-
1
-
-
0019029156
-
Polycyclic aromatic hydrocarbons: A review
-
Zedeck,M.S. (1980) Polycyclic aromatic hydrocarbons: A review. J. Environ. Pathol. Toxicol., 3, 537-567.
-
(1980)
J. Environ. Pathol. Toxicol.
, vol.3
, pp. 537-567
-
-
Zedeck, M.S.1
-
2
-
-
0028987872
-
The aryl hydrocarbon receptor complex
-
Hankinson,O. (1995) The aryl hydrocarbon receptor complex. Annu. Rev. Pharmacol. Toxicol., 35, 307-340.
-
(1995)
Annu. Rev. Pharmacol. Toxicol.
, vol.35
, pp. 307-340
-
-
Hankinson, O.1
-
3
-
-
0032832051
-
Cancer initiation by polycyclic aromatic hydrocarbons results from formation of stable DNA adducts rather than apurinic sites
-
Melendez-Colon,V.J., Luch,A., Seidel,A. and Baird,W.M. (1999) Cancer initiation by polycyclic aromatic hydrocarbons results from formation of stable DNA adducts rather than apurinic sites. Carcinogenesis, 20, 1885-1891.
-
(1999)
Carcinogenesis
, vol.20
, pp. 1885-1891
-
-
Melendez-Colon, V.J.1
Luch, A.2
Seidel, A.3
Baird, W.M.4
-
4
-
-
0033543728
-
A chemical inhibitor of p53 that protects mice from the side effects of cancer therapy
-
Komarov,P.G., Komarova,E.A., Kondratov,R.V., Christov-Tselkov,K., Coon,J.S., Chernov,M.V. and Gudkov,A.V. (1999) A chemical inhibitor of p53 that protects mice from the side effects of cancer therapy. Science, 285, 1733-1737.
-
(1999)
Science
, vol.285
, pp. 1733-1737
-
-
Komarov, P.G.1
Komarova, E.A.2
Kondratov, R.V.3
Christov-Tselkov, K.4
Coon, J.S.5
Chernov, M.V.6
Gudkov, A.V.7
-
5
-
-
0033632162
-
Suppression of p53: A new approach to overcome side effects of antitumor therapy
-
Komarova,E.A. and Gudkov,A.V. (2000) Suppression of p53: A new approach to overcome side effects of antitumor therapy. Biochemistry (Mosc), 65, 41-48.
-
(2000)
Biochemistry (Mosc)
, vol.65
, pp. 41-48
-
-
Komarova, E.A.1
Gudkov, A.V.2
-
6
-
-
1642413019
-
Polycyclic aromatic hydrocarbons modulate cell proliferation in rat hepatic epithelial stem-like WB-F344 cells
-
Chramostova,K., Vondracek,J., Sindlerova,L., Vojtesek,B., Kozubik,A. and Machala,M. (2004) Polycyclic aromatic hydrocarbons modulate cell proliferation in rat hepatic epithelial stem-like WB-F344 cells. Toxicol. Appl. Pharmacol., 196, 136-148.
-
(2004)
Toxicol. Appl. Pharmacol.
, vol.196
, pp. 136-148
-
-
Chramostova, K.1
Vondracek, J.2
Sindlerova, L.3
Vojtesek, B.4
Kozubik, A.5
Machala, M.6
-
7
-
-
33644983705
-
Activation of ERK1/2 and p38 kinases by polycyclic aromatic hydrocarbons in rat liver epithelial cells is associated with induction of apoptosis
-
in press
-
Andrysik,Z., Machala,M., Chramostova,K., Hofmanova,J., Kozubik,A. and Vondracek,J. (2005) Activation of ERK1/2 and p38 kinases by polycyclic aromatic hydrocarbons in rat liver epithelial cells is associated with induction of apoptosis. Toxicol. Appl. Pharmacol., in press.
-
(2005)
Toxicol. Appl. Pharmacol.
-
-
Andrysik, Z.1
Machala, M.2
Chramostova, K.3
Hofmanova, J.4
Kozubik, A.5
Vondracek, J.6
-
8
-
-
13444261149
-
Role of cell signaling in B[a]P-induced apoptosis: Characterization of unspecific effects of cell signaling inhibitors and apoptotic effects of B[a]P metabolites
-
Solhaug,A., Ovrebo,S., Mollerup,S., Lag,M., Schwarze,P.E., Nesnow,S. and Holme,J.A. (2005) Role of cell signaling in B[a]P-induced apoptosis: characterization of unspecific effects of cell signaling inhibitors and apoptotic effects of B[a]P metabolites. Chem. Biol. Interact., 151, 101-119.
