-
1
-
-
4143141823
-
The immunobiology of cancer immunosurveillance and immunoediting
-
Dunn GP, Old LJ, Schreiber RD. The immunobiology of cancer immunosurveillance and immunoediting. Immunity 2004;21:137-48.
-
(2004)
Immunity
, vol.21
, pp. 137-148
-
-
Dunn, G.P.1
Old, L.J.2
Schreiber, R.D.3
-
3
-
-
41149132390
-
Indoleamine 2,3-dioxygenase in T-cell tolerance and tumoral immune escape
-
Katz JB, Muller AJ, Metz R, Prendergast GC. Indoleamine 2,3-dioxygenase in T-cell tolerance and tumoral immune escape. Immunol Rev 2008;222:206-21.
-
(2008)
Immunol Rev
, vol.222
, pp. 206-221
-
-
Katz, J.B.1
Muller, A.J.2
Metz, R.3
Prendergast, G.C.4
-
4
-
-
46249124461
-
Immune escape as a fundamental trait of cancer: Focus on IDO
-
Prendergast GC. Immune escape as a fundamental trait of cancer: focus on IDO. Oncogene 2008;27:3889-900.
-
(2008)
Oncogene
, vol.27
, pp. 3889-3900
-
-
Prendergast, G.C.1
-
5
-
-
33644649659
-
Indoleamine 2,3-dioxygenase, tumor-induced tolerance and counter-regulation
-
Munn DH. Indoleamine 2,3-dioxygenase, tumor-induced tolerance and counter-regulation. Curr Opin Immunol 2006;18:220-5.
-
(2006)
Curr Opin Immunol
, vol.18
, pp. 220-225
-
-
Munn, D.H.1
-
6
-
-
46749110831
-
+ regulatory T cells is dependent on expression of heme oxygenase-1 in antigen-presenting cells
-
+ regulatory T cells is dependent on expression of heme oxygenase-1 in antigen-presenting cells. Am J Pathol 2008;173:154-60.
-
(2008)
Am J Pathol
, vol.173
, pp. 154-160
-
-
George, J.F.1
Braun, A.2
Brusko, T.M.3
-
7
-
-
70149101645
-
IDO activates regulatory T cells and blocks their conversion into Th17-like T cells
-
Baban B, Chandler PR, Sharma MD, et al. IDO activates regulatory T cells and blocks their conversion into Th17-like T cells. J Immunol 2009;183:2475-83.
-
(2009)
J Immunol
, vol.183
, pp. 2475-2483
-
-
Baban, B.1
Chandler, P.R.2
Sharma, M.D.3
-
8
-
-
0038418359
-
In vivo antitumor activity of pegylated zinc protoporphyrin: Targeted inhibition of heme oxygenase in solid tumor
-
Fang J, Sawa T, Akaike T, et al. In vivo antitumor activity of pegylated zinc protoporphyrin: targeted inhibition of heme oxygenase in solid tumor. Cancer Res 2003;63:3567-74.
-
(2003)
Cancer Res
, vol.63
, pp. 3567-3574
-
-
Fang, J.1
Sawa, T.2
Akaike, T.3
-
9
-
-
0842308157
-
Enhancement of chemotherapeutic response of tumor cells by a heme oxygenase inhibitor, pegylated zinc protoporphyrin
-
DOI 10.1002/ijc.11644
-
Fang J, Sawa T, Akaike T, Greish K, Maeda H. Enhancement of chemotherapeutic response of tumor cells by a heme oxygenase inhibitor, pegylated zinc protoporphyrin. Int J Cancer 2004;109:1-8. (Pubitemid 38165358)
-
(2004)
International Journal of Cancer
, vol.109
, Issue.1
, pp. 1-8
-
-
Fang, J.1
Sawa, T.2
Akaike, T.3
Greish, K.4
Maeda, H.5
-
10
-
-
33845696649
-
Inhibition of heme oxygenase-1 by zinc protoporphyrin IX reduces tumor growth of LL/2 lung cancer in C57BL mice
-
DOI 10.1002/ijc.22287
-
Hirai K, Sasahira T, Ohmori H, Fujii K, Kuniyasu H. Inhibition of heme oxygenase-1 by zinc protoporphyrin IX reduces tumor growth of LL/2 lung cancer in C57BL mice. Int J Cancer 2007;120:500-5. (Pubitemid 44969019)
-
(2007)
International Journal of Cancer
, vol.120
, Issue.3
, pp. 500-505
-
-
Hirai, K.1
Sasahira, T.2
Ohmori, H.3
Fujii, K.4
Kuniyasu, H.5
-
11
-
-
48249155029
-
Zinc protoporphyrin IX, a heme oxygenase-1 inhibitor, demonstrates potent antitumor effects but is unable to potentiate antitumor effects of chemotherapeutics in mice
-
Nowis D, Bugajski M, Winiarska M, et al. Zinc protoporphyrin IX, a heme oxygenase-1 inhibitor, demonstrates potent antitumor effects but is unable to potentiate antitumor effects of chemotherapeutics in mice. BMC Cancer 2008;8:197.
