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Volumn 56, Issue 24, 2013, Pages 10033-10044

Optimization of antitumor modulators of pre-mRNA splicing

Author keywords

[No Author keywords available]

Indexed keywords

4 DIALLYLAMINOMETHYLENE 1,3,4,7,10,11,12,13,14,15,16,17 DODECAHYDRO 6 HYDROXY 1 METHOXYMETHYL 10,13 DIMETHYL 3,7,17 TRIOXO 2 OXACYCLOPENTA[A]PHENANTHREN 11 YL ACETATE; BORTEZOMIB; CAMPTOTHECIN; DACTOLISIB; HARRINGTONINE; IMATINIB; MESSENGER RNA PRECURSOR; NATURAL PRODUCT; PACLITAXEL; PANOBINOSTAT; SILIBININ; SORAFENIB; SU 9516; SUDEMYCIN C1; SUDEMYCIN D1; SUDEMYCIN D6; SUDEMYCIN F1; TEMSIROLIMUS; UNCLASSIFIED DRUG;

EID: 84891323481     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm401370h     Document Type: Article
Times cited : (55)

References (49)
  • 1
    • 0029891101 scopus 로고    scopus 로고
    • The structure and function of proteins involved in mammalian pre-mRNA splicing
    • Kramer, A. The structure and function of proteins involved in mammalian pre-mRNA splicing Annu. Rev. Biochem. 1996, 65, 367-409
    • (1996) Annu. Rev. Biochem. , vol.65 , pp. 367-409
    • Kramer, A.1
  • 2
    • 0038670209 scopus 로고    scopus 로고
    • Molecular architecture of the multiprotein splicing factor SF3b
    • Golas, M. M.; Sander, B.; Will, C. L.; Luhrmann, R.; Stark, H. Molecular architecture of the multiprotein splicing factor SF3b Science 2003, 300, 980-984
    • (2003) Science , vol.300 , pp. 980-984
    • Golas, M.M.1    Sander, B.2    Will, C.L.3    Luhrmann, R.4    Stark, H.5
  • 3
    • 0032489021 scopus 로고    scopus 로고
    • Mechanical devices of the spliceosome: Motors, clocks, springs, and things
    • Staley, J. P.; Guthrie, C. Mechanical devices of the spliceosome: Motors, clocks, springs, and things Cell 1998, 92, 315-326
    • (1998) Cell , vol.92 , pp. 315-326
    • Staley, J.P.1    Guthrie, C.2
  • 5
    • 0030466895 scopus 로고    scopus 로고
    • New antitumor substances, FR901463, FR901464 and FR901465. II. Activities against experimental tumors in mice and mechanism of action
    • Nakajima, H.; Hori, Y.; Terano, H.; Okuhara, M.; Manda, T.; Matsumoto, S.; Shimomura, K. New antitumor substances, FR901463, FR901464 and FR901465. II. Activities against experimental tumors in mice and mechanism of action J. Antibiot. 1996, 49, 1204-1211
    • (1996) J. Antibiot. , vol.49 , pp. 1204-1211
    • Nakajima, H.1    Hori, Y.2    Terano, H.3    Okuhara, M.4    Manda, T.5    Matsumoto, S.6    Shimomura, K.7
  • 6
    • 0030461311 scopus 로고    scopus 로고
    • New antitumor substances, FR901463, FR901464 and FR901465. I. Taxonomy, fermentation, isolation, physico-chemical properties and biological activities
    • Nakajima, H.; Sato, B.; Fujita, T.; Takase, S.; Terano, H.; Okuhara, M. New antitumor substances, FR901463, FR901464 and FR901465. I. Taxonomy, fermentation, isolation, physico-chemical properties and biological activities J. Antibiot. 1996, 49, 1196-1203
    • (1996) J. Antibiot. , vol.49 , pp. 1196-1203
    • Nakajima, H.1    Sato, B.2    Fujita, T.3    Takase, S.4    Terano, H.5    Okuhara, M.6
  • 7
    • 0031054453 scopus 로고    scopus 로고
    • New antitumor substances, FR901463, FR901464 and FR901465. III. Structures of FR901463, FR901464 and FR901465
    • Nakajima, H.; Takase, S.; Terano, H.; Tanaka, H. New antitumor substances, FR901463, FR901464 and FR901465. III. Structures of FR901463, FR901464 and FR901465 J. Antibiot. 1997, 50, 96-99
    • (1997) J. Antibiot. , vol.50 , pp. 96-99
    • Nakajima, H.1    Takase, S.2    Terano, H.3    Tanaka, H.4
  • 8
    • 1842865013 scopus 로고    scopus 로고
    • Pladienolides, new substances from culture of Streptomyces platensis Mer-11107. III. in vitro and in vivo antitumor activities
