E. Olsen, Y. H. Kim, T. Kuzel et T. R. Pacheco, « Vorinostat (suberoylanilide hydroxamic acid, SAHA) is clinically active in advanced cutaneous T-cell lymphoma (CTCL): Results of a phase IIb trial », Journal of Clinical Oncology, vol. 24, no 18_suppl, , p. 7500–7500 (ISSN0732-183X, DOI10.1200/jco.2006.24.18_suppl.7500, lire en ligne, consulté le )
doi.org
dx.doi.org
Paul A. Marks et Ronald Breslow, « Dimethyl sulfoxide to vorinostat: development of this histone deacetylase inhibitor as an anticancer drug », Nature Biotechnology, vol. 25, no 1, , p. 84–90 (ISSN1087-0156, PMID17211407, DOI10.1038/nbt1272, lire en ligne, consulté le )
M. S. Finnin, J. R. Donigian, A. Cohen et V. M. Richon, « Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors », Nature, vol. 401, no 6749, , p. 188–193 (ISSN0028-0836, PMID10490031, DOI10.1038/43710, lire en ligne, consulté le )
E. Olsen, Y. H. Kim, T. Kuzel et T. R. Pacheco, « Vorinostat (suberoylanilide hydroxamic acid, SAHA) is clinically active in advanced cutaneous T-cell lymphoma (CTCL): Results of a phase IIb trial », Journal of Clinical Oncology, vol. 24, no 18_suppl, , p. 7500–7500 (ISSN0732-183X, DOI10.1200/jco.2006.24.18_suppl.7500, lire en ligne, consulté le )
Nancie M. Archin, Amy Espeseth, Daniel Parker et Manzoor Cheema, « Expression of latent HIV induced by the potent HDAC inhibitor suberoylanilide hydroxamic acid », AIDS research and human retroviruses, vol. 25, no 2, , p. 207–212 (ISSN1931-8405, PMID19239360, PMCIDPMC2853863, DOI10.1089/aid.2008.0191, lire en ligne, consulté le )
(en) V. M. Richon, « Cancer biology: mechanism of antitumour action of vorinostat (suberoylanilide hydroxamic acid), a novel histone deacetylase inhibitor », British Journal of Cancer, vol. 95, , S2–S6 (ISSN0007-0920, DOI10.1038/sj.bjc.6603463, lire en ligne, consulté le )
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C. Friend, M. C. Patuleia et E. De Harven, « Erythrocytic maturation in vitro of murine (Friend) virus-induced leukemic cells », National Cancer Institute Monograph, vol. 22, , p. 505–522 (ISSN0083-1921, PMID5923328, lire en ligne, consulté le )
Charlotte Friend, William Scher, J. G. Holland et Toru Sato, « Hemoglobin Synthesis in Murine Virus-Induced Leukemic Cells In Vitro: Stimulation of Erythroid Differentiation by Dimethyl Sulfoxide », Proceedings of the National Academy of Sciences of the United States of America, vol. 68, no 2, , p. 378–382 (ISSN0027-8424, PMID5277089, lire en ligne, consulté le )
Paul A. Marks et Ronald Breslow, « Dimethyl sulfoxide to vorinostat: development of this histone deacetylase inhibitor as an anticancer drug », Nature Biotechnology, vol. 25, no 1, , p. 84–90 (ISSN1087-0156, PMID17211407, DOI10.1038/nbt1272, lire en ligne, consulté le )
M. Tanaka, J. Levy, M. Terada et R. Breslow, « Induction of erythroid differentiation in murine virus infected eythroleukemia cells by highly polar compounds », Proceedings of the National Academy of Sciences of the United States of America, vol. 72, no 3, , p. 1003–1006 (ISSN0027-8424, PMID165480, lire en ligne, consulté le )
R C Reuben, R L Wife, R Breslow et R A Rifkind, « A new group of potent inducers of differentiation in murine erythroleukemia cells. », Proceedings of the National Academy of Sciences of the United States of America, vol. 73, no 3, , p. 862–866 (ISSN0027-8424, PMID1062798, lire en ligne, consulté le )
