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1.
Oncol Rep ; 36(4): 1875-85, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27509880

ABSTRACT

Epigenetic anticancer drugs such as histone deacetylase (HDAC) inhibitors have been combined with existing anticancer drugs for synergistic or additive effects. In the present study, we found that a very low concentration of depsipeptide, an HDAC inhibitor, potentiated the antitumor activity of 5-fluorouracil (5-FU) in a human colon cancer cell model using HCT-116, HT29, and SW48 cells via the inhibition of colony formation ability or cellular viability. Exposure to a combination of 5-FU (1.75 µM) and 1 nM depsipeptide for 24 and 48 h resulted in a 3- to 4-fold increase in activated caspase-3/7, while 5-FU alone failed to activate caspase-3/7. Microarray and subsequent gene ontology analyses revealed that compared to 5-FU or depsipeptide alone, the combination treatment of 5-FU and depsipeptide upregulated genes related to cell death and the apoptotic process consistent with the inhibition of colony formation and caspase-3/7 activation. These analyses indicated marked upregulation of antigen processing and presentation of peptide or polysaccharide antigen via major histocompatibility complex (MHC) class (GO:0002504) and MHC protein complex (GO:0042611). Compared with vehicle controls, the cells treated with the combination of 5-FU and depsipeptide showed marked induction (3- to 8.5-fold) of expression of MHC class II genes, but not of MHC class I genes. Furthermore, our global analysis of gene expression, which was focused on genes involved in the molecular regulation of MHC class II genes, showed enhancement of pro-apoptotic PCAF and CIITA after the combination of 5-FU and depsipeptide. These results may indicate a closer relationship between elevation of MHC class II expression and cellular apoptosis induced by the combination of depsipeptide and 5-FU. To the best of our knowledge, this is the first study to report that the combination of 5-FU and depsipeptide induces human colon cancer cell apoptosis in a concerted manner with the induction of MHC class II gene expression.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/pharmacology , Colonic Neoplasms/pathology , Depsipeptides/administration & dosage , Fluorouracil/pharmacology , Histocompatibility Antigens Class II/metabolism , Apoptosis/drug effects , Caspase 3/metabolism , Caspase 7/metabolism , Colonic Neoplasms/metabolism , Cyclin-Dependent Kinase Inhibitor p21/genetics , Drug Synergism , Enzyme Activation/drug effects , Gene Expression Regulation, Neoplastic , HCT116 Cells , Histone Deacetylase Inhibitors/administration & dosage , Humans , Oligonucleotide Array Sequence Analysis , Polymerase Chain Reaction , Transcriptional Activation/drug effects , Transcriptome , Up-Regulation
2.
Drug Metab Pharmacokinet ; 30(2): 188-97, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25989892

ABSTRACT

Constitutive androstane receptor (CAR) is one of the principal regulators of hepatic cytochrome P450s (CYPs) 3A (CYP3A). cDNA-mediated expression of a mature rat CAR (rCAR) into rat hepatoma cells induced CYP3A1 and CYP2B mRNAs. Aberrant rCAR failed in these inductions. Three important human CYP3A4 regulatory elements (REs), proximal ER6 (proER6), xenobiotic responsive enhancer module (XREM) and constitutive liver enhancer module (CLEM), support constitutive and inducible expression of CYP3As mediated by CAR and pregnane X receptor (PXR). NHR-scan software predicted proER6, XREM and CLEM at -255 b, -8 kb and -11.5 kb, respectively of CYP3A4, but neither XREM nor CLEM was predicted in rat CYP3A. A luciferase reporter construct carrying a 5'-flanking sequence of CYP3A1 (-31,739 to -31,585 from its transcription initiation site) revealed important for the rCAR-dependent transactivation of CYP3A1. This region includes two putative binding motifs of nuclear receptors (DR4 and DR2), a putative hepatocyte nuclear factor-1 binding motif (HNF1), nuclear factor-kappa B binding motif (NFκB), activator protein 1 binding motif (AP-1), and ecotropic viral integration site 1 binding motif (Evi1). We hereby conclude DR4 and/or DR2 motifs being primarily responsible and HNF1 being synergistically functioning elements for the rCAR-mediated transcription of CYP3A1.


