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来源于β-葡聚糖作为肿瘤微环境的新型调节剂:靶向巨噬细胞极化并诱导肺癌细胞铁死亡

-Derived β-Glucan as a Novel Modulator of Tumor Microenvironment: Targeting Macrophage Polarization and Inducing Ferroptosis in Lung Cancer.

作者信息

He Xiang, Ran Qin, Li Xiaolan, Xiong Anying, Zhang Lei, Jiang Manling, Bai Lingling, Peng Dan, Wang Junyi, Sun Baoqing, Li Guoping

机构信息

National Center for Respiratory Medicine, National Clinical Research Center for Respiratory Disease, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, 510120, People's Republic of China.

Laboratory of Allergy and Precision Medicine, Chengdu Institute of Respiratory Health, Affiliated Hospital of Southwest Jiaotong University, The Third People's Hospital of Chengdu, Chengdu, 610031, People's Republic of China.

出版信息

J Inflamm Res. 2024 Dec 6;17:10479-10494. doi: 10.2147/JIR.S489191. eCollection 2024.

Abstract

INTRODUCTION

Tumor-associated macrophages (TAMs) play a crucial role in the tumor microenvironment (TME), and their polarization state significantly influences patient outcomes. This study investigates the inhibitory effects of β-glucan extracted from Candida albicans on lung cancer progression, focusing on its impact on TAM polarization and the induction of ferroptosis, a form of regulated cell death.

METHODS

Utilizing both in vivo animal models and in vitro cellular assays, we assessed the impact of β-glucan on tumor growth, cellular proliferation, and migration. We evaluated TAM polarization by analyzing the expression of M1 and M2 markers and identified differentially expressed genes (DEGs) related to ferroptosis. The role of ferroptosis in TAM polarization was further confirmed by assessing the protein levels of ACSL4 and GPX4, intracellular ferrous ion levels, and lipid peroxides.

RESULTS

β-glucan treatment significantly reduced tumor size and weight, along with cellular proliferation and migration, suggesting a potent suppressive effect on lung cancer cell growth. β-glucan promoted an M1-like phenotype in TAMs, as evidenced by increased CD86 expression and decreased CD206 expression, and modulated cytokine mRNA levels. RNA sequencing analysis post β-glucan treatment identified a substantial number of DEGs enriched in the ferroptosis pathway. The induction of ferroptosis by β-glucan was further confirmed through the significant upregulation of ACSL4 and downregulation of GPX4, alongside increased intracellular ferrous ion levels and lipid peroxides. The ferroptosis inhibitor Fer-1 abrogated these effects, highlighting the specificity of β-glucan-mediated polarization.

CONCLUSION

These results collectively provide novel insights into the immunotherapeutic potential of β-glucan from Candida albicans and its role in modulating TAM polarization and lung cancer growth, offering a promising avenue for cancer treatment strategies.

摘要

引言

肿瘤相关巨噬细胞(TAM)在肿瘤微环境(TME)中起着关键作用,其极化状态显著影响患者预后。本研究调查了从白色念珠菌中提取的β-葡聚糖对肺癌进展的抑制作用,重点关注其对TAM极化和铁死亡(一种程序性细胞死亡形式)诱导的影响。

方法

利用体内动物模型和体外细胞试验,我们评估了β-葡聚糖对肿瘤生长、细胞增殖和迁移的影响。我们通过分析M1和M2标志物的表达来评估TAM极化,并鉴定了与铁死亡相关的差异表达基因(DEG)。通过评估ACSL4和GPX4的蛋白水平、细胞内亚铁离子水平和脂质过氧化物,进一步证实了铁死亡在TAM极化中的作用。

结果

β-葡聚糖处理显著降低了肿瘤大小和重量,以及细胞增殖和迁移,表明对肺癌细胞生长有强大的抑制作用。β-葡聚糖促进了TAM中类似M1的表型,CD86表达增加和CD206表达降低证明了这一点,并调节了细胞因子mRNA水平。β-葡聚糖处理后的RNA测序分析鉴定出大量富集在铁死亡途径中的DEG。β-葡聚糖诱导铁死亡通过ACSL4的显著上调和GPX4的下调进一步得到证实,同时细胞内亚铁离子水平和脂质过氧化物增加。铁死亡抑制剂Fer-1消除了这些作用,突出了β-葡聚糖介导的极化的特异性。

结论

这些结果共同为白色念珠菌β-葡聚糖的免疫治疗潜力及其在调节TAM极化和肺癌生长中的作用提供了新的见解,为癌症治疗策略提供了一个有前景的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d592/11630740/58185124cb6c/JIR-17-10479-g0001.jpg

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