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Volumn 4, Issue , 2013, Pages

Selective cancer targeting with prodrugs activated by histone deacetylases and a tumour-associated protease

Author keywords

[No Author keywords available]

Indexed keywords

BOC KAC PURO; HISTONE DEACETYLASE; PRODRUG; PROTEINASE; UNCLASSIFIED DRUG;

EID: 84889256327     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms3735     Document Type: Article
Times cited : (80)

References (40)
  • 1
    • 61849144810 scopus 로고    scopus 로고
    • HDAC family: What are the cancer relevant targets?
    • Witt, O., Deubzer, H. E., Milde, T. &Oehme, I. HDAC family: what are the cancer relevant targets? Cancer Lett. 277, 8-21 (2009).
    • (2009) Cancer Lett , vol.277 , pp. 8-21
    • Witt, O.1    Deubzer, H.E.2    Milde, T.3    Oehme, I.4
  • 3
    • 33748451151 scopus 로고    scopus 로고
    • Anticancer activities of histone deacetylase inhibitors
    • Bolden, J. E., Peart, M. J. &Johnstone, R. W. Anticancer activities of histone deacetylase inhibitors. Nat. Rev. Drug Discov. 5, 769-784 (2006).
    • (2006) Nat. Rev. Drug Discov , vol.5 , pp. 769-784
    • Bolden, J.E.1    Peart, M.J.2    Johnstone, R.W.3
  • 4
    • 30344477367 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer
    • Minucci, S. &Pelicci, P. G. Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer. Nat. Rev. Cancer 6, 38-51 (2006).
    • (2006) Nat. Rev. Cancer , vol.6 , pp. 38-51
    • Minucci, S.1    Pelicci, P.G.2
  • 5
    • 67650090545 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: Potential in cancer therapy
    • Marks, P. A. &Xu, W. S. Histone deacetylase inhibitors: Potential in cancer therapy. J. Cell Biochem. 107, 600-608 (2009).
    • (2009) J. Cell Biochem , vol.107 , pp. 600-608
    • Marks, P.A.1    Xu, W.S.2
  • 6
    • 79952262759 scopus 로고    scopus 로고
    • Histone deacetylase (HDAC) inhibitors in recent clinical trials for cancer therapy
    • Wagner, J. M., Hackanson, B., Lubbert, M. &Jung, M. Histone deacetylase (HDAC) inhibitors in recent clinical trials for cancer therapy. Clin. Epigenet. 1, 117-136 (2010).
    • (2010) Clin. Epigenet. , vol.1 , pp. 117-136
    • Wagner, J.M.1    Hackanson, B.2    Lubbert, M.3    Jung, M.4
  • 7
    • 77957091318 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor induces DNA damage, which normal but not transformed cells can repair
    • Lee, J. H., Choy, M. L., Ngo, L., Foster, S. S. &Marks, P. A. Histone deacetylase inhibitor induces DNA damage, which normal but not transformed cells can repair. Proc. Natl Acad. Sci. USA 107, 14639-14644 (2010).
    • (2010) Proc. Natl Acad. Sci. USA , vol.107 , pp. 14639-14644
    • Lee, J.H.1    Choy, M.L.2    Ngo, L.3    Foster, S.S.4    Marks, P.A.5
  • 8
    • 78249276172 scopus 로고    scopus 로고
    • Hdac3 is essential for the maintenance of chromatin structure and genome stability
    • Bhaskara, S. et al. Hdac3 is essential for the maintenance of chromatin structure and genome stability. Cancer Cell 18, 436-447 (2010).
    • (2010) Cancer Cell , vol.18 , pp. 436-447
    • Bhaskara, S.1
  • 9
    • 2342603891 scopus 로고    scopus 로고
    • Cathepsin cysteine proteases are effectors of invasive growth and angiogenesis during multistage tumorigenesis
    • Joyce, J. A. et al. Cathepsin cysteine proteases are effectors of invasive growth and angiogenesis during multistage tumorigenesis. Cancer Cell 5, 443-453 (2004).
