Yung-Chi Cheng, PhD
Henry Bronson Professor of PharmacologyCards
Appointments
Additional Titles
Chairman, Consortium for the Globalization of Chinese Medicine (CGCM)
Contact Info
Pharmacology
PO Box 208066, 333 Cedar Street
New Haven, CT 06520-8066
United States
Appointments
Additional Titles
Chairman, Consortium for the Globalization of Chinese Medicine (CGCM)
Contact Info
Pharmacology
PO Box 208066, 333 Cedar Street
New Haven, CT 06520-8066
United States
Appointments
Additional Titles
Chairman, Consortium for the Globalization of Chinese Medicine (CGCM)
Contact Info
Pharmacology
PO Box 208066, 333 Cedar Street
New Haven, CT 06520-8066
United States
About
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Titles
Henry Bronson Professor of Pharmacology
Chairman, Consortium for the Globalization of Chinese Medicine (CGCM)
Biography
The Cheng laboratory studies and develops novel anti-cancer and anti-viral drugs.
Areas of anti-cancer research include: hepatocellular carcinoma, pancreatic cancer, colorectal cancer, rectal cancer, lung cancer, and melanoma.
Areas of anti-viral research include: hepatitis B (HBV), hepatitis C (HCV), human immunodeficiency virus (HIV), Epstein Barr Virus (EBV), and cytomegalovirus (CMV)
Currently the lab is exploring systems biology approaches to developing multi-targeted medicines to treat cancer and other aging-related diseases.
Appointments
Pharmacology
ProfessorPrimary
Other Departments & Organizations
- Biochemistry, Quantitative Biology, Biophysics and Structural Biology (BQBS)
- Developmental Therapeutics
- Liver Center
- Microbiology
- Molecular Medicine, Pharmacology, and Physiology
- Pharmacology
- Primary Faculty
- Virology Laboratories
- Yale Cancer Center
- Yale Combined Program in the Biological and Biomedical Sciences (BBS)
- Yale Stem Cell Center
- Yale Ventures
Education & Training
- PhD
- Brown University (1972)
Research
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Overview
Medical Research Interests
Research at a Glance
Yale Co-Authors
Publications Timeline
Research Interests
Gang-Qing Yao, MD
Elijah Paintsil, FAAP, MD
Wing Lam, PhD
Barbara Burtness, MD
Fulan Guan, PhD
Kimberly L. Johung, MD, PhD
Neoplasms
Plant Extracts
Inflammation
Publications
2025
Cornuside ameliorates LPS induced cognitive dysfunction and microglial NLRP3 inflammasome activation by enhancing Sirt1-mediated autophagy
Lian W, Yuan X, Zhou F, Tong Z, Cheng Y, Zhang W, He J, Xu J. Cornuside ameliorates LPS induced cognitive dysfunction and microglial NLRP3 inflammasome activation by enhancing Sirt1-mediated autophagy. Journal Of Ethnopharmacology 2025, 355: 120615. PMID: 40962125, DOI: 10.1016/j.jep.2025.120615.Peer-Reviewed Original ResearchAltmetricConceptsSirt1-mediated autophagyAutophagy activationPro-caspase1Cognitive dysfunctionEffects of cornusideAD miceMorris water mazeStep-through testNLRP3 inflammasome activationAutophagyAnti-inflammatory effectsMicroglial NLRP3 inflammasome activationInflammasome activationWater mazeBehavioral performanceY-mazeTreatment of dementiaBehavioral testsCognitive functionLPS-stimulated BV2 cellsInhibitory effectFructusBV2 cellsCornusideStructural damage172P Final analysis of a randomized, double blind, phase II study of sorafenib with or without YIV-906 in patients with advanced HCC
Abou-Alfa G, Yen Y, Harding J, Whang-Peng J, Shi Y, Yuen M, Li X, Gu S, Liu C, Jeng L, Yen C, Pan C, Chen S, Hsieh J, Saif W, Liu S, Li F, Lam W, Chu E, Cheng Y. 172P Final analysis of a randomized, double blind, phase II study of sorafenib with or without YIV-906 in patients with advanced HCC. Annals Of Oncology 2025, 36: s72. DOI: 10.1016/j.annonc.2025.05.185.Peer-Reviewed Original ResearchSteamed panax notoginseng mitigates CA-MRSA USA300-induced necroptosis in human neutrophils
