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CCL5 derived from tumor-associated macrophages promotes prostate cancer stem cells and metastasis via activating β-catenin/STAT3 signaling

机译:源自肿瘤相关巨噬细胞的CCL5通过激活β-catenin/ STAT3信号传导促进前列腺癌干细胞和转移

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摘要

, The mRNA and protein expression differences of indicated genes between prostate cancer tumor tissues and para-carcinoma tissues (  = 3). Elisa assay indicated that the blood samples of prostate cancer patients (  = 30) exhibited elevated expression of CCL5 when compared with that of healthy male participants (  = 30). Prostate cancer patients with higher Gleason grade exhibited an increased CCL5 accumulation in the blood (  = 30). Tissue immunofluorescence assay suggested that CCL5 and the macrophage marker CD163 were co-localized in both the primary tumor and metastatic lymph node of prostate cancer patients. Scale bar, 10 μm. TAMs exhibited increased secretion of CCL5 than immature macrophages or prostate cancer cells. CCL5 concentrations in the cell culture supernatants of THP1-derived macrophages (M0), THP1-derived TAMs (M2), DU145 and PC3 cells were measured using Elisa method (  = 10). All values are presented as the mean ± SD. *  p
机译:,前列腺癌肿瘤组织和癌旁组织之间指示基因的mRNA和蛋白质表达差异(= 3)。 Elisa分析表明,与健康男性受试者(samples = 30)相比,前列腺癌患者的血液样本(= 30)显示出CCL5表达升高。格里森评分较高的前列腺癌患者血液中CCL5积累增加(increased = 30)。组织免疫荧光分析表明,CCL5和巨噬细胞标记CD163在前列腺癌患者的原发性肿瘤和转移性淋巴结中共定位。比例尺,10μm。与未成熟的巨噬细胞或前列腺癌细胞相比,TAM显示出增加的CCL5分泌。使用Elisa方法测量THP1来源的巨噬细胞(M0),THP1来源的TAM(M2),DU145和PC3细胞的细胞培养上清液中CCL5的浓度(= 10)。所有值均以平均值±SD表示。 * p

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