    • Mizui, Y.; Sakai, T.; Iwata, M.; Uenaka, T.; Okamoto, K.; Shimizu, H.; Yamori, T.; Yoshimatsu, K.; Asada, M. Pladienolides, new substances from culture of Streptomyces platensis Mer-11107. III. In vitro and in vivo antitumor activities J. Antibiot. 2004, 57, 188-196
    • (2004) J. Antibiot. , vol.57 , pp. 188-196
    • Mizui, Y.1    Sakai, T.2    Iwata, M.3    Uenaka, T.4    Okamoto, K.5    Shimizu, H.6    Yamori, T.7    Yoshimatsu, K.8    Asada, M.9
  • 13
    • 84876916289 scopus 로고    scopus 로고
    • Genomics-guided discovery of thailanstatins A, B, and C as pre-mRNA splicing inhibitors and antiproliferative agents from Burkholderia thailandensis MSMB43
    • Liu, X.; Biswas, S.; Berg, M. G.; Antapli, C. M.; Xie, F.; Wang, Q.; Tang, M. C.; Tang, G. L.; Zhang, L.; Dreyfuss, G.; Cheng, Y. Q. Genomics-guided discovery of thailanstatins A, B, and C as pre-mRNA splicing inhibitors and antiproliferative agents from Burkholderia thailandensis MSMB43 J. Nat. Prod. 2013, 76, 685-693
    • (2013) J. Nat. Prod. , vol.76 , pp. 685-693
    • Liu, X.1    Biswas, S.2    Berg, M.G.3    Antapli, C.M.4    Xie, F.5    Wang, Q.6    Tang, M.C.7    Tang, G.L.8    Zhang, L.9    Dreyfuss, G.10    Cheng, Y.Q.11
  • 16
    • 0036808433 scopus 로고    scopus 로고
    • GEX1 compounds, novel antitumor antibiotics related to herboxidiene, produced by Streptomyces sp. II. The effects on cell cycle progression and gene expression
    • Sakai, Y.; Tsujita, T.; Akiyama, T.; Yoshida, T.; Mizukami, T.; Akinaga, S.; Horinouchi, S.; Yoshida, M. GEX1 compounds, novel antitumor antibiotics related to herboxidiene, produced by Streptomyces sp. II. The effects on cell cycle progression and gene expression J. Antibiot. 2002, 55, 863-872
    • (2002) J. Antibiot. , vol.55 , pp. 863-872
    • Sakai, Y.1    Tsujita, T.2    Akiyama, T.3    Yoshida, T.4    Mizukami, T.5    Akinaga, S.6    Horinouchi, S.7    Yoshida, M.8
  • 17
    • 84871924824 scopus 로고    scopus 로고
    • The development and application of small molecule modulators of SF3b as therapeutic agents for cancer
    • Webb, T. R.; Joyner, A. S.; Potter, P. M. The development and application of small molecule modulators of SF3b as therapeutic agents for cancer Drug Discovery Today 2013, 18, 43-49
    • (2013) Drug Discovery Today , vol.18 , pp. 43-49
    • Webb, T.R.1    Joyner, A.S.2    Potter, P.M.3
  • 18
    • 7444220147 scopus 로고    scopus 로고
    • Aberrant and alternative splicing in cancer
    • Venables, J. P. Aberrant and alternative splicing in cancer Cancer Res. 2004, 64, 7647-7654
    • (2004) Cancer Res. , vol.64 , pp. 7647-7654
    • Venables, J.P.1
  • 21
    • 84868148842 scopus 로고    scopus 로고
    • Splicing factor mutations in myelodysplasia
    • Ogawa, S. Splicing factor mutations in myelodysplasia Int. J. Hematol. 2012, 96, 438-442
    • (2012) Int. J. Hematol. , vol.96 , pp. 438-442
    • Ogawa, S.1
  • 22
    • 84865861620 scopus 로고    scopus 로고
    • Spliceosome and other novel mutations in chronic lymphocytic leukemia and myeloid malignancies
    • Damm, F.; Nguyen-Khac, F.; Fontenay, M.; Bernard, O. A. Spliceosome and other novel mutations in chronic lymphocytic leukemia and myeloid malignancies Leukemia 2012, 26, 2027-2031
    • (2012) Leukemia , vol.26 , pp. 2027-2031
    • Damm, F.1    Nguyen-Khac, F.2    Fontenay, M.3    Bernard, O.A.4
  • 26
    • 84878061031 scopus 로고    scopus 로고
    • Chemical perturbation of Mcl-1 pre-mRNA splicing to induce apoptosis in cancer cells
    • Gao, Y.; Koide, K. Chemical perturbation of Mcl-1 pre-mRNA splicing to induce apoptosis in cancer cells ACS Chem. Biol. 2013, 8, 895-900
    • (2013) ACS Chem. Biol. , vol.8 , pp. 895-900
    • Gao, Y.1    Koide, K.2
