Center for Cancer Research and Genomic Medicine, The Daniel and Gloria Blumenthal Cancer Center, Paramus, New Jersey, United States of America.
PLoS One. 2013 Jun 6;8(6):e64456. doi: 10.1371/journal.pone.0064456. Print 2013.
The purpose of this study is to evaluate cytokine expression by peripheral blood mononuclear cells (PBMC) from stage I lung cancer patients and to confirm these expression patterns by exposing PBMCs to lung cancer cells in vitro. Five altered cytokines in stage I lung cancer patients (CCL3, IL8, IL1β, CXCL10, sIL2Rα) were identified in plasma from subjects (n = 15) before and after resection using a 30-plex panel protein assay. Gene expression studies using quantitative RT-qPCR were performed on PBMCs from stage I lung cancer patients (n = 62) before and after resection, and compared to non-cancer patients (n = 32) before and after surgery for benign disease. Co-culture experiments that exposed healthy donor PBMCs to lung cancer cells in vitro were performed to evaluate the effect on PBMC cytokine expression. PBMC gene expression of CCL3, IL8 and IL1β was higher in lung cancer patients compared to the same patients at each of four sequential timepoints after removal of their tumors, while CXCL10 and IL2Rα were essentially unchanged. This pattern was also detected when lung cancer patients were compared to non-cancer patients. When non-cancer patients underwent surgery for benign diseases, these cytokine expression changes were not demonstrable. Lung cancer cell lines, but not benign bronchial epithelial cells, induced similar changes in cytokine gene and protein expression by healthy donor PBMCs in an in vitro co-culture system. We conclude that PBMCs from stage I lung cancer patients possess distinct cytokine expression patterns compared to both non-cancer patients, and lung cancer patients following tumor removal. These expression patterns are replicated by healthy donor PBMCs exposed to lung cancer cell lines, but not benign bronchial epithelial cells in vitro. These findings have implications for understanding the immune response to lung cancer.
本研究旨在评估Ⅰ期肺癌患者外周血单个核细胞(PBMC)中的细胞因子表达,并通过体外暴露 PBMC 于肺癌细胞来确认这些表达模式。通过使用 30 plex 面板蛋白测定法,在术前和术后从受试者(n = 15)的血浆中鉴定了 5 种Ⅰ期肺癌患者中改变的细胞因子(CCL3、IL8、IL1β、CXCL10、sIL2Rα)。使用定量 RT-qPCR 对Ⅰ期肺癌患者(n = 62)的 PBMC 进行了基因表达研究,在手术前和手术后与非癌症患者(n = 32)进行了比较,用于良性疾病。进行了共培养实验,将健康供体 PBMC 暴露于体外的肺癌细胞,以评估对 PBMC 细胞因子表达的影响。与肿瘤切除后的四个连续时间点的同一患者相比,肺癌患者的 PBMC 基因表达 CCL3、IL8 和 IL1β 更高,而 CXCL10 和 IL2Rα 基本不变。当将肺癌患者与非癌症患者进行比较时,也观察到了这种模式。当非癌症患者因良性疾病进行手术时,这些细胞因子表达的变化无法检测到。在体外共培养系统中,肺癌细胞系而非良性支气管上皮细胞可诱导健康供体 PBMC 中的细胞因子基因和蛋白表达发生类似变化。我们得出结论,与非癌症患者和肿瘤切除后的肺癌患者相比,Ⅰ期肺癌患者的 PBMC 具有独特的细胞因子表达模式。这些表达模式在暴露于肺癌细胞系但未暴露于良性支气管上皮细胞的健康供体 PBMC 中得到复制。这些发现对理解对肺癌的免疫反应具有意义。