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Tumor Organoids Grown in Mixed-Composition Hydrogels Recapitulate the Plasticity of Pancreatic Cancers
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Minimally invasive determination of pancreatic ductal adenocarcinoma ( PDAC ) subtype by means of circulating cell‐free RNA
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3D Biomimetic Models to Reconstitute Tumor Microenvironment In Vitro: Spheroids, Organoids, and Tumor‐on‐a‐Chip
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A Self‐Assembled 3D Model Demonstrates How Stiffness Educates Tumor Cell Phenotypes and Therapy Resistance in Pancreatic Cancer
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Gemcitabine‐induced epithelial‐mesenchymal transition‐like changes sustain chemoresistance of pancreatic cancer cells of mesenchymal‐like phenotype
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Cell Detection with Star-Convex Polygons
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Cancer drug resistance induced by EMT: novel therapeutic strategies
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The differential effects of metronomic gemcitabine and antiangiogenic treatment in patient-derived xenografts of pancreatic cancer: treatment effects on metabolism, vascular function, cell proliferation, and tumor growth
inferredcites →https://doi.org/10.1016/j.actbio.2020.02.006openalex-snapshot
Breast cancer models: Engineering the tumor microenvironment
inferredcites →https://doi.org/10.1016/j.bbcan.2020.188356openalex-snapshot
Fibrosis and cancer: A strained relationship
inferredcites →https://doi.org/10.1016/j.bioactmat.2023.06.004openalex-snapshot
Recent advances in defined hydrogels in organoid research
inferredcites →https://doi.org/10.1016/j.biomaterials.2015.10.011openalex-snapshot
Proteomic analysis of naturally-sourced biological scaffolds
inferredcites →https://doi.org/10.1016/j.brainres.2019.146427openalex-snapshot
Mouse vs man: Organoid models of brain development & disease
inferredcites →https://doi.org/10.1016/j.canlet.2021.08.029openalex-snapshot
Tumor microenvironment and metabolic remodeling in gemcitabine‐based chemoresistance of pancreatic cancer
inferredcites →https://doi.org/10.1016/j.canlet.2023.216180openalex-snapshot
Patient-derived organoids in translational oncology and drug screening
inferredcites →https://doi.org/10.1016/j.cej.2024.155206openalex-snapshot
Hydrogels mimicking the viscoelasticity of extracellular matrix for regenerative medicine: Design, application, and molecular mechanism
inferredcites →https://doi.org/10.1016/j.cell.2014.12.021openalex-snapshot
Organoid Models of Human and Mouse Ductal Pancreatic Cancer
inferredcites →https://doi.org/10.1016/j.cellsig.2019.109487openalex-snapshot
Extracellular matrix-cell interactions: Focus on therapeutic applications
inferredcites →https://doi.org/10.1016/j.celrep.2024.114633openalex-snapshot
A CLIC1 network coordinates matrix stiffness and the Warburg effect to promote tumor growth in pancreatic cancer
inferredcites →https://doi.org/10.1016/j.drudis.2020.11.030openalex-snapshot
Addressing the tumour microenvironment in early drug discovery: a strategy to overcome drug resistance and identify novel targets for cancer therapy
inferredcites →https://doi.org/10.1016/j.ijbiomac.2023.128018openalex-snapshot
Collagen and derivatives-based materials as substrates for the establishment of glioblastoma organoids
inferredcites →https://doi.org/10.1016/j.tcb.2020.07.003openalex-snapshot
EMT, MET, Plasticity, and Tumor Metastasis
inferredcites →https://doi.org/10.1016/j.xcrm.2024.101557openalex-snapshot
GATA6 identifies an immune-enriched phenotype linked to favorable outcomes in patients with pancreatic cancer undergoing upfront surgery
inferredcites →https://doi.org/10.1016/j.ymeth.2016.09.016openalex-snapshot
TrackMate: An open and extensible platform for single-particle tracking
inferredcites →https://doi.org/10.1038/ncomms12819openalex-snapshot
Metastatic progression is associated with dynamic changes in the local microenvironment
inferredcites →https://doi.org/10.1038/ng.3398openalex-snapshot
Virtual microdissection identifies distinct tumor- and stroma-specific subtypes of pancreatic ductal adenocarcinoma
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nprot.2008.73openalex-snapshot
Analyzing real-time PCR data by the comparative CT method
