Qiang Shi
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Senior Staff Fellow
Also affiliated: Jiangxi University of Traditional Chinese Medicine (2025); Jiangnan University (2011–2013); Jiangsu University (2025); University of Science and Technology of China (2016–2026); Dalhousie University (2018); United States Food and Drug Administration (2008–2026); Zhejiang Sci-Tech University (2023); Center for Drug Evaluation and Research (2020); Shanghai Medical College of Fudan University (2023); North China University of Science and Technology (2022); Nanchang University (2022–2026); Johns Hopkins University (2024); China Three Gorges University (2022); Shanghai Jiao Tong University (2022); Capital Medical University (2007–2017); Liaocheng University (2022); Chinese Academy of Sciences (2022–2026); Shanghai University of Electric Power (2008); Fudan University (2016–2024); Johns Hopkins Medicine (2024); China-Japan Friendship Hospital (2017); Sir Run Run Shaw Hospital (2019); Tianjin Medical University General Hospital (2015); Chinese PLA General Hospital (2023); Soochow University (2022); Shanghai Stomatological Hospital (2023); Chongqing Bureau of Geology and Minerals Exploration (2021–2024); Changchun Institute of Applied Chemistry (2022–2026); Dalian University (2012); Fudan University Shanghai Cancer Center (2023); Ningbo No. 2 Hospital (2022); Hefei National Center for Physical Sciences at Nanoscale (2016); Shanghai Open University (2024); PAREXEL International (United States) (2012); Zhongshan Hospital (2016–2024); First Automotive Works (China) (2023); Changchun University of Chinese Medicine (2023); First Hospital of China Medical University (2009–2011); Shanghai Sixth People's Hospital (2022); Pfizer (China) (2012–2014); State Key Laboratory of Food Science and Technology (2022); State Key Laboratory of Polymer Physics and Chemistry (2022–2026); Center for Life Sciences (2023–2024); Shandong First Medical University (2022–2025); Dezhou University (2010–2013); Hebei University (2005); State Administration for Market Regulation (2026); Xinjiang Agricultural Vocational and Technical University (2022–2024); Jilin Animation Institute (2022); Tianjin Medical University (2015); Northwest Normal University (2023–2024); Zhejiang University (2006–2019); Shaanxi Normal University (2018); China Medical University (2009); Tsinghua University (2023–2024)
Research Areas
Biomedical Subjects
Links
Biography and Research Information
OverviewAI-generated summary
Qiang Shi's research focuses on drug safety evaluation and the prediction of drug-induced liver injury (DILI). He has contributed to guidelines for assay interpretation in autophagy monitoring and participated in the MicroArray Quality Control (MAQC)-II study, which examined common practices for developing and validating microarray-based predictive models. His work has also involved analyzing FDA-approved drug labeling specifically for the study of DILI and developing systems such as the Drug Induced Liver Injury Prediction System (DILIps) to translate clinical findings into knowledge for drug safety assessment.
Shi has investigated the effects of various compounds on biological systems, including the impact of 31 FDA-approved small-molecule kinase inhibitors on isolated rat liver mitochondria. His research interests also extend to understanding the toxicity of natural products, as indicated by his review of Usnic Acid and Usnea Barbata toxicity. Collaborations within the National Center for Toxicological Research have involved shared publications with researchers such as Laura K. Schnackenberg, Katy S Papineau, and Lijun Ren.
With a career marked by significant scholarly output, Shi has accumulated 209 total publications and 10,795 citations, resulting in an h-index of 36. He is recognized as a highly cited researcher. His work is characterized by investigations into cellular mechanisms, dose-response relationships, and the application of various experimental models, including those involving animals, to assess potential toxicological effects of chemical and drug substances.
