Ashekyan Ohanes, Shahbazyan Nerses, Bareghamyan Yeva, Kudryavzeva Anna, Mandel Daria, Schmidt Maria, Loeffler-Wirth Henry, Uduman Mohamed, Chand Dhan, Underwood Dennis, Armen Garo, Arakelyan Arsen, Nersisyan Lilit, Binder Hans
Armenian Bioinformatics Institute, 3/6 Nelson Stepanyan Str., Yerevan 0062, Armenia.
IZBI, Interdisciplinary Centre for Bioinformatics, Universität Leipzig, Härtelstr. 16-18, 04107 Leipzig, Germany.
Cancers (Basel). 2023 Jul 28;15(15):3835. doi: 10.3390/cancers15153835.
The molecular mechanisms of the liver metastasis of colorectal cancer (CRLM) remain poorly understood. Here, we applied machine learning and bioinformatics trajectory inference to analyze a gene expression dataset of CRLM. We studied the co-regulation patterns at the gene level, the potential paths of tumor development, their functional context, and their prognostic relevance. Our analysis confirmed the subtyping of five liver metastasis subtypes (LMS). We provide gene-marker signatures for each LMS, and a comprehensive functional characterization that considers both the hallmarks of cancer and the tumor microenvironment. The ordering of CRLMs along a pseudotime-tree revealed a continuous shift in expression programs, suggesting a developmental relationship between the subtypes. Notably, trajectory inference and personalized analysis discovered a range of epigenetic states that shape and guide metastasis progression. By constructing prognostic maps that divided the expression landscape into regions associated with favorable and unfavorable prognoses, we derived a prognostic expression score. This was associated with critical processes such as epithelial-mesenchymal transition, treatment resistance, and immune evasion. These factors were associated with responses to neoadjuvant treatment and the formation of an immuno-suppressive, mesenchymal state. Our machine learning-based molecular profiling provides an in-depth characterization of CRLM heterogeneity with possible implications for treatment and personalized diagnostics.
结直肠癌肝转移(CRLM)的分子机制仍未得到充分了解。在此,我们应用机器学习和生物信息学轨迹推断来分析CRLM的基因表达数据集。我们研究了基因水平的共调控模式、肿瘤发展的潜在路径、它们的功能背景及其预后相关性。我们的分析证实了五种肝转移亚型(LMS)的分型。我们为每种LMS提供了基因标记特征,以及一个综合的功能表征,该表征同时考虑了癌症特征和肿瘤微环境。沿着伪时间树对CRLMs进行排序揭示了表达程序的连续变化,表明各亚型之间存在发育关系。值得注意的是,轨迹推断和个性化分析发现了一系列影响和指导转移进展的表观遗传状态。通过构建将表达景观划分为与有利和不利预后相关区域的预后图谱,我们得出了一个预后表达评分。这与上皮-间质转化、治疗抵抗和免疫逃逸等关键过程相关。这些因素与新辅助治疗的反应以及免疫抑制性间充质状态的形成有关。我们基于机器学习的分子图谱提供了对CRLM异质性的深入表征,可能对治疗和个性化诊断具有启示意义。