Jędrzejewski Tomasz, Sobocińska Justyna, Maciejewski Bartosz, Spisz Paulina, Walczak-Skierska Justyna, Pomastowski Paweł, Wrotek Sylwia
Department of Immunology, Faculty of Biological and Veterinary Sciences, Nicolaus Copernicus University, Lwowska 1 Street, 87-100, Toruń, Poland.
Centre for Modern Interdisciplinary Technologies, Nicolaus Copernicus University in Toruń, Wileńska 4 Street, 87-100, Toruń, Poland.
Immunol Res. 2024 Dec 16;73(1):14. doi: 10.1007/s12026-024-09574-6.
Macrophages, the most abundant cells that participate in tumour progression, are the subject of a number of anticancer therapy approaches. Our previous results revealed that an extract of the fungus Coriolus versicolor (CV) has anti-cancer and immunomodulatory properties. The aim of the present study was to investigate whether CV extract-treated triple-negative breast cancer (TNBC) cells can release factors that can reprogram macrophages from pro-tumourigenic to anti-cancer subtypes. RAW 264.7 macrophages were cultured in a conditioned medium (CM) from non-treated 4T1 breast cancer cells (CM-NT) or CV extract-stimulated cells (CM-CV). After treatment, the following macrophage properties were evaluated: cell viability; M1/M2 phenotype (enzyme activities: iNOS and arginase 1; and expression of CD molecules: CD80 and CD163); cytokine concentrations: IL-6, TNF-α, IL-10, TGF-β, MCP-1 and VEGF; migration level; and ROS production. The results revealed that, compared with normal cells, TNBC cells stimulated with CV extract create a microenvironment that promotes a decrease in macrophage viability and migration, intracellular ROS production, and pro-angiogenic cytokine production (VEGF and MCP-1). Moreover, CM-CV decreased the expression of M2 macrophage markers (arginase 1 and CD163; IL-10 and TGF-β) but upregulated the expression of M1 cell markers (iNOS and CD80; IL-6 and TNF-α). We concluded that CV extract modifies the tumour microenvironment and changes macrophage polarisation toward functioning as an anti-tumour agent. Therefore, it is promising to use in the treatment of TNBC-associated macrophages.
巨噬细胞是参与肿瘤进展的最丰富的细胞,是多种抗癌治疗方法的研究对象。我们之前的结果表明,云芝提取物具有抗癌和免疫调节特性。本研究的目的是调查经云芝提取物处理的三阴性乳腺癌(TNBC)细胞是否能释放可将巨噬细胞从促肿瘤亚型重编程为抗癌亚型的因子。将RAW 264.7巨噬细胞培养于未处理的4T1乳腺癌细胞的条件培养基(CM-NT)或经云芝提取物刺激的细胞的条件培养基(CM-CV)中。处理后,评估以下巨噬细胞特性:细胞活力;M1/M2表型(酶活性:诱导型一氧化氮合酶和精氨酸酶1;以及CD分子表达:CD80和CD163);细胞因子浓度:白细胞介素-6、肿瘤坏死因子-α、白细胞介素-10、转化生长因子-β、单核细胞趋化蛋白-1和血管内皮生长因子;迁移水平;以及活性氧生成。结果显示,与正常细胞相比,经云芝提取物刺激的TNBC细胞创造了一个促进巨噬细胞活力和迁移降低、细胞内活性氧生成以及促血管生成细胞因子生成(血管内皮生长因子和单核细胞趋化蛋白-1)减少的微环境。此外,CM-CV降低了M2巨噬细胞标志物(精氨酸酶1和CD163;白细胞介素-10和转化生长因子-β)的表达,但上调了M1细胞标志物(诱导型一氧化氮合酶和CD80;白细胞介素-6和肿瘤坏死因子-α)的表达。我们得出结论,云芝提取物可改变肿瘤微环境,并使巨噬细胞极化转变为发挥抗肿瘤作用。因此,其在治疗TNBC相关巨噬细胞方面具有应用前景。