-
1
-
-
0032030770
-
Histone acetylation and transcriptional regulatory mechanisms
-
Struhl, K. Histone acetylation and transcriptional regulatory mechanisms. Genes Dev., 12: 599-606, 1998.
-
(1998)
Genes Dev.
, vol.12
, pp. 599-606
-
-
Struhl, K.1
-
2
-
-
0033565514
-
Transcriptional silencing of the p73 gene in acute lymphoblastic leukemia and Burkitt's lymphoma is associated with 5′ CpG island methylation
-
Corn, P. G., Kuerbitz, S. J., van Noesel, M. M., Esteller, M., Compitello, N., Baylin, S. B., and Herman, J. G. Transcriptional silencing of the p73 gene in acute lymphoblastic leukemia and Burkitt's lymphoma is associated with 5′ CpG island methylation. Cancer Res., 59: 3352-3356, 1999.
-
(1999)
Cancer Res.
, vol.59
, pp. 3352-3356
-
-
Corn, P.G.1
Kuerbitz, S.J.2
Van Noesel, M.M.3
Esteller, M.4
Compitello, N.5
Baylin, S.B.6
Herman, J.G.7
-
3
-
-
0034109902
-
Epigenetic silencing of maspin gene expression in human breast cancers
-
Domann, F. E., Rice, J. C., Hendrix, M. J., and Futscher, B. W. Epigenetic silencing of maspin gene expression in human breast cancers. Int. J. Cancer, 85: 805-810, 2000.
-
(2000)
Int. J. Cancer
, vol.85
, pp. 805-810
-
-
Domann, F.E.1
Rice, J.C.2
Hendrix, M.J.3
Futscher, B.W.4
-
4
-
-
0036644895
-
Frequent epigenetic silencing of the CpG island promoter of RASSF1A in thyroid carcinoma
-
Schagdarsurengin, U., Gimm, O., Hoang-Vu, C., Dralle, H., Pfeifer, G. P., and Dammann, R. Frequent epigenetic silencing of the CpG island promoter of RASSF1A in thyroid carcinoma. Cancer Res., 62: 3698-3701, 2002.
-
(2002)
Cancer Res.
, vol.62
, pp. 3698-3701
-
-
Schagdarsurengin, U.1
Gimm, O.2
Hoang-Vu, C.3
Dralle, H.4
Pfeifer, G.P.5
Dammann, R.6
-
5
-
-
18444408077
-
K-ras mutations and RASSF1A promoter methylation in colorectal cancer
-
van Engeland, M., Roemen, G. M., Brink, M., Pachen, M. M., Weijenberg, M. P., de Bruine, A. P., Arends, J. W., van den Brandt, P. A., de Goeij, A. F., and Herman, J. G. K-ras mutations and RASSF1A promoter methylation in colorectal cancer. Oncogene, 21: 3792-3795, 2002.
-
(2002)
Oncogene
, vol.21
, pp. 3792-3795
-
-
Van Engeland, M.1
Roemen, G.M.2
Brink, M.3
Pachen, M.M.4
Weijenberg, M.P.5
De Bruine, A.P.6
Arends, J.W.7
Van Den Brandt, P.A.8
De Goeij, A.F.9
Herman, J.G.10
-
6
-
-
85047699461
-
Coincident inactivation of 14-3-3σ and p16INK4a is an early event in vulval squamous neoplasia
-
Gasco, M., Sullivan, A., Repellin, C., Brooks, L., Farrell, P. J., Tidy, J. A., Dunne, B., Gusterson, B., Evans, D. J., and Crook, T. Coincident inactivation of 14-3-3σ and p16INK4a is an early event in vulval squamous neoplasia. Oncogene, 21: 1876-1881, 2002.