Subject(s)
5' Flanking Region , Cytochrome P-450 CYP3A/genetics , Hepatocytes/enzymology , Receptors, Cytoplasmic and Nuclear/genetics , Response Elements , Animals , Binding Sites , Carcinoma, Hepatocellular/enzymology , Carcinoma, Hepatocellular/genetics , Cell Line, Tumor , Constitutive Androstane Receptor , Cytochrome P-450 CYP3A/metabolism , Dexamethasone/pharmacology , Gene Expression Regulation, Enzymologic , Genes, Reporter , Hepatocyte Nuclear Factor 1/metabolism , Hepatocytes/drug effects , Liver Neoplasms/enzymology , Liver Neoplasms/genetics , Male , Protein Binding , RNA, Messenger/metabolism , Rats, Inbred F344 , Receptors, Cytoplasmic and Nuclear/metabolism , Transcription, Genetic , Transcriptional Activation , Transfection , Tricarboxylic Acids/pharmacology
3.
J Toxicol Sci ; 38(4): 611-7, 2013.
Article in English | MEDLINE | ID: mdl-23824016

ABSTRACT

We have previously demonstrated super-induced expression of the Grin2c gene encoding the N-methyl-D-aspartate receptor 2C subunit during the process of liver enlargement induced by phenobarbital, clofibrate, piperonyl butoxide, or lead nitrate. In the present study, hepatic Grin2c gene expression levels were assessed by real-time RT-PCR in male F344 rats fed for 3 days, 4 weeks, and 13 weeks a diet containing either ß-naphthoflavone (BNF) (5,000 ppm), indole-3-carbinol (I3C) (2,000 ppm), or acetaminophen (AA) (12,500 ppm until the first 14 days; 10,000 ppm from 15 days on), each of which is capable of inducing hepatocellular hypertrophy. Especially, either the 4-week or the 13-week treatment with each chemical, except for BNF, resulted in a drastic increase in the expression level of the Grin2c gene. DNA microarray analysis using RNAs of 13-week-treated rats showed that in the I3C- and AA-treated rats, the fold-increase rates of the Grin2c gene ranked second and first, respectively, among the genes analyzed. Histopathological analyses indicated that the slight hepatocellular hypertrophy in the periportal area and the hepatocellular necrosis in a portion of the centrilobular area developed in the BNF-treated and AA-treated rats, respectively. In addition, relative liver weight was significantly higher in the rats treated with BNF and I3C than in the control rats. The present findings suggest the possibility that the induction of Grin2c gene expression is not necessarily dependent on only the development of liver enlargement, although the significance of this induction remains unclear.


Subject(s)
Acetaminophen/pharmacology , Gene Expression/drug effects , Hepatomegaly/genetics , Indoles/pharmacology , Liver/metabolism , Receptors, N-Methyl-D-Aspartate/genetics , beta-Naphthoflavone/pharmacology , Animals , Hepatomegaly/pathology , Liver/drug effects , Male , Oligonucleotide Array Sequence Analysis , Rats , Rats, Inbred F344 , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction , Time Factors
4.
Toxicol Pathol ; 41(8): 1078-92, 2013.
Article in English | MEDLINE | ID: mdl-23531792

ABSTRACT

The constitutive androstane receptor (CAR) is essential for Cyp2b induction, liver hypertrophy, and hepatocarcinogenesis in response to phenobarbital (PB). Liver hypertrophy with Cyp2b induction is a major mode of action of hepatocarcinogenesis in rodents. However, it remains unclear whether CAR is involved in the response to many other nongenotoxic hepatocarcinogens besides PB. In this study, we investigated CAR involvement in liver hypertrophy and hepatocarcinogenesis of Cyp2b-inducing nongenotoxic hepatocarcinogens, piperonyl butoxide (PBO), and decabromodiphenyl ether (DBDE), using wild-type and CAR knockout (CARKO) male mice. PB was used as the positive control. In the wild-type mice, 4-week treatment with PBO, DBDE, or PB induced hepatocellular hypertrophy with increased Cyp2b10 messenger RNA and Cyp2b protein expression. In CARKO mice, only PBO showed liver hypertrophy with Cyp2b10 and Cyp3a11 induction. After 27-week treatment following diethylnitrosamine initiation, PBO and PB generated many eosinophilic altered foci/adenomas in wild-type mice; however, the lesions were far less frequent in CARKO mice. DBDE increased the multiplicity of basophilic altered foci/adenomas in wild-type and CARKO mice. Our findings indicate that murine CAR plays major roles in hepatocarcinogenesis but not in liver hypertrophy of PBO. DBDE may act via CAR-independent pathways during hepatocarcinogenesis.


