首页> 外文期刊>Biochemical and Biophysical Research Communications >Inhibition of PRL-3 gene expression in gastric cancer cell line SGC7901 via microRNA suppressed reduces peritoneal metastasis.
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Inhibition of PRL-3 gene expression in gastric cancer cell line SGC7901 via microRNA suppressed reduces peritoneal metastasis.

机译:通过抑制microRNA抑制胃癌细胞SGC7901中PRL-3基因表达可减少腹膜转移。

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摘要

High expression of PRL-3, a protein tyrosine phosphatase, is proved to be associated with lymph node metastasis in gastric carcinoma from previous studies. In this paper, we examined the relationship between PRL-3 expression and peritoneal metastasis in gastric carcinoma. We applied the artificial miRNA (pCMV-PRL3miRNA), which is based on the murine miR-155 sequence, to efficiently silence the target gene expression of PRL-3 in SGC7901 gastric cancer cells at both mRNA and protein levels. Then we observed that, in vitro, pCMV-PRL3miRNA significantly depressed the SGC7901 cell invasion and migration independent of cellular proliferation. In vivo, PRL-3 knockdown effectively suppressed the growth of peritoneal metastases and improved the prognosis in nude mice. Therefore, we concluded that artificial miRNA can depress the expression of PRL-3, and that PRL-3 might be a potential therapeutic target for gastric cancer peritoneal metastasis.
机译:以前的研究证明,蛋白酪氨酸磷酸酶PRL-3的高表达与胃癌的淋巴结转移有关。在本文中,我们研究了PRL-3表达与胃癌腹膜转移之间的关系。我们应用了基于小鼠miR-155序列的人工miRNA(pCMV-PRL3miRNA),以在mRNA和蛋白质水平上有效沉默SGC7901胃癌细胞中PRL-3的靶基因表达。然后我们观察到,在体外,pCMV-PRL3miRNA显着抑制了SGC7901细胞的侵袭和迁移,而与细胞增殖无关。在体内,PRL-3敲低可有效抑制腹膜转移的生长并改善裸鼠的预后。因此,我们得出的结论是,人造miRNA可以抑制PRL-3的表达,并且PRL-3可能是胃癌腹膜转移的潜在治疗靶标。

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