3-Ketone-4,6-diene ceramide analogs exclusively induce apoptosis in chemo-resistant cancer cells.
暂无分享,去创建一个
Ming Zhao | Jiawang Liu | M. Foroozesh | B. Beckman | J. Antoon | Barbara A Drew | Thong T Nguyen | Patrick S Dupart | Yuji Wang | Yong-Yu Liu | Kaustubh N. Bhinge | Tony Wang | Adharsh P. Ponnapakam
[1] A. Huwiler,et al. Effective inhibition of acid and neutral ceramidases by novel B-13 and LCL-464 analogues. , 2013, Bioorganic & medicinal chemistry.
[2] A. Bielawska,et al. LCL124, a Cationic Analog of Ceramide, Selectively Induces Pancreatic Cancer Cell Death by Accumulating in Mitochondria , 2013, The Journal of Pharmacology and Experimental Therapeutics.
[3] K. P. Bhabak,et al. Novel amide- and sulfonamide-based aromatic ethanolamines: effects of various substituents on the inhibition of acid and neutral ceramidases. , 2012, Bioorganic & medicinal chemistry.
[4] S. Morad,et al. Ceramide–Antiestrogen Nanoliposomal Combinations—Novel Impact of Hormonal Therapy in Hormone-Insensitive Breast Cancer , 2012, Molecular Cancer Therapeutics.
[5] K. Khoo,et al. Ceramide Glycosylation by Glucosylceramide Synthase Selectively Maintains the Properties of Breast Cancer Stem Cells* , 2012, The Journal of Biological Chemistry.
[6] F. Simbari,et al. 3-Deoxy-3,4-dehydro analogs of XM462. Preparation and activity on sphingolipid metabolism and cell fate. , 2012, Bioorganic & medicinal chemistry.
[7] B. Beckman,et al. Anti-proliferative effects of the novel ceramide analog (S)-2-(benzylideneamino)-3-hydroxy-N-tetrade-cylpropanamide in chemoresistant cancer. , 2012, Bioorganic & medicinal chemistry letters.
[8] A. Singh,et al. 3,4-Disubstituted oxazolidin-2-ones as constrained ceramide analogs with anticancer activities. , 2011, Bioorganic & medicinal chemistry.
[9] L. Rhodes,et al. Pharmacological inhibition of sphingosine kinase isoforms alters estrogen receptor signaling in human breast cancer. , 2011, Journal of molecular endocrinology.
[10] Steven Elliott,et al. Targeting NFĸB mediated breast cancer chemoresistance through selective inhibition of sphingosine kinase-2 , 2011, Cancer biology & therapy.
[11] A. Bielawska,et al. Synthesis, NMR characterization and divergent biological actions of 2'-hydroxy-ceramide/dihydroceramide stereoisomers in MCF7 cells. , 2010, Bioorganic & medicinal chemistry.
[12] L. Rhodes,et al. Antiestrogenic effects of the novel sphingosine kinase-2 inhibitor ABC294640. , 2010, Endocrinology.
[13] Jiawang Liu,et al. Novel anti-viability ceramide analogs: design, synthesis, and structure-activity relationship studies of substituted (S)-2-(benzylideneamino)-3-hydroxy-N-tetradecylpropanamides. , 2010, Bioorganic & medicinal chemistry.
[14] S. Pyne,et al. Sphingosine 1-phosphate and cancer , 2010, Nature Reviews Cancer.
[15] M. Cabot,et al. Direct quantitative determination of ceramide glycosylation in vivo: a new approach to evaluate cellular enzyme activity of glucosylceramide synthase , 2010, Journal of Lipid Research.
[16] M. Cabot,et al. Glucosylceramide synthase upregulates MDR1 expression in the regulation of cancer drug resistance through cSrc and β-catenin signaling , 2010, Molecular Cancer.
[17] Jiawang Liu,et al. Novel d-erythro N-octanoyl sphingosine analogs as chemo- and endocrine-resistant breast cancer therapeutics , 2010, Cancer Chemotherapy and Pharmacology.
[18] M. Cabot,et al. A New Mixed-Backbone Oligonucleotide against Glucosylceramide Synthase Sensitizes Multidrug-Resistant Tumors to Apoptosis , 2009, PloS one.
[19] Jiawang Liu,et al. Design, synthesis, and biological activity of a family of novel ceramide analogues in chemoresistant breast cancer cells. , 2009, Journal of medicinal chemistry.
[20] A. Melendez,et al. Synthesis and evaluation of sphingosine analogues as inhibitors of sphingosine kinases. , 2009, Journal of medicinal chemistry.
[21] A. Giuliano,et al. A role for ceramide in driving cancer cell resistance to doxorubicin , 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[22] Yusuf A. Hannun,et al. Principles of bioactive lipid signalling: lessons from sphingolipids , 2008, Nature Reviews Molecular Cell Biology.
[23] S. Saddoughi,et al. Roles of bioactive sphingolipids in cancer biology and therapeutics. , 2008, Sub-cellular biochemistry.
[24] Ming Zhao,et al. Dual-acting agents that possess reversing resistance and anticancer activities: Design, synthesis, MES-SA/Dx5 cell assay, and SAR of Benzyl 1,2,3,5,11,11a-hexahydro-3,3-dimethyl-1-oxo-6H-imidazo[3',4':1,2]pyridin[3,4-b]indol-2-substitutedacetates. , 2007, Bioorganic & medicinal chemistry.
[25] M. Cabot,et al. Glycosphingolipids and drug resistance. , 2006, Biochimica et biophysica acta.
[26] A. Llebaria,et al. Inhibitors of sphingolipid metabolism enzymes. , 2006, Biochimica et biophysica acta.
[27] W. Kamps,et al. PDMP sensitizes neuroblastoma to paclitaxel by inducing aberrant cell cycle progression leading to hyperploidy , 2006, Molecular Cancer Therapeutics.
[28] A. Giuliano,et al. Glucosylceramide synthase blockade down-regulates P-glycoprotein and resensitizes multidrug-resistant breast cancer cells to anticancer drugs. , 2005, Cancer research.
[29] Yan Tang,et al. Novel Ceramide Analogs as Potential Chemotherapeutic Agents in Breast Cancer , 2004, Journal of Pharmacology and Experimental Therapeutics.
[30] R. Bittman,et al. Synthesis of New Trans Double-Bond Sphingolipid Analogues: Δ4,6 and Δ6 Ceramides , 2002 .
[31] W. Kamps,et al. 1-phenyl-2-decanoylamino-3-morpholino-1-propanol chemosensitizes neuroblastoma cells for taxol and vincristine. , 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.
[32] K. M. Nicholson,et al. Preferential killing of multidrug-resistant KB cells by inhibitors of glucosylceramide synthase , 1999, British Journal of Cancer.
[33] S. Hakomori,et al. In vitro and in vivo induction of apoptosis by sphingosine and N, N-dimethylsphingosine in human epidermoid carcinoma KB-3-1 and its multidrug-resistant cells. , 1997, Clinical cancer research : an official journal of the American Association for Cancer Research.