Subject(s)
Halogenated Diphenyl Ethers/toxicity , Liver Neoplasms, Experimental/chemically induced , Liver Neoplasms, Experimental/metabolism , Piperonyl Butoxide/toxicity , Receptors, Cytoplasmic and Nuclear/metabolism , Animals , Aryl Hydrocarbon Hydroxylases/genetics , Aryl Hydrocarbon Hydroxylases/metabolism , Body Weight/drug effects , Cell Proliferation/drug effects , Constitutive Androstane Receptor , Liver/cytology , Liver/drug effects , Liver/pathology , Liver Neoplasms, Experimental/pathology , Male , Mice , Mice, Inbred C3H , Mice, Knockout , Organ Size/drug effects
5.
J Toxicol Sci ; 37(2): 281-6, 2012.
Article in English | MEDLINE | ID: mdl-22467018

ABSTRACT

The present study examined hepatic estrogen receptor (ER) and androgen receptor (AR) levels as well as estrogen-signaling status in a model of rat hepatic hypertrophy induced by phenobarbital (PB), chlofibrate (CF), or piperonyl butoxide (PBO). Male F344 rats were fed with PB at 2,500 ppm, CF at 2,500 ppm, and PBO at 20,000 ppm for 3 days, 4 weeks, and 13 weeks. CF and PBO induced diffuse hypertrophy, while centrilobular hypertrophy was observed with PB administration. The levels of mRNA for ERα, AR and leukemia inhibitory factor receptor (LIFR) which was found to be estrogen responsive in the present study, were determined by quantitative RT-PCR. In the CF and PBO groups, ERα mRNA expression was reduced, and consequently, the expression of a responsive gene, LIFR, was also decreased, while PB had no effect on ER mRNA levels. AR mRNA expression decreased in all the treated groups, but reduction was persistent only in PB group. Recently, LIFR was identified as a tumor suppressor gene in human HCC. Thus, LIFR may be one of the key mediators of hepatic carcinogenesis induced by CF and PBO, but PB appears to act via different mechanisms.


Subject(s)
Carcinogens/toxicity , Estrogen Receptor alpha/genetics , Hepatomegaly/metabolism , Receptors, Androgen/genetics , Animals , CD36 Antigens/genetics , Clofibrate/toxicity , Female , Hepatomegaly/chemically induced , Hepatomegaly/pathology , Leukemia Inhibitory Factor Receptor alpha Subunit/genetics , Liver/drug effects , Liver/metabolism , Liver/pathology , Male , Phenobarbital/toxicity , Piperonyl Butoxide/toxicity , RNA, Messenger/metabolism , Rats , Rats, Inbred F344
6.
J Toxicol Sci ; 36(5): 507-14, 2011 Oct.
Article in English | MEDLINE | ID: mdl-22008526

ABSTRACT

To identify gene expression that can be closely involved in chemical-induced hepatocellular hypertrophy, the hepatic gene expression profile was assessed by cDNA microarray analysis in male F344 rats fed for 3 days, 4 weeks, and 13 weeks a diet containing a hepatocellular hypertrophy inducer, either phenobarbital (500 ppm), clofibrate (2,500 ppm), or piperonyl butoxide (20,000 ppm). The results showed that, in all treatment groups, the increased expressional rate of the Grin2c gene, which encodes the N-methyl-D-aspartate receptor 2C subunit (NR2C), was the highest among those of all the genes tested, as compared with the corresponding gene expression in rats fed a normal diet. Moreover, real-time RT-PCR analysis showed that the expression levels of the Grin2c gene in rats fed with each chemical clearly increased in a chemical treatment period-dependent fashion, and that the increased rate was closely correlated with the grade of hypertrophy of hepatocytes rather than with the increased rate in liver weight. These results suggest the possibility that chemical-induced NR2C expression relates to the development of hepatocellular hypertrophy.


Subject(s)
Gene Expression/drug effects , Hepatomegaly/chemically induced , Receptors, N-Methyl-D-Aspartate/genetics , Animals , Clofibrate/toxicity , Disease Models, Animal , Hepatomegaly/genetics , Hepatomegaly/pathology , Liver/drug effects , Liver/metabolism , Liver/pathology , Male , Oligonucleotide Array Sequence Analysis , Organ Size/drug effects , Phenobarbital/toxicity , Piperonyl Butoxide/toxicity , Rats , Rats, Inbred F344 , Reverse Transcriptase Polymerase Chain Reaction
7.
J Toxicol Sci ; 36(5): 613-23, 2011 Oct.
Article in English | MEDLINE | ID: mdl-22008536

