Benzo[a]pyrene-induced changes in microRNA-mRNA networks.

Abstract:

:Toxicological studies assessing the safety of compounds for humans frequently use in vitro systems to characterize toxic responses in combination with transcriptomic analyses. Thus far, changes have mostly been investigated at the mRNA level. Recently, microRNAs have attracted attention because they are powerful negative regulators of mRNA levels and, thus, may be responsible for the modulation of important mRNA networks implicated in toxicity. This study aimed to identify possible microRNA-mRNA networks as novel interactions on the gene expression level after a genotoxic insult. We used benzo[a]pyrene (BaP), a polycyclic aromatic hydrocarbon, as a model genotoxic/carcinogenic compound. We analyzed time-dependent effects on mRNA and microRNA profiles in HepG2 cells, a widely used human liver cell line that expresses active p53 and is competent for the biotransformation of BaP. Changes in microRNA expression in response to BaP, in combination with multiple alterations of mRNA levels, were observed. Many of these altered mRNAs are targets of altered microRNAs. Using pathway analysis, we evaluated the relevance of such microRNA deregulations to genotoxicity. This revealed eight microRNAs that appear to participate in specific BaP-responsive pathways relevant to genotoxicity, such as apoptotic signaling, cell cycle arrest, DNA damage response, and DNA damage repair. Our results particularly highlight the potential of microRNA-29b, microRNA-26a-1*, and microRNA-122* as novel players in the BaP response. Therefore, this study demonstrates the added value of an integrated microRNA-mRNA approach for identifying molecular mechanisms induced by BaP in an in vitro human model.

journal_name

Chem Res Toxicol

authors

Lizarraga D,Gaj S,Brauers KJ,Timmermans L,Kleinjans JC,van Delft JH

doi

10.1021/tx2003799

subject

Has Abstract

pub_date

2012-04-16 00:00:00

pages

838-49

issue

4

eissn

0893-228X

issn

1520-5010

journal_volume

25

pub_type

杂志文章
  • Chemical reactivity and skin sensitization potential for benzaldehydes: can Schiff base formation explain everything?

    abstract::Skin sensitizers chemically modify skin proteins rendering them immunogenic. Sensitizing chemicals have been divided into applicability domains according to their suspected reaction mechanism. The widely accepted Schiff base applicability domain covers aldehydes and ketones, and detailed structure-activity-modeling fo...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx300278t

    authors: Natsch A,Gfeller H,Haupt T,Brunner G

    更新日期:2012-10-15 00:00:00

  • Thalidomide and Its Analogs Differentially Target Fibroblast Growth Factor Receptors: Thalidomide Suppresses FGFR Gene Expression while Pomalidomide Dampens FGFR2 Activity.

    abstract::Thalidomide is an infamous teratogen and it is continuously being explored for its anticancer properties. Fibroblast growth factor receptors (FGFRs) are implicated in embryo development and cancer pathophysiology. With striking similarities observed between FGFR implicated conditions and thalidomide embryopathy, we hy...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.8b00286

    authors: Sundaresan L,Kumar P,Manivannan J,Balaguru UM,Kasiviswanathan D,Veeriah V,Anishetty S,Chatterjee S

    更新日期:2019-04-15 00:00:00

  • Mass spectrometric strategies for the identification and characterization of human serum albumin covalently adducted by amoxicillin: ex vivo studies.

    abstract::This study addresses the detection and characterization of the modification of human serum albumin (HSA) by amoxicillin (AX) in ex vivo samples from healthy subjects under oral amoxicillin administration (acute intake of 1 g every 8 h for 48 h). To reach this goal, we used an analytical strategy based on targeted and ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx500210e

    authors: Garzon D,Ariza A,Regazzoni L,Clerici R,Altomare A,Sirtori FR,Carini M,Torres MJ,Pérez-Sala D,Aldini G

    更新日期:2014-09-15 00:00:00

  • Endogenous interleukin-4 regulates glutathione synthesis following acetaminophen-induced liver injury in mice.