-
(2005)
Chem. Biol. Interact.
, vol.151
, pp. 101-119
-
-
Solhaug, A.1
Ovrebo, S.2
Mollerup, S.3
Lag, M.4
Schwarze, P.E.5
Nesnow, S.6
Holme, J.A.7
-
9
-
-
1842740285
-
Cytochrome P450-dependent toxicity of environmental polycyclic aromatic hydrocarbons towards human macrophages
-
van Grevenynghe,J., Sparfel,L., Le Vee,M., Gilot,D., Drenou,B., Fauchet,R. and Fardel,O. (2004) Cytochrome P450-dependent toxicity of environmental polycyclic aromatic hydrocarbons towards human macrophages. Biochem. Biophys. Res. Commun., 317, 708-716.
-
(2004)
Biochem. Biophys. Res. Commun.
, vol.317
, pp. 708-716
-
-
van Grevenynghe, J.1
Sparfel, L.2
Le Vee, M.3
Gilot, D.4
Drenou, B.5
Fauchet, R.6
Fardel, O.7
-
10
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
Bradford,M.M. (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem., 72, 248-254.
-
(1976)
Anal. Biochem.
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
11
-
-
1842785906
-
Inhibition of carcinogen-bioactivating cytochrome P450 1 isoforms by amiloride derivatives
-
Sparfel,L., Huc,L., Le Vee,M., Desille,M., Lagadic-Gossmann,D. and Fardel,O. (2004) Inhibition of carcinogen-bioactivating cytochrome P450 1 isoforms by amiloride derivatives. Biochem. Pharmacol., 67, 1711-1719.
-
(2004)
Biochem. Pharmacol.
, vol.67
, pp. 1711-1719
-
-
Sparfel, L.1
Huc, L.2
Le Vee, M.3
Desille, M.4
Lagadic-Gossmann, D.5
Fardel, O.6
-
12
-
-
0022357068
-
Ethoxy-, pentoxy- and benzyloxyphenoxazones and homologues: A series of substrates to distinguish between different induced cytochromes P-450
-
Burke,M.D., Thompson,S., Elcombe,C.R., Halpert,J., Haaparanta,T. and Mayer,R.T. (1985) Ethoxy-, pentoxy- and benzyloxyphenoxazones and homologues: A series of substrates to distinguish between different induced cytochromes P-450. Biochem. Pharmacol., 34, 3337-3345.
-
(1985)
Biochem. Pharmacol.
, vol.34
, pp. 3337-3345
-
-
Burke, M.D.1
Thompson, S.2
Elcombe, C.R.3
Halpert, J.4
Haaparanta, T.5
Mayer, R.T.6
-
13
-
-
0031694273
-
Selectivity of polycyclic inhibitors for human cytochrome P450s 1A1, 1A2, and 1B1
-
Shimada,T., Yamazaki,H., Foroozesh,M., Hopkins,N.E., Alworth,W.L. and Guengerich,F.P. (1998) Selectivity of polycyclic inhibitors for human cytochrome P450s 1A1, 1A2, and 1B1. Chem. Res. Toxicol., 11, 1048-1056.
-
(1998)
Chem. Res. Toxicol.
, vol.11
, pp. 1048-1056
-
-
Shimada, T.1
Yamazaki, H.2
Foroozesh, M.3
Hopkins, N.E.4
Alworth, W.L.5
Guengerich, F.P.6
-
14
-
-
0025875527
-
The Ah receptor and the mechanism of dioxin toxicity
-
Landers,J.P. and Bunce,N.J. (1991) The Ah receptor and the mechanism of dioxin toxicity. Biochem. J., 276 (Pt 2), 273-287.
-
(1991)
Biochem. J.
