miR-575在卵巢癌中的临床意义及其对卵巢癌细胞的影响

Jie Wang, Wei-xin Zhou, Xilun Gan, Jianbo Yang
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引用次数: 0

摘要

卵巢癌(OC)是一种常见的妇科癌症,发病率逐年上升,严重威胁着患者的健康和安全。miR-575在多种肿瘤疾病中的关键作用已经得到了很好的证实。我们推测miRNA-575可能与OC的发生密切相关,并可能成为未来OC诊断和治疗的关键。为了验证这一假设,我们选择了68例入院的OC患者(研究组,或RG)和60例同期健康对照(对照组,或CG)作为研究参与者。本研究使用人OC细胞系A2780、OVCAR-3和SK-OV-3以及人正常卵巢上皮细胞IOSE80。采用纳米颗粒辅助聚合酶链反应(Nano-PCR)检测miRNA-575在OC中的表达及其诊断意义。研究miRNA-575在OC细胞中的表达及其对OC细胞生物学行为的影响,并探讨miR-575与磷酸酶和紧张素同源物(PTEN)的相关性。结果显示,miRNA-575在OC中高表达。转染miRNA-575后检测OC细胞的生物学行为。与阴性对照(NC)和抑制mirna -575组相比,mimics-miRNA-575组细胞增殖和侵袭能力增强,凋亡和凋亡蛋白计数显著下降(P < 0.05)。随后,观察到PTEN在OC细胞中表达较低。在线靶基因分析网站(http://www.targetscan.org/vert_72/)确定了miR-575与PTEN结合的相关位点。mir -575、mir -575抑制组和NC组PTEN蛋白检测结果显示,mir -575抑制组PTEN蛋白表达较NC组降低,而mir -575抑制组PTEN蛋白表达较NC组升高(P < 0.05)。因此,我们得出结论,miR-575的高表达可以促进OC细胞的增殖和侵袭,抑制凋亡,而miR-575对OC细胞的影响可能是通过靶向PTEN蛋白来实现的。miR-575作为OC的潜在治疗靶点,在OC诊断中具有重要的临床应用价值,是未来OC研究的重大突破。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Significance of miR-575 in Ovarian Cancer and Its Effect on Ovarian Cancer Cells
Ovarian cancer (OC) is a common form of gynecological cancer that increases in incidence annually, seriously threatening the health and safety of patients. The critical role of miR-575 in multiple neoplastic diseases has already been well established. We suspected that miRNA-575 may be strongly associated with the occurrence of OC and may be the key to OC diagnosis and treatment in the future. To test this hypothesis, we selected 68 OC patients (research group, or RG) who were admitted to our hospital and 60 concurrent healthy controls (control group, or CG) as the study participants. Human OC cell lines A2780, OVCAR-3, and SK-OV-3, and human normal ovarian epithelial cells IOSE80 were used in this study. Nanoparticle-assisted polymerase chain reaction (Nano-PCR), was used to identify miRNA-575 expression and its diagnostic implications in OC. miRNA-575 expression in OC cells and its influence on OC cell biological behaviors were investigated, and the correlation between miR-575 and the phosphatase and tensin homolog (PTEN) was discussed. The results revealed a highly expressed miRNA-575 in OC. Detection of biological behaviors was conducted after transfection of miRNA-575 into OC cells. Cell proliferation and invasion in the mimics-miRNA-575 group was statistically enhanced compared to the negative control (NC) and ininhibition-miRNA-575 groups, and the apoptosis and apoptosis protein count significantly declined (P < 0.05). Subsequently, PTEN was observed to present a lower expression in OC cells. Online target gene analysis website (http://www.targetscan.org/vert_72/) identified the related sites that could bind miR-575 and PTEN. PTEN protein detection in the mimics-miR-575, ininhibition-miR-575, and NC groups showed that the PTEN protein expression in the mimics-miR-575 group was reduced in comparison with that of the other groups, while that for ininhibition-miR-575 was elevated compared to that of the NC group (P < 0.05). Therefore, we came to the conclusion that a high expression of miR-575 can bolster OC cell proliferation and invasion and inhibit apoptosis, while the impact of miR-575 on OC cells may be achieved via targeting the PTEN protein. miR-575 presents important clinical applications in OC diagnosis as an underlying therapeutic target of OC and is a major breakthrough toward future OC research.
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来源期刊
Nanoscience and Nanotechnology Letters
Nanoscience and Nanotechnology Letters Physical, Chemical & Earth Sciences-MATERIALS SCIENCE, MULTIDISCIPLINARY
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