Kebin Liu

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Professor

Medical College of Georgia

United States

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About

Professor Kebin Liu serves at the Medical College of Georgia in the United States. His research areas focus on cancer immunotherapy, lipid nanoparticle gene therapy, and the mechanisms of action in tumor cell sensitivity. Recent publications include studies on the suppression of autoimmune conditions, enhancement of antitumor immunity, and innovative therapeutic approaches in cancer treatment.

Recent Grants

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Role of NF-kB in Fas-mediated Apoptosis and Tumor Suppression

Open Date: 2014-08-01

Close Date: 2019-07-31

Grant: Close

H3K9 Methylation and Pancreatic Cancer Chemoresistance

Open Date: 2014-06-04

Close Date: 2016-05-31

Grant: Close

Function of Verticillin A in Suppression of MDSC and CRC Stem Cells

Open Date: 2014-01-01

Close Date: 2017-12-31

Grant: Close

Role of IRF8 in Tumor Rejection and Suppression

Open Date: 2008-05-01

Close Date: 2020-06-30

Articles (15)

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2025

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2021

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2021

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2021

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Professor

Augusta University

UNITED STATES

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Kebin Liu

Research Interests

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About

Recent Grants

Articles (15)

Verticillin A-Loaded Surgical Buttresses Prevent Local Pancreatic Cancer Recurrence in a Murine Model

Lipid Nanoparticle Fas Gene Therapy Suppresses Autoimmune Lymphoproliferative Syndrome in Mice

In vitro antibody-mediated SARS-CoV-2 infection suppression through human ACE2 receptor blockade

Delivery of Interferon β-Encoding Plasmid via Lipid Nanoparticle Restores Interferon β Expression to Enhance Antitumor Immunity in Colon Cancer

Verticillins: fungal epipolythiodioxopiperazine alkaloids with chemotherapeutic potential

Caffeine Supplementation and FOXM1 Inhibition Enhance the Antitumor Effect of Statins in Neuroblastoma

5-Fluorouracil Suppresses Colon Tumor through Activating the p53-Fas Pathway to Sensitize Myeloid-Derived Suppressor Cells to FasL+ Cytotoxic T Lymphocyte Cytotoxicity

IRF8 Regulates Intrinsic Ferroptosis through Repressing p53 Expression to Maintain Tumor Cell Sensitivity to Cytotoxic T Lymphocytes

IRF8: Mechanism of Action and Health Implications

Restoring FAS Expression via Lipid-Encapsulated FAS DNA Nanoparticle Delivery Is Sufficient to Suppress Colon Tumor Growth In Vivo

WDR5-H3K4me3 epigenetic axis regulates OPN expression to compensate PD-L1 function to promote pancreatic cancer immune escape

Chemoenzymatic modular assembly of O-GalNAc glycans for functional glycomics

Osteopontin Blockade Immunotherapy Increases Cytotoxic T Lymphocyte Lytic Activity and Suppresses Colon Tumor Progression

MS4A1 expression and function in T cells in the colorectal cancer tumor microenvironment

Osteopontin: A Key Regulator of Tumor Progression and Immunomodulation

Collaborators (7)

Nicholas Oberlies

Jonathan Chekan

Han-Fei Ding

Zheng Dong

Roni Bollag

Mark Grinstaff

Huidong Shi

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