Many efforts have been made to discover tumor-specific microenvironment elements (TMEs) from immunostained tissue sections. However, the identification of yet unknown but relevant TMEs from multiplex immunostained tissues remains a challenge, due to the number of markers involved (tens) and the complexity of their spatial interactions. We present NaroNet, which uses machine learning to identify and annotate known as well as novel TMEs from self-supervised embeddings of cells, organized at different levels (local cell phenotypes and cellular neighborhoods). Then it uses the abundance of TMEs to classify patients based on biological or clinical features. We validate NaroNet using synthetic patient cohorts with adjustable incidence of different TMEs and two cancer patient datasets. In both synthetic and real datasets, NaroNet unsupervisedly identifies novel TMEs, relevant for the user-defined classification task. As NaroNet requires only patient-level information, it renders state-of-the-art computational methods accessible to a broad audience, accelerating the discovery of biomarker signatures.
翻译:已作出许多努力,以发现免疫性组织各部分的肿瘤特定微环境元素(TMEs),然而,由于涉及的标记数量(十)及其空间互动的复杂性,从多克斯免疫性组织中查明多发性免疫性组织中的未知但相关的TME(TMEs)仍是一个挑战。我们介绍NaroNet,它利用机器学习来识别和注释已知的以及自监督的细胞嵌入的新型TMEs,由不同层次(地方细胞型和细胞邻里)组织,然后利用大量TMEs对病人进行生物或临床特征的分类。我们验证NaroNet使用合成病人组群使用可调整的不同TMEs和两个癌症病人数据集。在合成和真实的数据集中,NaroNet不加监督地识别与用户定义的分类任务相关的新型TMEs。由于NaroNet仅需要病人级信息,它使广大受众可以使用最先进的计算方法,加速发现生物标记签名。