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Loan Vulliard

Publications and source records attributed to Loan Vulliard.

2 recordsLinked to original sources

Progress and new challenges in image-based profiling

For over two decades, image-based profiling has revolutionized cell phenotype analysis. Image-based profiling processes rich, high-throughput, microscopy data into thousands of unbiased measurements that reveal phenotypic patterns powerful for drug discovery, functional genomics, and cell state classification. Here, we review the evolving computational landscape of image-based profiling, detailing the bioinformatics processes involved from feature extraction to normalization and batch correction. We discuss how deep learning has fundamentally reshaped the field. We examine key methodological advancements, such as single-cell analysis, the development of robust similarity metrics, and the expansion into new modalities like optical pooled screening, temporal imaging, and 3D organoid profiling. We also highlight the growth of public benchmarks and open-source software ecosystems as a key driver for fostering reproducibility and collaboration. Despite these advances, the field still faces substantial challenges, particularly in developing methods for emerging temporal and 3D data modalities, establishing robust quality control standards and workflows, and interpreting the processed features. By focusing on the technical evolution of image-based profiling rather than the wide-ranging biological applications, our aim with this review is to provide researchers with a roadmap for navigating the progress and new challenges in this rapidly advancing domain.

q-bio.QM

Robust multicellular programs dissect the complex tumor microenvironment and track disease progression in colorectal adenocarcinomas

Colorectal cancer (CRC) is highly heterogeneous, with five-year survival rates dropping from $\sim$90% in localized disease to $\sim$15% with distant metastases. Disease progression is shaped not only by tumor-intrinsic alterations but also by the reorganization of the tumor microenvironment (TME). Metabolic, compositional, and spatial changes contribute to this progression, but considered individually they lack context and often fail as therapeutic targets. Understanding their coordination could reveal processes to alter the disease course. Here, we combined multiplexed ion beam imaging (MIBI) with machine learning to profile metabolic, functional and spatial states of 522 colorectal lesions with single-cell resolution. We observed recurrent stage-specific remodeling marked by a lymphoid-to-myeloid shift, stromal-cancer cooperation, and malignant metabolic shifts. Spatial organization of epithelial, stromal, and immune compartments provided stronger stratification of disease stage than tumor-intrinsic changes or bulk immune infiltration alone. To systematically model these coordinated changes, we condensed multimodal features into 10 latent factors of TME organization. These factors tracked disease progression, were conserved across cohorts, and revealed frequent multicellular metabolic niches and distinct, non-exclusive TME trajectories. Our framework MuVIcell exposes the elements that together drive CRC progression by grouping co-occurring changes across cell types and feature classes into coordinated multicellular programs. This creates a rational basis to therapeutically target TME reorganization. Importantly, the framework is scalable and flexible, offering a resource for studying multicellular organization in other solid tumors.

q-bio.QM