-
(2002)
Oncogene
, vol.21
, pp. 1876-1881
-
-
Gasco, M.1
Sullivan, A.2
Repellin, C.3
Brooks, L.4
Farrell, P.J.5
Tidy, J.A.6
Dunne, B.7
Gusterson, B.8
Evans, D.J.9
Crook, T.10
-
7
-
-
0035817688
-
Loss of p16Ink4a with retention of p19Arf predisposes mice to tumorigenesis
-
Sharpless, N. E., Bardeesy, N., Lee, K. H., Carrasco, D., Castrillon, D. H., Aguirre, A. J., Wu, E. A., Horner, J. W., and DePinho, R. A. Loss of p16Ink4a with retention of p19Arf predisposes mice to tumorigenesis. Nature (Lond.), 413: 86-91, 2001.
-
(2001)
Nature (Lond.)
, vol.413
, pp. 86-91
-
-
Sharpless, N.E.1
Bardeesy, N.2
Lee, K.H.3
Carrasco, D.4
Castrillon, D.H.5
Aguirre, A.J.6
Wu, E.A.7
Horner, J.W.8
DePinho, R.A.9
-
8
-
-
0036808073
-
Frequent epigenetic silencing of the p16 gene in non-small cell lung cancers of tobacco smokers
-
Yanagawa, N., Tamura, G., Oizumi, H., Takahashi, N., Shimazaki, Y., and Motoyama, T. Frequent epigenetic silencing of the p16 gene in non-small cell lung cancers of tobacco smokers. Jpn. J. Cancer Res., 93: 1107-1113, 2002.
-
(2002)
Jpn. J. Cancer Res.
, vol.93
, pp. 1107-1113
-
-
Yanagawa, N.1
Tamura, G.2
Oizumi, H.3
Takahashi, N.4
Shimazaki, Y.5
Motoyama, T.6
-
9
-
-
0036746906
-
Antineoplastic action of 5-aza-2′-deoxycytidine and phenylbutyrate on human lung carcinoma cells
-
Boivin, A. J., Momparler, L. F., Hurtubise, A., and Momparler, R. L. Antineoplastic action of 5-aza-2′-deoxycytidine and phenylbutyrate on human lung carcinoma cells. Anticancer Drugs, 13: 869-874, 2002.
-
(2002)
Anticancer Drugs
, vol.13
, pp. 869-874
-
-
Boivin, A.J.1
Momparler, L.F.2
Hurtubise, A.3
Momparler, R.L.4
-
10
-
-
0035819031
-
Increased susceptibility to tumorigenesis of ski-deficient heterozygous mice
-
Shinagawa, T., Nomura, T., Colmenares, C., Ohira, M., Nakagawara, A., and Ishii, S. Increased susceptibility to tumorigenesis of ski-deficient heterozygous mice. Oncogene, 20: 8100-8108, 2001.
-
(2001)
Oncogene
, vol.20
, pp. 8100-8108
-
-
Shinagawa, T.1
Nomura, T.2
Colmenares, C.3
Ohira, M.4
Nakagawara, A.5
Ishii, S.6
-
11
-
-
0037064089
-
Sp1 and Sp3 recruit histone deacetylase to repress transcription of human telomerase reverse transcriptase (hTERT) promoter in normal human somatic cells
-
Won, J., Yim, J., and Kim, T. K. Sp1 and Sp3 recruit histone deacetylase to repress transcription of human telomerase reverse transcriptase (hTERT) promoter in normal human somatic cells. J. Biol. Chem., 277: 38230-38238, 2002.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 38230-38238
-
-
Won, J.1
Yim, J.2
Kim, T.K.3
-
12
-
-
0034326799
-
Apicidin, a histone deacetylase inhibitor, inhibits proliferation of tumor cells via induction of p21WAF1/Cip1 and gelsolin
-
Han, J. W., Ahn, S. H., Park, S. H., Wang, S. Y., Bae, G. U., Seo, D. W., Kwon, H. K., Hong, S., Lee, H. Y., Lee, Y. W., and Lee, H. W. Apicidin, a histone deacetylase inhibitor, inhibits proliferation of tumor cells via induction of p21WAF1/Cip1 and gelsolin. Cancer Res., 60: 6068-6074, 2000.
-
(2000)
Cancer Res.
