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Volumn 60, Issue 23, 2017, Pages 9724-9738

Amphiphilic Modulation of Glycosylated Antitumor Ether Lipids Results in a Potent Triamino Scaffold against Epithelial Cancer Cell Lines and BT474 Cancer Stem Cells

Author keywords

[No Author keywords available]

Indexed keywords

1 (12 AMINODODECYL) 2,6 DIAMINO 2,6 DIDEOXY BETA DEXTRO GLUCOPYRANOSIDE; 1 O HEXADECYL 2 O METHYL 3 O [2' AMINO 6' N (12 AMINODODECYL) 2',6' DIDEOXY BETA DEXTRO GLUCOPYRANOSIDE] SN GLYCEROL; 1 O HEXADECYL 2 O METHYL 3 O [2' AMINO 6' N (3 AMINOPROPYL) 2',6' DIDEOXY BETA DEXTRO GLUCOPYRANOSIDE] SN GLYCEROL; 1 O HEXADECYL 2 O METHYL 3 O [2' N (12 AMINODODECYL) 6' AMINO 2',6' DIDEOXY BETA DEXTRO GLUCOPYRANOSIDE] SN GLYCEROL; 1 O HEXADECYL 2 O METHYL 3 O [2' N (3 AMINOPROPYL) 6' AMINO 2',6' DIDEOXY BETA DEXTRO GLUCOPYRANOSIDE] SN GLYCEROL; 1 O HEXADECYL 2 O METHYL 3 O [6' N (12 N CHLORAMBUCIL DODECYL) 2',6' DIAMINO 2',6' DIDEOXY BETA DEXTRO GLUCOPYRANOSIDE] SN GLYCEROL; AMINE; AMPHOPHILE; ANTINEOPLASTIC AGENT; CASPASE; CHLORAMBUCIL; CISPLATIN; DOXORUBICIN; ETHER LIPID; MONOAMINE; SALINOMYCIN; UNCLASSIFIED DRUG; LIPID;

EID: 85033439702     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/acs.jmedchem.7b01198     Document Type: Article
Times cited : (23)

References (52)
  • 1
    • 0036176510 scopus 로고    scopus 로고
    • Mechanism of cancer resistance
    • Gottesman, M. M. Mechanism of cancer resistance Annu. Rev. Med. 2002, 53, 615-627 10.1146/annurev.med.53.082901.103929
    • (2002) Annu. Rev. Med. , vol.53 , pp. 615-627
    • Gottesman, M.M.1
  • 2
    • 0036364467 scopus 로고    scopus 로고
    • Multidrug resistance in cancer: Role of ATP-dependent transporters
    • Gottesman, M. M.; Fojo, T.; Bates, S. E. Multidrug resistance in cancer: Role of ATP-dependent transporters Nat. Rev. Cancer 2002, 2, 48-58 10.1038/nrc706
    • (2002) Nat. Rev. Cancer , vol.2 , pp. 48-58
    • Gottesman, M.M.1    Fojo, T.2    Bates, S.E.3
  • 3
    • 13644254794 scopus 로고    scopus 로고
    • Molecular mechanisms of drug resistance
    • Longley, D. B.; Johnston, P. G. Molecular mechanisms of drug resistance J. Pathol. 2005, 205, 275-292 10.1002/path.1706
    • (2005) J. Pathol. , vol.205 , pp. 275-292
    • Longley, D.B.1    Johnston, P.G.2
  • 4
    • 84858608410 scopus 로고    scopus 로고
    • Cancer stem cells: Impact, heterogeneity, and uncertainty
    • Magee, J. A.; Piskounova, E.; Morrison, S. J. Cancer stem cells: Impact, heterogeneity, and uncertainty Cancer Cell 2012, 21, 283-296 10.1016/j.ccr.2012.03.003
    • (2012) Cancer Cell , vol.21 , pp. 283-296
    • Magee, J.A.1    Piskounova, E.2    Morrison, S.J.3
  • 6
    • 16844368698 scopus 로고    scopus 로고
    • Tumour stem cells and drug resistance
    • Dean, M.; Fojo, T.; Bates, S. Tumour stem cells and drug resistance Nat. Rev. Cancer 2005, 5, 275-284 10.1038/nrc1590
    • (2005) Nat. Rev. Cancer , vol.5 , pp. 275-284
    • Dean, M.1    Fojo, T.2    Bates, S.3
  • 7
    • 66449088004 scopus 로고    scopus 로고
    • A glycosylated antitumor ether lipid kills cells via paraptosis-like cell death
    • Samadder, P.; Bittman, R.; Byun, H.; Arthur, G. A glycosylated antitumor ether lipid kills cells via paraptosis-like cell death Biochem. Cell Biol. 2009, 87, 401-414 10.1139/O08-147