  • 27
    • 78651417715 scopus 로고    scopus 로고
    • Structural requirements for the antiproliferative activity of pre-mRNA splicing inhibitor FR901464
    • Osman, S.; Albert, B. J.; Wang, Y.; Li, M.; Czaicki, N. L.; Koide, K. Structural requirements for the antiproliferative activity of pre-mRNA splicing inhibitor FR901464 Chem.-Eur. J. 2011, 17, 895-904
    • (2011) Chem. - Eur. J. , vol.17 , pp. 895-904
    • Osman, S.1    Albert, B.J.2    Wang, Y.3    Li, M.4    Czaicki, N.L.5    Koide, K.6
  • 28
    • 0034715459 scopus 로고    scopus 로고
    • Convergent assembly of chiral components prepared by asymmetric catalysis
    • Thompson, C. F.; Jamison, T. F.; Jacobsen, E. N. Convergent assembly of chiral components prepared by asymmetric catalysis J. Am. Chem. Soc. 2000, 122, 10482-10483
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 10482-10483
    • Thompson, C.F.1    Jamison, T.F.2    Jacobsen, E.N.3
  • 30
    • 0035904404 scopus 로고    scopus 로고
    • FR901464: Total synthesis, proof of structure, and evaluation of synthetic analogues
    • Thompson, C. F.; Jamison, T. F.; Jacobsen, E. N. FR901464: Total synthesis, proof of structure, and evaluation of synthetic analogues J. Am. Chem. Soc. 2001, 123, 9974-9983
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 9974-9983
    • Thompson, C.F.1    Jamison, T.F.2    Jacobsen, E.N.3
  • 31
    • 33644959352 scopus 로고    scopus 로고
    • Total synthesis of FR901464, an antitumor agent that regulates the transcription of oncogenes and tumor suppressor genes
    • Albert, B. J.; Sivaramakrishnan, A.; Naka, T.; Koide, K. Total synthesis of FR901464, an antitumor agent that regulates the transcription of oncogenes and tumor suppressor genes J. Am. Chem. Soc. 2006, 128, 2792-2793
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 2792-2793
    • Albert, B.J.1    Sivaramakrishnan, A.2    Naka, T.3    Koide, K.4
  • 32
    • 33847668813 scopus 로고    scopus 로고
    • Total syntheses, fragmentation studies, and antitumor/antiproliferative activities of FR901464 and its low picomolar analogue
    • Albert, B. J.; Sivaramakrishnan, A.; Naka, T.; Czaicki, N. L.; Koide, K. Total syntheses, fragmentation studies, and antitumor/antiproliferative activities of FR901464 and its low picomolar analogue J. Am. Chem. Soc. 2007, 129, 2648-2659
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 2648-2659
    • Albert, B.J.1    Sivaramakrishnan, A.2    Naka, T.3    Czaicki, N.L.4    Koide, K.5
  • 35
    • 79961049732 scopus 로고    scopus 로고
    • Sudemycins, novel small molecule analogues of FR901464, induce alternative gene splicing
    • Fan, L.; Lagisetti, C.; Edwards, C. C.; Webb, T. R.; Potter, P. M. Sudemycins, novel small molecule analogues of FR901464, induce alternative gene splicing ACS Chem. Biol. 2011, 6, 582-589
    • (2011) ACS Chem. Biol. , vol.6 , pp. 582-589
    • Fan, L.1    Lagisetti, C.2    Edwards, C.C.3    Webb, T.R.4    Potter, P.M.5
  • 36
    • 80052376000 scopus 로고    scopus 로고
    • Design, synthesis and initial biological evaluation of a novel pladienolide analog scaffold
    • Gundluru, M. K.; Pourpak, A.; Cui, X.; Morris, S. W.; Webb, T. R. Design, synthesis and initial biological evaluation of a novel pladienolide analog scaffold MedChemCommun 2011, 2, 904-908
    • (2011) MedChemCommun , vol.2 , pp. 904-908
    • Gundluru, M.K.1    Pourpak, A.2    Cui, X.3    Morris, S.W.4    Webb, T.R.5
  • 37
    • 69149091031 scopus 로고    scopus 로고
    • Predicting outcome in melanoma: Where are we now?
    • Jennings, L.; Murphy, G. M. Predicting outcome in melanoma: where are we now? Br. J. Dermatol. 2009, 161, 496-503
    • (2009) Br. J. Dermatol. , vol.161 , pp. 496-503
    • Jennings, L.1    Murphy, G.M.2
