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Microvesicle-delivery miR-150 promotes tumorigenesis by up-regulating VEGF, and the neutralization of miR-150 attenuate tumor development

机译:微泡递送miR-150通过上调VEGF促进肿瘤发生,而miR-150的中和作用则减弱了肿瘤的发展

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Tumor-associated macrophages (TAMs) mostly exhibit M2-like (alternatively activated) properties and play positive roles in angiogenesis and tumorigenesis. Vascular endothelial growth factor (VEGF) is a key angiogenic factor. During tumor development, TAMs secrete VEGF and other factors to promote angiogenesis; thus, anti-treatment against TAMs and VEGF can repress cancer development, which has been demonstrated in clinical trials and on an experimental level. In the present work, we show that miR-150 is an oncomir because of its promotional effect on VEGF. MiR-150 targets TAMs to up-regulate their secretion of VEGF in vitro. With the utilization of cell-derived vesicles, named microvesicles (MVs), we transferred antisense RNA targeted to miR-150 into mice and found that the neutralization of miR-150 down-regulates miR-150 and VEGF levels in vivo and attenuates angiogenesis. Therefore, we proposed the therapeutic potential of neutralizing miR-150 to treat cancer and demonstrated a novel, natural, microvesicle-based method for the transfer of nucleic acids.
机译:肿瘤相关的巨噬细胞(TAM)大多表现出类似M2的特性(或激活),并在血管生成和肿瘤发生中发挥积极作用。血管内皮生长因子(VEGF)是关键的血管生成因子。在肿瘤发生过程中,TAM分泌VEGF和其他因子以促进血管生成。因此,针对TAM和VEGF的抗治疗可以抑制癌症的发展,这已在临床试验和实验水平上得到证实。在目前的工作中,我们表明miR-150是一种瘤,因为它对VEGF具有促进作用。 MiR-150靶向TAM,以在体外上调其VEGF的分泌。通过利用称为微囊泡(MVs)的细胞衍生囊泡,我们将针对miR-150的反义RNA转移到小鼠体内,发现miR-150的中和作用在体内下调了miR-150和VEGF的水平,并减弱了血管生成。因此,我们提出了中和miR-150来治疗癌症的治疗潜力,并证明了一种新颖的,基于天然微泡的核酸转移方法。

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