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The MSC-MCF-7 Duet Playing Tumor Vasculogenesis and Angiogenesis onto the Chick Embryo Chorioallantoic Membrane

机译:MSC-MCF-7二重唱在鸡胚荚膜内囊膜膜上玩肿瘤血管发生和血管生成

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摘要

Background/Aim: Human mesenchymal stem cells (hMSC) represent a versatile cell population, able to modulate the tumor microenvironment. Our aim was to recreate an open scene for the in vivo interaction between hMSC and the MCF-7 breast cancer cells (MCF-7), in order to enlighten the intimate involvement of hMSC in tumor vasculogenesis and angiogenesis. Materials and Methods: hMSC and MCF-7 were seeded onto the chick embryo chorioallantoic membrane (CAM) and incubated for 7 days. Consecutively, the morphology and the immunohistochemical profile of CAM were assessed. Results: Following this complex interaction, MCF-7 acquired a more aggressive phenotype, hMSC switched to a vascular precursor phenotype, while CAM underwent a major reset to an earlier stage, with hotspots of angiogenesis, vasculogenesis and hematopoiesis. Conclusion: The hallmark of this study was the establishment of a veritable in vivo experimental model of MSC involvement in tumor vasculogenesis and angiogenesis, allowing further analysis in the field.
机译:背景/目的:人间充质干细胞(HMSC)代表通用细胞群,能够调节肿瘤微环境。我们的目标是为HMSC和MCF-7乳腺癌细胞(MCF-7)之间的体内相互作用进行重建,以启发HMSC在肿瘤血管发生和血管生成中的敏感累及。材料和方法:将HMSC和MCF-7接种到鸡胚胚胎膜膜(凸轮)上并孵育7天。连续地,评估凸轮的形态和免疫组织化学谱。结果:在该复杂的相互作用之后,MCF-7获得了更具侵略性的表型,HMSC切换到血管前体表型,而CAM接受过较早阶段的重置重置,血管生成,血管生成和造血热点。结论:本研究的标志是建立在肿瘤血管生成和血管生成的MSC涉及的体内实验模型中的真实性模型,允许进一步分析该领域。

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