Suppr超能文献

骨肉瘤的基因组异质性——从单一候选基因到功能模块的转变

Genomic heterogeneity of osteosarcoma - shift from single candidates to functional modules.

作者信息

Poos Kathrin, Smida Jan, Maugg Doris, Eckstein Gertrud, Baumhoer Daniel, Nathrath Michaela, Korsching Eberhard

机构信息

Institute of Bioinformatics, University Hospital Münster, Münster, Germany.

Clinical Cooperation Group Osteosarcoma, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany; Children's Cancer Research Center and Department of Pediatrics, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

出版信息

PLoS One. 2015 Apr 7;10(4):e0123082. doi: 10.1371/journal.pone.0123082. eCollection 2015.

Abstract

Osteosarcoma (OS), a bone tumor, exhibit a complex karyotype. On the genomic level a highly variable degree of alterations in nearly all chromosomal regions and between individual tumors is observable. This hampers the identification of common drivers in OS biology. To identify the common molecular mechanisms involved in the maintenance of OS, we follow the hypothesis that all the copy number-associated differences between the patients are intercepted on the level of the functional modules. The implementation is based on a network approach utilizing copy number associated genes in OS, paired expression data and protein interaction data. The resulting functional modules of tightly connected genes were interpreted regarding their biological functions in OS and their potential prognostic significance. We identified an osteosarcoma network assembling well-known and lesser-known candidates. The derived network shows a significant connectivity and modularity suggesting that the genes affected by the heterogeneous genetic alterations share the same biological context. The network modules participate in several critical aspects of cancer biology like DNA damage response, cell growth, and cell motility which is in line with the hypothesis of specifically deregulated but functional modules in cancer. Further, we could deduce genes with possible prognostic significance in OS for further investigation (e.g. EZR, CDKN2A, MAP3K5). Several of those module genes were located on chromosome 6q. The given systems biological approach provides evidence that heterogeneity on the genomic and expression level is ordered by the biological system on the level of the functional modules. Different genomic aberrations are pointing to the same cellular network vicinity to form vital, but already neoplastically altered, functional modules maintaining OS. This observation, exemplarily now shown for OS, has been under discussion already for a longer time, but often in a hypothetical manner, and can here be exemplified for OS.

摘要

骨肉瘤(OS)是一种骨肿瘤,具有复杂的核型。在基因组水平上,可以观察到几乎所有染色体区域以及各个肿瘤之间存在高度可变的改变程度。这阻碍了骨肉瘤生物学中常见驱动因素的识别。为了确定参与骨肉瘤维持的常见分子机制,我们遵循这样的假设,即患者之间所有与拷贝数相关的差异都在功能模块水平上被拦截。该实现基于一种网络方法,利用骨肉瘤中与拷贝数相关的基因、配对表达数据和蛋白质相互作用数据。对紧密连接基因组成的功能模块进行了解释,涉及其在骨肉瘤中的生物学功能及其潜在的预后意义。我们确定了一个骨肉瘤网络,其中包含知名和不太知名的候选基因。所推导的网络显示出显著的连通性和模块性,表明受异质基因改变影响的基因共享相同的生物学背景。网络模块参与癌症生物学的几个关键方面,如DNA损伤反应、细胞生长和细胞运动,这与癌症中特定失调但功能模块的假设一致。此外,我们可以推断出在骨肉瘤中具有可能预后意义的基因以供进一步研究(例如EZR、CDKN2A、MAP3K5)。其中一些模块基因位于6号染色体q臂上。所给出的系统生物学方法提供了证据,表明基因组和表达水平上的异质性在功能模块水平上由生物系统进行了有序排列。不同的基因组畸变指向相同的细胞网络邻域,以形成维持骨肉瘤的重要但已发生肿瘤性改变的功能模块。这种观察结果,现在以骨肉瘤为例进行了说明,已经讨论了很长时间,但通常是以假设的方式,在这里可以以骨肉瘤为例进行具体说明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8b2/4388529/37a70e3a425e/pone.0123082.g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验