Jia‐Long Fang
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Also affiliated: Jiangnan University (2023–2025); United States Food and Drug Administration (2000–2026); University of South Florida (2002–2004); Karolinska Institutet (1995–1999); Moffitt Cancer Center (2002–2004); University of Illinois Chicago (2013); State Key Laboratory of Food Science and Technology (2023); Penn State Cancer Institute (2006)
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Jia-Long Fang investigates the toxicological effects and biological mechanisms of various chemical compounds, with a focus on potential carcinogenicity, metabolic disorders, and cellular responses. His research has examined the carcinogenicity of dyes such as gentian violet and malachite green, and the toxicity of polyethylene glycols in animal models. Fang has also explored the role of specific molecular pathways, including the thromboxane A2/thromboxane A2 receptor axis, in the development of hepatic insulin resistance and steatosis associated with non-alcoholic fatty liver disease. This work has led to the investigation of natural compounds like piperlongumine and ginkgolide B as potential therapeutic agents for ameliorating these conditions by targeting these pathways.
Further research by Fang delves into the metabolic transformations of compounds, such as the oxidation of 7-hydroxycannabidiol to a reactive metabolite by NAD(P)+-dependent alcohol oxidoreductases. His work also encompasses the impact of microbial metabolites, like indole-3-lactic acid produced by Lactiplantibacillus plantarum, on mitigating oxidative stress and intestinal aging. Fang's research network includes consistent collaborations with researchers at the National Center for Toxicological Research, including Frederick A. Beland, Mackean P. Maisha, Michelle M. Vanlandingham, and Robert P. Felton. With an h-index of 30 and over 3,187 citations across 65 publications, Fang is recognized as a highly cited researcher.
Metrics
- h-index: 30
- Publications: 63
- Citations: 3,238
Selected Publications
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Contribution of cytochrome P450-mediated metabolism to clavulanic acid-induced cytotoxicity in TK6-derived cytochrome P450-overexpressing cell lines (2026)
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NAD(P)+-dependent alcohol oxidoreductases oxidize 7-hydroxycannabidiol to a reactive formyl metabolite (2025)
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Flow cytometric analysis of the SARS coronavirus 2 antibodies in human plasma (2025)
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Two-year dermal carcinogenicity bioassay of triclosan in B6C3F1 mice (2023)
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Evaluation of association of anti-PEG antibodies with anaphylaxis after mRNA COVID-19 vaccination (2023)
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Evaluation of association of anti-PEG antibodies with anaphylaxis after mRNA COVID-19 vaccination (2023)
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Toxicity of high-molecular-weight polyethylene glycols in Sprague Dawley rats (2022)
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Flow cytometry analysis of anti-polyethylene glycol antibodies in human plasma (2020)
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Apoptosis contributes to the cytotoxicity induced by amodiaquine and its major metabolite N-desethylamodiaquine in hepatic cells (2019)
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Role of peroxisome proliferator-activated receptor alpha (PPARα) and PPARα-mediated species differences in triclosan-induced liver toxicity (2018)
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Effects of human sulfotransferases on the cytotoxicity of 12-hydroxynevirapine (2018)
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Cytochrome P450-mediated metabolism of triclosan attenuates its cytotoxicity in hepatic cells (2016)
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Effect of triclosan, triclocarban, 2,2′,4,4′-tetrabromodiphenyl ether, and bisphenol A on the iodide uptake, thyroid peroxidase activity, and expression of genes involved in thyroid hormone synthesis (2016)
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Human Sulfotransferases Enhance the Cytotoxicity of Tolvaptan (2015)
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Mechanisms of tolvaptan-induced toxicity in HepG2 cells (2015)
Collaboration Network
Top Collaborators
- Occurrence, Efficacy, Metabolism, and Toxicity of Triclosan
- Effect of ethanol on the tumorigenicity of urethane (ethyl carbamate) in B6C3F1 mice
- Effect of triclosan, triclocarban, 2,2′,4,4′-tetrabromodiphenyl ether, and bisphenol A on the iodide uptake, thyroid peroxidase activity, and expression of genes involved in thyroid hormone synthesis
- Quantification of Etheno-DNA Adducts Using Liquid Chromatography, On-Line Sample Processing, and Electrospray Tandem Mass Spectrometry