    • (2009) Biochem. Cell Biol. , vol.87 , pp. 401-414
    • Samadder, P.1    Bittman, R.2    Byun, H.3    Arthur, G.4
  • 8
    • 83055179599 scopus 로고    scopus 로고
    • An active endocytosis pathway is required for the cytotoxic effects of glycosylated antitumor ether lipids
    • Samadder, P.; Byun, H. S.; Bittman, R.; Arthur, G. An active endocytosis pathway is required for the cytotoxic effects of glycosylated antitumor ether lipids Anticancer Res. 2011, 31, 3809-3818
    • (2011) Anticancer Res. , vol.31 , pp. 3809-3818
    • Samadder, P.1    Byun, H.S.2    Bittman, R.3    Arthur, G.4
  • 9
    • 84897399896 scopus 로고    scopus 로고
    • Glycosylated antitumor ether lipids: Activity and mechanism of action
    • Arthur, G.; Bittman, R. Glycosylated antitumor ether lipids: Activity and mechanism of action Anti-Cancer Agents Med. Chem. 2014, 14, 592-606 10.2174/1871520614666140309231144
    • (2014) Anti-Cancer Agents Med. Chem. , vol.14 , pp. 592-606
    • Arthur, G.1    Bittman, R.2
  • 10
    • 84926431014 scopus 로고    scopus 로고
    • Non-apoptotic cell death associated with perturbations of macropinocytosis
    • Maltese, W. A.; Overmeyer, J. H. Non-apoptotic cell death associated with perturbations of macropinocytosis Front. Physiol. 2015, 6, 38 10.3389/fphys.2015.00038
    • (2015) Front. Physiol. , vol.6 , pp. 38
    • Maltese, W.A.1    Overmeyer, J.H.2
  • 11
    • 79957854823 scopus 로고    scopus 로고
    • A chalcone-related small molecule that induces methuosis, a novel form of non-apoptotic cell death, in glioblastoma cells
    • Overmeyer, J. H.; Young, A. M.; Bhanot, H.; Maltese, W. A. A chalcone-related small molecule that induces methuosis, a novel form of non-apoptotic cell death, in glioblastoma cells Mol. Cancer 2011, 10, 69-79 10.1186/1476-4598-10-69
    • (2011) Mol. Cancer , vol.10 , pp. 69-79
    • Overmeyer, J.H.1    Young, A.M.2    Bhanot, H.3    Maltese, W.A.4
  • 12
    • 84897448338 scopus 로고    scopus 로고
    • Cytotoxic properties of D-gluco-, D-galacto- and D-manno-configured 2-amino-2-deoxy-glycerolipids against epithelial cancer cell lines and BT-474 breast cancer stem cells
    • Samadder, P.; Xu, Y.; Schweizer, F.; Arthur, G. Cytotoxic properties of D-gluco-, D-galacto- and D-manno-configured 2-amino-2-deoxy-glycerolipids against epithelial cancer cell lines and BT-474 breast cancer stem cells Eur. J. Med. Chem. 2014, 78, 225-235 10.1016/j.ejmech.2014.03.057
    • (2014) Eur. J. Med. Chem. , vol.78 , pp. 225-235
    • Samadder, P.1    Xu, Y.2    Schweizer, F.3    Arthur, G.4
  • 13
    • 0030007483 scopus 로고    scopus 로고
    • Synthesis and evaluation of the antiproliferative effects of 1-O-hexadecyl-2-O-methyl-3-O-(2′-acetamido-2′-deoxy-β-D-glucopyranosyl)-sn-glycerol and 1-O-hexadecyl-2-O-methyl-3-O-(2′-amino-2′-deoxy-β-D-glucopyranosyl)-sn-glycerol on epithelial cancer
    • Erukulla, R. K.; Zhou, X.; Samadder, P.; Arthur, G.; Bittman, R. Synthesis and evaluation of the antiproliferative effects of 1-O-hexadecyl-2-O-methyl-3-O-(2′-acetamido-2′-deoxy-β-D-glucopyranosyl)-sn-glycerol and 1-O-hexadecyl-2-O-methyl-3-O-(2′-amino-2′-deoxy-β-D-glucopyranosyl)-sn-glycerol on epithelial cancer J. Med. Chem. 1996, 39, 1545-1548 10.1021/jm950928f
    • (1996) J. Med. Chem. , vol.39 , pp. 1545-1548
    • Erukulla, R.K.1    Zhou, X.2    Samadder, P.3    Arthur, G.4    Bittman, R.5