, vol.276
, Issue.PART 2
, pp. 273-287
-
-
Landers, J.P.1
Bunce, N.J.2
-
15
-
-
2442428432
-
Polycyclic aromatic hydrocarbons induce both apoptotic and anti-apoptotic signals in Hepa1c1c7 cells
-
Solhaug,A., Refsnes,M., Lag,M., Schwarze,P.E., Husoy,T. and Holme,J.A. (2004) Polycyclic aromatic hydrocarbons induce both apoptotic and anti-apoptotic signals in Hepa1c1c7 cells. Carcinogenesis, 25, 809-819.
-
(2004)
Carcinogenesis
, vol.25
, pp. 809-819
-
-
Solhaug, A.1
Refsnes, M.2
Lag, M.3
Schwarze, P.E.4
Husoy, T.5
Holme, J.A.6
-
16
-
-
22944470831
-
The p53 inhibitor pifithrin-alpha is a potent agonist of the aryl hydrocarbon receptor
-
Hoagland,M.S., Hoagland,E.M. and Swanson,H.I. (2005) The p53 inhibitor pifithrin-alpha is a potent agonist of the aryl hydrocarbon receptor. J. Pharmacol. Exp. Ther., 314, 603-610.
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.314
, pp. 603-610
-
-
Hoagland, M.S.1
Hoagland, E.M.2
Swanson, H.I.3
-
17
-
-
0037369909
-
Polycyclic aromatic hydrocarbons inhibit differentiation of human monocytes into macrophages
-
van Grevenynghe,J., Rion,S., Le Ferrec,E., Le Vee,M., Amiot,L., Fauchet,R. and Fardel,O. (2003) Polycyclic aromatic hydrocarbons inhibit differentiation of human monocytes into macrophages. J. Immunol., 170, 2374-2381.
-
(2003)
J. Immunol.
, vol.170
, pp. 2374-2381
-
-
van Grevenynghe, J.1
Rion, S.2
Le Ferrec, E.3
Le Vee, M.4
Amiot, L.5
Fauchet, R.6
Fardel, O.7
-
18
-
-
13644263678
-
Deregulation of cell proliferation by polycyclic aromatic hydrocarbons in human breast carcinoma MCF-7 cells reflects both genotoxic and nongenotoxic events
-
Pliskova,M., Vondracek,J., Vojtesek,B., Kozubik,A. and Machala,M. (2005) Deregulation of cell proliferation by polycyclic aromatic hydrocarbons in human breast carcinoma MCF-7 cells reflects both genotoxic and nongenotoxic events. Toxicol. Sci., 83, 246-256.
-
(2005)
Toxicol. Sci.
, vol.83
, pp. 246-256
-
-
Pliskova, M.1
Vondracek, J.2
Vojtesek, B.3
Kozubik, A.4
Machala, M.5
-
19
-
-
0028978675
-
p53 protein expression is correlated with benzo[a]pyrene-DNA adducts in carcinoma cell lines
-
Ramet,M., Castren,K., Jarvinen,K., Pekkala,K., Turpeenniemi-Hujanen,T., Soini,Y., Paakko,P. and Vahakangas,K. (1995) p53 protein expression is correlated with benzo[a]pyrene-DNA adducts in carcinoma cell lines. Carcinogenesis, 16, 2117-2124.
-
(1995)
Carcinogenesis
, vol.16
, pp. 2117-2124
-
-
Ramet, M.1
Castren, K.2
Jarvinen, K.3
Pekkala, K.4
Turpeenniemi-Hujanen, T.5
Soini, Y.6
Paakko, P.7
Vahakangas, K.8
-
20
-
-
13444287101
-
Role of cell signalling involved in induction of apoptosis by benzo[a]pyrene and cyclopenta[c,d]pyrene in Hepa1c1c7 cells
-
Solhaug,A., Refsnes,M. and Holme,J.A. (2004) Role of cell signalling involved in induction of apoptosis by benzo[a]pyrene and cyclopenta[c,d]pyrene in Hepa1c1c7 cells. J. Cell. Biochem., 93, 1143-1154.
-
(2004)
J. Cell. Biochem.
, vol.93
, pp. 1143-1154
-
-
Solhaug, A.1
Refsnes, M.2
Holme, J.A.3
-
21
-
-
0031048884
-
Radiation-enhanced expression of interferon-inducible genes in the KG1a primitive hematopoietic cell line
-
Clave,E., Carosella,E.D., Gluckman,E. and Socie,G. (1997) Radiation-enhanced expression of interferon-inducible genes in the KG1a primitive hematopoietic cell line. Leukemia, 11, 114-119.