    • (2004) Cancer Cell , vol.5 , pp. 443-453
    • Joyce, J.A.1
  • 10
    • 10044296973 scopus 로고    scopus 로고
    • Cysteine cathepsins in human cancer
    • Jedeszko, C. &Sloane, B. F. Cysteine cathepsins in human cancer. Biol. Chem. 385, 1017-1027 (2004).
    • (2004) Biol. Chem , vol.385 , pp. 1017-1027
    • Jedeszko, C.1    Sloane, B.F.2
  • 11
    • 80155174987 scopus 로고    scopus 로고
    • A new pathway that regulates 53BP1 stability implicates cathepsin L and vitamin D in DNA repair
    • Gonzalez-Suarez, I. et al. A new pathway that regulates 53BP1 stability implicates cathepsin L and vitamin D in DNA repair. EMBO J. 30, 3383-3396 (2011).
    • (2011) EMBO J , vol.30 , pp. 3383-3396
    • Gonzalez-Suarez, I.1
  • 12
    • 4544286160 scopus 로고    scopus 로고
    • Enhanced cathepsin L expression is mediated by different Ras effector pathways in fibroblasts and epithelial cells
    • Collette, J., Ulku, A. S., Der, C. J., Jones, A. &Erickson, A. H. Enhanced cathepsin L expression is mediated by different Ras effector pathways in fibroblasts and epithelial cells. Int. J. Cancer 112, 190-199 (2004).
    • (2004) Int. J. Cancer , vol.112 , pp. 190-199
    • Collette, J.1    Ulku, A.S.2    Der, C.J.3    Jones, A.4    Erickson, A.H.5
  • 13
    • 0023610145 scopus 로고
    • Cysteine proteinase cathepsin L expression correlates closely with the metastatic potential of H-ras-transformed murine fibroblasts
    • Denhardt, D. T., Greenberg, A. H., Egan, S. E., Hamilton, R. T. &Wright, J. A. Cysteine proteinase cathepsin L expression correlates closely with the metastatic potential of H-ras-transformed murine fibroblasts. Oncogene 2, 55-59 (1987).
    • (1987) Oncogene , vol.2 , pp. 55-59
    • Denhardt, D.T.1    Greenberg, A.H.2    Egan, S.E.3    Hamilton, T.R.4    Wright, J.A.5
  • 14
    • 0024008084 scopus 로고
    • Complete nucleotide and deduced amino acid sequences of human and murine preprocathepsin L An abundant transcript induced by transformation of fibroblasts
    • Joseph, L. J., Chang, L. C., Stamenkovich, D. &Sukhatme, V. P. Complete nucleotide and deduced amino acid sequences of human and murine preprocathepsin L. An abundant transcript induced by transformation of fibroblasts. J. Clin. Invest. 81, 1621-1629 (1988).
    • (1988) J. Clin. Invest , vol.81 , pp. 1621-1629
    • Joseph, L.J.1    Chang, L.C.2    Stamenkovich, D.3    Sukhatme, V.P.4
  • 15
    • 80052805542 scopus 로고    scopus 로고
    • Quantitative glycoproteomic analysis of optimal cutting temperature-embedded frozen tissues identifying glycoproteins associated with aggressive prostate cancer
    • Tian, Y., Bova, G. S. &Zhang, H. Quantitative glycoproteomic analysis of optimal cutting temperature-embedded frozen tissues identifying glycoproteins associated with aggressive prostate cancer. Anal. Chem. 83, 7013-7019 (2011).
    • (2011) Anal. Chem , vol.83 , pp. 7013-7019
    • Tian, Y.1    Bova, G.S.2    Zhang, H.3
  • 16
    • 84873050707 scopus 로고    scopus 로고
    • BRCA1 loss activates cathepsin L-mediated degradation of 53BP1 in breast cancer cells
    • Grotsky, D. A. et al. BRCA1 loss activates cathepsin L-mediated degradation of 53BP1 in breast cancer cells. J. Cell Biol. 200, 187-202 (2013).