    abstract::In a recent study, we reported that interleukin (IL)-4 had a protective role against acetaminophen (APAP)-induced liver injury (AILI), although the mechanism of protection was unclear. Here, we carried out more detailed investigations and have shown that one way IL-4 may control the severity of AILI is by regulating g...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx2003992

    authors: Ryan PM,Bourdi M,Korrapati MC,Proctor WR,Vasquez RA,Yee SB,Quinn TD,Chakraborty M,Pohl LR

    更新日期:2012-01-13 00:00:00

  • Identification of colchicine in placental blood from patients using herbal medicines.

    abstract::While characterizing natural antiinflammatory substances in human placental blood, we discovered a factor that affected human neutrophils and their adherence. Rigorous chemical and stereochemical analyses revealed this factor to be the well-known alkaloid, colchicine. When samples from individual patients were analyze...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx0155101

    authors: Petty HR,Fernando M,Kindzelskii AL,Zarewych BN,Ksebati MB,Hryhorczuk LM,Mobashery S

    更新日期:2001-09-01 00:00:00

  • Synthesis and characterization of bay region halohydrins derived from Benzo[a]pyrene diol epoxide and their role as intermediates in halide-catalyzed cis adduct formation.

    abstract::The bay region epoxide of benzo[a]pyrene (anti-BPDE) alkylates DNA to form adducts with >98% trans stereochemistry. Halide ions catalyze this reaction; however, this pathway is characterized by the formation of adducts with altered cis stereochemistry. Bay region halohydrins are possible intermediates in these reactio...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx980056v

    authors: Song Q,Negrete GR,Wolfe AR,Wang K,Meehan T

    更新日期:1998-09-01 00:00:00

  • Characterization of the transient oxaphosphetane BChE inhibitor formed from spontaneously activated ethephon.

    abstract::The major plant growth regulator ethephon degrades to ethylene and phosphate in aqueous solutions and plants and is spontaneously activated to a butyrylcholinesterase (BChE) inhibitor in alkaline solutions and animal tissues. In the present (31)P NMR kinetic study of the reactions of ethephon in pH 7.4 carbonate buffe...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx4002429

    authors: Lantz SR,Casida JE

    更新日期:2013-09-16 00:00:00

  • Surface modification of quartz inhibits toxicity, particle uptake, and oxidative DNA damage in human lung epithelial cells.

    abstract::Quartz (crystalline silica) is not consistently carcinogenic across different industries where similar quartz exposure occurs. In addition, there are reports that surface modification of quartz affects its cytotoxicity, inflammogenicity, and fibrogenicity. Taken together, these data suggest that the carcinogenicity of...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx025558u

    authors: Schins RP,Duffin R,Höhr D,Knaapen AM,Shi T,Weishaupt C,Stone V,Donaldson K,Borm PJ

    更新日期:2002-09-01 00:00:00

  • A novel pectenotoxin, PTX-12, in Dinophysis spp. and shellfish from Norway.

    abstract::Two novel pectenotoxins (PTXs) were detected by LC-MS in solid phase extracts of net hauls taken at Flødevigen, Norway, in June 2002 that were dominated by Dinophysis acuminata and Dinophysis norvegica. The new compounds were isolated as minor components from a large collection of a Dinophysis acuta-dominated bloom ob...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx049870a

    authors: Miles CO,Wilkins AL,Samdal IA,Sandvik M,Petersen D,Quilliam MA,Naustvoll LJ,Rundberget T,Torgersen T,Hovgaard P,Jensen DJ,Cooney JM

    更新日期:2004-11-01 00:00:00

  • Biotransformation and clearance of 3-(phenylamino)propane-1,2-diol, a compound present in samples related to toxic oil syndrome, in C57BL/6 and A/J mice.