  • 14
    • 84874318706 scopus 로고    scopus 로고
    • Structural-activity relationships of glucosamine-derived glycerolipids
    • Xu, Y.; Ogunsina, M.; Samadder, P.; Arthur, G.; Schweizer, F. Structural-activity relationships of glucosamine-derived glycerolipids ChemMedChem 2013, 8, 511-520 10.1002/cmdc.201200489
    • (2013) ChemMedChem , vol.8 , pp. 511-520
    • Xu, Y.1    Ogunsina, M.2    Samadder, P.3    Arthur, G.4    Schweizer, F.5
  • 16
    • 0025743796 scopus 로고
    • Elevated expression of phosphatidylserine in the outer membrane leaflet of human tumor cells and recognition by activated human blood monocytes
    • Utsugi, T.; Schroit, A. J.; Connor, J.; Bucana, C. D.; Fidler, I. J. Elevated expression of phosphatidylserine in the outer membrane leaflet of human tumor cells and recognition by activated human blood monocytes Cancer Res. 1991, 51, 3062-3066
    • (1991) Cancer Res. , vol.51 , pp. 3062-3066
    • Utsugi, T.1    Schroit, A.J.2    Connor, J.3    Bucana, C.D.4    Fidler, I.J.5
  • 17
    • 24144469847 scopus 로고    scopus 로고
    • Changes in electric charge and phospholipids composition in human colorectal cancer cells
    • Dobrzyńska, I.; Szachowicz-Petelska, B.; Sulkowski, S.; Figaszewski, Z. Changes in electric charge and phospholipids composition in human colorectal cancer cells Mol. Cell. Biochem. 2005, 276, 113-119 10.1007/s11010-005-3557-3
    • (2005) Mol. Cell. Biochem. , vol.276 , pp. 113-119
    • Dobrzyńska, I.1    Szachowicz-Petelska, B.2    Sulkowski, S.3    Figaszewski, Z.4
  • 18
    • 0029930750 scopus 로고    scopus 로고
    • Effect of O-glycosylated mucin on invasion and metastasis of HM7 human colon cancer cells
    • Yoon, W. H.; Park, H. D.; Lim, K.; Hwang, B. D. Effect of O-glycosylated mucin on invasion and metastasis of HM7 human colon cancer cells Biochem. Biophys. Res. Commun. 1996, 222, 694-699 10.1006/bbrc.1996.0806
    • (1996) Biochem. Biophys. Res. Commun. , vol.222 , pp. 694-699
    • Yoon, W.H.1    Park, H.D.2    Lim, K.3    Hwang, B.D.4
  • 19
    • 0030827120 scopus 로고    scopus 로고
    • Oligosaccharides expressed on MUC1 produced by pancreatic and colon tumor cell lines
    • Burdick, M. D.; Harris, A.; Reid, C. J.; Iwamura, T.; Hollingsworth, M. A. Oligosaccharides expressed on MUC1 produced by pancreatic and colon tumor cell lines J. Biol. Chem. 1997, 272, 24198-24202 10.1074/jbc.272.39.24198
    • (1997) J. Biol. Chem. , vol.272 , pp. 24198-24202
    • Burdick, M.D.1    Harris, A.2    Reid, C.J.3    Iwamura, T.4    Hollingsworth, M.A.5
  • 20
    • 53049110294 scopus 로고    scopus 로고
    • Mechanism of anticancer activity of buforin IIb, a histone H2A-derived peptide
    • Lee, H. S.; Park, C. B.; Kim, J. M.; Jang, S. A.; Park, I. Y.; Kim, M. S.; Cho, J. H.; Kim, S. C. Mechanism of anticancer activity of buforin IIb, a histone H2A-derived peptide Cancer Lett. 2008, 271, 47-55 10.1016/j.canlet.2008.05.041
    • (2008) Cancer Lett. , vol.271 , pp. 47-55
    • Lee, H.S.1    Park, C.B.2    Kim, J.M.3    Jang, S.A.4    Park, I.Y.5    Kim, M.S.6    Cho, J.H.7    Kim, S.C.8
  • 21
    • 0032213027 scopus 로고    scopus 로고
    • The cell-surface heparan sulfate proteoglycan glypican-1 regulates growth factor action in pancreatic carcinoma cells and is overexpressed in human pancreatic cancer
