Biomechanical interplay between anisotropic re-organization of cells and the surrounding matrix underlies transition to invasive cancer spread
The root cause of cancer mortality and morbidity is the metastatic spread of the primary tumor, but underlying mechanisms remain elusive. Here we investigate biomechanical interactions that may accompany invasive spread of melanoma cells. We find that metastatic cells can exert considerable traction...
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Published in | Scientific reports Vol. 8; no. 1; pp. 14210 - 10 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
21.09.2018
Nature Publishing Group |
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Abstract | The root cause of cancer mortality and morbidity is the metastatic spread of the primary tumor, but underlying mechanisms remain elusive. Here we investigate biomechanical interactions that may accompany invasive spread of melanoma cells. We find that metastatic cells can exert considerable traction forces and modify local collagen organization within a 3D matrix. When this re-organization is mimicked using a nano-fabricated model of aligned extracellular matrix fibers, metastatic cells, including less invasive melanoma cells, were in turn induced to align, elongate and migrate, guided by the local ridge orientations. Strikingly, we found that this aligned migration of melanoma cells was accompanied by long-range regulation of cytoskeletal remodeling that show anisotropic stiffening in the direction of fiber orientation suggestive of a positive feedback between ECM fiber alignment and forces exerted by cancer cells. Taken together, our findings suggest that the invasive spread of cancer cells can be defined by complex interplay with the surrounding matrix, during which they both modify the matrix and use the matrix alignment as a persistent migration cue, leading to more extensive and rapid invasive spread. |
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AbstractList | The root cause of cancer mortality and morbidity is the metastatic spread of the primary tumor, but underlying mechanisms remain elusive. Here we investigate biomechanical interactions that may accompany invasive spread of melanoma cells. We find that metastatic cells can exert considerable traction forces and modify local collagen organization within a 3D matrix. When this re-organization is mimicked using a nano-fabricated model of aligned extracellular matrix fibers, metastatic cells, including less invasive melanoma cells, were in turn induced to align, elongate and migrate, guided by the local ridge orientations. Strikingly, we found that this aligned migration of melanoma cells was accompanied by long-range regulation of cytoskeletal remodeling that show anisotropic stiffening in the direction of fiber orientation suggestive of a positive feedback between ECM fiber alignment and forces exerted by cancer cells. Taken together, our findings suggest that the invasive spread of cancer cells can be defined by complex interplay with the surrounding matrix, during which they both modify the matrix and use the matrix alignment as a persistent migration cue, leading to more extensive and rapid invasive spread. The root cause of cancer mortality and morbidity is the metastatic spread of the primary tumor, but underlying mechanisms remain elusive. Here we investigate biomechanical interactions that may accompany invasive spread of melanoma cells. We find that metastatic cells can exert considerable traction forces and modify local collagen organization within a 3D matrix. When this re-organization is mimicked using a nano-fabricated model of aligned extracellular matrix fibers, metastatic cells, including less invasive melanoma cells, were in turn induced to align, elongate and migrate, guided by the local ridge orientations. Strikingly, we found that this aligned migration of melanoma cells was accompanied by long-range regulation of cytoskeletal remodeling that show anisotropic stiffening in the direction of fiber orientation suggestive of a positive feedback between ECM fiber alignment and forces exerted by cancer cells. Taken together, our findings suggest that the invasive spread of cancer cells can be defined by complex interplay with the surrounding matrix, during which they both modify the matrix and use the matrix alignment as a persistent migration cue, leading to more extensive and rapid invasive spread.The root cause of cancer mortality and morbidity is the metastatic spread of the primary tumor, but underlying mechanisms remain elusive. Here we investigate biomechanical