, vol.60
, pp. 6068-6074
-
-
Han, J.W.1
Ahn, S.H.2
Park, S.H.3
Wang, S.Y.4
Bae, G.U.5
Seo, D.W.6
Kwon, H.K.7
Hong, S.8
Lee, H.Y.9
Lee, Y.W.10
Lee, H.W.11
-
13
-
-
0034596309
-
Histone deacetylase inhibitors: Inducers of differentiation or apoptosis of transformed cells
-
Marks, P. A., Richon, V. M., and Rifkind, R. A. Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells. J. Natl. Cancer Inst., 92: 1210-1216, 2000.
-
(2000)
J. Natl. Cancer Inst.
, vol.92
, pp. 1210-1216
-
-
Marks, P.A.1
Richon, V.M.2
Rifkind, R.A.3
-
14
-
-
0035023260
-
Histone deacetylase inhibitors promote apoptosis and differential cell cycle arrest in anaplastic thyroid cancer cells
-
Greenberg, V. L., Williams, J. M., Cogswell, J. P., Mendenhall, M., and Zimmer, S. G. Histone deacetylase inhibitors promote apoptosis and differential cell cycle arrest in anaplastic thyroid cancer cells. Thyroid, 11: 315-325, 2001.
-
(2001)
Thyroid
, vol.11
, pp. 315-325
-
-
Greenberg, V.L.1
Williams, J.M.2
Cogswell, J.P.3
Mendenhall, M.4
Zimmer, S.G.5
-
15
-
-
0036828101
-
MS-27-275, an inhibitor of histone deacetylase, has marked in vitro and in vivo antitumor activity against pediatric solid tumors
-
Jaboin, J., Wild, J., Hamidi, H., Khanna, C., Kim, C. J., Robey, R., Bates, S. E., and Thiele, C. J. MS-27-275, an inhibitor of histone deacetylase, has marked in vitro and in vivo antitumor activity against pediatric solid tumors. Cancer Res., 62: 6108-6115, 2002.
-
(2002)
Cancer Res.
, vol.62
, pp. 6108-6115
-
-
Jaboin, J.1
Wild, J.2
Hamidi, H.3
Khanna, C.4
Kim, C.J.5
Robey, R.6
Bates, S.E.7
Thiele, C.J.8
-
16
-
-
0035793107
-
Potent histone deacetylase inhibitors built from trichostatin A and cyclic tetrapeptide antibiotics including trapoxin
-
Furumai, R., Komatsu, Y., Nishino, N., Khochbin, S., Yoshida, M., and Horinouchi, S. Potent histone deacetylase inhibitors built from trichostatin A and cyclic tetrapeptide antibiotics including trapoxin. Proc. Natl. Acad. Sci. USA, 98: 87-92, 2001.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 87-92
-
-
Furumai, R.1
Komatsu, Y.2
Nishino, N.3
Khochbin, S.4
Yoshida, M.5
Horinouchi, S.6
-
17
-
-
0036681989
-
Sulfonamide anilides, a novel class of histone deacetylase inhibitors, are antiproliferative against human tumors
-
Fournel, M., Trachy-Bourget, M. C., Yan, P. T., Kalita, A., Bonfils, C., Beaulieu, C., Frechette, S., Leit, S., Abou-Khalil, E., Woo, S. H., Delorme, D., MacLeod, A. R., Besterman, J. M., and Li, Z. Sulfonamide anilides, a novel class of histone deacetylase inhibitors, are antiproliferative against human tumors. Cancer Res., 62: 4325-4330, 2002.
-
(2002)
Cancer Res.
, vol.62
, pp. 4325-4330
-
-
Fournel, M.1
Trachy-Bourget, M.C.2
Yan, P.T.3
Kalita, A.4
Bonfils, C.5
Beaulieu, C.6
Frechette, S.7
Leit, S.8
Abou-Khalil, E.9
Woo, S.H.10
Delorme, D.11
MacLeod, A.R.12
Besterman, J.M.13
Li, Z.14
-
18
-
-
0033767848
-
Mechanism of cell cycle arrest caused by histone deacetylase inhibitors in human cateinoma cells
-
Kim, Y. B., Ki, S. W., Yoshida, M., and Horinouchi, S. Mechanism of cell cycle arrest caused by histone deacetylase inhibitors in human cateinoma cells. J. Antibiot. (Tokyo), 53: 1191-1200, 2000.
