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Matrix Resistance Toward Proteolytic Cleavage Controls Contractility‐Dependent Migration Modes During Angiogenic Sprouting

Weiß, M. S., Trapani, G., Long, H., & Trappmann, B. (2024) · Advanced Science · doi:10.1002/advs.202305947 · Cited by 9

Multidimensional Imaging of Breast CancerPreprint

Rios, A. C., van Rheenen, J., & Scheele, C. L. G. J. (2022) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a041330 · Cited by 10

Volume imaging to interrogate cancer cell-tumor microenvironment interactions in space and time

Almagro, J., & Messal, H. A. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1176594 · Cited by 10

Evolution of phenotypic plasticity leads to tumor heterogeneity with implications for therapy

Syga, S., Jain, H. P., Krellner, M., Hatzikirou, H., & Deutsch, A. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012003 · Cited by 9

Enhanced extracellular matrix remodeling due to embedded spheroid fluidization

Zhang, T., Ameen, S., Ghosh, S., Kim, K., Pandey, M., Cheung, B. C. H., Thanh, M. T. H., Patteson, A. E., Wu, M., & Schwarz, J. (2025) · New Journal of Physics · doi:10.1088/1367-2630/ade81e · Cited by 9

Visualizing cellular interactions: intravital imaging in tumor microenvironment

Li, S., Liu, L., Shan, J., & Cheng, Q. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1630658 · Cited by 9

Impact of the ECM on the Mechanical Memory of Cancer Cells

Mierke, C. T. (2025) · Cells · doi:10.3390/cells14211707 · Cited by 10

A reusable single-cell patterning strategy based on an ultrathin metal microstencil

Song, Y., Tian, Q., Liu, J., Guo, W., Sun, Y., & Zhang, S. (2021) · Lab on a Chip · doi:10.1039/d0lc01175d · Cited by 9

BRPCA: Bounded Robust Principal Component Analysis to Incorporate Similarity Network for N7-Methylguanosine(m7G) Site-Disease Association Prediction

Ma, J., Zhang, L., Li, S., & Liu, H. (2021) · IEEE Transactions on Computational Biology and Bioinformatics · doi:10.1109/tcbb.2021.3109055 · Cited by 9

Collective directional migration drives the formation of heteroclonal cancer cell clusters

Palmiero, M., Cantarosso, I., di Blasio, L., Monica, V., Peracino, B., Primo, L., & Puliafito, A. (2023) · Molecular Oncology · doi:10.1002/1878-0261.13369 · Cited by 9

Matrix obstructions cause multiscale disruption in collective epithelial migration by suppressing leader cell function

Lee, Y. L., Mathur, J., Walter, C., Zmuda, H. M., & Pathak, A. (2023) · Molecular Biology of the Cell · doi:10.1091/mbc.e22-06-0226 · Cited by 9

Different contractility modes control cell escape from multicellular spheroids and tumor explants

Blauth, E., Grosser, S., Sauer, F., Merkel, M., Kubitschke, H., Warmt, E., Morawetz, E. W., Friedrich, P., Wolf, B., Briest, S., et al. (2024) · APL Bioengineering · doi:10.1063/5.0188186 · Cited by 8

Identifying Molecular Signatures of Distinct Modes of Collective Migration in Response to the Microenvironment Using Three-Dimensional Breast Cancer Models

Ardila, D. C., Aggarwal, V., Singh, M., Chattopadhyay, A., Chaparala, S., & Sant, S. (2021) · Cancers · doi:10.3390/cancers13061429 · Cited by 9

Cell jamming in a collagen-based interface assay is tuned by collagen density and proteolysis

Beunk, L., Wen, N., van Helvert, S., Bekker, B., Ran, L., Kang, R. J., Paulat, T., Syga, S., Deutsch, A., Friedl, P., et al. (2023) · Journal of Cell Science · doi:10.1242/jcs.260207 · Cited by 9

The cellular Potts model on disordered lattices

Nemati, H., & de Graaf, J. (2024) · Soft Matter · doi:10.1039/d4sm00445k · Cited by 10

Understanding the interplay between extracellular matrix topology and tumor-immune interactions: Challenges and opportunities

Fan, Y., Chiu, A., Zhao, F., & George, J. T. (2024) · Oncotarget · doi:10.18632/oncotarget.28666 · Cited by 10

Dual role of E-cadherin in the regulation of invasive collective migration of mammary carcinoma cells

Elisha, Y., Kalchenko, V., Kuznetsov, Y., & Geiger, B. (2018) · Scientific Reports · doi:10.1038/s41598-018-22940-3 · Cited by 74

Cell jamming: Collective invasion of mesenchymal tumor cells imposed by tissue confinement

Haeger, A., Krause, M., Wolf, K., & Friedl, P. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.03.020 · Cited by 302

Abstract A62: Unjamming and spreading of a cellular aggregate as a model of breast cancer migration

Wang, K., & Fredberg, J. J. (2017) · Cancer Research · doi:10.1158/1538-7445.epso16-a62

Modeling the Influence of the E-Cadherin-β-Catenin Pathway in Cancer Cell Invasion: A Multiscale Approach

Ramis-Conde, I., Drasdo, D., Anderson, A. R. A., & Chaplain, M. A. J. (2008) · Biophysical Journal · doi:10.1529/biophysj.107.114678 · Cited by 224

Cancer - from mechanisms of invasion to targeted therapy

Wicki, A. C. (2007) · edoc (University of Basel) · doi:10.5451/unibas-004261483