3D多路复用组织成像重建和通过通道嵌入的深度学习模型优化感兴趣区域(ROI)选择。

IF 2.8 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Frontiers in bioinformatics Pub Date : 2023-10-19 eCollection Date: 2023-01-01 DOI:10.3389/fbinf.2023.1275402
Erik Burlingame, Luke Ternes, Jia-Ren Lin, Yu-An Chen, Eun Na Kim, Joe W Gray, Young Hwan Chang
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引用次数: 0

摘要

引言:基于组织的采样和诊断被定义为从特定的有限空间中提取信息及其对特定对象的诊断意义。病理学家处理与肿瘤异质性相关的问题,因为分析单个样本并不一定能获得癌症的代表性描述,组织活检通常只显示肿瘤的一小部分。许多多重组织成像平台(MTI)假设包含二维(2D)组织切片的小核心样本的组织微阵列(TMA)是大块肿瘤的良好近似,尽管肿瘤不是2D的。然而,新兴的全玻片成像(WSI)或使用MTIs样循环免疫荧光(CyCIF)的3D肿瘤图谱强烈挑战了这一假设。尽管通过在WSI或3D中测量肿瘤微环境获得了额外的见解,但用CyCIF处理数十或数百个组织切片可能非常昂贵和耗时。即使资源不受限制,用于下游分析的组织中感兴趣区域(ROI)选择的标准在很大程度上仍然是定性和主观的,因为分层采样需要对象的知识并评估其特征。尽管TMA不能充分近似整个组织的特征,但存在一种理论上的组织亚采样,它可以最好地表示整个幻灯片图像中的肿瘤。方法:为了应对这些挑战,我们从两个方面提出了学习多模态图像翻译任务的深度学习方法:1)重建3D CyCIF表示的生成建模方法;2)共同嵌入CyCIF图像和苏木精和Eosin(H&E)部分,通过跨域翻译学习多模态映射,以选择最小代表性ROI。结果和讨论:我们证明,在训练时间给定一小部分成像数据的情况下,生成模型能够实现癌症样本的3D虚拟CyCIF重建。通过共同嵌入组织学和MTI特征,我们提出了一种用于客观ROI选择的简单凸优化。我们展示了ROI选择的潜在应用及其在细胞异质性方面的性能效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

3D multiplexed tissue imaging reconstruction and optimized region of interest (ROI) selection through deep learning model of channels embedding.

3D multiplexed tissue imaging reconstruction and optimized region of interest (ROI) selection through deep learning model of channels embedding.

3D multiplexed tissue imaging reconstruction and optimized region of interest (ROI) selection through deep learning model of channels embedding.

3D multiplexed tissue imaging reconstruction and optimized region of interest (ROI) selection through deep learning model of channels embedding.

Introduction: Tissue-based sampling and diagnosis are defined as the extraction of information from certain limited spaces and its diagnostic significance of a certain object. Pathologists deal with issues related to tumor heterogeneity since analyzing a single sample does not necessarily capture a representative depiction of cancer, and a tissue biopsy usually only presents a small fraction of the tumor. Many multiplex tissue imaging platforms (MTIs) make the assumption that tissue microarrays (TMAs) containing small core samples of 2-dimensional (2D) tissue sections are a good approximation of bulk tumors although tumors are not 2D. However, emerging whole slide imaging (WSI) or 3D tumor atlases that use MTIs like cyclic immunofluorescence (CyCIF) strongly challenge this assumption. In spite of the additional insight gathered by measuring the tumor microenvironment in WSI or 3D, it can be prohibitively expensive and time-consuming to process tens or hundreds of tissue sections with CyCIF. Even when resources are not limited, the criteria for region of interest (ROI) selection in tissues for downstream analysis remain largely qualitative and subjective as stratified sampling requires the knowledge of objects and evaluates their features. Despite the fact TMAs fail to adequately approximate whole tissue features, a theoretical subsampling of tissue exists that can best represent the tumor in the whole slide image. Methods: To address these challenges, we propose deep learning approaches to learn multi-modal image translation tasks from two aspects: 1) generative modeling approach to reconstruct 3D CyCIF representation and 2) co-embedding CyCIF image and Hematoxylin and Eosin (H&E) section to learn multi-modal mappings by a cross-domain translation for minimum representative ROI selection. Results and discussion: We demonstrate that generative modeling enables a 3D virtual CyCIF reconstruction of a colorectal cancer specimen given a small subset of the imaging data at training time. By co-embedding histology and MTI features, we propose a simple convex optimization for objective ROI selection. We demonstrate the potential application of ROI selection and the efficiency of its performance with respect to cellular heterogeneity.

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