inferredcites →https://doi.org/10.1038/nrm3758openalex-snapshot
Molecular mechanisms of epithelial–mesenchymal transition
inferredcites →https://doi.org/10.1038/onc.2013.23openalex-snapshot
WNT7B mediates autocrine Wnt/β-catenin signaling and anchorage-independent growth in pancreatic adenocarcinoma
inferredcites →https://doi.org/10.1038/onc.2016.358openalex-snapshot
ZEB1 induces LOXL2-mediated collagen stabilization and deposition in the extracellular matrix to drive lung cancer invasion and metastasis
inferredcites →https://doi.org/10.1038/oncsis.2017.54openalex-snapshot
Matrix stiffness induces epithelial–mesenchymal transition and promotes chemoresistance in pancreatic cancer cells
inferredcites →https://doi.org/10.1038/s12276-024-01272-5openalex-snapshot
Patient-derived tumor organoids: a new avenue for preclinical research and precision medicine in oncology
inferredcites →https://doi.org/10.1038/s41416-018-0327-zopenalex-snapshot
The clinical role of the TME in solid cancer
inferredcites →https://doi.org/10.1038/s41419-024-06697-4openalex-snapshot
Modulating extracellular matrix stiffness: a strategic approach to boost cancer immunotherapy
inferredcites →https://doi.org/10.1038/s41563-021-01057-5openalex-snapshot
Next-generation cancer organoids
inferredcites →https://doi.org/10.1038/s41580-022-00465-yopenalex-snapshot
Apical–basal polarity and the control of epithelial form and function
inferredcites →https://doi.org/10.1038/s41586-020-2612-2openalex-snapshot
Effects of extracellular matrix viscoelasticity on cellular behaviour
inferredcites →https://doi.org/10.1038/s41592-019-0650-1openalex-snapshot
CLIJ: GPU-accelerated image processing for everyone
inferredcites →https://doi.org/10.1038/s41596-020-0379-4openalex-snapshot
Establishment of patient-derived cancer organoids for drug-screening applications
inferredcites →https://doi.org/10.1038/s41598-019-54890-9openalex-snapshot
β-catenin activation down-regulates cell-cell junction-related genes and induces epithelial-to-mesenchymal transition in colorectal cancers
inferredcites →https://doi.org/10.1038/s41598-019-55687-6openalex-snapshot
Increased stiffness of the tumor microenvironment in colon cancer stimulates cancer associated fibroblast-mediated prometastatic activin A signaling
inferredcites →https://doi.org/10.1038/s42003-021-02910-8openalex-snapshot
Towards organoid culture without Matrigel
inferredcites →https://doi.org/10.1038/s43018-022-00349-2openalex-snapshot
Translational advances in pancreatic ductal adenocarcinoma therapy
inferredcites →https://doi.org/10.1039/d3bm00598dopenalex-snapshot
Matrix stiffness triggers chemoresistance through elevated autophagy in pancreatic ductal adenocarcinoma
inferredcites →https://doi.org/10.1073/pnas.1010396108openalex-snapshot
Contractility of the cell rear drives invasion of breast tumor cells in 3D Matrigel
inferredcites →https://doi.org/10.1073/pnas.1617037114openalex-snapshot
Modeling the two-way feedback between contractility and matrix realignment reveals a nonlinear mode of cancer cell invasion
inferredcites →https://doi.org/10.1084/jem.20151665openalex-snapshot
Metronomic chemotherapy prevents therapy-induced stromal activation and induction of tumor-initiating cells
inferredcites →https://doi.org/10.1089/ten.teb.2021.0186openalex-snapshot
Extracellular Microenvironmental Control for Organoid Assembly
inferredcites →https://doi.org/10.1093/bioinformatics/btw413openalex-snapshot
MorphoLibJ: integrated library and plugins for mathematical morphology with ImageJ
inferredcites →https://doi.org/10.1093/bioinformatics/btx180openalex-snapshot
Trainable Weka Segmentation: a machine learning tool for microscopy pixel classification
inferredcites →https://doi.org/10.1097/mpa.0000000000001432openalex-snapshot
Expression of Epithelial-Mesenchymal Transition Markers in Treated Pancreatic Ductal Adenocarcinoma
inferredcites →https://doi.org/10.1101/731877openalex-snapshot
openTSNE: a modular Python library for t-SNE dimensionality reduction and embedding
inferredcites →https://doi.org/10.1109/tsmc.1979.4310076openalex-snapshot
A Threshold Selection Method from Gray-Level Histograms
inferredcites →https://doi.org/10.1111/cas.15962openalex-snapshot
Increased mitochondria are responsible for the acquisition of gemcitabine resistance in pancreatic cancer cell lines
