-
1
-
-
0037371443
-
Pharmacogenetics of anticancer drug sensitivity in non-small cell lung cancer
-
Danesi R, de Braud F, Fogli S, et al. Pharmacogenetics of anticancer drug sensitivity in non-small cell lung cancer. Pharmacol Rev. 2003;55:57-103.
-
(2003)
Pharmacol Rev
, vol.55
, pp. 57-103
-
-
Danesi, R.1
de Braud, F.2
Fogli, S.3
-
2
-
-
33846457870
-
Cancer statistics, 2007
-
Jemal A, Siegel R, Ward E, Murray T, Xu J, Thun MJ. Cancer statistics, 2007. CA Cancer J Clin. 2007;57:43-66.
-
(2007)
CA Cancer J Clin
, vol.57
, pp. 43-66
-
-
Jemal, A.1
Siegel, R.2
Ward, E.3
Murray, T.4
Xu, J.5
Thun, M.J.6
-
3
-
-
25144483821
-
Phase 1 study of ABT-751, a novel microtubule inhibitor, in patients with refractory hematologic malignancies
-
Yee KW, Hagey A, Verstovsek S, et al. Phase 1 study of ABT-751, a novel microtubule inhibitor, in patients with refractory hematologic malignancies. Clin Cancer Res. 2005;11:6615-6624.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 6615-6624
-
-
Yee, K.W.1
Hagey, A.2
Verstovsek, S.3
-
4
-
-
0032570594
-
Microtubule-interfering agents activate c-Jun N-terminal kinase/stress-activated protein kinase through both Ras and apoptosis signal-regulating kinase pathways
-
Wang TH, Wang HS, Ichijo H, et al. Microtubule-interfering agents activate c-Jun N-terminal kinase/stress-activated protein kinase through both Ras and apoptosis signal-regulating kinase pathways. J Biol Chem. 1998;273:4928-4936.
-
(1998)
J Biol Chem
, vol.273
, pp. 4928-4936
-
-
Wang, T.H.1
Wang, H.S.2
Ichijo, H.3
-
5
-
-
3042740981
-
BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antitumoral activity in vivo
-
Kuo CC, Hsieh HP, Pan WY, et al. BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antitumoral activity in vivo. Cancer Res. 2004;64:4621-4628.
-
(2004)
Cancer Res
, vol.64
, pp. 4621-4628
-
-
Kuo, C.C.1
Hsieh, H.P.2
Pan, W.Y.3
-
6
-
-
33646428633
-
3,3′- Diindolylmethane is a novel mitochondrial H(+)-ATP synthase inhibitor that can induce p21(Cip1/Waf1) expression by induction of oxidative stress in human breast cancer cells
-
Gong Y, Sohn H, Xue L, Firestone GL, Bjeldanes LF. 3,3′- Diindolylmethane is a novel mitochondrial H(+)-ATP synthase inhibitor that can induce p21(Cip1/Waf1) expression by induction of oxidative stress in human breast cancer cells. Cancer Res. 2006;66:4880-4887.
-
(2006)
Cancer Res
, vol.66
, pp. 4880-4887
-
-
Gong, Y.1
Sohn, H.2
Xue, L.3
Firestone, G.L.4
Bjeldanes, L.F.5
-
7
-
-
0035984590
-
3,3′-Diindolylmethane (DIM) induces a G cell cycle arrest in human breast cancer cells that is accompanied by Sp1-mediated activation of p21(WAF1/CIP1) expression
-
Hong C, Kim HA, Firestone GL, Bjeldanes LF. 3,3′-Diindolylmethane (DIM) induces a G cell cycle arrest in human breast cancer cells that is accompanied by Sp1-mediated activation of p21(WAF1/CIP1) expression. Carcinogenesis. 2002;23:1297-1305.
