Stiborová M - Search Results

1

The first identification of the benzenediazonium ion formation from a non-aminoazo dye, 1-phenylazo-2-hydroxynaphthalene (Sudan I) by microsomes of rat livers.

Stiborová M, Asfaw B, Anzenbacher P, Leseticky L, Hodek P. Stiborová M, et al. Cancer Lett. 1988 Jun 30;40(3):319-26. doi: 10.1016/0304-3835(88)90091-2. Cancer Lett. 1988. PMID: 3383183

2

Expression of cytochrome P450 1A1 and its contribution to oxidation of a potential human carcinogen 1-phenylazo-2-naphthol (Sudan I) in human livers.

Stiborová M, Martínek V, Rýdlová H, Koblas T, Hodek P. Stiborová M, et al. Cancer Lett. 2005 Apr 8;220(2):145-54. doi: 10.1016/j.canlet.2004.07.036. Cancer Lett. 2005. PMID: 15766589

3

Peroxidase-mediated reaction of the carcinogenic non-aminoazo dye 1-phenylazo-2-hydroxynaphthalene with transfer ribonucleic acid.

Stiborová M, Frei E, Klokow K, Wiessler M, Safarík L, Anzenbacher P, Hradec J. Stiborová M, et al. Carcinogenesis. 1990 Oct;11(10):1789-94. doi: 10.1093/carcin/11.10.1789. Carcinogenesis. 1990. PMID: 2208592

4

Activation of carcinogens by peroxidase. Horseradish peroxidase-mediated formation of benzenediazonium ion from a non-aminoazo dye, 1-phenylazo-2-hydroxynaphthalene (Sudan I) and its binding to DNA.

Stiborová M, Asfaw B, Anzenbacher P. Stiborová M, et al. FEBS Lett. 1988 May 23;232(2):387-90. doi: 10.1016/0014-5793(88)80776-2. FEBS Lett. 1988. PMID: 3378630 Free article.

5

A new way to carcinogenicity of azo dyes: the benzenediazonium ion formed from a non-aminoazo dye, 1-phenylazo-2-hydroxynaphthalene(Sudan I) by microsomal enzymes binds to deoxyguanosine residues of DNA.

Stiborová M, Asfaw B, Anzenbacher P, Hodek P. Stiborová M, et al. Cancer Lett. 1988 Jun 30;40(3):327-33. doi: 10.1016/0304-3835(88)90092-4. Cancer Lett. 1988. PMID: 3383184

6

Benzenediazonium ion derived from Sudan I forms an 8-(phenylazo)guanine adduct in DNA.

Stiborová M, Asfaw B, Frei E, Schmeiser HH, Wiessler M. Stiborová M, et al. Chem Res Toxicol. 1995 Jun;8(4):489-98. doi: 10.1021/tx00046a002. Chem Res Toxicol. 1995. PMID: 7548728

7

Peroxidase-activated carcinogenic azo dye Sudan I (Solvent Yellow 14) binds to guanosine in transfer ribonucleic acid.

Stiborová M, Asfaw B, Frei E. Stiborová M, et al. Gen Physiol Biophys. 1995 Feb;14(1):39-49. Gen Physiol Biophys. 1995. PMID: 8529865

8

Sudan I is a potential carcinogen for humans: evidence for its metabolic activation and detoxication by human recombinant cytochrome P450 1A1 and liver microsomes.

Stiborová M, Martínek V, Rýdlová H, Hodek P, Frei E. Stiborová M, et al. Cancer Res. 2002 Oct 15;62(20):5678-84. Cancer Res. 2002. PMID: 12384524

9

Human hepatic and renal microsomes, cytochromes P450 1A1/2, NADPH:cytochrome P450 reductase and prostaglandin H synthase mediate the formation of aristolochic acid-DNA adducts found in patients with urothelial cancer.

Stiborová M, Frei E, Hodek P, Wiessler M, Schmeiser HH. Stiborová M, et al. Int J Cancer. 2005 Jan 10;113(2):189-97. doi: 10.1002/ijc.20564. Int J Cancer. 2005. PMID: 15386410

10

The binding of aristolochic acid I to the active site of human cytochromes P450 1A1 and 1A2 explains their potential to reductively activate this human carcinogen.

Stiborová M, Sopko B, Hodek P, Frei E, Schmeiser HH, Hudecek J. Stiborová M, et al. Cancer Lett. 2005 Nov 18;229(2):193-204. doi: 10.1016/j.canlet.2005.06.038. Epub 2005 Aug 24. Cancer Lett. 2005. PMID: 16125300

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