    abstract::In May 1981, a massive food-borne intoxication occurred in Spain. The so-called toxic oil syndrome (TOS) was associated with the consumption of aniline-denatured and refined rapeseed oil that was illegally sold as edible olive oil. Fatty acid anilides and fatty acid derivatives of 3-(phenylamino)propane-1,2-diol were ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx990105j

    authors: Ladona MG,Bujons J,Messeguer A,Ampurdanés C,Morató A,Corbella J

    更新日期:1999-12-01 00:00:00

  • In vitro reaction with DNA of the fjord-region diol epoxides of benzo[g]chrysene and benzo[c]phenanthrene as studied by 32P-postlabeling.

    abstract::The chemical reactivities of the optically-pure fjord-region syn- and anti-benzo[g]chrysene 11,12-dihydrodiol 13,14-epoxides (B[g]CDEs) toward DNA in vitro have been compared with those of the optically-pure fjord-region syn- and anti-benzo[c]phenanthrene 3,4-dihydrodiol 1,2-epoxides (B[c]PhDEs), using the standard 32...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00046a014

    authors: Giles AS,Seidel A,Phillips DH

    更新日期:1995-06-01 00:00:00

  • Metabolic studies on phencyclidine: characterization of a phencyclidine iminium ion metabolite.

    abstract::Studies on the metabolic bioactivation of the psychotomimetic amine phencyclidine have been pursued through the characterization of a new metabolite which is formed via initial cytochrome P-450 catalyzed oxidation of the parent drug to the corresponding iminium species. CI mass spectrometric and diode array UV and 1H ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00002a007

    authors: Hoag MK,Schmidt-Peetz M,Lampen P,Trevor A,Castagnoli N Jr

    更新日期:1988-03-01 00:00:00

  • Reevaluation of the effect of ellagic acid on N-methyl-N-nitrosourea DNA alkylation and mutagenicity.

    abstract::N-Methyl-N-nitrosourea (MNU) is a reactive, mutagenic methylating agent. MNU methylates DNA at various sites, including guanine N7, guanine O6, and adenine N3. Dixit and Gold [(1986) Proc. Natl. Acad. Sci. U.S.A. 83, 8039-8043] reported that ellagic acid, a phenolic natural product, inhibited the mutagenicity of MNU i...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00015a002

    authors: Lord HL,Josephy PD,Snieckus VA

    更新日期:1990-05-01 00:00:00

  • Sustained systemic delivery of green tea polyphenols by polymeric implants significantly diminishes benzo[a]pyrene-induced DNA adducts.

    abstract::The polyphenolics in green tea are believed to be the bioactive components. However, poor bioavailability following ingestion limits their efficacy in vivo. In this study, polyphenon E (poly E), a standardized green tea extract, was administered by sustained-release polycaprolactone implants (two, 2-cm implants; 20% d...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx2000625

    authors: Cao P,Vadhanam MV,Spencer WA,Cai J,Gupta RC

    更新日期:2011-06-20 00:00:00

  • Computational prediction of the chromosome-damaging potential of chemicals.

    abstract::We report on the generation of computer-based models for the prediction of the chromosome-damaging potential of chemicals as assessed in the in vitro chromosome aberration (CA) test. On the basis of publicly available CA-test results of more than 650 chemical substances, half of which are drug-like compounds, we gener...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx060136w

    authors: Rothfuss A,Steger-Hartmann T,Heinrich N,Wichard J

    更新日期:2006-10-01 00:00:00

  • Gamma-radiolysis and hydroxyl radical produce interstrand cross-links in DNA involving thymidine.

    abstract::Interstrand cross-links are minor components of the collection of products formed in DNA by ionizing radiation. Through their formation by other damaging agents, it is known that interstrand cross-links exert significant effects on replication and transcription. The structures of DNA interstrand cross-links produced a...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx7002307

    authors: Ding H,Greenberg MM

    更新日期:2007-11-01 00:00:00

  • Indirect cytotoxicity of flucloxacillin toward human biliary epithelium via metabolite formation in hepatocytes.

    abstract::Flucloxacillin, an isoxazolyl-penicillin, causes cholestasis and biliary epithelium injury. The aim of the study was to determine whether flucloxacillin, either directly or through metabolite formation, may induce cytotoxicity in hepatic or biliary cells. Cytotoxicity was assessed by lactate dehydrogenase release in p...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx0002435

    authors: Lakehal F,Dansette PM,Becquemont L,Lasnier E,Delelo R,Balladur P,Poupon R,Beaune PH,Housset C

