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Elucidation of the mechanism Underlying the promotion of ferroptosis and enhanced antitumor immunity by citrus polymethoxyflavones in CRC cells.

作者信息

Duan Yingying, Wu Yu, Tian Jiaqi, Yin Yuqin, Yuan Zhongwen, Zhu Wenting, Zhou Suyue, Li Chen, Feng Senling

机构信息

Guangdong Provincial Key Laboratory of Major Obstetric Diseases, Department of Pharmacy, Guangdong Provincial Clinical Research Center for Obstetrics and Gynecology, The Third Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.

School of Pharmaceutical Sciences, Guangzhou Medical University, Guangzhou, China.

出版信息

Front Pharmacol. 2025 Apr 11;16:1571178. doi: 10.3389/fphar.2025.1571178. eCollection 2025.


DOI:10.3389/fphar.2025.1571178
PMID:40290432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12021823/
Abstract

BACKGROUND: Colon cancer is a prevalent condition with a high mortality rate on a global scale. Research has indicated that Citrus polymethoxyflavones (PMFs), a class of flavonoids found in Citrus, possess the potential to demonstrate anti-tumor efficacy. Ferroptosis a form of cell death that is dependent on iron accumulation and lipid peroxidation. Immunotherapy is one of the most commonly used anti-tumor modalities in a clinical setting. Consequently, studies on the pharmacodynamic mechanism of Citrus to determine whether it can modulate tumor immunity through ferroptosis provide new ideas for the clinical treatment of colon cancer. PURPOSE: The objective of this study is to ascertain whether Citrus inhibits through ferroptosis and promotes tumor immunity among patients with colon cancer. METHODS: The inhibitory effect of PMFs on colon cancer was proved by experiment and model. In addition, the occurrence of ferroptosis was detected by measuring key ferroptosis indicators. Bioinformatics analysis was then performed to identify the crossover genes for Citrus polymethoxylflavonoids, colon cancer, and ferroptosis. Finally, key genes were identified by immunocorrelation analysis including WB, Q-PCR and flow cytometry. These experiments were designed to reveal the potential mechanisms of PMFs on ferroptosis and anti-tumor immunity. RESULTS: cell proliferation experiment and the growth of transplanted tumor mice showed that PMFs had inhibitory effect on colon cancer. In addition, the change of ferroptosis index showed that PMFs promoted the occurrence of ferroptosis, followed by Q-PCR and WB detection of and , the key genes screened by bioinformatics, found that PMFs inhibited by down-regulating , thus affecting colon cancer. Flow cytometry showed that CD4 T expression increased and CD8 T cell expression decreased after treatment, suggesting that anti-tumor immunity was activated. CONCLUSION: It is conceivable that the tumor immune microenvironment may be subject to regulation during the inhibition of colon cancer through ferroptosis in PMFs. The ferroptosis-related gene has been observed to regulate , thereby promoting anti-tumor immunity in colon cancer. However, further investigation is required to ascertain the underlyingprecise mechanisms.

摘要

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本文引用的文献

[1]
Sangerbox: A comprehensive, interaction-friendly clinical bioinformatics analysis platform.

Imeta. 2022-7-8

[2]
DEPDC5 protects CD8 T cells from ferroptosis by limiting mTORC1-mediated purine catabolism.

Cell Discov. 2024-5-20

[3]
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Front Immunol. 2023

[4]
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Technol Cancer Res Treat. 2023

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Network Pharmacological Analysis and Experimental Validation of the Effects of Silybin on Proliferation, Migration, and Immunotherapy of Papillary Thyroid Cancer.

Endocr Metab Immune Disord Drug Targets. 2024

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Cancer Immunol Immunother. 2023-12

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Sci Rep. 2023-8-25

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A Prognostic Model of Angiogenesis and Neutrophil Extracellular Traps Related Genes Manipulating Tumor Microenvironment in Colon Cancer.

J Cancer. 2023-7-9

[9]
5-Fluorouracil Suppresses Colon Tumor through Activating the p53-Fas Pathway to Sensitize Myeloid-Derived Suppressor Cells to FasL Cytotoxic T Lymphocyte Cytotoxicity.

Cancers (Basel). 2023-3-2

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