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      3D Microenvironment Stiffness Regulates Tumor Spheroid Growth and Mechanics via p21 and ROCK

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          Most cited references69

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          Global surveillance of trends in cancer survival 2000–14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries

          In 2015, the second cycle of the CONCORD programme established global surveillance of cancer survival as a metric of the effectiveness of health systems and to inform global policy on cancer control. CONCORD-3 updates the worldwide surveillance of cancer survival to 2014.
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            Tensional homeostasis and the malignant phenotype.

            Tumors are stiffer than normal tissue, and tumors have altered integrins. Because integrins are mechanotransducers that regulate cell fate, we asked whether tissue stiffness could promote malignant behavior by modulating integrins. We found that tumors are rigid because they have a stiff stroma and elevated Rho-dependent cytoskeletal tension that drives focal adhesions, disrupts adherens junctions, perturbs tissue polarity, enhances growth, and hinders lumen formation. Matrix stiffness perturbs epithelial morphogenesis by clustering integrins to enhance ERK activation and increase ROCK-generated contractility and focal adhesions. Contractile, EGF-transformed epithelia with elevated ERK and Rho activity could be phenotypically reverted to tissues lacking focal adhesions if Rho-generated contractility or ERK activity was decreased. Thus, ERK and Rho constitute part of an integrated mechanoregulatory circuit linking matrix stiffness to cytoskeletal tension through integrins to regulate tissue phenotype.
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              Fibroblasts in cancer.

              Tumours are known as wounds that do not heal - this implies that cells that are involved in angiogenesis and the response to injury, such as endothelial cells and fibroblasts, have a prominent role in the progression, growth and spread of cancers. Fibroblasts are associated with cancer cells at all stages of cancer progression, and their structural and functional contributions to this process are beginning to emerge. Their production of growth factors, chemokines and extracellular matrix facilitates the angiogenic recruitment of endothelial cells and pericytes. Fibroblasts are therefore a key determinant in the malignant progression of cancer and represent an important target for cancer therapies.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Advanced Biosystems
                Adv. Biosys.
                Wiley
                2366-7478
                2366-7478
                September 09 2019
                September 2019
                July 24 2019
                September 2019
                : 3
                : 9
                : 1900128
                Affiliations
                [1 ]TU DresdenCenter for Molecular and Cellular Bioengineering (CMCB) Fetscherstr. 105 01307 Dresden Germany
                [2 ]Max Planck Institute for the Science of LightMax‐Planck‐Zentrum für Physik und Medizin Staudtstr. 2 91058 Erlangen Germany
                [3 ]Leibniz Institute of Polymer Research DresdenMax Bergmann Center Hohe Str. 6 01069 Dresden Germany
                Article
                10.1002/adbi.201900128
                32648654
                d37404f8-dff7-4c97-bd95-7b5a55665eb7
                © 2019

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

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