首页> 美国卫生研究院文献>Marine Drugs >A Novel Peptide from Abalone (Haliotis discus hannai) to Suppress Metastasis and Vasculogenic Mimicry of Tumor Cells and Enhance Anti-Tumor Effect In Vitro
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A Novel Peptide from Abalone (Haliotis discus hannai) to Suppress Metastasis and Vasculogenic Mimicry of Tumor Cells and Enhance Anti-Tumor Effect In Vitro

机译:一种来自鲍鱼(Haliotis discus hannai)的新型肽可抑制肿瘤细胞的转移和血管生成拟态并增强体外抗肿瘤作用

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摘要

Vasculogenic mimicry (VM) formed by tumor cells plays a vital role in the progress of tumor, because it provides nutrition for tumor cells and takes away the metabolites. Therefore, the inhibition of VM is crucial to the clinical treatment of tumors. In this study, we investigated the anti-tumor effect of a novel peptide, KVEPQDPSEW (AATP), isolated from abalone (Haliotis discus hannai) on HT1080 cells by migration, invasion analysis and the mode of action. The results showed that AATP effectively inhibited MMPs by blocking MAPKs and NF-κB pathways, leading to the downregulation of metastasis of tumor cells. Moreover, AATP significantly inhibited VM and pro-angiogenic factors, including VEGF and MMPs by suppression of AKT/mTOR signaling. In addition, molecular docking was used to study the interaction of AATP and HIF-1α, and the results showed that AATP was combined with an active site of HIF-1α by a hydrogen bond. The effect of AATP on anti-metastatic and anti-vascular in HT1080 cells revealed that AATP may be a potential lead compound for treatment of tumors in the future.
机译:肿瘤细胞形成的血管生成模拟物(VM)在肿瘤的进展中起着至关重要的作用,因为它为肿瘤细胞提供了营养并带走了代谢物。因此,VM的抑制对于肿瘤的临床治疗至关重要。在这项研究中,我们通过迁移,侵袭分析和作用方式研究了从鲍鱼(Haliotis discus hannai)分离的新型肽KVEPQDPSEW(AATP)对HT1080细胞的抗肿瘤作用。结果表明,AATP通过阻断MAPKs和NF-κB途径有效抑制MMPs,从而导致肿瘤细胞转移的下调。此外,AATP通过抑制AKT / mTOR信号传导显着抑制VM和促血管生成因子,包括VEGF和MMP。此外,通过分子对接研究了AATP与HIF-1α的相互作用,结果表明AATP通过氢键与HIF-1α的活性位点结合。 AATP对HT1080细胞的抗转移和抗血管的作用表明,AATP可能是将来治疗肿瘤的潜在先导化合物。

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