Single-Walled vs. Multi-Walled Carbon Nanotubes: Influence of Physico-Chemical Properties on Toxicogenomics Responses in Mouse Lungs
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U. Vogel | K. Jensen | H. Wallin | S. Halappanavar | P. Clausen | S. S. Poulsen | K. B. Knudsen | P. Danielsen | A. Williams | Silvia Aidee Solorio-Rodriguez
[1] W. Wang,et al. SIRT1 prevents cigarette smoking-induced lung fibroblasts activation by regulating mitochondrial oxidative stress and lipid metabolism , 2022, Journal of translational medicine.
[2] K. Singh,et al. Do Carbon Nanotubes and Asbestos Fibers Exhibit Common Toxicity Mechanisms? , 2022, Nanomaterials.
[3] A. Markov,et al. Asthma and Post-Asthmatic Fibrosis: A Search for New Promising Molecular Markers of Transition from Acute Inflammation to Pulmonary Fibrosis , 2022, Biomedicines.
[4] M. Ohnishi,et al. Assessment of the toxicity and carcinogenicity of double-walled carbon nanotubes in the rat lung after intratracheal instillation: a two-year study , 2022, Particle and Fibre Toxicology.
[5] Yanan Du,et al. Mechanical communication in fibrosis progression. , 2021, Trends in cell biology.
[6] Hye-Youn Cho,et al. Transcriptomics Underlying Pulmonary Ozone Pathogenesis Regulated by Inflammatory Mediators in Mice , 2021, Antioxidants.
[7] J. Bourdon-Lacombe,et al. Potency ranking of per- and polyfluoroalkyl substances using high-throughput transcriptomic analysis of human liver spheroids. , 2021, Toxicological sciences : an official journal of the Society of Toxicology.
[8] U. Vogel,et al. In vitro-in vivo correlations of pulmonary inflammogenicity and genotoxicity of MWCNT , 2021, Particle and Fibre Toxicology.
[9] A. T. Saber,et al. In vitro-in vivo correlations of pulmonary inflammogenicity and genotoxicity of MWCNT , 2021, Particle and fibre toxicology.
[10] J. Thompson,et al. Transcriptome analysis reveals key genes modulated by ALK5 inhibition in a bleomycin model of systemic sclerosis , 2021, Rheumatology.
[11] E. Clini,et al. Pulmonary Stretch and Lung Mechanotransduction: Implications for Progression in the Fibrotic Lung , 2021, International journal of molecular sciences.
[12] N. Jacobsen,et al. Reactive oxygen species production, genotoxicity and telomere length in FE1-Muta™Mouse lung epithelial cells exposed to carbon nanotubes , 2021, Nanotoxicology.
[13] Nisha S. Sipes,et al. Benchmark Concentrations for Untargeted Metabolomics vs. Transcriptomics for Liver Injury Compounds in in Vitro Liver Models. , 2021, Toxicological sciences : an official journal of the Society of Toxicology.
[14] A. De Vizcaya-Ruiz,et al. In vitro cytotoxicity study of superparamagnetic iron oxide and silica nanoparticles on pneumocyte organelles. , 2020, Toxicology in vitro : an international journal published in association with BIBRA.
[15] K. Chinna,et al. Toxicity of Carbon Nanotubes: Molecular Mechanisms, Signaling Cascades, and Remedies in Biomedical Applications. , 2020, Chemical research in toxicology.
[16] M. Ohnishi,et al. Comparative carcinogenicity study of a thick, straight-type and a thin, tangled-type multi-walled carbon nanotube administered by intra-tracheal instillation in the rat , 2020, Particle and Fibre Toxicology.
[17] Mengjuan Zhang,et al. T Cells in Fibrosis and Fibrotic Diseases , 2020, Frontiers in Immunology.
[18] I. Garcia-Arcos,et al. Alveolar lipids in pulmonary disease. A review , 2020, Lipids in Health and Disease.
[19] Dongmei Wu,et al. 21st Century Tools for Nanotoxicology: Transcriptomic Biomarker Panel and Precision-Cut Lung Slice Organ Mimic System for the Assessment of Nanomaterial-Induced Lung Fibrosis. , 2020, Small.
[20] Nicklas Raun Jacobsen,et al. Acute Phase Response as a Biological Mechanism-of-Action of (Nano)particle-Induced Cardiovascular Disease. , 2020, Small.
[21] Chaobo Huang,et al. Multi-walled carbon nanotubes (MWCNTs) transformed THP-1 macrophages into foam cells: Impact of pulmonary surfactant component dipalmitoylphosphatidylcholine. , 2020, Journal of hazardous materials.