    • (2013) J. Cell Biol , vol.200 , pp. 187-202
    • Grotsky, D.A.1
  • 17
    • 1942470581 scopus 로고    scopus 로고
    • A cathepsin L isoform that is devoid of a signal peptide localizes to the nucleus in S phase and processes the CDP/Cux transcription factor
    • Goulet, B. et al. A cathepsin L isoform that is devoid of a signal peptide localizes to the nucleus in S phase and processes the CDP/Cux transcription factor. Mol. Cell 14, 207-219 (2004).
    • (2004) Mol. Cell , vol.14 , pp. 207-219
    • Goulet, B.1
  • 18
    • 34548689404 scopus 로고    scopus 로고
    • Increased expression and activity of nuclear cathepsin L in cancer cells suggests a novel mechanism of cell transformation
    • Goulet, B. et al. Increased expression and activity of nuclear cathepsin L in cancer cells suggests a novel mechanism of cell transformation. Mol. Cancer Res. 5, 899-907 (2007).
    • (2007) Mol. Cancer Res , vol.5 , pp. 899-907
    • Goulet, B.1
  • 19
    • 53549094681 scopus 로고    scopus 로고
    • Cathepsin L proteolytically processes histone H3 during mouse embryonic stem cell differentiation
    • Duncan, E. M. et al. Cathepsin L proteolytically processes histone H3 during mouse embryonic stem cell differentiation. Cell 135, 284-294 (2008).
    • (2008) Cell , vol.135 , pp. 284-294
    • Duncan, E.M.1
  • 20
    • 75549088309 scopus 로고    scopus 로고
    • Cathepsin L, target in cancer treatment?
    • Lankelma, J. M. et al. Cathepsin L, target in cancer treatment? Life Sci. 86, 225-233 (2010).
    • (2010) Life Sci , vol.86 , pp. 225-233
    • Lankelma, J.M.1
  • 21
    • 0141570564 scopus 로고    scopus 로고
    • Role of class i and class II histone deacetylases in carcinoma cells using siRNA
    • Glaser, K. B. et al. Role of class I and class II histone deacetylases in carcinoma cells using siRNA. Biochem. Biophys. Res. Commun. 310, 529-536 (2003).
    • (2003) Biochem. Biophys. Res. Commun , vol.310 , pp. 529-536
    • Glaser, K.B.1
  • 22
    • 2342603414 scopus 로고    scopus 로고
    • Induction of HDAC2 expression upon loss of APC in colorectal tumorigenesis
    • Zhu, P. et al. Induction of HDAC2 expression upon loss of APC in colorectal tumorigenesis. Cancer Cell 5, 455-463 (2004).
    • (2004) Cancer Cell , vol.5 , pp. 455-463
    • Zhu, P.1
  • 23
    • 33744956666 scopus 로고    scopus 로고
    • Histone deacetylase 3 (HDAC3) and other class i HDACs regulate colon cell maturation and p21 expression and are deregulated in human colon cancer
    • Wilson, A. J. et al. Histone deacetylase 3 (HDAC3) and other class I HDACs regulate colon cell maturation and p21 expression and are deregulated in human colon cancer. J. Biol. Chem. 281, 13548-13558 (2006).
    • (2006) J. Biol. Chem , vol.281 , pp. 13548-13558
    • Wilson, A.J.1
  • 25
    • 0037063176 scopus 로고    scopus 로고
    • Novel colon cancer cell lines leading to better understanding of the diversity of respective primary cancers
    • Vecsey-Semjen, B. et al. Novel colon cancer cell lines leading to better understanding of the diversity of respective primary cancers. Oncogene 21, 4646-4662 (2002).
