A LONG-TERM 10G-HYPERGRAVITY EXPOSURE PROMOTES CELL-CELL CONTACTS AND REDUCES ADHESIVENESS TO A SUBSTRATE, MIGRATION, AND INVASIVENESS OF MCF-7HUMAN BREAST CANCER CELLS

S Kannan, H Shailesh, H Mohamed, N Souchelnytskyi, S Souchelnytskyi
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Abstract

G-force is a fundamental force controlling human cells. Cancer is one of the 4 major health challenges in the Space missions. Cancer in Space project evaluates the reaction of human cancer cells to the conditions of the space flights, including an exposure to high g-forces.Explore an impact of 10 g force on the oncogenic properties of human breast adenocarcinoma cells MCF-7.Cells were exposed to 10 g force for 10 days, as part of a 6-week simulation of conditions of a space flight. Then the cells were cultured for one week under normal culture conditions, before performing tests. Cell proliferation, cell viability, cell-cell contact inhibition, migration, and invasiveness were measured. Immunoblotting was used to evaluate expression of proteins.Proliferation, cell-cell interaction and formation of 3D structures, migration, and invasiveness of cells exposed to 10 g were compared to parental cells cultured at 1 g condition. 10 g exposed cells showed a higher propensity for cell-cell contact inhibitions and lower for 3-dimensional growth in dense culture. This correlated with the decrease of proliferation in a dense culture as compared to the parental cells. The decrease of migration, adherence to a surface, and invasiveness was observed for cells subjected to the hypergravity, as compared to the parental MCF-7 cells. Enhanced expression of E-cadherin and phosphorylated pY576-FAK were observed in 10 g exposed cells but no impact on the expression of Erk, pErk, FAK and p53 was detected.The prolonged exposure of MCF-7 cells to 10 g force targets cell-cell and cell-substrate interactions.
长期的10g超重力暴露促进细胞间接触,降低mcf -7人乳腺癌细胞对基质的粘附性、迁移和侵袭性
重力是控制人体细胞的基本力量。癌症是太空任务中四大健康挑战之一。太空癌症项目评估人类癌细胞对太空飞行条件的反应,包括暴露在高重力下。探讨10 g力对人乳腺腺癌细胞MCF-7致癌特性的影响。细胞暴露在10g的力下10天,作为为期6周的太空飞行条件模拟的一部分。然后将细胞在正常培养条件下培养一周,然后进行测试。测量细胞增殖、细胞活力、细胞间接触抑制、迁移和侵袭性。免疫印迹法检测蛋白表达。将暴露于10g条件下的细胞的增殖、细胞间相互作用和3D结构的形成、迁移和侵袭性与在1g条件下培养的亲本细胞进行比较。10 g暴露的细胞在密集培养中表现出较高的细胞间接触抑制倾向和较低的三维生长倾向。与亲本细胞相比,这与密集培养中增殖的减少有关。与亲代MCF-7细胞相比,观察到受超重力作用的细胞迁移、粘附表面和侵袭性的减少。在10 g暴露的细胞中,E-cadherin和磷酸化pY576-FAK的表达增强,而Erk、pErk、FAK和p53的表达未受影响。MCF-7细胞长期暴露于10g力下,目标是细胞-细胞和细胞-底物相互作用。
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