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Decreased expression of peroxiredoxin1 inhibits proliferation, invasion, and metastasis of ovarian cancer cell

机译:Peroxiredoxin1的表达降低抑制卵巢癌细胞的增殖,侵袭和转移

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Aim: The aim of this study was to explore the expression of peroxiredoxin1 (PRDX1) in epithelial ovarian cancer, analyze the relationship between PRDX1 and clinicopathologic parameters of patients with ovarian cancer, including their prognosis, and describe changes and the mechanisms involved in malignant biologic behavior of ovarian cancer cells when PRDX1 expression is inhibited. Methods: The expression of PRDX1 was detected immunohistochemically in 15 samples of normal ovarian tissue, 21 benign, 11 borderline, and 101 malignant epithelial ovarian tumors. Changes in ovarian cancer cell proliferation, invasion, and metastasis before and after inhibiting PRDX1 expression were assessed by cell function assay. Additionally, gene set enrichment analysis (GSEA) of PRDX1 was performed by the Cancer Genome Atlas database. A protein–protein interaction network was then constructed and a pathway function analysis of the genes in the network was conducted. Results: PRDX1 expression was mainly localized to the cytoplasm, as well as the nucleus of cells. The expression rate of PRDX1 in epithelial ovarian malignant tissues (96.04%) was significantly higher than that in borderline (72.72%) and benign (57.14%) epithelial ovarian tumors, and normal ovarian tissue (20%; all P 0.05). Cox multivariate regression analysis indicated that advanced clinical stage, low tissue differentiation, and high expression of PRDX1 were independent risk factors affecting the prognosis of epithelial ovarian cancer (all P 0.05). Cell function assay verified that the decreased expression of PRDX1 inhibited ovarian cancer cell proliferation, invasion, and metastasis. GSEA analysis indicated that PRDX1 was significantly related to the Wnt signaling pathway. Western blot analysis confirmed that PRDX1 could regulate the expression of β-catenin in the Wnt pathway. Conclusion: Decreased expression of PRDX1 can attenuate cell proliferation, invasion, and metastasis of ovarian cancer cells. The expression of PRDX1 is related to the prognosis of patients with ovarian cancer and can therefore be used as a biomarker.
机译:目的:本研究旨在探讨peroxiredoxin1(PRDX1)在上皮性卵巢癌中的表达,分析PRDX1与卵巢癌患者的临床病理参数之间的关系,包括其预后,并描述其变化及其参与恶性生物学的机制PRDX1表达被抑制时卵巢癌细胞的行为。方法:采用免疫组织化学方法检测15例正常卵巢组织,21例良性,11例交界性和101例恶性上皮性卵巢肿瘤中PRDX1的表达。通过细胞功能测定评估抑制PRDX1表达前后卵巢癌细胞增殖,侵袭和转移的变化。此外,PRDX1的基因集富集分析(GSEA)由Cancer Genome Atlas数据库进行。然后构建了蛋白质-蛋白质相互作用网络,并对网络中的基因进行了通路功能分析。结果:PRDX1的表达主要定位于细胞质以及细胞核。 PRDX1在卵巢上皮恶性组织中的表达率(96.04%)显着高于交界性(72.72%)和良性(57.14%)的上皮性卵巢肿瘤和正常卵巢组织(20%;所有P <0.05)。 Cox多元回归分析表明,临床晚期,低组织分化和PRDX1高表达是影响上皮性卵巢癌预后的独立危险因素(所有P <0.05)。细胞功能测定证实PRDX1的表达降低抑制了卵巢癌细胞的增殖,侵袭和转移。 GSEA分析表明PRDX1与Wnt信号通路显着相关。 Western blot分析证实PRDX1可以调节Wnt途径中β-catenin的表达。结论:PRDX1的表达降低可以减弱卵巢癌细胞的增殖,侵袭和转移能力。 PRDX1的表达与卵巢癌患者的预后有关,因此可以用作生物标志物。

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