-
(2000)
J. Antibiot. (Tokyo)
, vol.53
, pp. 1191-1200
-
-
Kim, Y.B.1
Ki, S.W.2
Yoshida, M.3
Horinouchi, S.4
-
19
-
-
0035046529
-
Histone deacetylase inhibitors: Development of suberoylanilide hydroxamic acid (SAHA) for the treatment of cancers
-
Richon, V. M., Zhou, X., Rifkind, R. A., and Marks, P. A. Histone deacetylase inhibitors: development of suberoylanilide hydroxamic acid (SAHA) for the treatment of cancers. Blood Cells Mol. Dis., 27: 260-264, 2001.
-
(2001)
Blood Cells Mol. Dis.
, vol.27
, pp. 260-264
-
-
Richon, V.M.1
Zhou, X.2
Rifkind, R.A.3
Marks, P.A.4
-
20
-
-
0033520944
-
Histone deacetylase inhibition selectively alters the activity and expression of cell cycle proteins leading to specific chromatin acetylation and antiproliferative effects
-
Sambucetti, L. C., Fischer, D. D., Zabludoff, S., Kwon, P. O., Chamberlin, H., Trogani, N., Xu, H., and Cohen, D. Histone deacetylase inhibition selectively alters the activity and expression of cell cycle proteins leading to specific chromatin acetylation and antiproliferative effects. J. Biol. Chem., 274: 34940-34947, 1999.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 34940-34947
-
-
Sambucetti, L.C.1
Fischer, D.D.2
Zabludoff, S.3
Kwon, P.O.4
Chamberlin, H.5
Trogani, N.6
Xu, H.7
Cohen, D.8
-
21
-
-
0041532109
-
Cell cycle blockade and differentiation of ovarian cancer cells by the histone deacetylase inhibitor trichostatin A are associated with changes in p21, Rb, and Id proteins
-
Strait, K. A., Dabbas, B., Hammond, E. H., Warnick, C. T., Iistrup, S. J., and Ford, C. D. Cell cycle blockade and differentiation of ovarian cancer cells by the histone deacetylase inhibitor trichostatin A are associated with changes in p21, Rb, and Id proteins. Mol. Cancer Ther., 1: 1181-1190, 2002.
-
(2002)
Mol. Cancer Ther.
, vol.1
, pp. 1181-1190
-
-
Strait, K.A.1
Dabbas, B.2
Hammond, E.H.3
Warnick, C.T.4
Iistrup, S.J.5
Ford, C.D.6
-
22
-
-
0033003054
-
The biology and treatment of acute progranulocytic leukemia
-
Slack, J. L. The biology and treatment of acute progranulocytic leukemia. Curr. Opin. Oncol., 11: 9-13, 1999.
-
(1999)
Curr. Opin. Oncol.
, vol.11
, pp. 9-13
-
-
Slack, J.L.1
-
23
-
-
0034817075
-
ETO a target of t(8;21) in acute leukemia, makes distinct contacts with multiple histone deacetylases and binds mSin3A through its oligomerization domain
-
Amann, J. M., Nip, J., Strom, D. K., Lutterbach, B., Harada, H., Lenny, N., Downing, J. R., Meyers, S., and Hiebert, S. W. ETO, a target of t(8;21) in acute leukemia, makes distinct contacts with multiple histone deacetylases and binds mSin3A through its oligomerization domain. Mol. Cell. Biol., 21: 6470-6483, 2001.
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 6470-6483
-
-
Amann, J.M.1
Nip, J.2
Strom, D.K.3
Lutterbach, B.4
Harada, H.5
Lenny, N.6
Downing, J.R.7
Meyers, S.8
Hiebert, S.W.9
-
24
-
-
0031723957
-
Aberrant recruitment of the nuclear receptor corepressor-histone deacetylase complex by the acute myeloid leukemia fusion partner ETO
-
Gelmetti, V., Zhang, J., Fanelli, M., Minucci, S., Pelicci, P. G., and Lazar, M. A. Aberrant recruitment of the nuclear receptor corepressor-histone deacetylase complex by the acute myeloid leukemia fusion partner ETO. Mol. Cell. Biol., 18: 7185-7191, 1998.
