An X-ray micro-CT protocol enables non-destructive 3D visualization of glandular architecture in archived paraffin-embedded prostate cancer tissue

IF 4.1 2区 医学 Q1 PATHOLOGY
Santiago Laguna-Castro, Erna Mäkinen, Teemu Tolonen, Antti Kaipia, Jari Hyttinen
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引用次数: 0

Abstract

The prostate is organized as a complex glandular network, and prostate cancer is accompanied by architectural changes that cannot always be inferred from two-dimensional (2D) histology. The study of these features in three dimensions (3D) in cancerous tissue is important because glandular features have shown potential value for disease characterization and risk stratification beyond that obtained from individual 2D sections. Large collections of clinically annotated material preserved in paraffin remain an important research source. However, many 3D imaging methods require destructive or labor-intensive preparation, limiting access to valuable material that needs to be re-archived. In this proof-of-concept study, we developed an X-ray micro-computed tomography (micro-CT) workflow for direct 3D imaging of archived paraffin-embedded prostate specimens with near-zero sample manipulation. Imaging and denoising parameters were optimized to balance image quality with acquisition time. Paraffin-embedded prostate core punches (n = 5) from five radical prostatectomy specimens were imaged by micro-CT and subsequently processed for histology. Digitized histological sections were aligned with corresponding micro-CT planes for qualitative comparison, while pre-sectioning micro-CT data provided an intact geometric reference for exploratory assessment of histology-associated dimensional changes at the whole-core and glandular-lumen levels. The optimized workflow yielded micro-CT images with discernible glandular morphology and qualitative structural correspondence with matched histological sections. Exploratory measurements suggested modest dimensional change at the whole-core level and greater variability at the lumen level; none of the tested deformation metrics reached conventional statistical significance. Illustrative 3D segmentation presented the glandular epithelium and lumina as spatially continuous structures within a cancer-containing region. These findings support the feasibility of X-ray micro-CT as a non-destructive approach for 3D characterization of prostate glandular architecture directly from paraffin-embedded tissue, providing volumetric context for structures identified on histology while preserving the specimen for subsequent histological assessment.

x射线微ct协议使存档石蜡包埋前列腺癌组织的腺体结构的非破坏性三维可视化。
前列腺是一个复杂的腺体网络,前列腺癌伴随着结构变化,这些变化并不总是从二维组织学中推断出来。在癌组织中三维(3D)研究这些特征是很重要的,因为腺体特征在疾病表征和风险分层方面显示出潜在的价值,而不仅仅是单个二维切片。保存在石蜡中的大量临床注释材料仍然是一个重要的研究来源。然而,许多3D成像方法需要破坏性或劳动密集型的准备工作,限制了对需要重新存档的有价值材料的访问。在这项概念验证研究中,我们开发了一种x射线微计算机断层扫描(micro-CT)工作流程,用于对存档的石蜡包埋前列腺标本进行近零样本操作的直接3D成像。对成像和去噪参数进行了优化,以平衡图像质量和采集时间。对5例根治性前列腺切除术标本进行石蜡包埋前列腺核孔(n = 5)显微ct成像并进行组织学处理。数字化的组织学切片与相应的微ct平面对齐进行定性比较,而预切片的微ct数据为探索性评估全核和腺腔水平的组织学相关尺寸变化提供了完整的几何参考。优化后的工作流程产生的微ct图像具有可识别的腺体形态和与匹配的组织学切片的定性结构对应。探索性测量表明,在整个核心水平上有适度的尺寸变化,在流明水平上有更大的变异性;测试的变形指标均未达到常规统计显著性。说明性3D分割显示腺上皮和腔室在含癌区域内为空间连续结构。这些发现支持了x射线微ct作为直接从石蜡包埋组织中进行前列腺结构三维表征的非破坏性方法的可行性,为组织学上确定的结构提供了体积背景,同时保存标本用于后续的组织学评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Pathology Clinical Research
Journal of Pathology Clinical Research Medicine-Pathology and Forensic Medicine
CiteScore
7.40
自引率
2.40%
发文量
47
审稿时长
20 weeks
期刊介绍: The Journal of Pathology: Clinical Research and The Journal of Pathology serve as translational bridges between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The focus of The Journal of Pathology: Clinical Research is the publication of studies that illuminate the clinical relevance of research in the broad area of the study of disease. Appropriately powered and validated studies with novel diagnostic, prognostic and predictive significance, and biomarker discover and validation, will be welcomed. Studies with a predominantly mechanistic basis will be more appropriate for the companion Journal of Pathology.
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