256, 2012.
    • (2012) Neoplasma , vol.59 , pp. 248-256
    • Lin, X.1    Zhang, X.2    Wang, Q.3    Li, J.4    Zhang, P.5    Zhao, M.6    Li, X.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.