    更新日期:2001-06-01 00:00:00

  • Nitrosation and nitration of 2-amino-3-methylimidazo[4,5-f]quinoline by reactive nitrogen oxygen species.

    abstract::Both cooked red meat intake and chronic inflammation/infection are thought to play a role in the etiology of colon cancer. The heterocyclic amine 2-amino-3-methylimidazo[4,5-f ]quinoline (IQ) is formed during cooking of red meat and may be involved in initiation of colon cancer. Reactive nitrogen oxygen species (RNOS)...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx020008h

    authors: Lakshmi VM,Hsu FF,Zenser TV

    更新日期:2002-08-01 00:00:00

  • Relative Propensities of Cytochrome c Oxidase and Cobalt Corrins for Reaction with Cyanide and Oxygen: Implications for Amelioration of Cyanide Toxicity.

    abstract::In aqueous media at neutral pH, the binding of two cyanide molecules per cobinamide can be described by two formation constants, Kf1 = 1.1 (±0.6) × 105 M-1 and Kf2 = 8.5 (±0.1) × 104 M-1, or an overall cyanide binding constant of ∼1 × 1010 M-2. In comparison, the cyanide binding constants for cobalamin and a fully oxi...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.7b00275

    authors: Yuan Q,Pearce LL,Peterson J

    更新日期:2017-12-18 00:00:00

  • Toxicant Deposition and Transport in Alveolus: A Classical Density Functional Prediction.

    abstract::The deposition and transport of toxicants on pulmonary surfactant are important processes in human health and medical care. We have introduced classical density functional theory (CDFT) to provide insight into this process. Nine typical toxicants in PM2.5 were considered, and their free energy and structural informati...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.8b00272

    authors: Liu H,Liu Y,Shang Y,Liu H

    更新日期:2018-12-17 00:00:00

  • P450 3A-Catalyzed O-Dealkylation of Lapatinib Induces Mitochondrial Stress and Activates Nrf2.

    abstract::Lapatinib (LAP), an oral tyrosine kinase inhibitor for the treatment of metastatic breast cancer, has been associated with idiosyncractic hepatotoxicity. Recent investigations have implicated the importance of P450 3A4/5 enzymes in the formation of an electrophilic quinone imine (LAPQI) metabolite generated through fu...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.5b00524

    authors: Eno MR,El-Gendy Bel-D,Cameron MD

    更新日期:2016-05-16 00:00:00

  • The pattern of p53 mutations caused by PAH o-quinones is driven by 8-oxo-dGuo formation while the spectrum of mutations is determined by biological selection for dominance.

    abstract::PAHs (polycyclic aromatic hydrocarbons) are suspect lung cancer carcinogens that must be metabolically converted into DNA-reactive metabolites. P4501A1/P4501B1 plus epoxide hydrolase activate PAH to (+/-)- anti-benzo[ a]pyrene diol epoxide ((+/-)- anti-BPDE), which causes bulky DNA adducts. Alternatively, aldo-keto re...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx700404a

    authors: Park JH,Gelhaus S,Vedantam S,Oliva AL,Batra A,Blair IA,Troxel AB,Field J,Penning TM

    更新日期:2008-05-01 00:00:00

  • Enzyme-mediated dialdehyde formation: an alternative pathway for benzo[a]pyrene 7,8-dihydrodiol bioactivation.

    abstract::Polycyclic aromatic hydrocarbons, such as benzo[a]pyrene, are widespread environmental carcinogens of human concern. Several enzymatic systems have been shown to activate benzo[a]pyrene 7, 8-dihydrodiol, the proximate carcinogenic metabolite of benzo[a]pyrene, to a reactive species which produces both a chemiluminesce...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx000159p

    authors: Stansbury KH,Noll DM,Groopman JD,Trush MA

    更新日期:2000-11-01 00:00:00

  • Reactions of the Zn Proteome with Cd2+ and Other Xenobiotics: Trafficking and Toxicity.

