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Inhibition of peritoneal metastasis of human gastric cancer cells by dextran sulphate through the reduction in HIF-1α and ITGβ1 expression

机译:硫酸葡聚糖通过降低HIF-1α和ITGβ1表达来抑制人胃癌细胞的腹膜转移

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摘要

The aim of the present study was to investigate the effects of dextran sulphate (DS) on HIF-1α and integrin β1 (ITGβ1) expression in human gastric cancer cells, the correlation between HIF-1α and ITGβ1 expression and the influence of DS on the peritoneal metastasis of human gastric cancer cells. In in vitro experiments, BGC-823 cells in the experimental and control groups were administered DS and PBS, respectively, and exposed to hypoxic conditions for different periods. Immunocytochemistry, western blot and RT-PCR analyses were used to evaluate HIF-1α and ITGβ1 expression levels. In in vivo experiments, an animal model was established by injecting BGC-823 cells into nude mice. The experimental and control groups received DS and PBS injections, respectively. The mice were euthanized at different times, and the number of tumor nodules in the celiac implantation was recorded. Immunohistochemistry, RT-PCR and western blot analyses were used to detect HIF-1α and ITGβ1 expression in the tumor nodules of the greater omentum. The in vitro and in vivo results revealed that HIF-1α and ITGβ1 expression levels in the experimental group were significantly lower than those in the control group (P<0.05), and the expression levels of these factors were positively correlated with each other. The number of tumor nodules in the in vivo experiments was notably less in the experimental group than that noted in the control group (P<0.01). In conclusion, DS may act through inhibition of HIF-1α expression, which decreased ITGβ1 expression, consequently reducing tumor metastasis.
机译:本研究的目的是研究硫酸右旋糖酐(DS)对人胃癌细胞HIF-1α和整合素β1(ITGβ1)表达的影响,HIF-1α和ITGβ1表达之间的相关性以及DS对人胃癌细胞的影响。人胃癌细胞的腹膜转移。在体外实验中,分别对实验组和对照组的BGC-823细胞进行DS和PBS给药,并使其在不同时间的低氧条件下暴露。免疫细胞化学,Western印迹和RT-PCR分析用于评估HIF-1α和ITGβ1表达水平。在体内实验中,通过将BGC-823细胞注入裸鼠来建立动物模型。实验组和对照组分别接受DS和PBS注射。在不同时间对小鼠实施安乐死,并记录腹腔植入物中肿瘤结节的数量。免疫组织化学,RT-PCR和western blot分析检测大网膜肿瘤结节中HIF-1α和ITGβ1的表达。体内外实验结果表明,实验组HIF-1α和ITGβ1的表达水平明显低于对照组(P <0.05),且这些因子的表达水平呈正相关。体内实验中的肿瘤结节数明显少于对照组(P <0.01)。总之,DS可能通过抑制HIF-1α表达而起作用,从而降低了ITGβ1的表达,从而减少了肿瘤的转移。

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