    • Kleeff, J.; Ishiwata, T.; Kumbasar, A.; Friess, H.; Büchler, M. W.; Lander, A. D.; Korc, M. The cell-surface heparan sulfate proteoglycan glypican-1 regulates growth factor action in pancreatic carcinoma cells and is overexpressed in human pancreatic cancer J. Clin. Invest. 1998, 102, 1662-1673 10.1172/JCI4105
    • (1998) J. Clin. Invest. , vol.102 , pp. 1662-1673
    • Kleeff, J.1    Ishiwata, T.2    Kumbasar, A.3    Friess, H.4    Büchler, M.W.5    Lander, A.D.6    Korc, M.7
  • 22
    • 71749100398 scopus 로고    scopus 로고
    • Cationic amphiphilic peptides with cancer-selective toxicity
    • Schweizer, F. Cationic amphiphilic peptides with cancer-selective toxicity Eur. J. Pharmacol. 2009, 625, 190-194 10.1016/j.ejphar.2009.08.043
    • (2009) Eur. J. Pharmacol. , vol.625 , pp. 190-194
    • Schweizer, F.1
  • 23
    • 0037165196 scopus 로고    scopus 로고
    • Antimicrobial peptides of multicellular organisms
    • Zasloff, M. Antimicrobial peptides of multicellular organisms Nature 2002, 415, 389-395 10.1038/415389a
    • (2002) Nature , vol.415 , pp. 389-395
    • Zasloff, M.1
  • 24
    • 33845699790 scopus 로고    scopus 로고
    • Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies
    • Hancock, R. E. W.; Sahl, H.-G. Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies Nat. Biotechnol. 2006, 24, 1551-1557 10.1038/nbt1267
    • (2006) Nat. Biotechnol. , vol.24 , pp. 1551-1557
    • Hancock, R.E.W.1    Sahl, H.-G.2
  • 25
    • 50249103779 scopus 로고    scopus 로고
    • Antimicrobial peptides: Natural templates for synthetic membrane-active compounds
    • Giuliani, A.; Pirri, G.; Bozzi, A.; Di Giulio, A.; Aschi, M.; Rinaldi, A. C. Antimicrobial peptides: natural templates for synthetic membrane-active compounds Cell. Mol. Life Sci. 2008, 65, 2450-2460 10.1007/s00018-008-8188-x
    • (2008) Cell. Mol. Life Sci. , vol.65 , pp. 2450-2460
    • Giuliani, A.1    Pirri, G.2    Bozzi, A.3    Di Giulio, A.4    Aschi, M.5    Rinaldi, A.C.6
  • 26
    • 0344959559 scopus 로고    scopus 로고
    • ESR study of plasmatic membrane of the transplantable melanoma cells in relation to their biological properties
    • Kozłowska, K.; Nowak, J.; Kwiatkowski, B.; Cichorek, M. ESR study of plasmatic membrane of the transplantable melanoma cells in relation to their biological properties Exp. Toxicol. Pathol. 1999, 51, 89-92 10.1016/S0940-2993(99)80074-8
    • (1999) Exp. Toxicol. Pathol. , vol.51 , pp. 89-92
    • Kozłowska, K.1    Nowak, J.2    Kwiatkowski, B.3    Cichorek, M.4
  • 27
    • 0032938321 scopus 로고    scopus 로고
    • Membrane fluidity characteristics of human lung cancer
    • Sok, M.; Sentjurc, M.; Schara, M. Membrane fluidity characteristics of human lung cancer Cancer Lett. 1999, 139, 215-220 10.1016/S0304-3835(99)00044-0
    • (1999) Cancer Lett. , vol.139 , pp. 215-220
    • Sok, M.1    Sentjurc, M.2    Schara, M.3
  • 28
    • 84937426269 scopus 로고    scopus 로고
    • Synthetic glycosylated ether glycerolipids as anticancer agents
    • Jiménez-Barbero, J. Cañada, F. J. Martín-Santamaría, S. RSC: Cambridge, UK
    • Arthur, G.; Schweizer, F.; Ogunsina, M. Synthetic glycosylated ether glycerolipids as anticancer agents. In Carbohydrates in Drug Design and Discovery; Jiménez-Barbero, J.; Cañada, F. J.; Martín-Santamaría, S., Eds.; RSC: Cambridge, UK, 2015; pp 151-179.
