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Cored network biomarker of carcinogenesis from early and late stage bladder cancer samples

机译:来自早期和晚期膀胱癌样品的癌细胞生物标志物

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Cancers is the major cause of death around the world for a long time, and it occurs at DNA, RNA or protein level. In this study, we use the systems biology approach to construct the protein-protein interaction (PPI) networks for early and late stage bladder cancer. By comparing network of these two stage, core and specific network markers were identified by the intersection and distinction of key proteins. We identified 18 significant proteins(network marker) for the cored network and their carcinogenesis relevance values(CRVs) We construct the CPPIN and NPPIN network structures for both stage bladder cancer. We also identified 3388 cancer protein pairs and 3151 non-cancer protein pairs for the early stage bladder cancer, respectively. And build 634 cancer protein pairs and 1185 non cancer protein pairs for the late stage bladder cancer, respectively. Primary pathway analysis shows that proteins BRAC1 and CUL3 related to the function of cell growth, UBC should be only a housekeeping like protein because it does not involve in any important functions. More validation of these network markers by both literature and novel test set could help us reveal more mechanisms of bladder cancer in the future.
机译:癌症是世界周围死亡的主要原因很长一段时间,它发生在DNA,RNA或蛋白质水平。在这项研究中,我们使用系统生物学方法来构建早期和晚期膀胱癌的蛋白质 - 蛋白质相互作用(PPI)网络。通过比较这两个阶段的网络,通过关键蛋白的交叉点和区分核心和特定网络标记。我们鉴定了核网络的18例显着蛋白质(网络标记)及其致癌相关性值(CRV),我们构建了阶段膀胱癌的CPPIN和NPPIN网络结构。我们还分别鉴定了3388对癌症蛋白对和3151个非癌症蛋白对,用于早期膀胱癌。并分别构建634个癌症蛋白对和1185个非癌症蛋白对,用于晚期膀胱癌。主要途径分析表明,蛋白质Brac1和Cul3与细胞生长的功能有关,UBC应该只是蛋白质的家务,因为它不涉及任何重要功能。这些网络标记对这些网络标记的更多验证和新型测试集可以帮助我们在未来揭示更多膀胱癌的机制。

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