-
(1997)
Leukemia
, vol.11
, pp. 114-119
-
-
Clave, E.1
Carosella, E.D.2
Gluckman, E.3
Socie, G.4
-
22
-
-
0030008731
-
Activation of chemically diverse procarcinogens by human cytochrome P-450 1B1
-
Shimada,T., Hayes,C.L., Yamazaki,H., Amin,S., Hecht,S.S., Guengerich,F.P. and Sutter,T.R. (1996) Activation of chemically diverse procarcinogens by human cytochrome P-450 1B1. Cancer Res., 56, 2979-2984.
-
(1996)
Cancer Res.
, vol.56
, pp. 2979-2984
-
-
Shimada, T.1
Hayes, C.L.2
Yamazaki, H.3
Amin, S.4
Hecht, S.S.5
Guengerich, F.P.6
Sutter, T.R.7
-
23
-
-
0142231975
-
Discovery of cytochrome P450 1B1 inhibitors as new promising anti-cancer agents
-
Chun,Y.J. and Kim,S. (2003) Discovery of cytochrome P450 1B1 inhibitors as new promising anti-cancer agents. Med. Res. Rev., 23, 657-668.
-
(2003)
Med. Res. Rev.
, vol.23
, pp. 657-668
-
-
Chun, Y.J.1
Kim, S.2
-
24
-
-
0037292971
-
Cytochrome P450 1B1: A target for inhibition in anticarcinogenesis strategies
-
Guengerich,F.P., Chun,Y.J., Kim,D., Gillam,E.M. and Shimada,T. (2003) Cytochrome P450 1B1: A target for inhibition in anticarcinogenesis strategies. Mutat. Res., 523-524, 173-182.
-
(2003)
Mutat. Res.
, vol.523-524
, pp. 173-182
-
-
Guengerich, F.P.1
Chun, Y.J.2
Kim, D.3
Gillam, E.M.4
Shimada, T.5
-
25
-
-
0037206613
-
Inhibition of human cytochrome P450 1B1, 1A1 and 1A2 by antigenotoxic compounds, purpurin and alizarin
-
Takahashi,E., Fujita,K., Kamataki,T., Arimoto-Kobayashi,S., Okamoto,K. and Negishi,T. (2002) Inhibition of human cytochrome P450 1B1, 1A1 and 1A2 by antigenotoxic compounds, purpurin and alizarin. Mutat. Res., 508, 147-156.
-
(2002)
Mutat. Res.
, vol.508
, pp. 147-156
-
-
Takahashi, E.1
Fujita, K.2
Kamataki, T.3
Arimoto-Kobayashi, S.4
Okamoto, K.5
Negishi, T.6
-
26
-
-
0035890772
-
A new selective and potent inhibitor of human cytochrome P450 1B1 and its application to antimutagenesis
-
[Erratum (2002) Cancer Res., 62, 1232.]
-
Chun,Y.J., Kim,S., Kim,D., Lee,S.K. and Guengerich,F.P. (2001) A new selective and potent inhibitor of human cytochrome P450 1B1 and its application to antimutagenesis [Erratum (2002) Cancer Res., 62, 1232.]. Cancer Res., 61, 8164-8170.
-
(2001)
Cancer Res.
, vol.61
, pp. 8164-8170
-
-
Chun, Y.J.1
Kim, S.2
Kim, D.3
Lee, S.K.4
Guengerich, F.P.5
-
27
-
-
0033014568
-
The flavonoid galangin is an inhibitor of CYP1A1 activity and an agonist/antagonist of the aryl hydrocarbon receptor
-
Ciolino,H.P. and Yeh,G.C. (1999) The flavonoid galangin is an inhibitor of CYP1A1 activity and an agonist/antagonist of the aryl hydrocarbon receptor. Br. J. Cancer, 79, 1340-1346.