ABSTRACT

The purpose of our study was to examine the altered gene expression associated with nongenotoxic chemical-mediated liver hypertrophy and successive liver tumor promotion. Five-week-old male rats were fed a basal diet or a diet containing phenobarbital (PB) or clofibrate (CF) for 3 days, 4 weeks, and 13 weeks. Hepatic expression profiling of cell growth- and stress-related genes, as well as those involved in xenobiotic metabolism, was performed by DNA microarray and/or real time quantitative reverse transcription-polymerase chain reaction. The induction of liver hypertrophy and hepatic cytochrome P450 (CYP) isoforms (CYP2B1/2B2 for PB and CYP4A1 for CF) by PB and CF were clearly observed at all the treatment periods examined. Genes encoding DNA damage-inducible 45 (GADD45) family proteins, in particular GADD45g (GADD45 gamma) were down-regulated by treatment with either PB or CF for 4 and 13 weeks. The chemical-mediated development of liver hypertrophy, induction of hepatic CYPs, and suppression of hepatic GADD45g gene at week 13 disappeared at 4 weeks following cessation of the chemical treatment. Additionally, DNA microarray data indicated that cell cycle-related genes such as cyclins CCNB1 and CCNA2 and cyclin-dependent kinase inhibitor CDKN3 were also down-regulated by treatment with either PB or CF at 13 weeks. Since GADD45 functions as a chemical and radiation stress sensor by interacting with cyclins and cyclin-dependent kinase inhibitors, the decrease in the gene expression of GADD45g mRNA observed in this study, may be associated with nongenotoxic chemical-induced tumor promotion of hepatocarcinogenesis rather than liver hypertrophy.


Subject(s)
Cell Cycle Proteins/genetics , DNA Damage , Gene Expression/drug effects , Hepatomegaly/chemically induced , Liver Neoplasms, Experimental/chemically induced , Liver/drug effects , Nuclear Proteins/genetics , Animals , Clofibrate/toxicity , Cytochrome P-450 Enzyme System/biosynthesis , DNA Damage/genetics , Down-Regulation , Enzyme Induction , Gene Expression Profiling , Hepatomegaly/genetics , Hepatomegaly/pathology , Isoenzymes , Liver/enzymology , Liver/metabolism , Liver/pathology , Liver Neoplasms, Experimental/genetics , Liver Neoplasms, Experimental/pathology , Male , Oligonucleotide Array Sequence Analysis , Phenobarbital/toxicity , Rats , Rats, Inbred F344 , Real-Time Polymerase Chain Reaction , Time Factors , Xenobiotics/toxicity
8.
Drug Metab Pharmacokinet ; 26(6): 577-83, 2011.
Article in English | MEDLINE | ID: mdl-21878739

ABSTRACT

Cross-talk between the aryl hydrocarbon receptor (AhR) pathway and the typical stress response is thought to be an important signal transduction in response to nutrient-stress conditions, such as glucose deprivation in liver cells. In the present study, we demonstrate that reduction of glucose concentration in the medium of HepG2 cells, a human hepatocellular carcinoma cell line, induces the CYP1 family and Nrf2. RNAi for AhR abolishes the induction of expression of CYP1 and Nrf2. These inductions are accompanied by the translocation of AhR into the nucleus in response to low-glucose conditions. Endogenous compounds are recruited as AhR ligands to induce various gene expressions, and our present results suggest that an endogenous AhR ligand is produced under low-glucose conditions and that the role of AhR as a transcription factor is related to the low-glucose response. The recommended glucose concentration (4.5 g/L) in the medium for culture of HepG2 was used as the high-glucose concentration in this study. We adopted 1.0 g/L as the low-glucose condition for elucidation of mechanisms of the stress response. These results will be useful to understand the relationship between drug-metabolizing enzymes and mechanisms of the anti-stress response of tumor cells, and will also be useful for investigating preventive remedies against tumor angiogenesis.


Subject(s)
Cell Nucleus/metabolism , Cytochrome P-450 Enzyme System/biosynthesis , Receptors, Aryl Hydrocarbon/biosynthesis , Carcinoma, Hepatocellular/enzymology , Carcinoma, Hepatocellular/genetics , Carcinoma, Hepatocellular/metabolism , Cell Line, Tumor , Cell Nucleus/enzymology , Cell Nucleus/genetics , Cytochrome P-450 Enzyme System/genetics , Gene Expression Regulation, Enzymologic , Gene Expression Regulation, Neoplastic , Gene Knockdown Techniques/methods , Glucose/metabolism , Hep G2 Cells , Humans , Inactivation, Metabolic , Ligands , Liver Neoplasms/enzymology , Liver Neoplasms/genetics , Liver Neoplasms/metabolism , NF-E2-Related Factor 2/genetics , NF-E2-Related Factor 2/metabolism , Protein Transport , Receptors, Aryl Hydrocarbon/genetics , Receptors, Aryl Hydrocarbon/metabolism , Signal Transduction
9.
Oncogene ; 21(38): 5823-34, 2002 Aug 29.
Article in English | MEDLINE | ID: mdl-12185581

