Kalamohan Kalaivani, Rathinam Dhanasekaran, Panneerpandian Ponmathi, Ganesan Kumaresan
Unit of Excellence in Cancer Genetics, Department of Genetics, School of Biological Sciences, Centre for Excellence in Genomic Sciences, Madurai Kamaraj University, Madurai, 625021, India.
Cancer Immunol Immunother. 2017 Jul;66(7):941-954. doi: 10.1007/s00262-017-1998-7. Epub 2017 Apr 12.
The existing large number of gene expression profiles of tumour samples offers a great advantage for the integrative functional genomic exploration of molecular dysregulation in cancers. The clusters of genes (modules) derived from a gastric cancer (GC) coexpression network were explored to understand their clinical and functional significance. Among the modules derived from the GC mRNA expression network, six modules were relatively highly expressed in diffuse type gastric tumours. Elevated expression of genes related to extracellular matrix (ECM), angiogenesis, collagen and intracellular cytoskeletal components and immune response were identified in these modules. ECM-related modules exhibited an inverse correlation with modules representing the expression of immune response genes. A reduced expression of immune response genes was identified as the key factor associated with the aggressive features of diffuse gastric tumours, which is indicative of tumour progression involving the escape from immune surveillance in diffuse tumours. A part of the identified aggressive factors was common between intestinal and diffuse type tumours. The coexpressed modules and their expression patterns delineate the fine transition involved in cancer progression in the later stages of tumours. The identified modules could serve as surrogate gene-sets, indicating the molecular staging of GC aggressiveness with underlying biological interaction.
现有的大量肿瘤样本基因表达谱为癌症分子失调的综合功能基因组探索提供了巨大优势。我们探索了源自胃癌(GC)共表达网络的基因簇(模块),以了解其临床和功能意义。在源自GC mRNA表达网络的模块中,有六个模块在弥漫型胃肿瘤中相对高表达。在这些模块中,鉴定出与细胞外基质(ECM)、血管生成、胶原蛋白、细胞内细胞骨架成分和免疫反应相关的基因表达升高。与ECM相关的模块与代表免疫反应基因表达的模块呈负相关。免疫反应基因表达降低被确定为与弥漫性胃肿瘤侵袭性特征相关的关键因素,这表明肿瘤进展涉及弥漫性肿瘤逃避免疫监视。部分已鉴定出的侵袭性因素在肠型和弥漫型肿瘤中是共同的。共表达模块及其表达模式描绘了肿瘤后期癌症进展中所涉及的精细转变。所鉴定出的模块可作为替代基因集,指示具有潜在生物学相互作用的GC侵袭性的分子分期。