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首页> 外文期刊>Cellular and Molecular Neurobiology >miR-373 Inhibits Glioma Cell U251 Migration and Invasion by Down-Regulating CD44 and TGFBR2
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miR-373 Inhibits Glioma Cell U251 Migration and Invasion by Down-Regulating CD44 and TGFBR2

机译:miR-373通过下调CD44和TGFBR2抑制胶质瘤细胞U251迁移和侵袭

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摘要

Glioblastoma multiforme (GBM) is the most malignant glioma, unveiling the underlying mechanisms of its aggressiveness could promote the discovery of potential targets for effective treatment. MicroRNAs (miRNAs) are important participants in both development and disease, its involvement in cancers has long been recognized. In this study, we investigated the role of miRNA-373 (miR-373) in GBM cell line U251, demonstrated that although miR-373 does not affect cell growth of U251, it inhibits migration and invasion of U251. Forced expression of miR-373 down-regulates the expressions CD44 and TGFBR2, while knockdown of CD44 and TGFBR2 presents the similar phenotype as miR-373 overexpression, suggesting that CD44 and TGFBR2 are functional targets of miR-373, down-regulation of CD44 and TGFBR2 by miR-373 are partly responsible for the migration, and invasion suppressive role of miR-373 in U251.
机译:多形胶质母细胞瘤(GBM)是最恶性的神经胶质瘤,揭示其侵袭性的潜在机制可促进发现有效治疗的潜在靶标。微小RNA(miRNA)是发育和疾病的重要参与者,长期以来它就参与了癌症的研究。在这项研究中,我们研究了miRNA-373(miR-373)在GBM细胞系U251中的作用,证明了尽管miR-373不影响U251的细胞生长,但它抑制了U251的迁移和侵袭。强迫表达miR-373下调CD44和TGFBR2的表达,而敲除CD44和TGFBR2则表现出与miR-373过表达相似的表型,这表明CD44和TGFBR2是miR-373的功能靶标,下调CD44和TGFBR2。 miR-373的TGFBR2部分负责miR-373在U251中的迁移和侵袭抑制作用。

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