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Pathways Regulating Spheroid Formation of Human Follicular Thyroid Cancer Cells under Simulated Microgravity Conditions: A Genetic Approach

机译:模拟微重力条件下调节人卵泡甲状腺癌细胞球状形成的途径:遗传方法。

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摘要

Microgravity induces three-dimensional (3D) growth in numerous cell types. Despite substantial efforts to clarify the underlying mechanisms for spheroid formation, the precise molecular pathways are still not known. The principal aim of this paper is to compare static 1g-control cells with spheroid forming (MCS) and spheroid non-forming (AD) thyroid cancer cells cultured in the same flask under simulated microgravity conditions. We investigated the morphology and gene expression patterns in human follicular thyroid cancer cells (UCLA RO82-W-1 cell line) after a 24 h-exposure on the Random Positioning Machine (RPM) and focused on 3D growth signaling processes. After 24 h, spheroid formation was observed in RPM-cultures together with alterations in the F-actin cytoskeleton. qPCR indicated more changes in gene expression in MCS than in AD cells. Of the 24 genes analyzed VEGFA, VEGFD, MSN, and MMP3 were upregulated in MCS compared to 1g-controls, whereas ACTB, ACTA2, KRT8, TUBB, EZR, RDX, PRKCA, CAV1, MMP9, PAI1, CTGF, MCP1 were downregulated. A pathway analysis revealed that the upregulated genes code for proteins, which promote 3D growth (angiogenesis) and prevent excessive accumulation of extracellular proteins, while genes coding for structural proteins are downregulated. Pathways regulating the strength/rigidity of cytoskeletal proteins, the amount of extracellular proteins, and 3D growth may be involved in MCS formation.
机译:微重力在许多细胞类型中诱导三维(3D)生长。尽管做出了大量努力来澄清球体形成的潜在机制,但确切的分子途径仍然未知。本文的主要目的是比较在模拟微重力条件下,在同一烧瓶中培养的带有1个球形和非球形(甲状腺)甲状腺癌细胞的静态1g对照细胞。我们在随机定位机(RPM)上暴露24小时后,研究了人类滤泡性甲状腺癌细胞(UCLA RO82-W-1细胞系)的形态和基因表达模式,并重点研究了3D生长信号传导过程。 24小时后,在RPM培养物中观察到球状形成以及F-肌动蛋白细胞骨架的改变。 qPCR表明,与AD细胞相比,MCS中基因表达的变化更多。与1g对照相比,在分析的24个基因中,VEGFS,VEGFD,MSN和MMP3在MCS中上调,而ACTB,ACTA2,KRT8,TUBB,EZR,RDX,PRCAA,CAV1,MMP9,PAI1, CTGF MCP1 下调。通路分析表明,上调的基因编码蛋白质,从而促进3D生长(血管生成)并防止细胞外蛋白质的过度积累,而编码结构蛋白的基​​因则被下调。调节细胞骨架蛋白的强度/刚度,细胞外蛋白的量和3D生长的途径可能与MCS的形成有关。

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