  • 39
    • 33746857820 scopus 로고    scopus 로고
    • Polymethylhydrosiloxane: A versatile reducing agent for organic synthesis
    • Lawrence, N. J.; Drew, M. D.; Bushell, S. M. Polymethylhydrosiloxane: A versatile reducing agent for organic synthesis J. Chem. Soc., Perkin Trans. 1 1999, 0, 3381-3391
    • (1999) J. Chem. Soc., Perkin Trans. 1 , vol.0 , pp. 3381-3391
    • Lawrence, N.J.1    Drew, M.D.2    Bushell, S.M.3
  • 40
    • 34848850746 scopus 로고    scopus 로고
    • An efficient, inexpensive, and shelf-stable diazotransfer reagent: Imidazole-1-sulfonyl azide hydrochloride
    • Goddard-Borger, E. D.; Stick, R. V. An efficient, inexpensive, and shelf-stable diazotransfer reagent: Imidazole-1-sulfonyl azide hydrochloride Org. Lett. 2007, 9, 3797-3800
    • (2007) Org. Lett. , vol.9 , pp. 3797-3800
    • Goddard-Borger, E.D.1    Stick, R.V.2
  • 42
    • 67650488269 scopus 로고    scopus 로고
    • Synergistic drug combinations tend to improve therapeutically relevant selectivity
    • Lehar, J.; Krueger, A. S.; Avery, W.; Heilbut, A. M.; Johansen, L. M.; Price, E. R.; Rickles, R. J.; Short, G. F., 3rd.; Staunton, J. E.; Jin, X.; Lee, M. S.; Zimmermann, G. R.; Borisy, A. A. Synergistic drug combinations tend to improve therapeutically relevant selectivity Nat. Biotechnol. 2009, 27, 659-666
    • (2009) Nat. Biotechnol. , vol.27 , pp. 659-666
    • Lehar, J.1    Krueger, A.S.2    Avery, W.3    Heilbut, A.M.4    Johansen, L.M.5    Price, E.R.6    Rickles, R.J.7
  • 44
    • 43049131769 scopus 로고    scopus 로고
    • Targeting the PI3K/Akt/mTOR pathway: Effective combinations and clinical considerations
    • LoPiccolo, J.; Blumenthal, G. M.; Bernstein, W. B.; Dennis, P. A. Targeting the PI3K/Akt/mTOR pathway: Effective combinations and clinical considerations Drug Resist. Updates 2008, 11, 32-50
    • (2008) Drug Resist. Updates , vol.11 , pp. 32-50
    • Lopiccolo, J.1    Blumenthal, G.M.2    Bernstein, W.B.3    Dennis, P.A.4
  • 45
    • 68849131434 scopus 로고    scopus 로고
    • Sorafenib has soluble epoxide hydrolase inhibitory activity, which contributes to its effect profile in vivo
    • Liu, J. Y.; Park, S. H.; Morisseau, C.; Hwang, S. H.; Hammock, B. D.; Weiss, R. H. Sorafenib has soluble epoxide hydrolase inhibitory activity, which contributes to its effect profile in vivo Mol. Cancer Ther. 2009, 8, 2193-2203
    • (2009) Mol. Cancer Ther. , vol.8 , pp. 2193-2203
    • Liu, J.Y.1    Park, S.H.2    Morisseau, C.3    Hwang, S.H.4    Hammock, B.D.5    Weiss, R.H.6
  • 46
    • 64249112966 scopus 로고    scopus 로고
    • Mammalian epoxide hydrolases in xenobiotic metabolism and signalling
    • Decker, M.; Arand, M.; Cronin, A. Mammalian epoxide hydrolases in xenobiotic metabolism and signalling Arch. Toxicol. 2009, 83, 297-318
    • (2009) Arch. Toxicol. , vol.83 , pp. 297-318
    • Decker, M.1    Arand, M.2    Cronin, A.3
  • 47
    • 0021118703 scopus 로고
    • Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors
    • Chou, T. C.; Talalay, P. Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors Adv. Enzyme Regul. 1984, 22, 27-55
    • (1984) Adv. Enzyme Regul. , vol.22 , pp. 27-55
    • Chou, T.C.1    Talalay, P.2
  • 48
    • 84875463958 scopus 로고    scopus 로고
    • The role of human carboxylesterases in drug metabolism: Have we overlooked their importance?
    • Laizure, S. C.; Herring, V.; Hu, Z.; Witbrodt, K.; Parker, R. B. The role of human carboxylesterases in drug metabolism: Have we overlooked their importance? Pharmacotherapy 2013, 33, 210-222
    • (2013) Pharmacotherapy , vol.33 , pp. 210-222
    • Laizure, S.C.1    Herring, V.2    Hu, Z.3    Witbrodt, K.4    Parker, R.B.5


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