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      Structural centrosome aberrations promote non‐cell‐autonomous invasiveness

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          Abstract

          Centrosomes are the main microtubule‐organizing centers of animal cells. Although centrosome aberrations are common in tumors, their consequences remain subject to debate. Here, we studied the impact of structural centrosome aberrations, induced by deregulated expression of ninein‐like protein ( NLP), on epithelial spheres grown in Matrigel matrices. We demonstrate that NLP‐induced structural centrosome aberrations trigger the escape (“budding”) of living cells from epithelia. Remarkably, all cells disseminating into the matrix were undergoing mitosis. This invasive behavior reflects a novel mechanism that depends on the acquisition of two distinct properties. First, NLP‐induced centrosome aberrations trigger a re‐organization of the cytoskeleton, which stabilizes microtubules and weakens E‐cadherin junctions during mitosis. Second, atomic force microscopy reveals that cells harboring these centrosome aberrations display increased stiffness. As a consequence, mitotic cells are pushed out of mosaic epithelia, particularly if they lack centrosome aberrations. We conclude that centrosome aberrations can trigger cell dissemination through a novel, non‐cell‐autonomous mechanism, raising the prospect that centrosome aberrations contribute to the dissemination of metastatic cells harboring normal centrosomes.

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          An improved technique for determining hardness and elastic modulus using load and displacement sensing indentation experiments

          The indentation load-displacement behavior of six materials tested with a Berkovich indenter has been carefully documented to establish an improved method for determining hardness and elastic modulus from indentation load-displacement data. The materials included fused silica, soda–lime glass, and single crystals of aluminum, tungsten, quartz, and sapphire. It is shown that the load–displacement curves during unloading in these materials are not linear, even in the initial stages, thereby suggesting that the flat punch approximation used so often in the analysis of unloading data is not entirely adequate. An analysis technique is presented that accounts for the curvature in the unloading data and provides a physically justifiable procedure for determining the depth which should be used in conjunction with the indenter shape function to establish the contact area at peak load. The hardnesses and elastic moduli of the six materials are computed using the analysis procedure and compared with values determined by independent means to assess the accuracy of the method. The results show that with good technique, moduli can be measured to within 5%.
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            Morphogenesis and oncogenesis of MCF-10A mammary epithelial acini grown in three-dimensional basement membrane cultures.

            The three-dimensional culture of MCF-10A mammary epithelial cells on a reconstituted basement membrane results in formation of polarized, growth-arrested acini-like spheroids that recapitulate several aspects of glandular architecture in vivo. Oncogenes introduced into MCF-10A cells disrupt this morphogenetic process, and elicit distinct morphological phenotypes. Recent studies analyzing the mechanistic basis for phenotypic heterogeneity observed among different oncogenes (e.g., ErbB2, cyclin D1) have illustrated the utility of this three-dimensional culture system in modeling the biological activities of cancer genes, particularly with regard to their ability to disrupt epithelial architecture during the early aspects of carcinoma formation. Here we provide a collection of protocols to culture MCF-10A cells, to establish stable pools expressing a gene of interest via retroviral infection, as well as to grow and analyze MCF-10A cells in three-dimensional basement membrane culture.
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              Why don't we get more cancer? A proposed role of the microenvironment in restraining cancer progression.

              Tumors are like new organs and are made of multiple cell types and components. The tumor competes with the normal microenvironment to overcome antitumorigenic pressures. Before that battle is won, the tumor may exist within the organ unnoticed by the host, referred to as 'occult cancer'. We review how normal tissue homeostasis and architecture inhibit progression of cancer and how changes in the microenvironment can shift the balance of these signals to the procancerous state. We also include a discussion of how this information is being tailored for clinical use.
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                Author and article information

                Contributors
                erich.nigg@unibas.ch
                Journal
                EMBO J
                EMBO J
                10.1002/(ISSN)1460-2075
                EMBJ
                embojnl
                The EMBO Journal
                John Wiley and Sons Inc. (Hoboken )
                0261-4189
                1460-2075
                22 March 2018
                02 May 2018
                22 March 2018
                : 37
                : 9 ( doiID: 10.1002/embj.v37.9 )
                : e98576
                Affiliations
                [ 1 ] Biozentrum University of Basel Basel Switzerland
                [ 2 ] Swiss Nanoscience Institute University of Basel Basel Switzerland
                [ 3 ]Present address: Department of Medicine I Medical Center – University of Freiburg Faculty of Medicine University of Freiburg Freiburg Germany
                Author notes
                [*] [* ]Corresponding author. Tel: +41 61 207 16 56; E‐mail: erich.nigg@ 123456unibas.ch
                [†]

                These authors contributed equally to this work

                Author information
                http://orcid.org/0000-0003-4835-5719
                Article
                EMBJ201798576
                10.15252/embj.201798576
                5920242
                29567643
                6107be72-db90-4c4b-b031-ee61b7a54e16
                © 2018 The Authors. Published under the terms of the CC BY NC ND 4.0 license

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 07 November 2017
                : 14 February 2018
                : 27 February 2018
                Page count
                Figures: 12, Tables: 0, Pages: 19, Words: 13907
                Funding
                Funded by: University of Basel.
                Funded by: Argovia Professorship
                Funded by: Biozentrum
                Funded by: Swiss Nanoscience Institute
                Funded by: Swiss National Science Foundation Nanotera Project
                Funded by: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF)
                Award ID: 310030B_149641
                Categories
                Article
                Articles
                Custom metadata
                2.0
                embj201798576
                02 May 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.3.7 mode:remove_FC converted:27.04.2018

                Molecular biology
                biomechanical properties,invasiveness,multicellular cooperation,non‐cell‐autonomous process,structural centrosome aberrations,cancer,cell adhesion, polarity & cytoskeleton,cell cycle

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