inferredcites →https://doi.org/10.1126/sciadv.abe1969openalex-snapshot
Microrheology reveals simultaneous cell-mediated matrix stiffening and fluidization that underlie breast cancer invasion
inferredcites →https://doi.org/10.1126/sciadv.abg6467openalex-snapshot
Oncogenic RAS instructs morphological transformation of human epithelia via differential tissue mechanics
inferredcites →https://doi.org/10.1152/ajpendo.00457.2019openalex-snapshot
A pipeline for multidimensional confocal analysis of mitochondrial morphology, function, and dynamics in pancreatic β-cells
inferredcites →https://doi.org/10.1155/2019/8472712openalex-snapshot
Development of Collagen-Based 3D Matrix for Gastrointestinal Tract-Derived Organoid Culture
inferredcites →https://doi.org/10.1158/0008-5472.can-12-4384openalex-snapshot
Canonical Wnt Signaling Is Required for Pancreatic Carcinogenesis
inferredcites →https://doi.org/10.1158/1078-0432.ccr-21-0640openalex-snapshot
Molecular Subtypes of Pancreatic Cancer: A Proteomics Approach
inferredcites →https://doi.org/10.1186/s12967-022-03405-8openalex-snapshot
Patient-derived xenograft (PDX) models, applications and challenges in cancer research
inferredcites →https://doi.org/10.1186/s13046-023-02926-4openalex-snapshot
Exploring the interaction between extracellular matrix components in a 3D organoid disease model to replicate the pathophysiology of breast cancer
inferredcites →https://doi.org/10.1186/s40170-022-00285-wopenalex-snapshot
Metabolic flux analysis of 3D spheroids reveals significant differences in glucose metabolism from matched 2D cultures of colorectal cancer and pancreatic ductal adenocarcinoma cell lines
inferredcites →https://doi.org/10.1186/s40170-024-00357-zopenalex-snapshot
Pancreatic cancer tumor organoids exhibit subtype-specific differences in metabolic profiles
inferredcites →https://doi.org/10.1371/journal.pone.0171417openalex-snapshot
Characterization of three-dimensional cancer cell migration in mixed collagen-Matrigel scaffolds using microfluidics and image analysis
inferredcites →https://doi.org/10.1371/journal.pone.0195820openalex-snapshot
Combined experimental and computational characterization of crosslinked collagen-based hydrogels
inferredcites →https://doi.org/10.1371/journal.pone.0220019openalex-snapshot
The use of mixed collagen-Matrigel matrices of increasing complexity recapitulates the biphasic role of cell adhesion in cancer cell migration: ECM sensing, remodeling and forces at the leading edge of cancer invasion
inferredcites →https://doi.org/10.14701/ahbps.23-052openalex-snapshot
Enhancing generation efficiency of liver organoids in a collagen scaffold using human chemically derived hepatic progenitors
inferredcites →https://doi.org/10.15252/embr.202256380openalex-snapshot
Calculation of ATP production rates using the Seahorse XF Analyzer
inferredcites →https://doi.org/10.15283/ijsc21190openalex-snapshot
Engineering the Extracellular Matrix for Organoid Culture
inferredcites →https://doi.org/10.21105/joss.03021openalex-snapshot
seaborn: statistical data visualization
inferredcites →https://doi.org/10.3389/fcell.2019.00135openalex-snapshot
Mechanochemical Signaling of the Extracellular Matrix in Epithelial-Mesenchymal Transition
inferredcites →https://doi.org/10.3389/fcell.2021.740574openalex-snapshot
Research Progress, Challenges, and Breakthroughs of Organoids as Disease Models
inferredcites →https://doi.org/10.3389/fcell.2021.751301openalex-snapshot
Extracellular Matrix Signals as Drivers of Mitochondrial Bioenergetics and Metabolic Plasticity of Cancer Cells During Metastasis
inferredcites →https://doi.org/10.3389/fmolb.2022.1020888openalex-snapshot
Culprits of PDAC resistance to gemcitabine and immune checkpoint inhibitor: Tumour microenvironment components
inferredcites →https://doi.org/10.3389/fphy.2020.579168openalex-snapshot
Quantification of Visco-Elastic Properties of a Matrigel for Organoid Development as a Function of Polymer Concentration
inferredcites →https://doi.org/10.3390/bioengineering8030037openalex-snapshot
Hydrogel Models with Stiffness Gradients for Interrogating Pancreatic Cancer Cell Fate
inferredcites →https://doi.org/10.3390/cancers13174442openalex-snapshot
The Extracellular Matrix in Pancreatic Cancer: Description of a Complex Network and Promising Therapeutic Options
inferredcites →https://doi.org/10.3390/cancers13174451openalex-snapshot
