|1.||El-Kadi, Ayman O S: 4 articles (04/2010 - 09/2004)|
|2.||Izzotti, A: 2 articles (05/2015 - 03/2001)|
|3.||Shibutani, Makoto: 2 articles (02/2010 - 06/2009)|
|4.||Mitsumori, Kunitoshi: 2 articles (02/2010 - 06/2009)|
|5.||Dewa, Yasuaki: 2 articles (02/2010 - 06/2009)|
|6.||Jinno, Hideto: 2 articles (08/2006 - 08/2002)|
|7.||Tanaka-Kagawa, Toshiko: 2 articles (08/2006 - 08/2002)|
|8.||Korashy, Hesham M: 2 articles (11/2004 - 09/2004)|
|9.||Elbekai, Reem H: 2 articles (11/2004 - 10/2004)|
|10.||Luo, Wei-Cheng: 1 article (12/2015)|
06/01/2009 - "Molecular expression analysis of beta-naphthoflavone-induced hepatocellular tumors in rats."
01/01/1981 - "NMRI Swiss strain exhibits a natural high sensitivity to the carcinogenic effect of the hydrocarbon, and the pretreatment of mice be beta-naphthoflavone leads to a large decrease of the formation of tumors. "
05/01/2006 - "The results demonstrated that DMBA-DNA adduct formation in both cancer cell lines was inhibited by SA at concentrations of > or = 2.5 mM. CYP1A was undetectable in RMTCs while CYP1A induction by beta-naphthoflavone in MCF-7 cells was significantly inhibited by SA in a concentration-dependent manner. "
07/01/2000 - "Liver tumor-promoting effect of beta-naphthoflavone, a strong CYP 1A1/2 inducer, and the relationship between CYP 1A1/2 induction and Cx32 decrease in its hepatocarcinogenesis in the rat."
10/01/1988 - "Tumor induction was inhibited by indole-3-carbinol (27.5% incidence, 1.89 tumors per tumor-bearing fish) but enhanced by beta-naphthoflavone (91.8% incidence, 3.60 tumors per tumor-bearing fish). "
|2.||Hepatocellular Carcinoma (Hepatoma)
02/25/2015 - "H4IIE rat hepatoma cells were challenged with high ROS levels after exposure to CuNPs, while the AhR-induced cellular anti-oxidant defence was simultaneously activated by the AhR ligand beta-Naphthoflavone (ßNF). "
08/01/2006 - "In this study, we focused on UGT1A isoforms (UGT1A1, UGT1A6 and UGT1A9), mainly expressed in the human liver, and examined the inducibility of UGT1As by beta-naphthoflavone (BNF) in human hepatoma HepG2 cells. "
07/01/1989 - "At least two cis-regulatory elements were identified in the 5'-flanking region of the Ya gene: one, responsible for the basal level of expression, is present in the sequence up to -0.2 kb; another, responsible for the inducible expression by aromatic compounds such as beta-naphthoflavone and 3-methylcholanthrene, is located in the sequence from -0.2 kb to -1.6 kb. The inducible element was functional only in cells with normal aromatic compound receptors, and it retained responsiveness to beta-naphthoflavone when transfected into homologous (mouse) or heterologous (rat, human) hepatoma cells. "
11/01/2004 - "Benzo[a]pyrene, 3-methylcholanthrene and beta-naphthoflavone induce oxidative stress in hepatoma hepa 1c1c7 Cells by an AHR-dependent pathway."
08/09/2002 - "DNA microarrays and real time PCR were used to analyze the mechanism of gene induction by CYP1A1 inducers, beta-naphthoflavone, and omeprazole, in the human hepatocellular carcinoma HepG2 cells. "
05/20/1994 - "Large variations were noticed for expression of the NQO2 and NQO1 genes among various tissues, 1336 bp of the 5'-flanking region of the NQO2 gene containing ARE and XRE was found sufficient to increase expression of the CAT gene in response to beta-naphthoflavone and tCDD in transfected human hepatoblastoma (Hep-G2) cells."
07/25/1992 - "Deletion mutagenesis and transfection studies into hepatic (mouse hepatoma (Hepa-1) and human hepatoblastoma (Hep-G2)) and nonhepatic (HeLa) cells indicated that high levels of expression of the human NAD(P)H:quinone oxidoreductase gene in tumor cells and its induction by beta-naphthoflavone and 3-(2)-tert-butyl-4-hydroxyanisole are mediated by human antioxidant response element (hARE) located in the region between -470 and -445. "
09/01/1989 - "Induction of the cytochrome P-450 monooxygenase system with beta-naphthoflavone did not alter venular contractions induced by hypoxia or anoxia. "
06/01/1998 - "In this study, we analyzed the effects of beta-naphthoflavone (beta-NF) and hypoxia on these parameters and expression of key enzymes of glucose metabolism. "
|3.||Cytochrome P-450 Enzyme System (Cytochrome P450)
|5.||DNA (Deoxyribonucleic Acid)
|6.||Messenger RNA (mRNA)
|7.||Butylated Hydroxyanisole (BHA)
|9.||Protein Isoforms (Isoforms)