-
(2002)
Carcinogenesis
, vol.23
, pp. 1297-1305
-
-
Hong, C.1
Kim, H.A.2
Firestone, G.L.3
Bjeldanes, L.F.4
-
8
-
-
31544436372
-
Indole-3-carbinol activates the ATM signaling pathway independent of DNA damage to stabilize p53 and induce G1 arrest of human mammary epithelial cells
-
Brew CT, Aronchik I, Hsu JC, et al. Indole-3-carbinol activates the ATM signaling pathway independent of DNA damage to stabilize p53 and induce G1 arrest of human mammary epithelial cells. Int J Cancer. 2006;118:857-868.
-
(2006)
Int J Cancer
, vol.118
, pp. 857-868
-
-
Brew, C.T.1
Aronchik, I.2
Hsu, J.C.3
-
9
-
-
29144499032
-
CAN and iodine-catalyzed reaction of indole or 1-methylindole with α,β-unsaturated ketone or aldehyde
-
Ko S, Lin C, Tu Z, Wang YF, Wang CC, Yao CF. CAN and iodine-catalyzed reaction of indole or 1-methylindole with α,β-unsaturated ketone or aldehyde. Tetrahedron Lett. 2006;47:487-492.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 487-492
-
-
Ko, S.1
Lin, C.2
Tu, Z.3
Wang, Y.F.4
Wang, C.C.5
Yao, C.F.6
-
10
-
-
33846821661
-
D-501036, a novel selenophene-based triheterocycle derivative, exhibits potent in vitro and in vivo antitumoral activity which involves DNA damage and ataxia telangiectasia-mutated nuclear protein kinase activation
-
Juang SH, Lung CC, Hsu PC, et al. D-501036, a novel selenophene-based triheterocycle derivative, exhibits potent in vitro and in vivo antitumoral activity which involves DNA damage and ataxia telangiectasia-mutated nuclear protein kinase activation. Mol Cancer Ther. 2007;6:193-202.
-
(2007)
Mol Cancer Ther
, vol.6
, pp. 193-202
-
-
Juang, S.H.1
Lung, C.C.2
Hsu, P.C.3
-
11
-
-
2342517643
-
Arsenic trioxide induces apoptosis in peripheral blood T lymphocyte subsets by inducing oxidative stress: A role of Bcl-2
-
Gupta S, Yel L, Kim D, Kim C, Chiplunkar S, Gollapudi S. Arsenic trioxide induces apoptosis in peripheral blood T lymphocyte subsets by inducing oxidative stress: a role of Bcl-2. Mol Cancer Ther. 2003;2:711-719.
-
(2003)
Mol Cancer Ther
, vol.2
, pp. 711-719
-
-
Gupta, S.1
Yel, L.2
Kim, D.3
Kim, C.4
Chiplunkar, S.5
Gollapudi, S.6
-
12
-
-
0035078341
-
Reactive oxygen species (ROS) mediates the mitochondrial-dependent apoptosis induced by transforming growth factor (beta) in fetal hepatocytes
-
Herrera B, Alvarez AM, Sanchez A, et al. Reactive oxygen species (ROS) mediates the mitochondrial-dependent apoptosis induced by transforming growth factor (beta) in fetal hepatocytes. FASEB J. 2001;15:741-751.
-
(2001)
FASEB J
, vol.15
, pp. 741-751
-
-
Herrera, B.1
Alvarez, A.M.2
Sanchez, A.3
-
13
-
-
18144363210
-
Farnesyltransferase inhibitors induce DNA damage via reactive oxygen species in human cancer cells
-
Pan J, She M, Xu ZX, Sun L, Yeung SC. Farnesyltransferase inhibitors induce DNA damage via reactive oxygen species in human cancer cells. Cancer Res. 2005;65:3671-3681.