    • (2015) Carbohydrates in Drug Design and Discovery , pp. 151-179
    • Arthur, G.1    Schweizer, F.2    Ogunsina, M.3
  • 29
    • 84890948458 scopus 로고    scopus 로고
    • Structure activity relationships of N-linked and diglycosylated glucosamine-based antitumor glycerolipids
    • Ogunsina, M.; Pan, H.; Samadder, P.; Arthur, G.; Schweizer, F. Structure activity relationships of N-linked and diglycosylated glucosamine-based antitumor glycerolipids Molecules 2013, 18, 15288-15304 10.3390/molecules181215288
    • (2013) Molecules , vol.18 , pp. 15288-15304
    • Ogunsina, M.1    Pan, H.2    Samadder, P.3    Arthur, G.4    Schweizer, F.5
  • 30
    • 84994523284 scopus 로고    scopus 로고
    • Design, synthesis and evaluation of cytotoxic properties of bisamino glucosylated antitumor ether lipids against cancer cells and cancer stem cells
    • Ogunsina, M.; Samadder, P.; Idowu, T.; Arthur, G.; Schweizer, F. Design, synthesis and evaluation of cytotoxic properties of bisamino glucosylated antitumor ether lipids against cancer cells and cancer stem cells MedChemComm 2016, 7, 2100-2110 10.1039/C6MD00328A
    • (2016) MedChemComm , vol.7 , pp. 2100-2110
    • Ogunsina, M.1    Samadder, P.2    Idowu, T.3    Arthur, G.4    Schweizer, F.5
  • 31
    • 84954386847 scopus 로고    scopus 로고
    • Design, synthesis and antitumor properties of glycosylated antitumor ether lipid (GAEL)-chlorambucil-hybrids
    • Idowu, T.; Samadder, P.; Arthur, G.; Schweizer, F. Design, synthesis and antitumor properties of glycosylated antitumor ether lipid (GAEL)-chlorambucil-hybrids Chem. Phys. Lipids 2016, 194, 139-148 10.1016/j.chemphyslip.2015.07.003
    • (2016) Chem. Phys. Lipids , vol.194 , pp. 139-148
    • Idowu, T.1    Samadder, P.2    Arthur, G.3    Schweizer, F.4
  • 32
    • 85015081962 scopus 로고    scopus 로고
    • Replacing D-glucosamine with its L-enantiomer in glycosylated antitumor ether lipids (GAELs) retains cytotoxic effects against epithelial cancer cells and cancer stem cells
    • Ogunsina, M.; Samadder, P.; Idowu, T.; Arthur, G.; Schweizer, F. Replacing D-glucosamine with its L-enantiomer in glycosylated antitumor ether lipids (GAELs) retains cytotoxic effects against epithelial cancer cells and cancer stem cells J. Med. Chem. 2017, 60, 2142-2147 10.1021/acs.jmedchem.6b01773
    • (2017) J. Med. Chem. , vol.60 , pp. 2142-2147
    • Ogunsina, M.1    Samadder, P.2    Idowu, T.3    Arthur, G.4    Schweizer, F.5
  • 34
    • 77957329669 scopus 로고    scopus 로고
    • Cationic amphiphiles, a new generation of antimicrobials inspired by the natural antimicrobial peptide scaffold
    • Findlay, B.; Zhanel, G. G.; Schweizer, F. Cationic amphiphiles, a new generation of antimicrobials inspired by the natural antimicrobial peptide scaffold Antimicrob. Agents Chemother. 2010, 54, 4049-4058 10.1128/AAC.00530-10
    • (2010) Antimicrob. Agents Chemother. , vol.54 , pp. 4049-4058
    • Findlay, B.1    Zhanel, G.G.2    Schweizer, F.3
  • 35
    • 2942652871 scopus 로고    scopus 로고