Metrics
- h-index: 36
- Publications: 197
- Citations: 10,783
Positions
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Senior Staff Fellow 2023–presentUS Food and Drug Administration, National Center for Toxicological Research Division of Systems Biology ORCID
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Visiting Scientist 2010–2023National Center for Toxicological Research Systems Biology ORCID
Selected Publications
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Challenges and solutions in measuring commonly used biomarkers for drug-induced liver injury in a liver-on-a-chip platform (2025)
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Toxicity of ubiquitous tire rubber antiozonant N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD) and its transformation product 6PPD-quinone (6PPD-Q) in primary human hepatocytes and liver spheroids (2025)
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Pexidartinib impairs liver mitochondrial functions causing cell death in primary human hepatocytes at clinically relevant concentrations (2025)
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Considerations from the pharmaceutical industry (IQ MPS affiliate) workshop on animal microphysiological systems and 3Rs in drug development (2025)
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New Alternative Methods in Drug Safety Assessment (2023)
Collaboration Network
Top Collaborators
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Sensitivity to hepatotoxicity due to epigallocatechin gallate is affected by genetic background in diversity outbred mice
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Identification of Urinary microRNA Profiles in Rats That May Diagnose Hepatotoxicity
- Circulating MicroRNA and Long Noncoding RNA as Biomarkers of Cardiovascular Diseases
Showing 5 of 24 shared publications
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Identification of Urinary microRNA Profiles in Rats That May Diagnose Hepatotoxicity
- Green tea extract can potentiate acetaminophen-induced hepatotoxicity in mice
- Drug-Induced Liver Injury in Children: Clinical Observations, Animal Models, and Regulatory Status
Showing 5 of 13 shared publications
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Identification of Urinary microRNA Profiles in Rats That May Diagnose Hepatotoxicity
- Green tea extract can potentiate acetaminophen-induced hepatotoxicity in mice
- Regorafenib impairs mitochondrial functions, activates AMP-activated protein kinase, induces autophagy, and causes rat hepatocyte necrosis
Showing 5 of 13 shared publications
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Regorafenib impairs mitochondrial functions, activates AMP-activated protein kinase, induces autophagy, and causes rat hepatocyte necrosis
- Cytotoxicity of 34 FDA approved small-molecule kinase inhibitors in primary rat and human hepatocytes
- Green tea epigallocatechin gallate binds to and inhibits respiratory complexes in swelling but not normal rat hepatic mitochondria
Showing 5 of 11 shared publications
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Identification of Urinary microRNA Profiles in Rats That May Diagnose Hepatotoxicity
- Circulating extracellular vesicles as a potential source of new biomarkers of drug-induced liver injury
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Green tea epigallocatechin gallate binds to and inhibits respiratory complexes in swelling but not normal rat hepatic mitochondria
Showing 5 of 10 shared publications
- Effects of 31 FDA approved small-molecule kinase inhibitors on isolated rat liver mitochondria
- Cytotoxicity of 34 FDA approved small-molecule kinase inhibitors in primary rat and human hepatocytes
- Co‐Culture of Human Primary Hepatocytes and Nonparenchymal Liver Cells in the Emulate® Liver‐Chip for the Study of Drug‐Induced Liver Injury
- Performance of high-throughput CometChip assay using primary human hepatocytes: a comparison of DNA damage responses with in vitro human hepatoma cell lines
- Hepatic Transcript Profiles of Cytochrome P450 Genes Predict Sex Differences in Drug Metabolism
Showing 5 of 9 shared publications
- The MicroArray Quality Control (MAQC)-II study of common practices for the development and validation of microarray-based predictive models
- FDA-approved drug labeling for the study of drug-induced liver injury
- Translating Clinical Findings into Knowledge in Drug Safety Evaluation - Drug Induced Liver Injury Prediction System (DILIps)