-
(2008)
BMC Cancer
, vol.8
, pp. 197
-
-
Nowis, D.1
Bugajski, M.2
Winiarska, M.3
-
12
-
-
34547643025
-
Novel tryptophan catabolic enzyme IDO2 is the preferred biochemical target of the antitumor IDO inhibitory compound D-1MT
-
Metz R, DuHadaway JB, Kamasani U, Laury-Kleintop L, Muller AJ, Prendergast GC. Novel tryptophan catabolic enzyme IDO2 is the preferred biochemical target of the antitumor IDO inhibitory compound D-1MT. Cancer Res 2007;67:7082-7.
-
(2007)
Cancer Res
, vol.67
, pp. 7082-7087
-
-
Metz, R.1
Duhadaway, J.B.2
Kamasani, U.3
Laury-Kleintop, L.4
Muller, A.J.5
Prendergast, G.C.6
-
13
-
-
31544482454
-
Structure-activity study of brassinin derivatives as indoleamine 2,3-dioxygenase inhibitors
-
DOI 10.1021/jm0508888
-
Gaspari P, Banerjee T, Malachowski WP, et al. Structure-activity study of brassinin derivatives as indoleamine 2,3-dioxygenase inhibitors. J Med Chem 2006;49:684-92. (Pubitemid 43157498)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.2
, pp. 684-692
-
-
Gaspari, P.1
Banerjee, T.2
Malachowski, W.P.3
Muller, A.J.4
Prendergast, G.C.5
Duhadaway, J.6
Bennett, S.7
Donovan, A.M.8
-
14
-
-
1842507884
-
Indoleamine 2,3-dioxygenase expression is restricted to fetal trophoblast giant cells during murine gestation and is maternal genome specific
-
DOI 10.1016/j.jri.2003.11.003, PII S0165037803001530
-
Baban B, Chandler P, McCool D, Marshall B, Munn DH, Mellor AL. Indoleamine 2,3-dioxygenase expression is restricted to fetal trophoblast giant cells during murine gestation and is maternal genome specific. J Reprod Immunol 2004;61:67-77. (Pubitemid 38446980)
-
(2004)
Journal of Reproductive Immunology
, vol.61
, Issue.2
, pp. 67-77
-
-
Baban, B.1
Chandler, P.2
McCool, D.3
Marshall, B.4
Munn, D.H.5
Mellor, A.L.6
-
15
-
-
33846689594
-
Inhibition of indoleamine 2,3-dioxygenase in dendritic cells by stereoisomers of 1-methyl-tryptophan correlates with antitumor responses
-
Hou DY, Muller AJ, Sharma MD, et al. Inhibition of indoleamine 2,3-dioxygenase in dendritic cells by stereoisomers of 1-methyl-tryptophan correlates with antitumor responses. Cancer Res 2007;67:792-801.
-
(2007)
Cancer Res
, vol.67
, pp. 792-801
-
-
Hou, D.Y.1
Muller, A.J.2
Sharma, M.D.3
-
16
-
-
23644447237
-
Indoleamine 2,3-dioxygenase in cancer: Targeting pathological immune tolerance with small-molecule inhibitors
-
Muller AJ, Malachowski WP, Prendergast GC. Indoleamine 2,3-dioxygenase in cancer: targeting pathological immune tolerance with small-molecule inhibitors. Expert Opin Ther Targets 2005;9:831-49.
-
(2005)
Expert Opin Ther Targets
, vol.9
, pp. 831-849
-
-
Muller, A.J.1
Malachowski, W.P.2
Prendergast, G.C.3
-
17
-
-
16244408626
-
Inhibition of indoleamine 2,3-dioxygenase, an immunoregulatory target of the cancer suppression gene Bin1, potentiates cancer chemotherapy
-
DOI 10.1038/nm1196
-
Muller AJ, DuHadaway JB, Sutanto-Ward E, Donover PS, Prendergast GC. Inhibition of indoleamine 2,3-dioxygenase, an immunomodulatory target of the tumor suppressor gene Bin1, potentiates cancer chemotherapy. Nat Med 2005;11:312-9. (Pubitemid 40460560)
-
(2005)
Nature Medicine
, vol.11
, Issue.3
, pp. 312-319
-
-
Muller, A.J.1
Duhadaway, J.B.2
Donover, P.S.3
Sutanto-Ward, E.4
Prendergast, G.C.5
-
18
-
-
77950192174
-
Immunotherapeutic suppression of IDO and tumor growth by ethyl pyruvate
-
Muller AJ, DuHadaway JB, Jaller D, Curtis P, Metz R, Prendergast GC. Immunotherapeutic suppression of IDO and tumor growth by ethyl pyruvate. Cancer Res 2010;70:1845-53.