V. M. Richon, R. G. Ramsay, R. A. Rifkind et P. A. Marks, « Modulation of the c-myb, c-myc and p53 mRNA and protein levels during induced murine erythroleukemia cell differentiation », Oncogene, vol. 4, no 2, , p. 165–173 (ISSN0950-9232, PMID2648254, lire en ligne, consulté le )
P. A. Marks, M. Sheffery et R. A. Rifkind, « Induction of transformed cells to terminal differentiation and the modulation of gene expression », Cancer Research, vol. 47, no 3, , p. 659–666 (ISSN0008-5472, PMID3542191, lire en ligne, consulté le )
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V. M. Richon, Y. Webb, R. Merger et T. Sheppard, « Second generation hybrid polar compounds are potent inducers of transformed cell differentiation », Proceedings of the National Academy of Sciences of the United States of America, vol. 93, no 12, , p. 5705–5708 (ISSN0027-8424, PMID8650156, lire en ligne, consulté le )
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M. S. Finnin, J. R. Donigian, A. Cohen et V. M. Richon, « Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors », Nature, vol. 401, no 6749, , p. 188–193 (ISSN0028-0836, PMID10490031, DOI10.1038/43710, lire en ligne, consulté le )
E. Olsen, Y. H. Kim, T. Kuzel et T. R. Pacheco, « Vorinostat (suberoylanilide hydroxamic acid, SAHA) is clinically active in advanced cutaneous T-cell lymphoma (CTCL): Results of a phase IIb trial », Journal of Clinical Oncology, vol. 24, no 18_suppl, , p. 7500–7500 (ISSN0732-183X, DOI10.1200/jco.2006.24.18_suppl.7500, lire en ligne, consulté le )
Nancie M. Archin, Amy Espeseth, Daniel Parker et Manzoor Cheema, « Expression of latent HIV induced by the potent HDAC inhibitor suberoylanilide hydroxamic acid », AIDS research and human retroviruses, vol. 25, no 2, , p. 207–212 (ISSN1931-8405, PMID19239360, PMCIDPMC2853863, DOI10.1089/aid.2008.0191, lire en ligne, consulté le )
(en) V. M. Richon, « Cancer biology: mechanism of antitumour action of vorinostat (suberoylanilide hydroxamic acid), a novel histone deacetylase inhibitor », British Journal of Cancer, vol. 95, , S2–S6 (ISSN0007-0920, DOI10.1038/sj.bjc.6603463, lire en ligne, consulté le )
Oscar Moradei, Christiane R. Maroun, Isabelle Paquin et Arkadii Vaisburg, « Histone deacetylase inhibitors: latest developments, trends and prospects », Current Medicinal Chemistry. Anti-Cancer Agents, vol. 5, no 5, , p. 529–560 (ISSN1568-0118, PMID16178777, lire en ligne, consulté le )
nature.com
(en) V. M. Richon, « Cancer biology: mechanism of antitumour action of vorinostat (suberoylanilide hydroxamic acid), a novel histone deacetylase inhibitor », British Journal of Cancer, vol. 95, , S2–S6 (ISSN0007-0920, DOI10.1038/sj.bjc.6603463, lire en ligne, consulté le )
nih.gov
ncbi.nlm.nih.gov
C. Friend, M. C. Patuleia et E. De Harven, « Erythrocytic maturation in vitro of murine (Friend) virus-induced leukemic cells », National Cancer Institute Monograph, vol. 22, , p. 505–522 (ISSN0083-1921, PMID5923328, lire en ligne, consulté le )
Charlotte Friend, William Scher, J. G. Holland et Toru Sato, « Hemoglobin Synthesis in Murine Virus-Induced Leukemic Cells In Vitro: Stimulation of Erythroid Differentiation by Dimethyl Sulfoxide », Proceedings of the National Academy of Sciences of the United States of America, vol. 68, no 2, , p. 378–382 (ISSN0027-8424, PMID5277089, lire en ligne, consulté le )
Paul A. Marks et Ronald Breslow, « Dimethyl sulfoxide to vorinostat: development of this histone deacetylase inhibitor as an anticancer drug », Nature Biotechnology, vol. 25, no 1, , p. 84–90 (ISSN1087-0156, PMID17211407, DOI10.1038/nbt1272, lire en ligne, consulté le )