- Biomarkers for drug-induced liver injury
- A testing strategy to predict risk for drug-induced liver injury in humans using high-content screen assays and the ‘rule-of-two’ model
Showing 5 of 7 shared publications
- Review of Usnic Acid and Usnea Barbata Toxicity
- Gene expression profiling in the developing rat brain exposed to ketamine
- A testing strategy to predict risk for drug-induced liver injury in humans using high-content screen assays and the ‘rule-of-two’ model
- Endoplasmic Reticulum Stress and Store-Operated Calcium Entry Contribute to Usnic Acid-Induced Toxicity in Hepatic Cells
- Assessment of usnic acid toxicity in rat primary hepatocytes using 13C isotopomer distribution analysis of lactate, glutamate and glucose
Showing 5 of 7 shared publications
- A comprehensive study of the association between drug hepatotoxicity and daily dose, liver metabolism, and lipophilicity using 975 oral medications
- Regorafenib impairs mitochondrial functions, activates AMP-activated protein kinase, induces autophagy, and causes rat hepatocyte necrosis
- Circulating extracellular vesicles as a potential source of new biomarkers of drug-induced liver injury
- Green tea epigallocatechin gallate binds to and inhibits respiratory complexes in swelling but not normal rat hepatic mitochondria
- Mechanisms for epigallocatechin gallate induced inhibition of drug metabolizing enzymes in rat liver microsomes
Showing 5 of 6 shared publications
- Potential of extracellular microRNAs as biomarkers of acetaminophen toxicity in children
- Assessment of usnic acid toxicity in rat primary hepatocytes using 13C isotopomer distribution analysis of lactate, glutamate and glucose
- Hepatic Transcript Profiles of Cytochrome P450 Genes Predict Sex Differences in Drug Metabolism
- Circulating Mitochondrial Biomarkers for Drug-Induced Liver Injury
- FDA-approved drug labeling for the study of drug-induced liver injury
- Translating Clinical Findings into Knowledge in Drug Safety Evaluation - Drug Induced Liver Injury Prediction System (DILIps)
- A testing strategy to predict risk for drug-induced liver injury in humans using high-content screen assays and the ‘rule-of-two’ model
- Unravelling Sex Differences in Drug‐Induced Liver Injury
- Gene expression profiling in the developing rat brain exposed to ketamine
- Toxicity of ubiquitous tire rubber antiozonant N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD) and its transformation product 6PPD-quinone (6PPD-Q) in primary human hepatocytes and liver spheroids
- Challenges and solutions in measuring commonly used biomarkers for drug-induced liver injury in a liver-on-a-chip platform
- Confirmation of the mode of action of anesthetic‐induced developmental neurotoxicity with gene expression studies
- Review of Usnic Acid and Usnea Barbata Toxicity
- Endoplasmic Reticulum Stress and Store-Operated Calcium Entry Contribute to Usnic Acid-Induced Toxicity in Hepatic Cells
- Gene expression profiling in male B6C3F1 mouse livers exposed to kava identifies – Changes in drug metabolizing genes and potential mechanisms linked to kava toxicity
- Performance of high-throughput CometChip assay using primary human hepatocytes: a comparison of DNA damage responses with in vitro human hepatoma cell lines
- Gene expression profiling in male B6C3F1 mouse livers exposed to kava identifies – Changes in drug metabolizing genes and potential mechanisms linked to kava toxicity
- Quantitation of DNA reactive pyrrolic metabolites of senecionine – A carcinogenic pyrrolizidine alkaloid by LC/MS/MS analysis
- Effects of glutathione and cysteine on pyrrolizidine alkaloid-induced hepatotoxicity and DNA adduct formation in rat primary hepatocytes
- Metabolism of carcinogenic pyrrolizidine alkaloids and pyrrolizidine alkaloidN-oxides by rat primary hepatocytes generate the same characteristic DHP-DNA adducts
- Gene expression profiling in male B6C3F1 mouse livers exposed to kava identifies – Changes in drug metabolizing genes and potential mechanisms linked to kava toxicity
- Quantitation of DNA reactive pyrrolic metabolites of senecionine – A carcinogenic pyrrolizidine alkaloid by LC/MS/MS analysis
- Effects of glutathione and cysteine on pyrrolizidine alkaloid-induced hepatotoxicity and DNA adduct formation in rat primary hepatocytes
- Metabolism of carcinogenic pyrrolizidine alkaloids and pyrrolizidine alkaloidN-oxides by rat primary hepatocytes generate the same characteristic DHP-DNA adducts
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