    • Mechanisms of tamoxifen resistance: Increased estrogen receptor-HER2/neu cross-talk in ER/HER2-positive breast cancer
    • Shou, J.; Massarweh, S.; Osborne, C. K.; Wakeling, A. E.; Ali, S.; Weiss, H.; Schiff, R. Mechanisms of tamoxifen resistance: increased estrogen receptor-HER2/neu cross-talk in ER/HER2-positive breast cancer J. Natl. Cancer Inst. 2004, 96, 926-935 10.1093/jnci/djh166
    • (2004) J. Natl. Cancer Inst. , vol.96 , pp. 926-935
    • Shou, J.1    Massarweh, S.2    Osborne, C.K.3    Wakeling, A.E.4    Ali, S.5    Weiss, H.6    Schiff, R.7
  • 36
    • 84859424942 scopus 로고    scopus 로고
    • Clinicopathologic signature of TNBC patients with good prognosis
    • Korea Breast Cancer Society
    • Kim, K.; Lee, E.; Lee, J.; Bae, J.; Korea Breast Cancer Society Clinicopathologic signature of TNBC patients with good prognosis Cancer Res. 2009, 69, 4065-4065 10.1158/0008-5472.SABCS-09-4065
    • (2009) Cancer Res. , vol.69 , pp. 4065
    • Kim, K.1    Lee, E.2    Lee, J.3    Bae, J.4
  • 40
    • 72949118673 scopus 로고    scopus 로고
    • High aldehyde dehydrogenase and expression of cancer stem cell markers selects for breast cancer cells with enhanced malignant and metastatic ability
    • Croker, A. K.; Goodale, D.; Chu, J.; Postenka, C.; Hedley, B. D.; Hess, D. A.; Allan, A. L. High aldehyde dehydrogenase and expression of cancer stem cell markers selects for breast cancer cells with enhanced malignant and metastatic ability J. Cell. Mol. Med. 2009, 13, 2236-2252 10.1111/j.1582-4934.2008.00455.x
    • (2009) J. Cell. Mol. Med. , vol.13 , pp. 2236-2252
    • Croker, A.K.1    Goodale, D.2    Chu, J.3    Postenka, C.4    Hedley, B.D.5    Hess, D.A.6    Allan, A.L.7
  • 42
    • 0033168928 scopus 로고    scopus 로고
    • Cisplatin-induced apoptosis proceeds by caspase-3-dependent and -independent pathways in cisplatin-resistant and -sensitive human ovarian cancer cell lines
    • Henkels, K. M.; Turchi, J. J. Cisplatin-induced apoptosis proceeds by caspase-3-dependent and -independent pathways in cisplatin-resistant and -sensitive human ovarian cancer cell lines Cancer Res. 1999, 59, 3077-3083
    • (1999) Cancer Res. , vol.59 , pp. 3077-3083
    • Henkels, K.M.1    Turchi, J.J.2
  • 43
    • 84856066278 scopus 로고    scopus 로고
    • Salinomycin: A new cancer drug candidate
    • Huczynski, A. Salinomycin: A new cancer drug candidate Chem. Biol. Drug Des. 2012, 79, 235-238 10.1111/j.1747-0285.2011.01287.x
    • (2012) Chem. Biol. Drug Des. , vol.79 , pp. 235-238
    • Huczynski, A.1
  • 44
    • 68749099671 scopus 로고    scopus 로고
    • Identification of selective inhibitors of cancer stem cells by high-throughput screening
    • Gupta, P. B.; Onder, T. T.; Jiang, G.; Tao, K.; Kuperwasser, C.; Weinberg, R. A.; Lander, E. S. Identification of selective inhibitors of cancer stem cells by high-throughput screening Cell 2009, 138, 645-659 10.1016/j.cell.2009.06.034
    • (2009) Cell , vol.138 , pp. 645-659
    • Gupta, P.B.1    Onder, T.T.2    Jiang, G.3    Tao, K.4    Kuperwasser, C.5    Weinberg, R.A.6    Lander, E.S.7
  • 45
    • 0041666539 scopus 로고    scopus 로고