-
(1999)
Br. J. Cancer
, vol.79
, pp. 1340-1346
-
-
Ciolino, H.P.1
Yeh, G.C.2
-
28
-
-
6444222048
-
Resveratrol inhibits TCDD-induced expression of CYP1A1 and CYP1B1 and catechol estrogen-mediated oxidative DNA damage in cultured human mammary epithelial cells
-
Chen,Z.H., Hurh,Y.J., Na,H.K., Kim,J.H., Chun,Y.J., Kim,D.H., Kang,K.S., Cho,M.H. and Surh,Y.J. (2004) Resveratrol inhibits TCDD-induced expression of CYP1A1 and CYP1B1 and catechol estrogen-mediated oxidative DNA damage in cultured human mammary epithelial cells. Carcinogenesis, 25, 2005-2013.
-
(2004)
Carcinogenesis
, vol.25
, pp. 2005-2013
-
-
Chen, Z.H.1
Hurh, Y.J.2
Na, H.K.3
Kim, J.H.4
Chun, Y.J.5
Kim, D.H.6
Kang, K.S.7
Cho, M.H.8
Surh, Y.J.9
-
29
-
-
0038807711
-
Flavonoids: Promising anticancer agents
-
Ren,W., Qiao,Z., Wang,H., Zhu,L. and Zhang,L. (2003) Flavonoids: promising anticancer agents. Med. Res. Rev., 23, 519-534.
-
(2003)
Med. Res. Rev.
, vol.23
, pp. 519-534
-
-
Ren, W.1
Qiao, Z.2
Wang, H.3
Zhu, L.4
Zhang, L.5
-
30
-
-
2142673078
-
The p53-inhibitor pifithrin-alpha inhibits firefly luciferase activity in vivo and in vitro
-
Rocha,S., Campbell,K.J., Roche,K.C. and Perkins,N.D. (2003) The p53-inhibitor pifithrin-alpha inhibits firefly luciferase activity in vivo and in vitro. BMC Mol. Biol., 4, 9.
-
(2003)
BMC Mol. Biol.
, vol.4
, pp. 9
-
-
Rocha, S.1
Campbell, K.J.2
Roche, K.C.3
Perkins, N.D.4
-
31
-
-
0037507247
-
p53 inhibitor pifithrin alpha can suppress heat shock and glucocorticoid signaling pathways
-
Komarova,E.A., Neznanov,N., Komarov,P.G., Chemov,M.V., Wang,K. and Gudkov,A.V. (2003) p53 inhibitor pifithrin alpha can suppress heat shock and glucocorticoid signaling pathways. J. Biol. Chem., 278, 15465-15468.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 15465-15468
-
-
Komarova, E.A.1
Neznanov, N.2
Komarov, P.G.3
Chemov, M.V.4
Wang, K.5
Gudkov, A.V.6
-
32
-
-
0141569519
-
Reciprocal inhibition of p53 and nuclear factor-kappaB transcriptional activities determines cell survival or death in neurons
-
Culmsee,C., Siewe,J., Junker,V., Retiounskaia,M., Schwarz,S., Camandola,S., El-Metainy,S., Behnke,H., Mattson,M.P. and Krieglstein,J. (2003) Reciprocal inhibition of p53 and nuclear factor-kappaB transcriptional activities determines cell survival or death in neurons. J. Neurosci., 23, 8586-8595.
-
(2003)
J. Neurosci.
, vol.23
, pp. 8586-8595
-
-
Culmsee, C.1
Siewe, J.2
Junker, V.3
Retiounskaia, M.4
Schwarz, S.5
Camandola, S.6
El-Metainy, S.7
Behnke, H.8
Mattson, M.P.9
Krieglstein, J.10
-
33
-
-
18144428775
-
Prospective therapeutic applications of p53 inhibitors
-
Gudkov,A.V. and Komarova,E.A. (2005) Prospective therapeutic applications of p53 inhibitors. Biochem. Biophys. Res. Commun., 331, 726-736.
-
(2005)
Biochem. Biophys. Res. Commun.
, vol.331
, pp. 726-736
-
-
Gudkov, A.V.1
Komarova, E.A.2
-
35
-
-
0026561121
-
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours
-
Donehower,L.A., Harvey,M., Slagle,B.L., McArthur,M.J., Montgomery,C.A.Jr, Butel,J.S. and Bradley,A. (1992) Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours. Nature, 356, 215-221.
-
(1992)
Nature
, vol.356
, pp. 215-221
-
-
Donehower, L.A.1
Harvey, M.2
Slagle, B.L.3
McArthur, M.J.4
Montgomery Jr., C.A.5
Butel, J.S.6
Bradley, A.7
|