M. Tanaka, J. Levy, M. Terada et R. Breslow, « Induction of erythroid differentiation in murine virus infected eythroleukemia cells by highly polar compounds », Proceedings of the National Academy of Sciences of the United States of America, vol. 72, no 3, , p. 1003–1006 (ISSN0027-8424, PMID165480, lire en ligne, consulté le )
R C Reuben, R L Wife, R Breslow et R A Rifkind, « A new group of potent inducers of differentiation in murine erythroleukemia cells. », Proceedings of the National Academy of Sciences of the United States of America, vol. 73, no 3, , p. 862–866 (ISSN0027-8424, PMID1062798, lire en ligne, consulté le )
V. M. Richon, R. G. Ramsay, R. A. Rifkind et P. A. Marks, « Modulation of the c-myb, c-myc and p53 mRNA and protein levels during induced murine erythroleukemia cell differentiation », Oncogene, vol. 4, no 2, , p. 165–173 (ISSN0950-9232, PMID2648254, lire en ligne, consulté le )
P. A. Marks, M. Sheffery et R. A. Rifkind, « Induction of transformed cells to terminal differentiation and the modulation of gene expression », Cancer Research, vol. 47, no 3, , p. 659–666 (ISSN0008-5472, PMID3542191, lire en ligne, consulté le )
M. Andreeff, R. Stone, J. Michaeli et C. W. Young, « Hexamethylene bisacetamide in myelodysplastic syndrome and acute myelogenous leukemia: a phase II clinical trial with a differentiation-inducing agent », Blood, vol. 80, no 10, , p. 2604–2609 (ISSN0006-4971, PMID1421378, lire en ligne, consulté le )
V. M. Richon, Y. Webb, R. Merger et T. Sheppard, « Second generation hybrid polar compounds are potent inducers of transformed cell differentiation », Proceedings of the National Academy of Sciences of the United States of America, vol. 93, no 12, , p. 5705–5708 (ISSN0027-8424, PMID8650156, lire en ligne, consulté le )
M. Yoshida, M. Kijima, M. Akita et T. Beppu, « Potent and specific inhibition of mammalian histone deacetylase both in vivo and in vitro by trichostatin A », The Journal of Biological Chemistry, vol. 265, no 28, , p. 17174–17179 (ISSN0021-9258, PMID2211619, lire en ligne, consulté le )
V. M. Richon, S. Emiliani, E. Verdin et Y. Webb, « A class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases », Proceedings of the National Academy of Sciences of the United States of America, vol. 95, no 6, , p. 3003–3007 (ISSN0027-8424, PMID9501205, lire en ligne, consulté le )
M. S. Finnin, J. R. Donigian, A. Cohen et V. M. Richon, « Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors », Nature, vol. 401, no 6749, , p. 188–193 (ISSN0028-0836, PMID10490031, DOI10.1038/43710, lire en ligne, consulté le )
Nancie M. Archin, Amy Espeseth, Daniel Parker et Manzoor Cheema, « Expression of latent HIV induced by the potent HDAC inhibitor suberoylanilide hydroxamic acid », AIDS research and human retroviruses, vol. 25, no 2, , p. 207–212 (ISSN1931-8405, PMID19239360, PMCIDPMC2853863, DOI10.1089/aid.2008.0191, lire en ligne, consulté le )
Oscar Moradei, Christiane R. Maroun, Isabelle Paquin et Arkadii Vaisburg, « Histone deacetylase inhibitors: latest developments, trends and prospects », Current Medicinal Chemistry. Anti-Cancer Agents, vol. 5, no 5, , p. 529–560 (ISSN1568-0118, PMID16178777, lire en ligne, consulté le )
pubmed.ncbi.nlm.nih.gov
C. Friend, M. C. Patuleia et E. De Harven, « Erythrocytic maturation in vitro of murine (Friend) virus-induced leukemic cells », National Cancer Institute Monograph, vol. 22, , p. 505–522 (ISSN0083-1921, PMID5923328, lire en ligne, consulté le )