Decreased E‐Cadherin in MCF7 Human Breast Cancer Cells Forming Multicellular Spheroids Exposed to Simulated Microgravity |
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Authors: | Jayashree Sahana Mohamed Zakaria Nassef Markus Wehland Sascha Kopp Marcus Krüger Thomas J Corydon Manfred Infanger Johann Bauer Daniela Grimm |
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Institution: | 1. Department of Biomedicine, Aarhus University, 8000 Aarhus C, Denmark;2. Clinic for Plastic, Aesthetic and Hand Surgery, Otto‐von‐Guericke‐University Magdeburg, 39120 Magdeburg, Germany;3. Department of Ophthalmology, Aarhus University Hospital, 8000 Aarhus C, Denmark;4. Max‐Planck Institute of Biochemistry, 82152 Martinsried, Germany;5. Gravitational Biology and Translational Regenerative Medicine, Faculty of Medicine and Mechanical Engineering, Otto‐von‐Guericke‐University Magdeburg, 39120 Magdeburg, Germany |
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Abstract: | MCF7 human breast cancer cells were cultured under normal gravity (1 g) and on a random positioning machine (RPM) preventing sedimentation. After 2 weeks, adherent 1 g‐control and adherent RPM cells (AD) as well as multicellular spheroids (MCS) were harvested. AD and MCS had been exposed to the RPM in the same culture flask. In a subsequent proteome analysis, the majority of the proteins detected showed similar label‐free quantification (LFQ) scores in each of the respective subpopulations, but in both AD or MCS cultures, proteins were also found whose LFQs deviated at least twofold from their counterparts in the 1 g‐control cells. They included the cell junction protein E‐cadherin, which was diminished in MCS cells, where proteins of the E‐cadherin autodegradation pathway were enhanced and c‐Src (proto‐oncogene tyrosine‐protein kinase c‐Src) was detected. Spheroid formation was prevented by inhibition of c‐Src but promoted by antibodies blocking E‐cadherin activity. An interaction analysis of the detected proteins that are involved in forming and regulating junctions or adhesion complexes and in E‐cadherin autodegradation indicated connections between the two protein groups. This suggests that the balance of proteins that up‐ or downregulate E‐cadherin mediates the tendency of MCF7 cells to form MCS during RPM exposure. |
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Keywords: | cell interaction ISG15 proteome data Reactome signaling pathways simulated microgravity |
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