Genomic Heterogeneity of Pancreatic Ductal Adenocarcinoma and Its Clinical Impact
inferredcites →https://doi.org/10.3390/cancers13205086openalex-snapshot
TGFβ Signaling in the Pancreatic Tumor Microenvironment
inferredcites →https://doi.org/10.3390/cancers13215532openalex-snapshot
Epithelial to Mesenchymal Transition: Key Regulator of Pancreatic Ductal Adenocarcinoma Progression and Chemoresistance
inferredcites →https://doi.org/10.3390/cancers13246204openalex-snapshot
TGFβ Drives Metabolic Perturbations during Epithelial Mesenchymal Transition in Pancreatic Cancer: TGFβ Induced EMT in PDAC
inferredcites →https://doi.org/10.3390/cancers14010190openalex-snapshot
3D Cell Culture Models as Recapitulators of the Tumor Microenvironment for the Screening of Anti-Cancer Drugs
inferredcites →https://doi.org/10.3390/cancers14010238openalex-snapshot
The Functional Role of Extracellular Matrix Proteins in Cancer
inferredcites →https://doi.org/10.3390/cancers14092155openalex-snapshot
Divergent Roles of Mitochondria Dynamics in Pancreatic Ductal Adenocarcinoma
inferredcites →https://doi.org/10.3390/cancers16223863openalex-snapshot
Altered Mechanobiology of PDAC Cells with Acquired Chemoresistance to Gemcitabine and Paclitaxel
inferredcites →https://doi.org/10.3390/cells10030497openalex-snapshot
The Role of Mitochondria in the Chemoresistance of Pancreatic Cancer Cells
inferredcites →https://doi.org/10.3390/cells9041040openalex-snapshot
E-Cadherin in Pancreatic Ductal Adenocarcinoma: A Multifaceted Actor during EMT
inferredcites →https://doi.org/10.3390/diagnostics13020215openalex-snapshot
Current Status of the Diagnosis of Early-Stage Pancreatic Ductal Adenocarcinoma
inferredcites →https://doi.org/10.3390/gels7010017openalex-snapshot
Modeling the Mechanobiology of Cancer Cell Migration Using 3D Biomimetic Hydrogels
inferredcites →https://doi.org/10.3390/ijms19010181openalex-snapshot
Halfway between 2D and Animal Models: Are 3D Cultures the Ideal Tool to Study Cancer-Microenvironment Interactions?
inferredcites →https://doi.org/10.3390/ph14080740openalex-snapshot
Epithelial to Mesenchymal Transition in Patients with Pancreatic Ductal Adenocarcinoma: State-of-the-Art and Therapeutic Opportunities
inferredcites →https://doi.org/10.5555/1953048.2078195openalex-snapshot
Scikit-learn: Machine Learning in Python
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/adhm.71452openalex-snapshot
A Lightweight, 3D‐Printable, Low‐Cost, “One‐Click” Dorsal Skin Window for High‐Quality Long‐Term Multimodal Subcutaneous Tumor Imaging
inferred← citeshttps://doi.org/10.1002/jbma.70028openalex-snapshot
Advances in 3D Organoids and Organ‐on‐a‐Chip Systems for Biomedical Research
inferred← citeshttps://doi.org/10.1002/mdr2.70048openalex-snapshot
Tumor Organoids: Breakthroughs in Clinical Decision Making, Drug Development, and Translational Advances Beyond Conventional Models
inferred← citeshttps://doi.org/10.1016/j.addr.2026.115836openalex-snapshot
Matrix-integrated microfluidic tumor models for evaluating drug delivery systems and pre-clinical testing
inferred← citeshttps://doi.org/10.1016/j.isci.2026.116487openalex-snapshot
Bioengineering advances in pancreatic cancer organoids for reproducible tumor microenvironment modeling
inferred← citeshttps://doi.org/10.1016/j.isci.2026.116756openalex-snapshot
The application and progress of AI-based image analysis in tumor organoid research
inferred← citeshttps://doi.org/10.1093/procel/pwag007openalex-snapshot
Harnessing human tumor organoids for cancer modeling and precision therapy
inferred← citeshttps://doi.org/10.1186/s12967-026-08763-1openalex-snapshot
Three-dimensional spheroid models in breast cancer: tumor microenvironment complexity, cancer stem cell-driven resistance, and translational model integration
inferred← citeshttps://doi.org/10.1186/s40170-025-00413-2openalex-snapshot
Matrix composition and glucose availability cooperatively determine cancer spheroid bioenergetics in 3D hydrogels
inferred← citeshttps://doi.org/10.26779/2786-832x.2025.5.70openalex-snapshot
Exosomal delivery of CRISPR/Cas9 complexes for targeted editing of KRAS^G12D in pancreatic cancer: prerequisites for clinical surgical application
inferred← citeshttps://doi.org/10.3389/fcell.2026.1890385openalex-snapshot
Advances in organoids for personalized medicine: from technological development to clinical application
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