Background:
Collagen VI is a structural component of the extracellular matrix that regulates cellular processes, including adhesion, migration and signaling, that contribute to tumor growth and migration. In malignancies, such as Hodgkin lymphoma, changes in collagen deposition and its spatial arrangement are indicative of tumor-associated stromal remodeling. Traditional histopathology does not adequately capture the spatial organization of collagen networks. This study presents a reproducible digital pathology workflow using ImageJ to quantify collagen VI cellular spatial interactions in diseased tissue.
Aim: To develop and validate a digital pathology workflow using ImageJ for quantitative assessment of collagen VI-cellular spatial arrangements in cancer-related tissue remodeling.
Methods:
A Hodgkin lymphoma tissue image was used to establish workflow, which was subsequently applied to a COVID-19 lung tissue cohort. Structural elements were binarized and skeletonized; branching-related topological parameters were quantified. Architectural complexity was summarized using a composite Branching Complexity Index (BCI), alongside density-based metrics including branch and junction densities. Collagen fractional area was quantified using color thresholding. Distributional analyses and Spearman’s rank correlation assessed metric robustness and associations with collagen deposition. Reproducibility was evaluated using Bland–Altman and Spearman correlation analyses.
Results:
Branching-derived metrics were extracted and showed broad distributions with stable variability. BCI showed no meaningful association with collagen fractional area in normal lung tissue, whereas COVID-19 lung tissue demonstrated a positive association between BCI and collagen deposition, supporting the biological plausibility of the framework. Density-based metrics showed cohort-specific relationships with collagen fractional area, suggesting that branching abundance and network connectivity capture aspects of architectural remodeling. Bland-Altman analysis confirmed reproducibility for distance measurements.
Conclusion:
Skeleton-based branching analysis provides an approach for quantifying lung architectural remodeling in cancer. Branching metrics show associations with collagen deposition while extending beyond conventional area-based measures. This framework supports future integration with clinical data and application inother diseases involving tissue remodeling.
Acknowledgement:
We acknowledge the work done on the study titled "Multi-omic spatial profiling reveals the unique SARS-CoV-2 lung microenvironment and collagen VI as a predictive biomarker in severe COVID-19" to be the background of this study.