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Graph clustering techniques applied to the glycomic response in glioblastoma cells to treatments with STAT3 phosphorylation inhibition and fetal bovine serum

机译:图聚类技术应用于胶质母细胞瘤细胞对STAT3磷酸化抑制和胎牛血清的糖代谢反应

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Cancer stem cells (CSC) represent a very small percentage of the total tumor population however they pose a big challenge in treating cancer. Glycans play a key role in cancer therapeutics since overexpression of them depending on the glycan type can lead either to cell death or more invasive metastasis. Two major components, fetal bovine serum (FBS) and STAT3, are known to up- or down-regulate certain glycolipid or phospholipid compositions found in glioblastoma CSCs. The analysis and the understanding of the global interactional behavior of lipidomic networks remains a challenging task and can not be accomplished solely based on intuitive reasoning. The present contribution aims at applying graph clustering networks to analyze the functional aspects of certain activators or inhibitors at the molecular level in glioblastoma stem cells (GSCs). This research enhances our understanding of the differences in phenotype changes and determining the responses of glycans to certain treatments for the aggressive GSCs, and represents together with a quantitative phosphoproteomic study1 the most detailed systems biology study of GSCs differentiation known so far. Thus, these new paradigms are providing unique understanding of the mechanisms involved in GSC maintenance and tumorigenicity and are thus opening a new window to biomedical frontiers
机译:癌症干细胞(CSC)仅占总肿瘤人口的很小一部分,但在治疗癌症方面却构成了巨大挑战。聚糖在癌症治疗中起着关键作用,因为取决于聚糖类型的过表达可能导致细胞死亡或更具侵袭性的转移。已知两种主要成分,胎牛血清(FBS)和STAT3,可以上调或下调胶质母细胞瘤CSC中发现的某些糖脂或磷脂成分。对脂质组学网络的整体相互作用行为的分析和理解仍然是一项艰巨的任务,不能仅凭直觉推理就可以完成。本文稿旨在应用图聚类网络在胶质母细胞瘤干细胞(GSC)的分子水平上分析某些激活剂或抑制剂的功能方面。这项研究增进了我们对表型变化差异的理解,并确定了糖对侵略性GSC某些治疗的反应,并与定量磷酸化蛋白质组学研究一起代表了迄今为止已知的最详细的GSCs分化系统生物学研究。因此,这些新范例为GSC维持和致瘤性的机制提供了独特的理解,从而为生物医学领域开辟了新窗口

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