    • Q-VD-OPh, a broad spectrum caspase inhibitor with potent antiapoptotic properties
    • Caserta, T. M.; Smith, A. N.; Gultice, A. D.; Reedy, M. A.; Brown, T. L. Q-VD-OPh, a broad spectrum caspase inhibitor with potent antiapoptotic properties Apoptosis 2003, 8, 345-352 10.1023/A:1024116916932
    • (2003) Apoptosis , vol.8 , pp. 345-352
    • Caserta, T.M.1    Smith, A.N.2    Gultice, A.D.3    Reedy, M.A.4    Brown, T.L.5
  • 46
    • 0001213485 scopus 로고
    • Role of hydrogen peroxide and hydroxyl radical formation in the killing of ehrlich tumor cells by anticancer quinones
    • Doroshow, J. H. Role of hydrogen peroxide and hydroxyl radical formation in the killing of ehrlich tumor cells by anticancer quinones Proc. Natl. Acad. Sci. U. S. A. 1986, 83, 4514-4518 10.1073/pnas.83.12.4514
    • (1986) Proc. Natl. Acad. Sci. U. S. A. , vol.83 , pp. 4514-4518
    • Doroshow, J.H.1
  • 48
    • 70349564137 scopus 로고    scopus 로고
    • Cell death pathways-potential therapeutic targets
    • MacFarlane, M. Cell death pathways-potential therapeutic targets Xenobiotica 2009, 39, 616-624 10.1080/00498250903137990
    • (2009) Xenobiotica , vol.39 , pp. 616-624
    • MacFarlane, M.1
  • 49
    • 0018413113 scopus 로고
    • Ethidium dimer: A new reagent for the fluorimetric determination of nucleic acids
    • Markovits, J.; Roques, B. P.; Le Pecq, J.-B. Ethidium dimer: A new reagent for the fluorimetric determination of nucleic acids Anal. Biochem. 1979, 94, 259-264 10.1016/0003-2697(79)90357-9
    • (1979) Anal. Biochem. , vol.94 , pp. 259-264
    • Markovits, J.1    Roques, B.P.2    Le Pecq, J.-B.3
  • 50
    • 52549087785 scopus 로고    scopus 로고
    • Cancer stem cells in solid tumours: Accumulating evidence and unresolved questions
    • Visvader, J. E.; Lindeman, G. J. Cancer stem cells in solid tumours: Accumulating evidence and unresolved questions Nat. Rev. Cancer 2008, 8, 755-768 10.1038/nrc2499
    • (2008) Nat. Rev. Cancer , vol.8 , pp. 755-768
    • Visvader, J.E.1    Lindeman, G.J.2
  • 51
    • 84896125494 scopus 로고    scopus 로고
    • Evolution of the cancer stem cell model
    • Kreso, A.; Dick, J. E. Evolution of the cancer stem cell model Cell Stem Cell 2014, 14, 275-291 10.1016/j.stem.2014.02.006
    • (2014) Cell Stem Cell , vol.14 , pp. 275-291
    • Kreso, A.1    Dick, J.E.2
  • 52
    • 85019177780 scopus 로고    scopus 로고
    • Amphiphilic tobramycin-lysine conjugates sensitize multidrug resistant gram-negative bacteria to rifampicin and minocycline
    • Lyu, Y.; Yang, X.; Goswami, S.; Gorityala, B. K.; Idowu, T.; Domalaon, R.; Zhanel, G. G.; Shan, A.; Schweizer, F. Amphiphilic tobramycin-lysine conjugates sensitize multidrug resistant gram-negative bacteria to rifampicin and minocycline J. Med. Chem. 2017, 60, 3684-3702 10.1021/acs.jmedchem.6b01742
    • (2017) J. Med. Chem. , vol.60 , pp. 3684-3702
    • Lyu, Y.1    Yang, X.2    Goswami, S.3    Gorityala, B.K.4    Idowu, T.5    Domalaon, R.6    Zhanel, G.G.7    Shan, A.8    Schweizer, F.9


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