[22] E. Bargagli,et al. Serum amyloid A: A potential biomarker of lung disorders. , 2019, Respiratory investigation.
[23] Gennady Korotkevich,et al. Fast gene set enrichment analysis , 2019, bioRxiv.
[24] D. Corry,et al. Electronic cigarettes disrupt lung lipid homeostasis and innate immunity independent of nicotine. , 2019, The Journal of clinical investigation.
[25] U. Vogel,et al. Acute phase response and inflammation following pulmonary exposure to low doses of zinc oxide nanoparticles in mice , 2019, Nanotoxicology.
[26] M. Bell,et al. Circadian rhythms in skin and other elastic tissues. , 2019, Matrix biology : journal of the International Society for Matrix Biology.
[27] H. Fukui,et al. Comparison of the effects of multiwall carbon nanotubes on the epithelial cells and macrophages , 2019, Nanotoxicology.
[28] A. Naiki‐Ito,et al. MWCNT‐7 administered to the lung by intratracheal instillation induces development of pleural mesothelioma in F344 rats , 2019, Cancer science.
[29] D. Greco,et al. Surface PEGylation suppresses pulmonary effects of CuO in allergen-induced lung inflammation , 2019, Particle and Fibre Toxicology.
[30] Andrew Williams,et al. Ranking of nanomaterial potency to induce pathway perturbations associated with lung responses , 2019, NanoImpact.
[31] C. D. Dela Cruz,et al. BPIFA1 regulates lung neutrophil recruitment and interferon signaling during acute inflammation. , 2019, American journal of physiology. Lung cellular and molecular physiology.
[32] Satish K. Sharma,et al. Oxidative damage of SP‐D abolishes control of eosinophil extracellular DNA trap formation , 2018, Journal of leukocyte biology.
[33] Q. Ma,et al. Type 2 Immune Mechanisms in Carbon Nanotube-Induced Lung Fibrosis , 2018, Front. Immunol..
[34] Håkan Wallin,et al. Influence of dispersion medium on nanomaterial-induced pulmonary inflammation and DNA strand breaks: investigation of carbon black, carbon nanotubes and three titanium dioxide nanoparticles , 2017, Mutagenesis.
[35] Dongmei Wu,et al. Multi-walled carbon nanotube-induced genotoxic, inflammatory and pro-fibrotic responses in mice: Investigating the mechanisms of pulmonary carcinogenesis. , 2017, Mutation research.
[36] Andrew Williams,et al. Application of bi-clustering of gene expression data and gene set enrichment analysis methods to identify potentially disease causing nanomaterials , 2017, Data in brief.
[37] H. Kataura,et al. A 104-week pulmonary toxicity assessment of long and short single-wall carbon nanotubes after a single intratracheal instillation in rats , 2017, Inhalation toxicology.
[38] Dongmei Wu,et al. Stat-6 signaling pathway and not Interleukin-1 mediates multi-walled carbon nanotube-induced lung fibrosis in mice: insights from an adverse outcome pathway framework , 2017, Particle and Fibre Toxicology.
[39] R. Bowler,et al. Gene and metabolite time-course response to cigarette smoking in mouse lung and plasma , 2017, PloS one.
[40] Håkan Wallin,et al. Multi-walled carbon nanotube-physicochemical properties predict the systemic acute phase response following pulmonary exposure in mice , 2017, PloS one.
[41] R. Pavlović,et al. Gene expression profiles among murine strains segregate with distinct differences in the progression of radiation-induced lung disease , 2017, Disease Models & Mechanisms.
[42] Jacqueline P. Williams,et al. Radiation induced pulmonary fibrosis as a model of progressive fibrosis: Contributions of DNA damage, inflammatory response and cellular senescence genes , 2017, Experimental lung research.
[43] S. Kralj,et al. Harmful at non-cytotoxic concentrations: SiO2-SPIONs affect surfactant metabolism and lamellar body biogenesis in A549 human alveolar epithelial cells , 2017, Nanotoxicology.
[44] S. Halappanavar,et al. Toxicogenomics analysis of mouse lung responses following exposure to titanium dioxide nanomaterials reveal their disease potential at high doses , 2016, Mutagenesis.
[45] Andrew Williams,et al. A framework for the use of single-chemical transcriptomics data in predicting the hazards associated with complex mixtures of polycyclic aromatic hydrocarbons , 2016, Archives of Toxicology.
[46] H. Kato,et al. Pulmonary and pleural inflammation after intratracheal instillation of short single-walled and multi-walled carbon nanotubes. , 2016, Toxicology letters.