    abstract::Understanding the molecular basis of inorganic chemical toxicity has lagged behind the proliferation of detailed mechanisms that explain the biochemical toxicology of many organic xenobiotics. In this perspective, general barriers to explicating the bioinorganic chemistry of toxic metals are considered, followed by a ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.6b00328

    authors: Petering DH

    更新日期:2017-01-17 00:00:00

  • The nutritional supplement chromium(III) tris(picolinate) cleaves DNA.

    abstract::Chromium(III) tris(picolinate) [Cr(pic)3] is currently a very popular nutritional supplement; however, its safety has recently been questioned, especially with regard to its ability to act as a clastogen. At physiologically relevant concentrations, Cr(pic)3 is reduced by biological reductants, including ascorbate and ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx9900167

    authors: Speetjens JK,Collins RA,Vincent JB,Woski SA

    更新日期:1999-06-01 00:00:00

  • Biotransformation pathways of biocides and pharmaceuticals in freshwater crustaceans based on structure elucidation of metabolites using high resolution mass spectrometry.

    abstract::So far, there is limited information on biotransformation mechanisms and products of polar contaminants in freshwater crustaceans. In the present study, metabolites of biocides and pharmaceuticals formed in Gammarus pulex and Daphnia magna were identified using liquid chromatography-high resolution mass spectrometry. ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx300457f

    authors: Jeon J,Kurth D,Hollender J

    更新日期:2013-03-18 00:00:00

  • Redox properties and activity of iron-citrate complexes: evidence for redox cycling.

    abstract::Iron in iron overload disease is present as non-transferrin-bound iron, consisting of iron, citrate, and albumin. We investigated the redox properties of iron citrate by electrochemistry, by the kinetics of its reaction with ascorbate, by ESR, and by analyzing the products of reactions of ascorbate with iron citrate c...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx500377b

    authors: Adam FI,Bounds PL,Kissner R,Koppenol WH

    更新日期:2015-04-20 00:00:00

  • Thiol oxidation by 1,2,3-oxadiazolinium ions, presumed carcinogens.

    abstract::3-Alkyl-1,2,3-oxadiazolinium ions 1 have been proposed as reactive intermediates in the activation of (2-hydroxyethyl)nitrosamines. The reaction of 3-methyl-1,2,3-oxadiazolinium tosylate (1a), 2-ethyl-1-methoxy-2-phenyldiazenium tetrafluoroborate (3), and 3-phenyl-1,2,3-oxadiazolinium triflate (1b) with thiols was inv...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00048a001

    authors: Loeppky RN,Srinivasan A

    更新日期:1995-09-01 00:00:00

  • Bezafibrate induces a mitochondrial derangement in human cell lines: a PPAR-independent mechanism for a peroxisome proliferator.

    abstract::Bezafibrate is a hypolipidemic drug that belongs to the group of peroxisome proliferators because it binds to peroxisome proliferator-activated receptors type alpha (PPARs). Peroxisome proliferators produce a myriad of extraperoxisomal effects, which are not necessarily dependent on their interaction with PPARs. An in...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx0341052

    authors: Scatena R,Bottoni P,Vincenzoni F,Messana I,Martorana GE,Nocca G,De Sole P,Maggiano N,Castagnola M,Giardina B

    更新日期:2003-11-01 00:00:00

  • Qualitative analysis of the role of metabolites in inhibitory drug-drug interactions: literature evaluation based on the metabolism and transport drug interaction database.

    abstract::Guidance from the Food and Drug Administration on drug interaction studies does not include a specific section on contributions of metabolites to observed inhibitory drug-drug interactions, and the quantitative role of drug metabolites in inhibitory drug-drug interactions is not presently known. The current work was u...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章,评审

    doi:10.1021/tx800491e

    authors: Isoherranen N,Hachad H,Yeung CK,Levy RH

    更新日期:2009-02-01 00:00:00