Si Chen Ph.D.
Staff Fellow — Division of Biochemical Toxicology
Si Chen, Ph.D.
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About | Publications | Lab Members
Dr. Si Chen graduated from Sun Yat-sen University (China) in 2006 with a bachelor’s degree in preventive medicine, and then received a master’s degree in immunology in 2009. In 2012, she received a Ph.D. in biochemistry and molecular biology from Nankai University (China). Dr. Chen joined FDA’s National Center for Toxicological Research (NCTR) in the Division of Biochemical Toxicology as an Oak Ridge Institute of Science and Education (ORISE) fellow in 2012. In 2015, she was recruited to be a member of the Over-the-Counter Monographs Team, a joint program between FDA’s Center for Drug Evaluation and Research and NCTR, and was converted to a staff fellow. During her research career, Dr. Chen has published more than 50 articles in peer-reviewed journals and eight book chapters. Her work has been cited more than 1,000 times, with an H-index of 27.
A major focus of Dr. Chen’s research is elucidating the molecular mechanisms of drug and herbal dietary supplement-associated liver toxicity. Dr. Chen has conducted several mechanistic studies on the hepatotoxic effects of FDA-regulated products, including goldenseal, Ginkgo biloba, usnic acid, sertraline, dronedarone, and nitroxides. Another major focus of Dr. Chen’s research is screening and identifying the micro ribonucleic acids (miRNA) that are responsible for drug resistance in ovarian cancer and investigating the underlying molecular mechanisms of candidate miRNAs using both bioinformatics and biochemical approaches.
Professional Societies/National and International Groups
Society of Toxicology
2012 – Present
Characterization of Cytochrome P450s (CYP)-Overexpressing HepG2 Cells for Assessing Drug and Chemical-Induced Liver Toxicity.
Chen S., Wu Q., Li X., Li D., Mei N., Ning B., Puig M., Ren Z., Tolleson W.H., and Guo L.
J Environ Sci Health C Toxicol Carcinog. 2021, 39(1):68-86.
The Role of Hepatic Cytochrome P450s in the Cytotoxicity of Sertraline
Chen S., Wu Q., Li X., Li D., Fan M., Ren Z., Bryant M., Mei N., Ning B., and Guo L.
Arch Toxicol. 2020, 94(7):2401-2411.
MicroRNAs hsa-miR-495-3p and hsa-miR-486-5p Suppress Basal and Rifampicin-induced Expression of Human Sulfotransferase 2A1 (SULT2A1) by Facilitating mRNA Degradation.
Li D., Knox B., Chen S., Wu L., Tolleson W.H., Liu Z., Yu D., Guo L., Tong W., and Ning B.
Biochem Pharmacol. 2019, doi: 10.1016/j.bcp.2019.08.019. Epub 2019 Aug 22.
The Role of Hepatic Cytochrome P450s in the Cytotoxicity of Dronedarone.
Chen S., Wu Q., Ning B., Bryant M., and Guo L.
Arch Toxicol. 2018, 92(6):1969-1981.
DNA Damage-induced Apoptosis and Mitogen-activated Protein Kinase Pathway Contribute to the Toxicity of Dronedarone in Hepatic Cells.
Chen S., Ren Z., Yu D., Ning B., and Guo L.
Environ Mol Mutagen. 2018, 59(4):278-289.
ROS Generation and JNK Activation Contribute to 4-methoxy-TEMPO-induced Cytotoxicity, Autophagy, and DNA Damage in HepG2 Cells.
Zhang Z., Ren Z., Chen S., Guo X., Liu F., Guo L., and Mei N.
Arch Toxicol. 2018, 92(2):717-728.
Endoplasmic Reticulum Stress and MAPK Signaling Pathway Activation Underlie Leflunomide-induced Toxicity in HepG2 Cells.
Ren Z., Chen S., Qing T., Xuan J., Couch L., Yu D., Ning B., Shi L., and Guo L.
Toxicology. 2017, 392:11-21.
