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Inhibition of ovarian cancer cell metastasis by a fusion polypeptide Tat-ELP

机译:融合多肽Tat-ELP抑制卵巢癌细胞的转移

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Tumor cell metastasis is a complex, multi-step process that is a major cause of death and morbidity amongst cancer patients. Cell adhesion plays a critical role in the development of metastatic cancer, and it is mediated by interactions between receptors on the cell surface and ligands of the extracellular matrix or other surfaces. Therefore, inhibition of the cell adhesion process appears to be an effective method of preventing metastasis. This work describes a genetically engineered polypeptide with the potential to prevent cell adhesion and inhibit metastasis. We have found that the cell penetrating peptide Tat, fused with elastin-like polypeptide (ELP) inhibited adhesion, spreading, invasion and migration of SKOV-3 ovarian cancer cells in cell culture. Furthermore, we have also confirmed that Tat-ELP has anti-metastatic potential in an experimental ovarian cancer metastasis model in vivo, causing approximately 80% reduction in the tumor burden. Since cell attachment is an important step in tumor cell invasion and metastasis, these results suggest a novel role of Tat-ELP as a therapeutic intervention in cancer metastasis.
机译:肿瘤细胞转移是一个复杂的,多步骤的过程,是癌症患者死亡和发病的主要原因。细胞粘附在转移性癌症的发展中起着至关重要的作用,它是由细胞表面受体与细胞外基质或其他表面配体之间的相互作用介导的。因此,抑制细胞粘附过程似乎是预防转移的有效方法。这项工作描述了一种基因工程多肽,具有防止细胞粘附和抑制转移的潜力。我们已经发现,与弹性蛋白样多肽(ELP)融合的细胞穿透肽Tat在细胞培养中抑制SKOV-3卵巢癌细胞的粘附,扩散,侵袭和迁移。此外,我们还证实,Tat-ELP在体内实验性卵巢癌转移模型中具有抗转移潜力,可减轻肿瘤负担约80%。由于细胞附着是肿瘤细胞侵袭和转移的重要步骤,因此这些结果表明,Tat-ELP作为癌症转移的治疗干预手段具有新的作用。

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