Görke Robert, Meyer-Bäse Anke, Wagner Dorothea, He Huan, Emmett Mark R, Conrad Charles A
Department of Computer Science, Karlsruhe Institute of Technology, Karlsruhe D-76128, Germany.
BMC Syst Biol. 2010 Sep 7;4:126. doi: 10.1186/1752-0509-4-126.
Intelligent and multitiered quantitative analysis of biological systems rapidly evolves to a key technique in studying biomolecular cancer aspects. Newly emerging advances in both measurement as well as bio-inspired computational techniques have facilitated the development of lipidomics technologies and offer an excellent opportunity to understand regulation at the molecular level in many diseases.
We present computational approaches to study the response of glioblastoma U87 cells to gene- and chemo-therapy. To identify distinct biomarkers and differences in therapeutic outcomes, we develop a novel technique based on graph-clustering. This technique facilitates the exploration and visualization of co-regulations in glioblastoma lipid profiling data. We investigate the changes in the correlation networks for different therapies and study the success of novel gene therapies targeting aggressive glioblastoma.
The novel computational paradigm provides unique "fingerprints" by revealing the intricate interactions at the lipidome level in glioblastoma U87 cells with induced apoptosis (programmed cell death) and thus opens a new window to biomedical frontiers.
生物系统的智能和多层次定量分析正迅速发展成为研究生物分子癌症方面的一项关键技术。测量技术以及受生物启发的计算技术方面新出现的进展推动了脂质组学技术的发展,并为理解多种疾病的分子水平调控提供了绝佳机会。
我们提出了用于研究胶质母细胞瘤U87细胞对基因治疗和化学治疗反应的计算方法。为了识别不同的生物标志物和治疗结果差异,我们开发了一种基于图聚类的新技术。该技术有助于探索和可视化胶质母细胞瘤脂质谱数据中的共调控。我们研究了不同疗法相关网络的变化,并研究了针对侵袭性胶质母细胞瘤的新型基因疗法的成效。
这种新颖的计算范式通过揭示胶质母细胞瘤U87细胞脂质组水平上诱导凋亡(程序性细胞死亡)时的复杂相互作用,提供了独特的“指纹”,从而为生物医学前沿打开了一扇新窗口。