Ruosaari Salla, Hienonen-Kempas Tuija, Puustinen Anne, Sarhadi Virinder K, Hollmén Jaakko, Knuutila Sakari, Saharinen Juha, Wikman Harriet, Anttila Sisko
Biological Mechanisms and Prevention of Work-related Diseases, Health and Work Ability, Finnish Institute of Occupational Health, Topeliuksenkatu 41aA, FI-00250 Helsinki, Finland.
BMC Med Genomics. 2008 Nov 11;1:55. doi: 10.1186/1755-8794-1-55.
Studies on asbestos-induced tumourigenesis have indicated the role of, e.g., reactive oxygen/nitrogen species, mitochondria, as well as NF-kappaB and MAPK signalling pathways. The exact molecular mechanisms contributing to asbestos-mediated carcinogenesis are, however, still to be characterized.
In this study, gene expression data analyses together with gene annotation data from the Gene Ontology (GO) database were utilized to identify pathways that are differentially regulated in lung and tumour tissues between asbestos-exposed and non-exposed lung cancer patients. Differentially regulated pathways were identified from gene expression data from 14 asbestos-exposed and 14 non-exposed lung cancer patients using custom-made software and Iterative Group Analysis (iGA). Western blotting was used to further characterize the findings, specifically to determine the protein levels of UBA1 and UBA7.
Differences between asbestos-related and non-related lung tumours were detected in pathways associated with, e.g., ion transport, NF-kappaB signalling, DNA repair, as well as spliceosome and nucleosome complexes. A notable fraction of the pathways down-regulated in both normal and tumour tissue of the asbestos-exposed patients were related to protein ubiquitination, a versatile process regulating, for instance, DNA repair, cell cycle, and apoptosis, and thus being also a significant contributor of carcinogenesis. Even though UBA1 or UBA7, the early enzymes involved in protein ubiquitination and ubiquitin-like regulation of target proteins, did not underlie the exposure-related deregulation of ubiquitination, a difference was detected in the UBA1 and UBA7 levels between squamous cell carcinomas and respective normal lung tissue (p = 0.02 and p = 0.01) without regard to exposure status.
Our results indicate alterations in protein ubiquitination related both to cancer type and asbestos. We present for the first time pathway analysis results on asbestos-associated lung cancer, providing important insight into the most relevant targets for future research.
关于石棉诱导肿瘤发生的研究表明了活性氧/氮物种、线粒体以及核因子κB(NF-κB)和丝裂原活化蛋白激酶(MAPK)信号通路等的作用。然而,导致石棉介导的致癌作用的确切分子机制仍有待阐明。
在本研究中,利用基因表达数据分析以及来自基因本体论(GO)数据库的基因注释数据,以识别在石棉暴露和未暴露的肺癌患者的肺组织和肿瘤组织中差异调节的通路。使用定制软件和迭代组分析(iGA),从14例石棉暴露和14例未暴露的肺癌患者的基因表达数据中识别差异调节的通路。蛋白质印迹法用于进一步表征研究结果,特别是确定泛素激活酶1(UBA1)和泛素样修饰激活酶7(UBA7)的蛋白质水平。
在与离子转运、NF-κB信号传导、DNA修复以及剪接体和核小体复合物等相关的通路中,检测到石棉相关和非相关肺肿瘤之间的差异。在石棉暴露患者的正常组织和肿瘤组织中均下调的通路中,有相当一部分与蛋白质泛素化有关,蛋白质泛素化是一个多功能过程,例如调节DNA修复、细胞周期和细胞凋亡,因此也是致癌作用的重要因素。尽管参与蛋白质泛素化和靶蛋白泛素样调节的早期酶UBA1或UBA7并非暴露相关的泛素化失调的基础,但在鳞状细胞癌和相应的正常肺组织之间检测到UBA1和UBA7水平存在差异(p = 0.02和p = 0.01),且与暴露状态无关。
我们 的结果表明蛋白质泛素化的改变与癌症类型和石棉均相关。我们首次展示了石棉相关肺癌的通路分析结果,为未来研究的最相关靶点提供了重要见解。