[47] P. Bushel,et al. Effects of mannose-binding lectin on pulmonary gene expression and innate immune inflammatory response to ozone. , 2016, American journal of physiology. Lung cellular and molecular physiology.
[48] Per Axel Clausen,et al. Multi-walled carbon nanotube physicochemical properties predict pulmonary inflammation and genotoxicity , 2016, Nanotoxicology.
[49] Q. Ma,et al. In vivo activation of a T helper 2-driven innate immune response in lung fibrosis induced by multi-walled carbon nanotubes , 2016, Archives of Toxicology.
[50] Naveena Yanamala,et al. Integrated Analysis of Dysregulated ncRNA and mRNA Expression Profiles in Humans Exposed to Carbon Nanotubes , 2016, PloS one.
[51] Jeffrey J. Sutherland,et al. Assessing Concordance of Drug-Induced Transcriptional Response in Rodent Liver and Cultured Hepatocytes , 2016, PLoS Comput. Biol..
[52] Manuel C. Peitsch,et al. Comprehensive systems biology analysis of a 7-month cigarette smoke inhalation study in C57BL/6 mice , 2016, Scientific Data.
[53] M. Ohnishi,et al. Lung carcinogenicity of inhaled multi-walled carbon nanotube in rats , 2015, Particle and Fibre Toxicology.
[54] Andrew Williams,et al. Nano-risk Science: application of toxicogenomics in an adverse outcome pathway framework for risk assessment of multi-walled carbon nanotubes , 2015, Particle and Fibre Toxicology.
[55] J. Pitroda,et al. A Critical Review on Carbon Nanotubes , 2016 .
[56] Andrew Williams,et al. Application of biclustering of gene expression data and gene set enrichment analysis methods to identify potentially disease causing nanomaterials , 2015, Beilstein journal of nanotechnology.
[57] U. Vogel,et al. Carbon black nanoparticles induce biphasic gene expression changes associated with inflammatory responses in the lungs of C57BL/6 mice following a single intratracheal instillation , 2015, Toxicology and Applied Pharmacology.
[58] K. Walters,et al. Prior infection with Type A Francisella tularensis antagonizes the pulmonary transcriptional response to an aerosolized Toll-like receptor 4 agonist , 2015, BMC Genomics.
[59] I. Rahman,et al. Circadian clock-coupled lung cellular and molecular functions in chronic airway diseases. , 2015, American journal of respiratory cell and molecular biology.
[60] Andrew Williams,et al. MWCNTs of different physicochemical properties cause similar inflammatory responses, but differences in transcriptional and histological markers of fibrosis in mouse lungs. , 2015, Toxicology and applied pharmacology.
[61] Nicklas Raun Jacobsen,et al. Transcriptional profiling identifies physicochemical properties of nanomaterials that are determinants of the in vivo pulmonary response , 2015, Environmental and molecular mutagenesis.
[62] Vittorio Fortino,et al. Inhalation of rod-like carbon nanotubes causes unconventional allergic airway inflammation , 2014, Particle and Fibre Toxicology.
[63] Oliver Eickelberg,et al. Cigarette smoke-induced iBALT mediates macrophage activation in a B cell-dependent manner in COPD. , 2014, American journal of physiology. Lung cellular and molecular physiology.
[64] Håkan Wallin,et al. Particle-induced pulmonary acute phase response may be the causal link between particle inhalation and cardiovascular disease , 2014, Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology.
[65] Feng Yang,et al. Effect of multi-walled carbon nanotube surface modification on bioactivity in the C57BL/6 mouse model , 2014, Nanotoxicology.
[66] Liying Wang,et al. Effect of Fiber Length on Carbon Nanotube-Induced Fibrogenesis , 2014, International journal of molecular sciences.
[67] Y. Bossé,et al. Impact of Cigarette Smoke on the Human and Mouse Lungs: A Gene-Expression Comparison Study , 2014, PloS one.
[68] David Bechtold,et al. The circadian clock regulates rhythmic activation of the NRF2/glutathione-mediated antioxidant defense pathway to modulate pulmonary fibrosis , 2014, Genes & development.
[69] Milind B. Suraokar,et al. Radiation-Enhanced Lung Cancer Progression in a Transgenic Mouse Model of Lung Cancer Is Predictive of Outcomes in Human Lung and Breast Cancer , 2014, Clinical Cancer Research.
[70] Dongmei Wu,et al. Transcriptomic Analysis Reveals Novel Mechanistic Insight into Murine Biological Responses to Multi-Walled Carbon Nanotubes in Lungs and Cultured Lung Epithelial Cells , 2013, PloS one.