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 7185-7191
-
-
Gelmetti, V.1
Zhang, J.2
Fanelli, M.3
Minucci, S.4
Pelicci, P.G.5
Lazar, M.A.6
-
25
-
-
0035132140
-
Histone deacetylase-targeted treatment restores retinoic acid signaling and differentiation in acute myeloid leukemia
-
Ferrara, F. F., Fazi, F., Bianchini, A., Padula, F., Gehnetti, V., Minucci, S., Mancini, M, Pelicci, P. G., Lo, C. F., and Nervi, C. Histone deacetylase-targeted treatment restores retinoic acid signaling and differentiation in acute myeloid leukemia. Cancer Res., 61: 2-7, 2001.
-
(2001)
Cancer Res.
, vol.61
, pp. 2-7
-
-
Ferrara, F.F.1
Fazi, F.2
Bianchini, A.3
Padula, F.4
Gehnetti, V.5
Minucci, S.6
Mancini, M.7
Pelicci, P.G.8
Lo, C.F.9
Nervi, C.10
-
26
-
-
17344388929
-
Complete remission through blast cell differentiation in PLZF/RARα-positive acute promyelocytic leukemia: In vitro and in vivo studies
-
Petti, M. C., Fazi, F., Gentile, M., Diverio, D., De Fabritiis, P., De Propris, M. S., Fiorini, R., Spiriti, M. A., Padula, F., Pelicci, P. G., Nervi, C., and Lo, C. F. Complete remission through blast cell differentiation in PLZF/RARα-positive acute promyelocytic leukemia: in vitro and in vivo studies. Blood, 10: 1065-1067, 2002.
-
(2002)
Blood
, vol.10
, pp. 1065-1067
-
-
Petti, M.C.1
Fazi, F.2
Gentile, M.3
Diverio, D.4
De Fabritiis, P.5
De Propris, M.S.6
Fiorini, R.7
Spiriti, M.A.8
Padula, F.9
Pelicci, P.G.10
Nervi, C.11
Lo, C.F.12
-
27
-
-
0033551152
-
A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors
-
Saito, A., Yamashita, T., Mariko, Y., Nosaka, Y., Tsuchiya, K., Ando, T., Suzuki, T., Tsuruo, T., and Nakanishi, O. A synthetic inhibitor of histone deacetylase, MS-27-275, with marked in vivo antitumor activity against human tumors. Proc. Natl. Acad. Sci. USA, 96: 4592-4597, 1999.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 4592-4597
-
-
Saito, A.1
Yamashita, T.2
Mariko, Y.3
Nosaka, Y.4
Tsuchiya, K.5
Ando, T.6
Suzuki, T.7
Tsuruo, T.8
Nakanishi, O.9
-
28
-
-
0034770423
-
Histone deacetylase inhibitors increase p21(WAF1) and induce apoptosis of human myeloma cell lines independent of decreased IL-6 receptor expression
-
Lavelle, D., Chen, Y. H., Hankewych, M., and DeSimone, J. Histone deacetylase inhibitors increase p21(WAF1) and induce apoptosis of human myeloma cell lines independent of decreased IL-6 receptor expression. Am. J. Hematol., 68: 170-178, 2001.
-
(2001)
Am. J. Hematol.
, vol.68
, pp. 170-178
-
-
Lavelle, D.1
Chen, Y.H.2
Hankewych, M.3
DeSimone, J.4
-
29
-
-
0034672294
-
Effect of trichostatin A on cell growth and expression of cell cycle- and apoptosis-related molecules in human gastric and oral carcinoma cell lines
-
Suzuki, T., Yokozaki, H., Kuniyasu, H., Hayashi, K., Naka, K., Ono, S., Ishikawa, T., Tahara, E., and Yasui, W. Effect of trichostatin A on cell growth and expression of cell cycle- and apoptosis-related molecules in human gastric and oral carcinoma cell lines. Int. J. Cancer, 88: 992-997, 2000.