interactions that may accompany invasive spread of melanoma cells. We find that metastatic cells can exert considerable traction forces and modify local collagen organization within a 3D matrix. When this re-organization is mimicked using a nano-fabricated model of aligned extracellular matrix fibers, metastatic cells, including less invasive melanoma cells, were in turn induced to align, elongate and migrate, guided by the local ridge orientations. Strikingly, we found that this aligned migration of melanoma cells was accompanied by long-range regulation of cytoskeletal remodeling that show anisotropic stiffening in the direction of fiber orientation suggestive of a positive feedback between ECM fiber alignment and forces exerted by cancer cells. Taken together, our findings suggest that the invasive spread of cancer cells can be defined by complex interplay with the surrounding matrix, during which they both modify the matrix and use the matrix alignment as a persistent migration cue, leading to more extensive and rapid invasive spread. |
ArticleNumber | 14210 |
Author | Kim, Deok-Ho Ewald, Andrew J. Kshitiz Su, Chia-Yi Seo, Jayhyun Park, JinSeok Gray, Ryan S. Levchenko, Andre An, Steven S. Kwak, Moonkyu |
Author_xml | – sequence: 1 givenname: Deok-Ho surname: Kim fullname: Kim, Deok-Ho email: deokho@uw.edu organization: Department of Bioengineering, University of Washington, Department of Biomedical Engineering, Johns Hopkins University – sequence: 2 givenname: Andrew J. surname: Ewald fullname: Ewald, Andrew J. organization: Department of Biomedical Engineering, Johns Hopkins University, Department of Cell Biology, Johns Hopkins University, Department of Oncology, the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine – sequence: 3 givenname: JinSeok surname: Park fullname: Park, JinSeok organization: Department of Biomedical Engineering, Yale University, Yale Systems Biology Institute, Yale University – sequence: 4 surname: Kshitiz fullname: Kshitiz organization: Department of Bioengineering, University of Washington, Department of Biomedical Engineering, Johns Hopkins University, Department of Biomedical Engineering, Yale University, Yale Systems Biology Institute, Yale University – sequence: 5 givenname: Moonkyu surname: Kwak fullname: Kwak, Moonkyu organization: School of Mechanical Engineering, Kyungpook National University – sequence: 6 givenname: Ryan S. orcidid: 0000-0001-9668-6497 surname: Gray fullname: Gray, Ryan S. organization: Department of Cell Biology, Johns Hopkins University – sequence: 7 givenname: Chia-Yi orcidid: 0000-0002-9483-4510 surname: Su fullname: Su, Chia-Yi organization: Department of Bioengineering, University of Washington – sequence: 8 givenname: Jayhyun surname: Seo fullname: Seo, Jayhyun organization: Department of Environmental Health and Engineering, Johns Hopkins Bloomberg School of Public Health – sequence: 9 givenname: Steven S. surname: An fullname: An, Steven S. email: san@jhu.edu organization: Department of Environmental Health and Engineering, Johns Hopkins Bloomberg School of Public Health, Department of Chemical and Biomolecular Engineering, Johns Hopkins Whiting School of Engineering, Department of Oncology, the Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine – sequence: 10 givenname: Andre surname: Levchenko fullname: Levchenko, Andre email: andre.levchenko@yale.edu organization: Department of Biomedical Engineering, Johns Hopkins University, Department of Biomedical Engineering, Yale University, Yale Systems Biology Institute, Yale University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30242256$$D View this record in MEDLINE/PubMed |
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Keywords | Groove Surface Melanoma Cell Invasion Local Ridge Orientation Cell wM1 Anisotropic Stiffness |
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Snippet | The root cause of cancer mortality and morbidity is the metastatic spread of the primary tumor, but underlying mechanisms remain elusive. Here we investigate... |
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SubjectTerms | 14 631/57/343/1361 631/67/327 Anisotropy Biomechanics Cancer Cell migration Collagen Cytoskeleton Extracellular matrix Fibers Humanities and Social Sciences Invasiveness Melanoma Metastases Metastasis Morbidity multidisciplinary Science Science (multidisciplinary) |
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Title | Biomechanical interplay between anisotropic re-organization of cells and the surrounding matrix underlies transition to invasive cancer spread |
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