[71] U. Vogel,et al. Validation of freezing tissues and cells for analysis of DNA strand break levels by comet assay , 2013, Mutagenesis.
[72] U. Shankavaram,et al. Role of type II pneumocyte senescence in radiation-induced lung fibrosis. , 2013, Journal of the National Cancer Institute.
[73] U. Vogel,et al. Carbon Black Nanoparticle Intratracheal Instillation Does Not Alter Cardiac Gene Expression , 2013, Cardiovascular Toxicology.
[74] Jacob S. Lamson,et al. Particle-Induced Pulmonary Acute Phase Response Correlates with Neutrophil Influx Linking Inhaled Particles and Cardiovascular Risk , 2013, PloS one.
[75] U. Vogel,et al. Pulmonary instillation of low doses of titanium dioxide nanoparticles in mice leads to particle retention and gene expression changes in the absence of inflammation. , 2013, Toxicology and applied pharmacology.
[76] Andrew Williams,et al. Mice exposed in situ to urban air pollution exhibit pulmonary alterations in gene expression in the lipid droplet synthesis pathways , 2013, Environmental and molecular mutagenesis.
[77] Carla M. T. Bauer,et al. Bleomycin Induces Molecular Changes Directly Relevant to Idiopathic Pulmonary Fibrosis: A Model for “Active” Disease , 2013, PloS one.
[78] Zongxi Li,et al. Surface charge and cellular processing of covalently functionalized multiwall carbon nanotubes determine pulmonary toxicity. , 2013, ACS nano.
[79] T. Luedde,et al. miR-199a-5p Is Upregulated during Fibrogenic Response to Tissue Injury and Mediates TGFbeta-Induced Lung Fibroblast Activation by Targeting Caveolin-1 , 2013, PLoS genetics.
[80] J. Samet,et al. Particulate matter induces cardiac arrhythmias via dysregulation of carotid body sensitivity and cardiac sodium channels. , 2012, American journal of respiratory cell and molecular biology.
[81] M. Hayashi,et al. In vivo genotoxicity study of single-wall carbon nanotubes using comet assay following intratracheal instillation in rats. , 2012, Regulatory toxicology and pharmacology : RTP.
[82] T. Moritake,et al. Strain-dependent damage in mouse lung after carbon ion irradiation. , 2012, International journal of radiation oncology, biology, physics.
[83] Yong Qian,et al. Multiwalled Carbon Nanotube-Induced Gene Signatures in the Mouse Lung: Potential Predictive Value for Human Lung Cancer Risk and Prognosis , 2012, Journal of toxicology and environmental health. Part A.
[84] Dongmei Wu,et al. Exposure of pregnant mice to carbon black by intratracheal instillation: toxicogenomic effects in dams and offspring. , 2012, Mutation research.
[85] S. Auerbach,et al. Differential Transcriptomic Analysis of Spontaneous Lung Tumors in B6C3F1 Mice: Comparison to Human Non–Small Cell Lung Cancer , 2012, Toxicologic pathology.
[86] Errol M. Thomson,et al. Overexpression of tumor necrosis factor-α in the lungs alters immune response, matrix remodeling, and repair and maintenance pathways. , 2012, The American journal of pathology.
[87] Ivana V. Yang,et al. Novel regulators of the systemic response to lipopolysaccharide. , 2011, American journal of respiratory cell and molecular biology.
[88] G. Wu,et al. FIZZ2/RELM-β Induction and Role in Pulmonary Fibrosis , 2011, The Journal of Immunology.
[89] S. Kleeberger,et al. Identification of Candidate Genes Downstream of TLR4 Signaling after Ozone Exposure in Mice: A Role for Heat-Shock Protein 70 , 2011, Environmental health perspectives.
[90] Andrew Williams,et al. Environmental and Molecular Mutagenesis 52:425^439 (2011) Research Article Pulmonary Response to Surface-Coated Nanotitanium Dioxide Particles Includes Induction of Acute Phase Response Genes, Inflammatory Cascades, and Changes in MicroRNAs: A Toxicogenom , 2022 .
[91] S. Moghaddam,et al. Interleukin 6, but Not T Helper 2 Cytokines, Promotes Lung Carcinogenesis , 2010, Cancer Prevention Research.
[92] J. Fostel,et al. Protective Role of Interleukin-10 in Ozone-Induced Pulmonary Inflammation , 2010, Environmental health perspectives.