- Long-Term Exposure to Zidovudine Delays Cell Cycle Progression, Induces Apoptosis, and Decreases Telomerase Activity in Human Hepatocytes
Showing 5 of 26 shared publications
- Effect of triclosan, triclocarban, 2,2′,4,4′-tetrabromodiphenyl ether, and bisphenol A on the iodide uptake, thyroid peroxidase activity, and expression of genes involved in thyroid hormone synthesis
- Cytochrome P450-mediated metabolism of triclosan attenuates its cytotoxicity in hepatic cells
- Mechanisms of tolvaptan-induced toxicity in HepG2 cells
- Role of peroxisome proliferator-activated receptor alpha (PPARα) and PPARα-mediated species differences in triclosan-induced liver toxicity
- Extracellular signal-regulated kinases 1/2 and Akt contribute to triclosan-stimulated proliferation of JB6 Cl 41-5a cells
Showing 5 of 7 shared publications
- Cytotoxicity and inhibitory effects of low-concentration triclosan on adipogenic differentiation of human mesenchymal stem cells
- Methysticin and 7,8-Dihydromethysticin are Two Major Kavalactones in Kava Extract to Induce CYP1A1
- Differential effects of triclosan on the activation of mouse and human peroxisome proliferator-activated receptor alpha
- XPC is essential for nucleotide excision repair of zidovudine-induced DNA damage in human hepatoma cells
- Differential gene expression in human hepatocyte cell lines exposed to the antiretroviral agent zidovudine
Showing 5 of 7 shared publications
- Review of Usnic Acid and Usnea Barbata Toxicity
- Mitochondrial Dysfunction Induced by Sertraline, an Antidepressant Agent
- Mechanisms of tolvaptan-induced toxicity in HepG2 cells
- Methysticin and 7,8-Dihydromethysticin are Two Major Kavalactones in Kava Extract to Induce CYP1A1
- Differential gene expression in human hepatocyte cell lines exposed to the antiretroviral agent zidovudine
- Absorption and metabolism of triclosan after application to the skin of B 6 C 3 F 1 mice
- Role of peroxisome proliferator-activated receptor alpha (PPARα) and PPARα-mediated species differences in triclosan-induced liver toxicity
- Dose–response assessment of the dermal toxicity of triclosan in B6C3F1 mice
- Toxicity of high-molecular-weight polyethylene glycols in Sprague Dawley rats
- Two-year dermal carcinogenicity bioassay of triclosan in B6C3F1 mice
- Absorption and metabolism of triclosan after application to the skin of B 6 C 3 F 1 mice
- Cytochrome P450-mediated metabolism of triclosan attenuates its cytotoxicity in hepatic cells
- Toxicity of high-molecular-weight polyethylene glycols in Sprague Dawley rats
- Human Sulfotransferases Enhance the Cytotoxicity of Tolvaptan
- Effects of human sulfotransferases on the cytotoxicity of 12-hydroxynevirapine
- Role of peroxisome proliferator-activated receptor alpha (PPARα) and PPARα-mediated species differences in triclosan-induced liver toxicity
- Dose–response assessment of the dermal toxicity of triclosan in B6C3F1 mice
- Toxicity of high-molecular-weight polyethylene glycols in Sprague Dawley rats
- Two-year dermal carcinogenicity bioassay of triclosan in B6C3F1 mice
- Effect of ethanol on the tumorigenicity of urethane (ethyl carbamate) in B6C3F1 mice
- Quantification of Etheno-DNA Adducts Using Liquid Chromatography, On-Line Sample Processing, and Electrospray Tandem Mass Spectrometry
- Quantitative Analysis of Etheno-2‘-Deoxycytidine DNA Adducts Using On-Line Immunoaffinity Chromatography Coupled With LC/ES-MS/MS Detection
- Cytochrome P450-mediated metabolism of triclosan attenuates its cytotoxicity in hepatic cells
- Human Sulfotransferases Enhance the Cytotoxicity of Tolvaptan
- Effects of human sulfotransferases on the cytotoxicity of 12-hydroxynevirapine
- Flow cytometry analysis of anti-polyethylene glycol antibodies in human plasma
- Role of peroxisome proliferator-activated receptor alpha (PPARα) and PPARα-mediated species differences in triclosan-induced liver toxicity
- Apoptosis contributes to the cytotoxicity induced by amodiaquine and its major metabolite N-desethylamodiaquine in hepatic cells
- Quantification of Etheno-DNA Adducts Using Liquid Chromatography, On-Line Sample Processing, and Electrospray Tandem Mass Spectrometry
- Quantitative Analysis of Etheno-2‘-Deoxycytidine DNA Adducts Using On-Line Immunoaffinity Chromatography Coupled With LC/ES-MS/MS Detection
- Dose–response assessment of the dermal toxicity of triclosan in B6C3F1 mice
- Toxicity of high-molecular-weight polyethylene glycols in Sprague Dawley rats
- Mechanisms of tolvaptan-induced toxicity in HepG2 cells
- Human Sulfotransferases Enhance the Cytotoxicity of Tolvaptan
- Chemogenomic Analysis Identifies Geldanamycins as Substrates and Inhibitors of ABCB1
- Pharmacogenomics Approach Reveals MRP1 (ABCC1)-Mediated Resistance to Geldanamycins
- Chemogenomic Analysis Identifies Geldanamycins as Substrates and Inhibitors of ABCB1
- Pharmacogenomics Approach Reveals MRP1 (ABCC1)-Mediated Resistance to Geldanamycins
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