-
(2000)
Int. J. Cancer
, vol.88
, pp. 992-997
-
-
Suzuki, T.1
Yokozaki, H.2
Kuniyasu, H.3
Hayashi, K.4
Naka, K.5
Ono, S.6
Ishikawa, T.7
Tahara, E.8
Yasui, W.9
-
30
-
-
1542588471
-
Second generation hybrid polar compounds are potent inducers of transformed cell differentiation
-
Richon, V. M., Webb, Y., Merger, R., Sheppard, T., Jursic, B., Ngo, L., Civoli, F., Breslow, R., Rifkind, R. A., and Marks, P. A. Second generation hybrid polar compounds are potent inducers of transformed cell differentiation. Proc. Natl. Acad. Sci. USA, 93(12): 5705-5708, 1996.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, Issue.12
, pp. 5705-5708
-
-
Richon, V.M.1
Webb, Y.2
Merger, R.3
Sheppard, T.4
Jursic, B.5
Ngo, L.6
Civoli, F.7
Breslow, R.8
Rifkind, R.A.9
Marks, P.A.10
-
31
-
-
0038627550
-
Psammaplins from the sponge Pseudoceratina purpurea: Inhibition of both histone deacetylase and DNA methyltransferase
-
Pina, I. C., Gautschi, J. T., Wang, G. Y., Sanders, M. L., Schmitz, F. J., France, D., Cornell-Kennon, S., Sambucetti, L. C., Remiszewski, S. W., Perez, L. B., Bair, K. W., and Crews, P. Psammaplins from the sponge Pseudoceratina purpurea: inhibition of both histone deacetylase and DNA methyltransferase. J. Org. Chem., 68(10): 3866-3873, 2003.
-
(2003)
J. Org. Chem.
, vol.68
, Issue.10
, pp. 3866-3873
-
-
Pina, I.C.1
Gautschi, J.T.2
Wang, G.Y.3
Sanders, M.L.4
Schmitz, F.J.5
France, D.6
Cornell-Kennon, S.7
Sambucetti, L.C.8
Remiszewski, S.W.9
Perez, L.B.10
Bair, K.W.11
Crews, P.12
-
32
-
-
0141953928
-
The discovery of NVP-LAQ824: From concept to clinic
-
Remiszewski, S. W. The discovery of NVP-LAQ824: from concept to clinic. Curr. Med. Chem., 10(22): 2393-402, 2003.
-
(2003)
Curr. Med. Chem.
, vol.10
, Issue.22
, pp. 2393-2402
-
-
Remiszewski, S.W.1
-
33
-
-
0001811191
-
Histone deacetylase as a new target for cancer chemotherapy
-
Yoshida, M., Furumai, R., Nishiyama, M., Komatsu, Y., Nishino, N., and Horinouchi, S. Histone deacetylase as a new target for cancer chemotherapy. Cancer Chemother. Pharmacol., 48 Suppl 1: S20-S26, 2001.
-
(2001)
Cancer Chemother. Pharmacol.
, vol.48
, Issue.SUPPL. 1
-
-
Yoshida, M.1
Furumai, R.2
Nishiyama, M.3
Komatsu, Y.4
Nishino, N.5
Horinouchi, S.6
-
34
-
-
0035755974
-
Histone deacetylases and cancer: Causes and therapies
-
Marks, P., Rifkind, R. A., Richon, V. M., Breslow, R., Miller, T., and Kelly, W. K. Histone deacetylases and cancer: causes and therapies. Nat. Rev. Cancer 1: 194-202, 2001.
-
(2001)
Nat. Rev. Cancer
, vol.1
, pp. 194-202
-
-
Marks, P.1
Rifkind, R.A.2
Richon, V.M.3
Breslow, R.4
Miller, T.5
Kelly, W.K.6
-
35
-
-
0036652874
-
A new class of anti-cancer drugs: HDAC-inhibitors
-
Pelicci, P. G. A new class of anti-cancer drugs: HDAC-inhibitors. Suppl. Tumori, 1: S66, 2002.