Activation of the Nrf2 Signaling Pathway in Usnic Acid-induced Toxicity in HepG2 Cells.
Chen S., Zhang Z., Qing T., Ren Z., Yu D., Couch L., Ning B., Mei N., Shi L., Tolleson W.H., and Guo L.
Arch Toxicol. 2017, 91(3):1293-1307.
Endoplasmic Reticulum Stress Induction and ERK1/2 Activation Contribute to Nefazodone-induced Toxicity in Hepatic Cells.
Ren Z., Chen S., Zhang J., Doshi U., Li A.P., and Guo L.
Toxicol Sci. 2016,154(2):368-380.
Development of HepG2-derived Cells Expressing Cytochrome P450s for Assessing Metabolism-associated Drug-induced Liver Toxicity.
Xuan J., Chen S., Ning B., Tolleson W., and Guo L.
Chem Biol Interact. 2016, 255:63-73.
MicroRNAs as Pharmacogenomic Biomarkers for Drug Efficacy and Drug Safety Assessment.
Koturbash I., Tolleson W.H., Guo L., Yu D., Chen S., Hong H., Mattes W., and Ning B.
Biomark Med. 2015, 9(11):1153-76.
Ginkgo biloba Leaf Extract Induces DNA Damage by Inhibiting Topoisomerase II Activity in Human Hepatic Cells.
Zhang Z., Chen S., Mei H., Xuan J., Guo X., Couch L., Guo L., and Mei N.
Sci Rep. 2015, 5:14633.
Endoplasmic Reticulum Stress and Store-operated Calcium Entry Contribute to Usnic Acid-induced Toxicity in Hepatic Cells.
Chen S., Zhang Z., Wu Y., Shi Q., Yan H., Mei N., Tolleson W.H., and Guo L.
Toxicol Sci. 2015,146(1):116-26.
Reactive Oxygen Species and c-Jun N-terminal Kinases Contribute to TEMPO-induced Apoptosis in L5178Y Cells.
Guo X., Chen S., Zhang Z., Dobrovolsky V.N., Dial S., Guo L., and Mei N.
Chem Biol Interact. 2015, 235:27-36.
Mechanisms of Tolvaptan-induced Toxicity in HepG2 Cells.
Wu Y., Beland F.A., Chen S., Liu F., Guo L., and Fang J.L.
Biochem Pharmacol. 2015, 95(4):324-36.
The Role of Autophagy in Usnic Acid-induced Toxicity in Hepatic Cells.
Chen S., Dobrovolsky V.N., Liu F., Wu Y., Mei N., and Guo L.
Toxicol Sci. 2014,142(1):33-44.
Sertraline Induces Endoplasmic Reticulum Stress in Hepatic Cells.
Chen S., Xuan J., Couch L., Iyer A., Wu Y., Li Q., and Guo L.
Toxicology. 2014, 322:78-88.
Autophagy in Drug-induced Liver Toxicity.
Chen S., Melchior W.B., Jr., Wu Y., and Guo L.
J Food Drug Anal. 2014, 22(2):161–168.
Sertraline, an Antidepressant, Induces Apoptosis in Hepatic Cells Through the Mitogen-activated Protein Kinase Pathway.
Chen S., Xuan J., Wan L., Lin H., Couch L., Mei N., Dobrovolsky V.N., and Guo L.
Toxicol Sci. 2014,137(2):404-15.
Endoplasmic Reticulum Stress in Drug- and Environmental Toxicant-induced Liver Toxicity.
Chen S., Melchior W.B., Jr., and Guo L.
J Environ Sci Health C Environ Carcinog Ecotoxicol Rev. 2014, 32(1):83-104.
Contact information for all lab members:
Lei Guo, Ph.D.
Yuxi Li, Ph.D.
ORISE Postdoctoral Fellow
Zhen Ren, Ph.D.
- Contact Information
- Si Chen
ExpertiseApproachDomainTechnology & DisciplineToxicology