Mo Qianxing, Wan Lixin, Schell Michael J, Jim Heather, Tworoger Shelley S, Peng Guang
Department of Biostatistics & Bioinformatics, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Department of Molecular Oncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Cancers (Basel). 2021 Dec 7;13(24):6168. doi: 10.3390/cancers13246168.
By iCluster analysis, we found that the integrative molecular classification of the UM was primarily driven by DNA copy number variation on chromosomes 3, 6 and 8, differential methylation and expression of genes involved in the immune system, cell morphogenesis, movement and migration, and differential mutation of genes including , , , and . Integrative analysis revealed that pathways including IL6/JAK/STAT3 signaling, angiogenesis, allograft rejection, inflammatory response and interferon gamma response were hypomethylated and up-regulated in the M3 iSubtype, which was associated with a worse overall survival, compared to the D3 iSubtype. Using two independent gene expression datasets, we demonstrated that the subtype-driving genes had an excellent prognostic power in classifying UM into high- or low-risk groups for metastasis. Integrative analysis of UM multi-omics data provided a comprehensive view of UM biology for understanding the underlying mechanism leading to UM metastasis. The concordant molecular alterations at multi-omics levels revealed by our integrative analysis could be used for patient stratification towards personalized management and surveillance.
通过iCluster分析,我们发现葡萄膜黑色素瘤(UM)的综合分子分类主要由3号、6号和8号染色体上的DNA拷贝数变异、免疫系统、细胞形态发生、运动和迁移相关基因的差异甲基化和表达,以及包括、、、和在内的基因的差异突变驱动。综合分析显示,与D3 i亚型相比,M3 i亚型中包括IL6/JAK/STAT3信号传导、血管生成、同种异体移植排斥、炎症反应和干扰素γ反应等通路发生低甲基化并上调,这与较差的总生存期相关。使用两个独立的基因表达数据集,我们证明亚型驱动基因在将UM分为转移高风险或低风险组方面具有出色的预后能力。对UM多组学数据的综合分析为理解导致UM转移的潜在机制提供了UM生物学的全面视图。我们的综合分析揭示的多组学水平上一致的分子改变可用于患者分层,以实现个性化管理和监测。