胶质母细胞瘤病理图像的高性能计算分析与数据库支持识别分子和生存相关。

Jun Kong, Fusheng Wang, George Teodoro, Lee Cooper, Carlos S Moreno, Tahsin Kurc, Tony Pan, Joel Saltz, Daniel Brat
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引用次数: 11

摘要

在本文中,我们提出了一个新的框架,用于核显微图像分析、数据管理和高性能计算,以支持涉及核形态学特征、分子数据和临床结果的转化研究。我们的图像分析流水线由核分割和特征计算组成,通过高性能计算在多核cpu和图形处理器单元(gpu)上协同执行。所有来自图像分析的数据都在空间关系数据库中进行管理,支持高效的科学查询。我们将图像分析工作流程应用于来自癌症基因组图谱数据集的159个胶质母细胞瘤(GBM)。通过综合研究,我们发现四种特定核特征的统计数据与患者生存显著相关。此外,我们将核特征与分子数据联系起来,发现了支持病理领域知识的有趣结果。结果表明,前向亚型GBMs的核偏心率平均值最小,核范围和核轴长平均值最大。我们还发现干细胞标记物MYC和细胞增殖制造者MKI67的基因表达与核特征相关。为了补充和告知病理学家相关的诊断特征,我们根据遗传和转录分类查询了每个患者群体中最具代表性的核实例。我们的研究结果表明,特定的核特征具有预后意义,并与转录和遗传类别相关,突出了高通量病理图像分析作为基于人类的审查和转化研究的补充方法的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-Performance Computational Analysis of Glioblastoma Pathology Images with Database Support Identifies Molecular and Survival Correlates.

High-Performance Computational Analysis of Glioblastoma Pathology Images with Database Support Identifies Molecular and Survival Correlates.

High-Performance Computational Analysis of Glioblastoma Pathology Images with Database Support Identifies Molecular and Survival Correlates.

High-Performance Computational Analysis of Glioblastoma Pathology Images with Database Support Identifies Molecular and Survival Correlates.

In this paper, we present a novel framework for microscopic image analysis of nuclei, data management, and high performance computation to support translational research involving nuclear morphometry features, molecular data, and clinical outcomes. Our image analysis pipeline consists of nuclei segmentation and feature computation facilitated by high performance computing with coordinated execution in multi-core CPUs and Graphical Processor Units (GPUs). All data derived from image analysis are managed in a spatial relational database supporting highly efficient scientific queries. We applied our image analysis workflow to 159 glioblastomas (GBM) from The Cancer Genome Atlas dataset. With integrative studies, we found statistics of four specific nuclear features were significantly associated with patient survival. Additionally, we correlated nuclear features with molecular data and found interesting results that support pathologic domain knowledge. We found that Proneural subtype GBMs had the smallest mean of nuclear Eccentricity and the largest mean of nuclear Extent, and MinorAxisLength. We also found gene expressions of stem cell marker MYC and cell proliferation maker MKI67 were correlated with nuclear features. To complement and inform pathologists of relevant diagnostic features, we queried the most representative nuclear instances from each patient population based on genetic and transcriptional classes. Our results demonstrate that specific nuclear features carry prognostic significance and associations with transcriptional and genetic classes, highlighting the potential of high throughput pathology image analysis as a complementary approach to human-based review and translational research.

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