A pancreatic cancer organoid-in-matrix platform shows distinct sensitivities to T cell killing

• Published in: Scientific reports 2024-04, Vol.14 (1), p.9377-9377, Article 9377
• Main Authors: Lahusen, Anton, Cai, Jierui, Schirmbeck, Reinhold, Wellstein, Anton, Kleger, Alexander, Seufferlein, Thomas, Eiseler, Tim, Lin, Yuan-Na
• Format: Article
• Language: English
• Subjects: 631/67/2329; 631/67/327; 631/67/580; 631/67/70; Adenocarcinoma; Animals; Carcinoma, Pancreatic Ductal - genetics; Carcinoma, Pancreatic Ductal - immunology; Carcinoma, Pancreatic Ductal - metabolism; Carcinoma, Pancreatic Ductal - pathology; Cell culture; Cell Line, Tumor; Coculture Techniques - methods; Heterogeneity; Humanities and Social Sciences; Humans; Lymphocytes; Lymphocytes T; Mice; Molecular modelling; multidisciplinary; Organoids; Organoids - metabolism; Organoids - pathology; Pancreatic cancer; Pancreatic Neoplasms - genetics; Pancreatic Neoplasms - immunology; Pancreatic Neoplasms - metabolism; Pancreatic Neoplasms - pathology; Phenotypes; Science; Science (multidisciplinary); Stromal cells; T-Lymphocytes - immunology; T-Lymphocytes - metabolism; Transcriptomics; Tumor Microenvironment; Tumors
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-60107-5

Poor treatment responses of pancreatic ductal adenocarcinoma (PDAC) are in large part due to tumor heterogeneity and an immunosuppressive desmoplastic tumor stroma that impacts interactions with cells in the tumor microenvironment (TME). Thus, there is a pressing need for models to probe the contributions of cellular and noncellular crosstalk. Organoids are promising model systems with the potential to generate a plethora of data including phenotypic, transcriptomic and genomic characterization but still require improvements in culture conditions mimicking the TME. Here, we describe an INTERaction with Organoid-in-MatriX ("InterOMaX") model system, that presents a 3D co-culture-based platform for investigating matrix-dependent cellular crosstalk. We describe its potential to uncover new molecular mechanisms of T cell responses to murine KPC ( LSL- Kras G12D /+27 /Trp53 tm1Tyj/J /p48 Cre/ + ) PDAC cells as well as PDAC patient-derived organoids (PDOs). For this, a customizable matrix and homogenously sized organoid-in-matrix positioning of cancer cells were designed based on a standardized agarose microwell chip array system and established for co-culture with T cells and inclusion of stromal cells. We describe the detection and orthogonal analysis of murine and human PDAC cell populations with distinct sensitivity to T cell killing that is corroborated in vivo . By enabling both identification and validation of gene candidates for T cell resistance, this platform sets the stage for better mechanistic understanding of cancer cell-intrinsic resistance phenotypes in PDAC.