-
(2002)
Suppl. Tumori
, vol.1
-
-
Pelicci, P.G.1
-
36
-
-
0036176617
-
Histone deacetylase inhibitors in cancer treatment
-
Vigushin, D. M., and Coombes, R. C. Histone deacetylase inhibitors in cancer treatment. Anticancer Drugs, 13: 1-13, 2002.
-
(2002)
Anticancer Drugs
, vol.13
, pp. 1-13
-
-
Vigushin, D.M.1
Coombes, R.C.2
-
37
-
-
17744416444
-
Histone deacetylase inhibitor activates the WAF1/Cip1 gene promoter through the Sp1 sites
-
Sowa, Y., Orita, T., Minamikawa, S., Nakano, K., Mizuno, T., Nomura, H., and Sakai, T. Histone deacetylase inhibitor activates the WAF1/Cip1 gene promoter through the Sp1 sites. Biochem. Biophys. Res. Commun., 241: 142-150, 1997.
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.241
, pp. 142-150
-
-
Sowa, Y.1
Orita, T.2
Minamikawa, S.3
Nakano, K.4
Mizuno, T.5
Nomura, H.6
Sakai, T.7
-
38
-
-
0034086168
-
Histone deacetylase inhibitors trigger a G2 checkpoint in normal cells that is defective in tumor cells
-
Qiu, L., Burgess, A., Fairlie, D. P., Leonard, H., Parsons, P. G., and Gabrielli, B. G. Histone deacetylase inhibitors trigger a G2 checkpoint in normal cells that is defective in tumor cells. Mol. Biol. Cell, 11: 2069-2083, 2000.
-
(2000)
Mol. Biol. Cell
, vol.11
, pp. 2069-2083
-
-
Qiu, L.1
Burgess, A.2
Fairlie, D.P.3
Leonard, H.4
Parsons, P.G.5
Gabrielli, B.G.6
-
39
-
-
0033199896
-
Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma
-
Glick, R. D., Swendeman, S. L., Coffey, D. C., Rifkind, R. A., Marks, P. A., Richon, V. M., and La Quaglia, M. P. Hybrid polar histone deacetylase inhibitor induces apoptosis and CD95/CD95 ligand expression in human neuroblastoma. Cancer Res., 59: 4392-4399, 1999.
-
(1999)
Cancer Res.
, vol.59
, pp. 4392-4399
-
-
Glick, R.D.1
Swendeman, S.L.2
Coffey, D.C.3
Rifkind, R.A.4
Marks, P.A.5
Richon, V.M.6
La Quaglia, M.P.7
-
40
-
-
0036584375
-
Histone deacetylase inhibitors sensitize human colonic adenocarcinoma cell lines to TNF-related apoptosis inducing ligand-mediated apoptosis
-
Inoue, H., Shiraki, K., Ohmori, S., Sakai, T., Deguchi, M., Yamanaka, T., Okano, H., and Nakano, T. Histone deacetylase inhibitors sensitize human colonic adenocarcinoma cell lines to TNF-related apoptosis inducing ligand-mediated apoptosis. Int. J. Mol. Med., 9: 521-525, 2002.
-
(2002)
Int. J. Mol. Med.
, vol.9
, pp. 521-525
-
-
Inoue, H.1
Shiraki, K.2
Ohmori, S.3
Sakai, T.4
Deguchi, M.5
Yamanaka, T.6
Okano, H.7
Nakano, T.8
-
41
-
-
0033614993
-
Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives
-
Suzuki, T., Ando, T., Tsuchiya, K., Fukazawa, N., Saito, A., Mariko, Y., Yamashita, T., and Nakanishi, O. Synthesis and histone deacetylase inhibitory activity of new benzamide derivatives. J. Med. Chem., 42(15): 3001-3003, 1999.
-
(1999)
J. Med. Chem.
, vol.42
, Issue.15
, pp. 3001-3003
-
-
Suzuki, T.1
Ando, T.2
Tsuchiya, K.3
Fukazawa, N.4
Saito, A.5
Mariko, Y.6
Yamashita, T.7
Nakanishi, O.8
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