[93] M. Kashon,et al. Response of the mouse lung transcriptome to welding fume: effects of stainless and mild steel fumes on lung gene expression in A/J and C57BL/6J mice , 2010, Respiratory research.
[94] A. Sweet-Cordero,et al. Loss of p130 accelerates tumor development in a mouse model for human small-cell lung carcinoma. , 2010, Cancer research.
[95] Stephan Gebel,et al. The transcriptome of Nrf2-/- mice provides evidence for impaired cell cycle progression in the development of cigarette smoke-induced emphysematous changes. , 2010, Toxicological sciences : an official journal of the Society of Toxicology.
[96] S. Hester,et al. Differential Transcriptional Changes in Mice Exposed to Chemically Distinct Diesel Samples , 2010, Biomedical informatics insights.
[97] Jürgen Pauluhn,et al. Subchronic 13-week inhalation exposure of rats to multiwalled carbon nanotubes: toxic effects are determined by density of agglomerate structures, not fibrillar structures. , 2010, Toxicological sciences : an official journal of the Society of Toxicology.
[98] T. Xia,et al. Understanding biophysicochemical interactions at the nano-bio interface. , 2009, Nature materials.
[99] Shyam Biswal,et al. Cigarette smoke-induced emphysema in A/J mice is associated with pulmonary oxidative stress, apoptosis of lung cells, and global alterations in gene expression. , 2009, American journal of physiology. Lung cellular and molecular physiology.
[100] A. Loudon,et al. Circadian timing in the lung; a specific role for bronchiolar epithelial cells. , 2009, Endocrinology.
[101] Nicklas Raun Jacobsen,et al. Lung inflammation and genotoxicity following pulmonary exposure to nanoparticles in ApoE-/- mice , 2009, Particle and Fibre Toxicology.
[102] Steve Horvath,et al. WGCNA: an R package for weighted correlation network analysis , 2008, BMC Bioinformatics.
[103] J. Samet,et al. Murine Lung Responses to Ambient Particulate Matter: Genomic Analysis and Influence on Airway Hyperresponsiveness , 2008, Environmental health perspectives.
[104] Ivana V. Yang,et al. Fibroproliferation in LPS-induced airway remodeling and bleomycin-induced fibrosis share common patterns of gene expression , 2008, Immunogenetics.
[105] A. Scott,et al. Hookworm-Induced Persistent Changes to the Immunological Environment of the Lung , 2008, Infection and Immunity.
[106] S. Hester,et al. Increased transcription of immune and metabolic pathways in naive and allergic mice exposed to diesel exhaust. , 2008, Toxicological sciences : an official journal of the Society of Toxicology.
[107] D. Voehringer,et al. Disease-specific gene expression profiling in multiple models of lung disease. , 2008, American journal of respiratory and critical care medicine.
[108] T. Wynn,et al. Cellular and molecular mechanisms of fibrosis , 2008, The Journal of pathology.
[109] V. Beral,et al. IARC MONOGRAPHS PROGRAMME ON THE EVALUATION OF CARelNOGENIC RISKS TO HUMANS' , 2008 .
[110] Russell S. Thomas,et al. Application of genomic biomarkers to predict increased lung tumor incidence in 2-year rodent cancer bioassays. , 2007, Toxicological sciences : an official journal of the Society of Toxicology.
[111] P. Finn,et al. Hubs in biological interaction networks exhibit low changes in expression in experimental asthma , 2007, Molecular systems biology.
[112] A. Scott,et al. Innate Immune Responses to Lung-Stage Helminth Infection Induce Alternatively Activated Alveolar Macrophages , 2006, Infection and Immunity.
[113] M. O'connell,et al. Carbon Nanotubes Properties and Applications , 2006 .
[114] T. Niewold,et al. Acute phase reaction and acute phase proteins. , 2005, Journal of Zhejiang University. Science. B.
[115] X. Cui,et al. Improved statistical tests for differential gene expression by shrinking variance components estimates. , 2005, Biostatistics.
[116] G. Parmigiani,et al. The Analysis of Gene Expression Data , 2003 .
[117] Hao Wu,et al. MAANOVA: A Software Package for the Analysis of Spotted cDNA Microarray Experiments , 2003 .
[118] G. Churchill,et al. Statistical design and the analysis of gene expression microarray data. , 2001, Genetical research.
[119] B. Spellberg,et al. Type 1/Type 2 immunity in infectious diseases. , 2001, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[120] Y. Benjamini,et al. Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .
[121] S. R. Searle,et al. Population Marginal Means in the Linear Model: An Alternative to Least Squares Means , 1980 .