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首页> 外文期刊>Peptides: An International Journal >The anti-tumor effects of the recombinant toxin protein rLj-RGD3 from Lampetra japonica on pancreatic carcinoma Panc-1 cells in nude mice
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The anti-tumor effects of the recombinant toxin protein rLj-RGD3 from Lampetra japonica on pancreatic carcinoma Panc-1 cells in nude mice

机译:Realombinant Toxin蛋白RLJ-RGD3在裸鼠胰腺癌Panc-1细胞上的重组毒素蛋白RLJ-RGD3的抗肿瘤作用

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摘要

Recombinant Lampetra japonica RGD peptide (rLj-RGD3) is a soluble toxin protein with three RGD (Arg-Gly-Asp) motifs and a molecular weight of 13.5 kDa. The aim of this study was to investigate the effects and mechanisms of rLj-RGD3 on tumor growth and survival in pancreatic carcinoma Panc-1 cell-bearing mice. A Panc-1 human pancreatic carcinoma-bearing nude mouse model was successfully generated, and the animals were treated with different doses of rLj-RGD3 for 3 weeks. The volume and weight of the subcutaneous tumors, the survival of the nude mice, histopathological changes, the intratumoral MVD, the number of apoptotic Panc-1 cells, and apoptosis-related proteins and gene expressions were determined. rLj-RGD3 significantly decreased the tumor volumes and weights, and the maximum tumor volume and weight IR values were 53.2% (p < 0.001) and 55.9% (p < 0.001), respectively. The life expectancy of Panc-1-bearing nude mice treated with rLj-RGD3 was increased by 56.3% (p <0.001). Meanwhile, rLjRGD3 promoted the expression of Bax, caspase-3, and caspase-9 and inhibited Bcl-2 and VEGF expression. In addition, rLj-RGD3 did not change FAK, PI3K and Akt expression, but p-FAK, p-PI3K and p-Akt, levels were down-regulated. These results show that rLj-RGD3 induced potent anti-tumor activity in vivo and suppressed the growth of transplanted Panc-1 cells in a nude mouse model, implying that rLj-RGD3 may serve as a potent clinical therapeutic agent for human pancreatic carcinoma. (C) 2016 Elsevier Inc. All rights reserved.
机译:重组Lampetra Japonica RGD肽(RLJ-RGD3)是一种具有三种RGD(Arg-Gly-ASP)基序的可溶性毒素蛋白,分子量为13.5kDa。本研究的目的是探讨RLJ-RGD3对胰腺癌Panc-1细胞小鼠肿瘤生长和存活的影响和机制。成功地生成了Panc-1人胰腺癌裸鼠模型,并用不同剂量的RLJ-RGD3处理了动物3周。测定了皮下肿瘤的体积和重量,裸鼠的存活,组织病理学变化,脑内MVD,凋亡PANC-1细胞的数量和凋亡相关蛋白质和基因表达。 RLJ-RGD3显着降低了肿瘤体积和重量,并且最大肿瘤体积和重量IR值分别为53.2%(P <0.001)和55.9%(P <0.001)。用RLJ-RGD3处理的Panc-1携带裸鼠的预期寿命增加56.3%(P <0.001)。同时,RLJRGD3促进了Bax,Caspase-3和Caspase-9的表达并抑制Bcl-2和VEGF表达。此外,RLJ-RGD3没有改变FAK,PI3K和AKT表达,但P-FAK,P-PI3K和P-AKT,水平降调。这些结果表明,RLJ-RGD3诱导体内有效的抗肿瘤活性并抑制了裸鼠模型中移植的PANC-1细胞的生长,暗示RLJ-RGD3可以用作人类胰腺癌的有效临床治疗剂。 (c)2016年Elsevier Inc.保留所有权利。

著录项

  • 来源
    《Peptides: An International Journal》 |2017年第2017期|共10页
  • 作者单位

    Dalian Med Univ Dept Pharmacol Dalian 116044 Liaoning Provin Peoples R China;

    Liaoning Normal Univ Sch Life Sci Dalian 116029 Liaoning Provin Peoples R China;

    Dalian Med Univ Dept Pharmacol Dalian 116044 Liaoning Provin Peoples R China;

    Dalian Med Univ Dept Pharmacol Dalian 116044 Liaoning Provin Peoples R China;

    Dalian Med Univ Dept Pharmacol Dalian 116044 Liaoning Provin Peoples R China;

    Dalian Med Univ Dept Pharmacol Dalian 116044 Liaoning Provin Peoples R China;

    Liaoning Normal Univ Sch Life Sci Dalian 116029 Liaoning Provin Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

    rLj-RGD3; Pancreatic carcinoma; Panc-1 cells; Anti-tumor; Mice;

    机译:RLJ-RGD3;胰腺癌;Panc-1细胞;抗肿瘤;小鼠;

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