    • (2002) Oncogene , vol.21 , pp. 4646-4662
    • Vecsey-Semjen, B.1
  • 26
    • 0029662049 scopus 로고    scopus 로고
    • TGF-beta1 and Ha-Ras collaborate in modulating the phenotypic plasticity and invasiveness of epithelial tumor cells
    • Oft, M. et al. TGF-beta1 and Ha-Ras collaborate in modulating the phenotypic plasticity and invasiveness of epithelial tumor cells. Genes Dev. 10, 2462-2477 (1996).
    • (1996) Genes Dev , vol.10 , pp. 2462-2477
    • Oft, M.1
  • 27
    • 0024996768 scopus 로고
    • Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A
    • Yoshida, M., Kijima, M., Akita, M. &Beppu, T. Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A. J. Biol. Chem. 265, 17174-17179 (1990).
    • (1990) J. Biol. Chem , vol.265 , pp. 17174-17179
    • Yoshida, M.1    Kijima, M.2    Akita, M.3    Beppu, T.4
  • 28
    • 0035126973 scopus 로고    scopus 로고
    • Resistance to butyrate-induced cell differentiation and apoptosis during spontaneous Caco-2 cell differentiation
    • Mariadason, J. M., Velcich, A., Wilson, A. J., Augenlicht, L. H. &Gibson, P. R. Resistance to butyrate-induced cell differentiation and apoptosis during spontaneous Caco-2 cell differentiation. Gastroenterology 120, 889-899 (2001).
    • (2001) Gastroenterology , vol.120 , pp. 889-899
    • Mariadason, J.M.1    Velcich, A.2    Wilson, A.J.3    Augenlicht, L.H.4    Gibson, P.R.5
  • 29
    • 0037253808 scopus 로고    scopus 로고
    • A fluorogenic histone deacetylase assay well suited for high-throughput activity screening
    • Wegener, D., Wirsching, F., Riester, D. &Schwienhorst, A. A fluorogenic histone deacetylase assay well suited for high-throughput activity screening. Chem. Biol. 10, 61-68 (2003).
    • (2003) Chem. Biol , vol.10 , pp. 61-68
    • Wegener, D.1    Wirsching, F.2    Riester, D.3    Schwienhorst, A.4
  • 30
    • 50349087906 scopus 로고    scopus 로고
    • Evaluation of the pharmacodynamic effects of MGCD0103 from preclinical models to human using a novel HDAC enzyme assay
    • Bonfils, C. et al. Evaluation of the pharmacodynamic effects of MGCD0103 from preclinical models to human using a novel HDAC enzyme assay. Clin. Cancer Res. 14, 3441-3449 (2008).
    • (2008) Clin. Cancer Res , vol.14 , pp. 3441-3449
    • Bonfils, C.1
  • 31
    • 37849019672 scopus 로고    scopus 로고
    • Determination of the class and isoform selectivity of smallmolecule histone deacetylase inhibitors
    • Khan, N. et al. Determination of the class and isoform selectivity of smallmolecule histone deacetylase inhibitors. Biochem. J. 409, 581-589 (2008).
    • (2008) Biochem. J , vol.409 , pp. 581-589
    • Khan, N.1
  • 32
    • 72549086620 scopus 로고    scopus 로고
    • JNJ-26481585, a novel second-generation oral histone deacetylase inhibitor, shows broad-spectrum preclinical antitumoral activity
    • Arts, J. et al. JNJ-26481585, a novel second-generation oral histone deacetylase inhibitor, shows broad-spectrum preclinical antitumoral activity. Clin. Cancer Res. 15, 6841-6851 (2009).
    • (2009) Clin. Cancer Res , vol.15 , pp. 6841-6851
    • Arts, J.1
  • 33
    • 67650083046 scopus 로고    scopus 로고
    • Selective class II HDAC inhibitors impair myogenesis by modulating the stability and activity of HDAC-MEF2 complexes
    • Nebbioso, A. et al. Selective class II HDAC inhibitors impair myogenesis by modulating the stability and activity of HDAC-MEF2 complexes. EMBO Rep. 10, 776-782 (2009).