-
(2005)
Cancer Res
, vol.65
, pp. 3671-3681
-
-
Pan, J.1
She, M.2
Xu, Z.X.3
Sun, L.4
Yeung, S.C.5
-
14
-
-
3142707088
-
Biological consequences of oxidative stress-induced DNA damage in Saccharomyces cerevisiae
-
Salmon TB, Evert BA, Song B, Doetsch PW. Biological consequences of oxidative stress-induced DNA damage in Saccharomyces cerevisiae. Nucleic Acids Res. 2004;32:3712-3723.
-
(2004)
Nucleic Acids Res
, vol.32
, pp. 3712-3723
-
-
Salmon, T.B.1
Evert, B.A.2
Song, B.3
Doetsch, P.W.4
-
15
-
-
14844327760
-
Reactive oxygen species promote TNFalpha-induced death and sustained JNK activation by inhibiting MAP kinase phosphatases
-
Kamata H, Honda S, Maeda S, Chang L, Hirata H, Karin M. Reactive oxygen species promote TNFalpha-induced death and sustained JNK activation by inhibiting MAP kinase phosphatases. Cell. 2005;120:649-661.
-
(2005)
Cell
, vol.120
, pp. 649-661
-
-
Kamata, H.1
Honda, S.2
Maeda, S.3
Chang, L.4
Hirata, H.5
Karin, M.6
-
17
-
-
26444560960
-
Caspases: Pharmacological manipulation of cell death
-
Lavrik IN, Golks A, Krammer PH. Caspases: pharmacological manipulation of cell death. J Clin Invest. 2005;115:2665-2672.
-
(2005)
J Clin Invest
, vol.115
, pp. 2665-2672
-
-
Lavrik, I.N.1
Golks, A.2
Krammer, P.H.3
-
18
-
-
20044361991
-
Mitochondrial O2*- and H2O2 mediate glucose deprivation-induced stress in human cancer cells
-
Ahmad IM, Aykin-Burns N, Sim JE, et al. Mitochondrial O2*- and H2O2 mediate glucose deprivation-induced stress in human cancer cells. J Biol Chem. 2005;280:4254-4263.
-
(2005)
J Biol Chem
, vol.280
, pp. 4254-4263
-
-
Ahmad, I.M.1
Aykin-Burns, N.2
Sim, J.E.3
-
19
-
-
0034607702
-
Requirement of JNK for stress-induced activation of the cytochrome c-mediated death pathway
-
Tournier C, Hess P, Yang DD, et al. Requirement of JNK for stress-induced activation of the cytochrome c-mediated death pathway. Science. 2000;288:870-874.
-
(2000)
Science
, vol.288
, pp. 870-874
-
-
Tournier, C.1
Hess, P.2
Yang, D.D.3
-
20
-
-
0036269755
-
The Bax subfamily of Bcl2-related proteins is essential for apoptotic signal transduction by c-Jun NH-terminal kinase
-
Lei K, Nimnual A, Zong WX, et al. The Bax subfamily of Bcl2-related proteins is essential for apoptotic signal transduction by c-Jun NH-terminal kinase. Mol Cell Biol. 2002;22:4929-4942.
-
(2002)
Mol Cell Biol
, vol.22
, pp. 4929-4942
-
-
Lei, K.1
Nimnual, A.2
Zong, W.X.3
-
21
-
-
0037174934
-
JNK phosphorylation and activation of BAD couples the stress-activated signaling pathway to the cell death machinery
-
Donovan N, Becker EB, Konishi Y, Bonni A. JNK phosphorylation and activation of BAD couples the stress-activated signaling pathway to the cell death machinery. J Biol Chem. 2002;277:40944-40949.
-
(2002)
J Biol Chem
, vol.277
, pp. 40944-40949
-
-
Donovan, N.1
Becker, E.B.2
Konishi, Y.3
Bonni, A.4
-
22
-
-
33744956666
-
Histone deacetylase 3 (HDAC3) and other class I HDACs regulate colon cell maturation and p21 expression and are deregulated in human colon cancer
-
Wilson AJ, Byun DS, Popova N, 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. 2006;281:13548-13558.