-
(2010)
Cancer Res
, vol.70
, pp. 1845-1853
-
-
Muller, A.J.1
Duhadaway, J.B.2
Jaller, D.3
Curtis, P.4
Metz, R.5
Prendergast, G.C.6
-
19
-
-
4043092238
-
Expression of indoleamine 2,3-dioxygenase by plasmacytoid dendritic cells in tumor-draining lymph nodes
-
DOI 10.1172/JCI200421583
-
Munn DH, Sharma MD, Hou D, et al. Expression of indoleamine 2,3-dioxygenase by plasmacytoid dendritic cells in tumor-draining lymph nodes. J Clin Invest 2004;114:280-90. (Pubitemid 39071633)
-
(2004)
Journal of Clinical Investigation
, vol.114
, Issue.2
, pp. 280-290
-
-
Munn, D.H.1
Sharma, M.D.2
Hou, D.3
Baban, B.4
Lee, J.R.5
Antonia, S.J.6
Messina, J.L.7
Chandler, P.8
Koni, P.A.9
Mellor, A.L.10
-
20
-
-
46249121758
-
Antitumor properties of chemopreventive natural product brassinin are based upon inhibition of indoleamine 2,3-dioxygenase (IDO)
-
Banerjee T, DuHadaway JB, Gaspari P, et al. Antitumor properties of chemopreventive natural product brassinin are based upon inhibition of indoleamine 2,3-dioxygenase (IDO). Oncogene 2007;27:2851-7.
-
(2007)
Oncogene
, vol.27
, pp. 2851-2857
-
-
Banerjee, T.1
Duhadaway, J.B.2
Gaspari, P.3
-
21
-
-
41149180179
-
Indoleamine 2,3-dioxygenase is the anticancer target for a novel series of potent naphthoquinone-based inhibitors
-
DOI 10.1021/jm7014155
-
Kumar S, Malachowski WP, DuHadaway JB, et al. Indoleamine 2,3- dioxygenase is the anticancer target for a novel series of potent naphthoquinone-based inhibitors. J Med Chem 2008;51:1706-18. (Pubitemid 351438852)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.6
, pp. 1706-1718
-
-
Kumar, S.1
Malachowski, W.P.2
Duhadaway, J.B.3
Lalonde, J.M.4
Carroll, P.J.5
Jaller, D.6
Metz, R.7
Prendergast, G.C.8
Muller, A.J.9
-
22
-
-
77953417182
-
Naphthaquinone-based compounds as potent inhibitors of immunoregulatory enzyme indoleamine 23-dioxygenase and cancer
-
Kumar S, Malachowski WP, DuHadaway JB, et al. Naphthaquinone-based compounds as potent inhibitors of immunoregulatory enzyme indoleamine 2,3-dioxygenase and cancer. J Med Chem 2007;51:1709-18.
-
(2007)
J Med Chem
, vol.51
, pp. 1709-1718
-
-
Kumar, S.1
Malachowski, W.P.2
Duhadaway, J.B.3
-
23
-
-
58549107152
-
SOCS3 drives proteasomal degradation of indoleamine 2,3-dioxygenase (IDO) and antagonizes IDO-dependent tolerogenesis
-
Orabona C, Pallotta MT, Volpi C, et al. SOCS3 drives proteasomal degradation of indoleamine 2,3-dioxygenase (IDO) and antagonizes IDO-dependent tolerogenesis. Proc Natl Acad Sci U S A 2008;105:20828-33.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 20828-20833
-
-
Orabona, C.1
Pallotta, M.T.2
Volpi, C.3
-
24
-
-
0032710987
-
Zinc protoporphyrin: A metabolite with a mission
-
Labbe RF, Vreman HJ, Stevenson DK. Zinc protoporphyrin: a metabolite with a mission. Clin Chem 1999;45:2060-72.
-
(1999)
Clin Chem
, vol.45
, pp. 2060-2072
-
-
Labbe, R.F.1
Vreman, H.J.2
Stevenson, D.K.3
|