首页> 外文期刊>Molecular Therapy - Oncolytics >Pseudostellaria heterophylla Extract Polysaccharide H-1-2 Suppresses Pancreatic Cancer by Inhibiting Hypoxia-Induced AG2
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Pseudostellaria heterophylla Extract Polysaccharide H-1-2 Suppresses Pancreatic Cancer by Inhibiting Hypoxia-Induced AG2

机译:Pseudostellaria heterophylla提取多糖H-1-2通过抑制缺氧诱导的ag2来抑制胰腺癌

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We aimed to examine the therapeutic potential of polysaccharide H-1-2, a bioactive component of Pseudostellaria heterophylla , against pancreatic cancer, as well as to demonstrate the underlying molecular mechanisms. Invasion and migration of pancreatic cells treated with H-1-2 were evaluated. A xenograft tumor mouse model was established to assess the effect of H-1-2 on tumor growth. Expression levels of hypoxic inducible factor-1α (HIF1α) and anterior gradient 2 (AGR2) were measured in pancreatic cells after H-1-2 treatment. Luciferase report and chromatin immunoprecipitation assays were conducted to investigate HIF1α regulation on AGR2. AGR2 expression was re-introduced into pancreatic cells to assess the role of AGR2 as a downstream effector of hypoxia after H-1-2 treatment. H-1-2 inhibited invasion and migration of pancreatic cancer cells, repressed xenograft pancreatic tumor growth, and increased survival of mice. H-1-2 repressed AGR2 expression in pancreatic cancer cells through the hypoxia response element (HRE) in its promoter region. Ectopic AGR2 expression partially negated the H-1-2 inhibitory effect on invasion and migration of pancreatic cells and on xenograft pancreatic tumors growth, and it also compromised the H-1-2 promotional effect on survival of mice. We conclude that H-1-2 suppresses pancreatic cancer by inhibiting hypoxia-induced AGR2 expression, supporting further investigation into its efficacy against pancreatic cancer in clinical settings.
机译:我们的目的是检查多糖H-1-2的治疗潜力,抗胰腺癌的假脑胰蛋白杂志的生物活性成分,以及证明潜在的分子机制。评价用H-1-2治疗的胰腺细胞的侵袭和迁移。建立了异种移植肿瘤小鼠模型,以评估H-1-2对肿瘤生长的影响。在H-1-2处理后,在胰腺细胞中测量缺氧诱导因子-1α(HIF1α)和前梯度2(AGR2)的表达水平。进行荧光素酶报告和染色质免疫沉淀测定以研究AGR2对HIF1α调节。将Agr2表达重新引入胰腺细胞中,以评估AGR2作为H-1-2治疗后缺氧的下游效应器的作用。 H-1-2抑制胰腺癌细胞的侵袭和迁移,抑制异种移植胰腺肿瘤生长,并增加小鼠的存活率。通过其启动子区中的缺氧响应元素(HRE)在胰腺癌细胞中抑制AGR2表达。异位AGR2表达部分否定了H-1-2对胰腺细胞的侵袭和迁移和异种移植物胰腺肿瘤生长的抑制作用,并且还损害了对小鼠存活的H-1-2促进作用。我们得出结论,H-1-2通过抑制缺氧诱导的AGR2表达来抑制胰腺癌,在临床环境中支持进一步调查其对胰腺癌的疗效。

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