-
(2006)
J Biol Chem
, vol.281
, pp. 13548-13558
-
-
Wilson, A.J.1
Byun, D.S.2
Popova, N.3
-
23
-
-
30344477367
-
Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer
-
Minucci S, Pelicci PG. Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer. Nat Rev. 2006;6:38-51.
-
(2006)
Nat Rev
, vol.6
, pp. 38-51
-
-
Minucci, S.1
Pelicci, P.G.2
-
24
-
-
25144440127
-
Rational development of histone deacetylase inhibitors as anticancer agents: A review
-
Acharya MR, Sparreboom A, Venitz J, Figg WD. Rational development of histone deacetylase inhibitors as anticancer agents: a review. Mol Pharmacol. 2005;68:917-932.
-
(2005)
Mol Pharmacol
, vol.68
, pp. 917-932
-
-
Acharya, M.R.1
Sparreboom, A.2
Venitz, J.3
Figg, W.D.4
-
25
-
-
33846220751
-
Simvastatin attenuates cisplatin-induced kidney and liver damage in rats
-
Iseri S, Ercan F, Gedik N, Yuksel M, Alican I. Simvastatin attenuates cisplatin-induced kidney and liver damage in rats. Toxicology. 2007;230:256-264.
-
(2007)
Toxicology
, vol.230
, pp. 256-264
-
-
Iseri, S.1
Ercan, F.2
Gedik, N.3
Yuksel, M.4
Alican, I.5
-
26
-
-
0041342015
-
Drug-induced hepatotoxicity
-
Lee WM. Drug-induced hepatotoxicity. N Engl J Med. 2003;349:474-485.
-
(2003)
N Engl J Med
, vol.349
, pp. 474-485
-
-
Lee, W.M.1
-
27
-
-
0019182003
-
Metabolism of drugs by the kidney
-
Anders MW. Metabolism of drugs by the kidney. Kidney Int. 1980;18:636-647.
-
(1980)
Kidney Int
, vol.18
, pp. 636-647
-
-
Anders, M.W.1
-
28
-
-
0036554871
-
Akt inactivation is a key event in indole-3-carbinol-induced apoptosis in PC-3 cells
-
Chinni SR, Sarkar FH. Akt inactivation is a key event in indole-3-carbinol-induced apoptosis in PC-3 cells. Clin Cancer Res. 2002;8:1228-1236.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 1228-1236
-
-
Chinni, S.R.1
Sarkar, F.H.2
-
29
-
-
33646386136
-
Gene expression profiling revealed survivin as a target of 3,3′-diindolylmethane-induced cell growth inhibition and apoptosis in breast cancer cells
-
Rahman KW, Li Y, Wang Z, Sarkar SH, Sarkar FH. Gene expression profiling revealed survivin as a target of 3,3′-diindolylmethane-induced cell growth inhibition and apoptosis in breast cancer cells. Cancer Res. 2006;66: 4952-4960.
-
(2006)
Cancer Res
, vol.66
, pp. 4952-4960
-
-
Rahman, K.W.1
Li, Y.2
Wang, Z.3
Sarkar, S.H.4
Sarkar, F.H.5
-
30
-
-
0028242313
-
Anticarcinogenic activity of indole-3-carbinol acid products: Ultrasensitive bioassay by trout embryo microinjection
-
Dashwood RH, Fong AT, Arbogast DN, Bjeldanes LF, Hendricks JD, Bailey GS. Anticarcinogenic activity of indole-3-carbinol acid products: ultrasensitive bioassay by trout embryo microinjection. Cancer Res. 1994;54:3617-3619.
-
(1994)
Cancer Res
, vol.54
, pp. 3617-3619
-
-
Dashwood, R.H.1
Fong, A.T.2
Arbogast, D.N.3
Bjeldanes, L.F.4
Hendricks, J.D.5
Bailey, G.S.6
|