ABSTRACT

Shc family of docking proteins, ShcA, ShcB and ShcC, play roles in cellular signal transduction by binding to phosphotyrosine residues of various activated receptor tyrosine kinases. Both ShcB and ShcC proteins are selectively expressed in the neural system of adult mouse tissues. In most of neuroblastoma cells, obvious tyrosine phosphorylation of ShcC was observed, whereas expression of ShcB was considerably low. Phosphoproteins associated with hyperphosphorylated ShcC were purified from neuroblastoma cell lines, and identified by mass-spectrometry. Anaplastic lymphoma kinase (ALK), which turned out to be one of these phosphoproteins, was constitutively activated and associated with the PTB domain of ShcC in three neuroblastoma cells. In vitro kinase assay revealed that ShcC is a potent substrate of the activated ALK kinase. The ALK gene locus was significantly amplified in both of these cell lines, suggesting that gene amplification leads to constitutive activation of the ALK kinase, which results in hyperphosphorylation of ShcC. Constitutive activation of ALK appeared to interfere with signals from other receptor tyrosine kinases. ALK-ShcC signal activation, possibly caused by co-amplification with the N-myc gene, might give additional effects on malignant tumor progression of neuroblastoma.


Subject(s)
Nerve Tissue Proteins/metabolism , Neuroblastoma/metabolism , Neuropeptides , Protein-Tyrosine Kinases/metabolism , Receptor Protein-Tyrosine Kinases/metabolism , Adult , Anaplastic Lymphoma Kinase , Animals , Chromatography, Affinity/methods , Enzyme Activation , Humans , Infant , Male , Mice , Mice, Nude , Nervous System Neoplasms/metabolism , Neuroblastoma/genetics , Phosphoproteins/isolation & purification , Phosphoproteins/metabolism , Phosphorylation , Protein-Tyrosine Kinases/genetics , Receptor Protein-Tyrosine Kinases/genetics , Shc Signaling Adaptor Proteins , Signal Transduction , Src Homology 2 Domain-Containing, Transforming Protein 3 , Tumor Cells, Cultured , Tyrosine/metabolism
10.
Leuk Lymphoma ; 43(2): 415-20, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11999578

ABSTRACT

A chimeric gene, AML1-MTG16, showing high homology to AML1-MTG8, was recently identified in adult leukemic patients with the abnormal karyotype t(16;21)(q24;q22). We recently saw a child patient of 11 years of age who developed acute myelogenous leukemia with the karyotype t(16;21)(q24;q22), 11 months after autologous peripheral blood stem-cell transplantation (PBSCT) for acute promyelocytic leukemia with karyotype t(15;17)(q22;q11). The reciprocal translocation was localized by fluorescence in situ hybridization (FISH) analysis, reverse transcription polymerase chain reaction (RT-PCR), and Southern blot analysis of bone marrow blood cells and peripheral blood cells. FISH analysis identified a reciprocal translocation between chromosomes 16 and 21. RT-PCR analysis identified expression of the chimeric gene AML1-MTG16. Southern blot analysis revealed a breakpoint occurring at a 1.4 kb Eco RI fragment between exons 3 and 4 of MTG16. The breakpoint is within the same region as that of secondary leukemias, which has been reported previously. This case suggests the possibility that the region of the breakpoint of MTG16 is a characteristic of secondary leukemia.


Subject(s)
Leukemia, Myeloid, Acute/genetics , Neoplasms, Second Primary/genetics , Oncogene Proteins, Fusion/genetics , Transcription Factors/genetics , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Bone Marrow Transplantation , Child , Chromosome Breakage , Chromosomes, Human, Pair 16 , Chromosomes, Human, Pair 21 , Core Binding Factor Alpha 2 Subunit , Cytogenetic Analysis , Humans , Leukemia, Myeloid, Acute/diagnosis , Leukemia, Myeloid, Acute/therapy , Leukemia, Promyelocytic, Acute/pathology , Leukemia, Promyelocytic, Acute/therapy , Neoplasms, Second Primary/diagnosis , Neoplasms, Second Primary/pathology , Translocation, Genetic
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