    • (2009) EMBO Rep , vol.10 , pp. 776-782
    • Nebbioso, A.1
  • 34
    • 0022596895 scopus 로고
    • Expression in mammalian cells of a gene from Streptomyces alboniger conferring puromycin resistance
    • Vara, J. A., Portela, A., Ortin, J. &Jimenez, A. Expression in mammalian cells of a gene from Streptomyces alboniger conferring puromycin resistance. Nucleic Acids Res. 14, 4617-4624 (1986).
    • (1986) Nucleic Acids Res , vol.14 , pp. 4617-4624
    • Vara, J.A.1    Portela, A.2    Ortin, J.3    Jimenez, A.4
  • 35
    • 0015502063 scopus 로고
    • Studies on transfer ribonucleic acid-ribosome complexes XXI. Effect of antibiotics on peptidylpuromycin synthesis by mammalian polyribosomes
    • Pestka, S., Rosenfeld, H., Harris, R. &Hintikka, H. Studies on transfer ribonucleic acid-ribosome complexes. XXI. Effect of antibiotics on peptidylpuromycin synthesis by mammalian polyribosomes. J. Biol. Chem. 247, 6895-6900 (1972).
    • (1972) J. Biol. Chem , vol.247 , pp. 6895-6900
    • Pestka, S.1    Rosenfeld, H.2    Harris, R.3    Hintikka, H.4
  • 36
    • 63949084607 scopus 로고    scopus 로고
    • SUnSET, a nonradioactive method to monitor protein synthesis
    • Schmidt, E. K., Clavarino, G., Ceppi, M. &Pierre, P. SUnSET, a nonradioactive method to monitor protein synthesis. Nat. Methods 6, 275-277 (2009).
    • (2009) Nat. Methods , vol.6 , pp. 275-277
    • Schmidt, E.K.1    Clavarino, G.2    Ceppi, M.3    Pierre, P.4
  • 37
    • 70949086288 scopus 로고    scopus 로고
    • Synthesis, crystallization, and biological evaluation of an orally active prodrug of gemcitabine
    • Bender, D. M. et al. Synthesis, crystallization, and biological evaluation of an orally active prodrug of gemcitabine. J. Med. Chem. 52, 6958-6961 (2009).
    • (2009) J. Med. Chem , vol.52 , pp. 6958-6961
    • Bender, D.M.1
  • 38
    • 33745644988 scopus 로고    scopus 로고
    • Enhanced cellular uptake of Ara-C via a peptidomimetic prodrug, L-valyl-ara-C in Caco-2 cells
    • Cheon, E. P., Hong, J. H. &Han, H. K. Enhanced cellular uptake of Ara-C via a peptidomimetic prodrug, L-valyl-ara-C in Caco-2 cells. J. Pharm. Pharmacol. 58, 927-932 (2006).
    • (2006) J. Pharm. Pharmacol , vol.58 , pp. 927-932
    • Cheon, E.P.1    Hong, J.H.2    Han, H.K.3
  • 39
    • 84873076698 scopus 로고    scopus 로고
    • Imaging of protein synthesis: In vitro and in vivo evaluation of 44)Sc-DOTA-puromycin
    • Eigner, S. et al. Imaging of protein synthesis: in vitro and in vivo evaluation of (44)Sc-DOTA-puromycin. Mol. Imaging Biol. 15, 79-86 (2013).
    • (2013) Mol. Imaging Biol. , vol.15 , pp. 79-86
    • Eigner, S.1
  • 40
    • 3342935872 scopus 로고    scopus 로고
    • A general approach to detect protein expression in vivo using fluorescent puromycin conjugates
    • Starck, S. R., Green, H. M., Alberola-Ila, J. &Roberts, R. W. A general approach to detect protein expression in vivo using fluorescent puromycin conjugates. Chem. Biol. 11, 999-1008 (2004).
    • (2004) Chem. Biol , vol.11 , pp. 999-1008
    • Starck, S.R.1    Green, H.M.2    Alberola-Ila, J.3    Roberts, R.W.4


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