Zhang L, Feng X, An H, Yang W, Xia Y, Wen B, Zheng H, Chen Y, Cheng Y, Jiang C, Lu C, Tan Y. Steamed panax notoginseng mitigates CA-MRSA USA300-induced necroptosis in human neutrophils. Frontiers In Pharmacology 2025, 16: 1546652. PMID: 40520183, PMCID: PMC12163054, DOI: 10.3389/fphar.2025.1546652.Peer-Reviewed Original ResearchAltmetricConceptsCA-MRSAVirulence factorsCommunity-associated methicillin-resistant Staphylococcus aureus (CAQuorum-sensing signaling pathwayPolymorphonuclear neutrophil countMethicillin-resistant Staphylococcus aureus (MRPhagocytic function of polymorphonuclear neutrophilsGenes of MRSAPolymorphonuclear neutrophilsSignaling pathwayCA-MRSA infectionsHost innate immune responseBacterial virulence factorsDrug-resistant bacterial infectionsMCP-1IL-1BIL-8Pro-inflammatory cytokines IL-1bDisrupt innate immunityInnate immune responseRNA-seqFunctions of polymorphonuclear neutrophilsPathogenic microbial infectionsPanax notoginsengCytokines IL-1bCorrection: Cornuside alleviates cognitive impairments induced by Aβ1−42 through attenuating NLRP3-mediated neurotoxicity by promoting mitophagy
Zhou F, Lian W, Yuan X, Wang Z, Xia C, Yan Y, Wang W, Tong Z, Cheng Y, Xu J, He J, Zhang W. Correction: Cornuside alleviates cognitive impairments induced by Aβ1−42 through attenuating NLRP3-mediated neurotoxicity by promoting mitophagy. Alzheimer's Research & Therapy 2025, 17: 63. PMID: 40108656, PMCID: PMC11921720, DOI: 10.1186/s13195-025-01715-9.Peer-Reviewed Original ResearchCitationsAltmetricConceptsCornuside alleviates cognitive impairments induced by Aβ1−42 through attenuating NLRP3-mediated neurotoxicity by promoting mitophagy
Zhou F, Lian W, Yuan X, Wang Z, Xia C, Yan Y, Wang W, Tong Z, Cheng Y, Xu J, He J, Zhang W. Cornuside alleviates cognitive impairments induced by Aβ1−42 through attenuating NLRP3-mediated neurotoxicity by promoting mitophagy. Alzheimer's Research & Therapy 2025, 17: 47. PMID: 39972387, PMCID: PMC11837312, DOI: 10.1186/s13195-025-01695-w.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsMitochondrial functionMitochondrial membrane potential depolarizationNLRP3 inflammasome activationInflammasome activationAlzheimer's diseasePromotion of mitophagyAnti-AD candidateBNIP3 pathwayFormation of autophagosomesDamaged mitochondriaProgressive neurodegenerative disorderProduction of ROSMitophagy fluxOxidative phosphorylationMitophagyMembrane potential depolarizationPINK1/Parkin signalingIncreased colocalizationMitochondrial dysfunctionNLRP3 inflammasomeAD miceSynaptic damageEt ZuccCaspase-1Neurodegenerative disorders
2024
Selective inhibition of tumor microvascular permeability by cavtratin blocks tumor progression in mice
Gratton J, Lin M, Yu J, Weiss E, Jiang Z, Fairchild T, Iwakiri Y, Groszmann R, Claffey K, Cheng Y, Sessa W. Selective inhibition of tumor microvascular permeability by cavtratin blocks tumor progression in mice. Cancer Cell 2024, 42: 1127. PMID: 38821059, DOI: 10.1016/j.ccell.2024.05.009.Peer-Reviewed Original ResearchAltmetricSafety evaluation of traditional Chinese medicine: new era, new strategy
Zhao X, Bai Z, Zhan X, Wang J, Cheng Y, Xiao X. Safety evaluation of traditional Chinese medicine: new era, new strategy. Acupuncture And Herbal Medicine 2024, 4: 171-175. DOI: 10.1097/hm9.0000000000000119.Peer-Reviewed Original ResearchCitations
2023
YIV-818-A: a novel therapeutic agent in prostate cancer management through androgen receptor downregulation, glucocorticoid receptor inhibition, epigenetic regulation, and enhancement of apalutamide, darolutamide, and enzalutamide efficacy
