The Inhibitory Mechanisms of Tumor PD-L1 Expression by Natural Bioactive Gallic Acid in Non-Small-Cell Lung Cancer (NSCLC) Cells

• Published in: Cancers 2020-03, Vol.12 (3), p.727
• Main Authors: Kang, Dong Young, Sp, Nipin, Jo, Eun Seong, Rugamba, Alexis, Hong, Dae Young, Lee, Hong Ghi, Yoo, Ji-Seung, Liu, Qing, Jang, Kyoung-Jin, Yang, Young Mok
• Format: Article
• Language: English
• Subjects: 1-Phosphatidylinositol 3-kinase; AKT protein; Angiogenesis; Apoptosis; Binding sites; Cell culture; Cell cycle; Cell growth; Cell migration; Chemotherapy; Cytotoxicity; Epidermal growth factor; Epidermal growth factor receptors; Gallic acid; Growth factors; Immunotherapy; Kinases; Ligands; Lung cancer; Monoclonal antibodies; Non-small cell lung carcinoma; p53 Protein; PD-1 protein; PD-L1 protein; Peripheral blood; Phosphorylation; Proteins; Signal transduction; Small cell lung carcinoma; Studies; Trihydroxybenzoic acid
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers12030727

Non-small-cell lung cancer (NSCLC) is the most common lung cancer subtype and accounts for more than 80% of all lung cancer cases. Epidermal growth factor receptor (EGFR) phosphorylation by binding growth factors such as EGF activates downstream prooncogenic signaling pathways including KRAS-ERK, JAK-STAT, and PI3K-AKT. These pathways promote the tumor progression of NSCLC by inducing uncontrolled cell cycle, proliferation, migration, and programmed death-ligand 1 (PD-L1) expression. New cytotoxic drugs have facilitated considerable progress in NSCLC treatment, but side effects are still a significant cause of mortality. Gallic acid (3,4,5-trihydroxybenzoic acid; GA) is a phenolic natural compound, isolated from plant derivatives, that has been reported to show anticancer effects. We demonstrated the tumor-suppressive effect of GA, which induced the decrease of PD-L1 expression through binding to EGFR in NSCLC. This binding inhibited the phosphorylation of EGFR, subsequently inducing the inhibition of PI3K and AKT phosphorylation, which triggered the activation of p53. The p53-dependent upregulation of miR-34a induced PD-L1 downregulation. Further, we revealed the combination effect of GA and anti-PD-1 monoclonal antibody in an NSCLC-cell and peripheral blood mononuclear-cell coculture system. We propose a novel therapeutic application of GA for immunotherapy and chemotherapy in NSCLC.