Graf John F, Zavodszky Maria I
GE Global Research, Niskayuna, New York, United States of America.
PLoS One. 2017 Nov 30;12(11):e0188878. doi: 10.1371/journal.pone.0188878. eCollection 2017.
Tumor heterogeneity can manifest itself by sub-populations of cells having distinct phenotypic profiles expressed as diverse molecular, morphological and spatial distributions. This inherent heterogeneity poses challenges in terms of diagnosis, prognosis and efficient treatment. Consequently, tools and techniques are being developed to properly characterize and quantify tumor heterogeneity. Multiplexed immunofluorescence (MxIF) is one such technology that offers molecular insight into both inter-individual and intratumor heterogeneity. It enables the quantification of both the concentration and spatial distribution of 60+ proteins across a tissue section. Upon bioimage processing, protein expression data can be generated for each cell from a tissue field of view.
The Multi-Omics Heterogeneity Analysis (MOHA) tool was developed to compute tissue heterogeneity metrics from MxIF spatially resolved tissue imaging data. This technique computes the molecular state of each cell in a sample based on a pathway or gene set. Spatial states are then computed based on the spatial arrangements of the cells as distinguished by their respective molecular states. MOHA computes tissue heterogeneity metrics from the distributions of these molecular and spatially defined states. A colorectal cancer cohort of approximately 700 subjects with MxIF data is presented to demonstrate the MOHA methodology. Within this dataset, statistically significant correlations were found between the intratumor AKT pathway state diversity and cancer stage and histological tumor grade. Furthermore, intratumor spatial diversity metrics were found to correlate with cancer recurrence.
MOHA provides a simple and robust approach to characterize molecular and spatial heterogeneity of tissues. Research projects that generate spatially resolved tissue imaging data can take full advantage of this useful technique. The MOHA algorithm is implemented as a freely available R script (see supplementary information).
肿瘤异质性可通过具有不同表型特征的细胞亚群表现出来,这些表型特征以多样的分子、形态和空间分布形式呈现。这种内在的异质性在诊断、预后和有效治疗方面带来了挑战。因此,人们正在开发工具和技术来准确表征和量化肿瘤异质性。多重免疫荧光(MxIF)就是这样一种技术,它能从分子层面洞察个体间和肿瘤内的异质性。它能够量化组织切片上60多种蛋白质的浓度和空间分布。经过生物图像处理后,可以从组织视野中的每个细胞生成蛋白质表达数据。
开发了多组学异质性分析(MOHA)工具,用于从MxIF空间分辨组织成像数据中计算组织异质性指标。该技术基于一条信号通路或一组基因来计算样本中每个细胞的分子状态。然后根据细胞的空间排列计算空间状态,这些细胞通过各自的分子状态得以区分。MOHA根据这些分子和空间定义状态的分布来计算组织异质性指标。展示了一个约700名患有MxIF数据的结直肠癌队列,以证明MOHA方法。在这个数据集中,发现肿瘤内AKT信号通路状态多样性与癌症分期和组织学肿瘤分级之间存在统计学上的显著相关性。此外,发现肿瘤内空间多样性指标与癌症复发相关。
MOHA提供了一种简单而稳健的方法来表征组织的分子和空间异质性。生成空间分辨组织成像数据的研究项目可以充分利用这项有用的技术。MOHA算法以免费可用的R脚本形式实现(见补充信息)。