Lam W, Arammash M, Cai W, Guan F, Jiang Z, Liu S, Cheng P, Cheng Y. YIV-818-A: a novel therapeutic agent in prostate cancer management through androgen receptor downregulation, glucocorticoid receptor inhibition, epigenetic regulation, and enhancement of apalutamide, darolutamide, and enzalutamide efficacy. Frontiers In Pharmacology 2023, 14: 1244655. PMID: 37860121, PMCID: PMC10582333, DOI: 10.3389/fphar.2023.1244655.Peer-Reviewed Original ResearchCitationsAltmetricConceptsCastration-resistant prostate cancerAR target genesActive compoundsAnti-prostate cancer drugProstate cancerSynergistic effectGlucocorticoid receptorPotential drug candidatesDrug discovery platformRA-VIILuciferase activityKey active compoundsGlucocorticoid receptor inhibitionProstate cancer managementNovel therapeutic agentsRA-VDrug candidatesCompoundsDeprivation therapySafety profileCancer deathExtra-terminal (BET) proteinsGR activityReceptor inhibitionAR inhibitionBiologically active secoiridoids: A comprehensive update
Peng Z, He J, Cheng Y, Xu J, Zhang W. Biologically active secoiridoids: A comprehensive update. Medicinal Research Reviews 2023, 43: 1201-1252. PMID: 36899490, DOI: 10.1002/med.21949.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsOxime compoundsValuable precursorsCyclic ethersHemiacetal structureNatural productsBasic skeletonStructural diversityMonoterpene derivativesAntitumor drug developmentBiological activityPhenolic secoiridoidsSecoiridoidsCompoundsPharmacological investigationsOpen new areasDrug developmentBetter drugsEtherSynthesisDerivativesPrecursorsWide rangeBioactivityRingMultiple molecular targetsCelastrol attenuates hepatitis C virus translation and inflammatory response in mice by suppressing heat shock protein 90β
Chen S, Li Z, Xu J, Ding M, Shan Y, Cheng Y, Zhang G, Sun Y, Wang Y, Wang Y. Celastrol attenuates hepatitis C virus translation and inflammatory response in mice by suppressing heat shock protein 90β. Acta Pharmacologica Sinica 2023, 44: 1637-1648. PMID: 36882503, PMCID: PMC10374583, DOI: 10.1038/s41401-023-01067-w.Peer-Reviewed Original ResearchCitationsAltmetricMeSH Keywords and ConceptsConceptsHepatic inflammatory responseInflammatory responseHepatocellular carcinomaHCC patientsHCV-positive HCC patientsHepatitis C virus infectionHepatitis B virus-associated hepatocellular carcinomaExpression levelsVirus-associated hepatocellular carcinomaPositive HCC patientsC virus infectionHCV translationAnti-HCV activityHCV RNA-dependent RNA polymeraseHeat shock protein 90βHepatic expression levelsEndoplasmic reticulum stressPositive HCVNatural Product CelastrolHepatic inflammationCirrhosis patientsImmune cellsHepatitis C virus translationCelastrol doseVirus infection
Academic Achievements & Community Involvement
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Activities
activity Globalization of Chinese Medicine
01/01/2008 - PresentResearchDetailsChina; Hong KongAbstract/SynopsisProfessor Yung-chi Cheng of the Yale School of Medicine has been working with the University of Hong Kong, Peking University, Tsinghua University, and a number of other prominent Chinese institutions to form a Consortium for the Globalization of Chinese Medicine. The Consortium brings together a network of academic, industrial and regulatory agencies to advance the field of Chinese medicine.
Honors
honor Honorary Prof Chang Chun University of Traditional Chinese Med; Honorary Professor Hua Qiao University; Cheung on Tak Intl Award for Outstanding Contribution to Chinese Medicine
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Pharmacology
PO Box 208066, 333 Cedar Street
New Haven, CT 06520-8066
United States