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<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">PAR</journal-id><journal-title-group><journal-title>Proceedings of Anticancer Research</journal-title></journal-title-group><issn>2208-3545</issn><eissn>2208-3553</eissn><publisher><publisher-name>Bio-Byword Scientific Publishing Pty. Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.26689/par.v8i5.8323</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Immunoregulatory Effect and Mechanism of Epigallocatechin-3-Gallate in A Mouse Oral Cancer Model</title><url>https://artdesignp.com/journal/PAR/8/5/10.26689/par.v8i5.8323</url><author>LiYizhen,HuangSiyi,LingYanzi,FuLiyan,ZhengRuyue,DuanXinwei,LuoYueji</author><pub-date pub-type="publication-year"><year>2024</year></pub-date><volume>8</volume><issue>5</issue><history><date date-type="pub"><published-time>2024-09-26</published-time></date></history><abstract>Objective: This investigation delineates the anti-cancer potency of epigallocatechin-3-gallate (EGCG) in an oral cancer mouse model, with a focus on its effect on T-cell activation. Methods: An oral cancer model was established in male Balb/c mice using 4-nitroquinoline 1-oxide (4-NQO). The mice were systematically grouped and administered graded concentrations of EGCG. Key parameters such as body weight, hydration levels, tumor volume, and mass were meticulously tracked. T-cell activity and cytokine expression profiles, focusing on interleukin-2 (IL-2), interferon-gamma (IFN-γ), and tumor necrosis factor-alpha (TNF-α), were quantified using ELISA. A comprehensive statistical evaluation included one-way ANOVA, Tukey’s HSD multiple comparison test, and the Kruskal-Wallis non-parametric assessment. Results: EGCG-administered cohorts exhibited a pronounced reduction in tumor size and mass, with the high-dose group showing the greatest efficacy. ELISA findings corroborated a significant increase in T-cell activity and concomitant upregulation of key cytokines, including IL-2, IFN-γ, and TNF-α (P &amp;lt; 0.05). Conclusion: This investigation confirms the tumor-suppressive efficacy of EGCG in a murine oral squamous cell carcinoma model. The therapeutic effects of EGCG are mediated through T-cell activation and the upregulation of pivotal cytokine expression, highlighting its potential immunomodulatory role in oral cancer treatment.</abstract><keywords/></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>Sung H, Ferlay J, Siegel RL, et al., Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin, 71(3): 209–249. https://doi.org/10.3322/caac.21660</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B2" content-type="article"><label>2</label><element-citation publication-type="journal"><p>Fang Y, Yu Y, Wu DW, et al., 2020, A Review of Immune-Related Adverse Events Associated with Immunotherapy. 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