Glover Kyle P, Chen Zhongqiang, Markell Lauren K, Han Xing
DuPont Haskell Global Centers for Health & Environmental Sciences, Newark, Delaware, United States of America; Department of Biological Sciences, Cell and Molecular Biology Graduate Program, University of the Sciences, Philadelphia, Pennsylvania, United States of America.
DuPont Industrial Biosciences, Wilmington, Delaware, United States of America.
PLoS One. 2015 Oct 2;10(10):e0139850. doi: 10.1371/journal.pone.0139850. eCollection 2015.
Activation of stress response pathways in the tumor microenvironment can promote the development of cancer. However, little is known about the synergistic tumor promoting effects of stress response pathways simultaneously induced in the tumor microenvironment. Therefore, the purpose of this study was to establish gene expression signatures representing the interaction of pathways deregulated by tumor promoting agents and pathways induced by DNA damage. Human lymphoblastoid TK6 cells were pretreated with the protein kinase C activating tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA) and exposed to UVC-irradiation. The time and dose-responsive effects of the co-treatment were captured with RNA-sequencing (RNA-seq) in two separate experiments. TK6 cells exposed to both TPA and UVC had significantly more genes differentially regulated than the theoretical sum of genes induced by either stress alone, thus indicating a synergistic effect on global gene expression patterns. Further analysis revealed that TPA+UVC co-exposure caused synergistic perturbation of specific genes associated with p53, AP-1 and inflammatory pathways important in carcinogenesis. The 17 gene signature derived from this model was confirmed with other PKC-activating tumor promoters including phorbol-12,13-dibutyrate, sapintoxin D, mezerein, (-)-Indolactam V and resiniferonol 9,13,14-ortho-phenylacetate (ROPA) with quantitative real-time PCR (QPCR). Here we show a novel gene signature that may represent a synergistic interaction in the tumor microenvironment that is relevant to the mechanisms of chemical induced tumor promotion.
肿瘤微环境中应激反应通路的激活可促进癌症发展。然而,对于肿瘤微环境中同时诱导的应激反应通路的协同促肿瘤作用却知之甚少。因此,本研究的目的是建立基因表达特征,以代表由促肿瘤剂失调的通路与DNA损伤诱导的通路之间的相互作用。用人淋巴母细胞TK6细胞预先用蛋白激酶C激活的肿瘤启动子12-O-十四烷酰佛波醇-13-乙酸酯(TPA)处理,然后暴露于紫外线C(UVC)照射。在两个独立实验中通过RNA测序(RNA-seq)捕获联合处理的时间和剂量反应效应。暴露于TPA和UVC的TK6细胞中差异调节的基因明显多于单独一种应激诱导的基因理论总和,从而表明对整体基因表达模式有协同作用。进一步分析表明,TPA+UVC共同暴露导致与致癌作用中重要的p53、AP-1和炎症通路相关的特定基因发生协同扰动。用包括佛波醇-12,13-二丁酸酯、沙品毒素D、大戟二萜醇、(-)-吲哚内酰胺V和9,13,14-邻苯乙酸树脂大戟醇(ROPA)在内的其他PKC激活肿瘤启动子通过定量实时PCR(QPCR)证实了从该模型衍生的17个基因特征。在这里,我们展示了一种新的基因特征,它可能代表了肿瘤微环境中与化学诱导肿瘤促进机制相关的协同相互作用。