首页> 美国卫生研究院文献>Cancer Microenvironment >Three-Dimensional Cellular Arrangement in Epithelial Ovarian Cancer Cell Lines TOV-21G and SKOV-3 is Associated with Apoptosis-Related miRNA Expression Modulation
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Three-Dimensional Cellular Arrangement in Epithelial Ovarian Cancer Cell Lines TOV-21G and SKOV-3 is Associated with Apoptosis-Related miRNA Expression Modulation

机译:上皮性卵巢癌细胞系TOV-21G和SKOV-3中的三维细胞排列与凋亡相关的miRNA表达调节相关。

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摘要

Epithelial ovarian cancer (EOC) is the most lethal gynecological malignancy, and the lack of chemoresistance biomarkers contributes to the poor prognosis. Cancer stem cells (CSC) have been investigated in EOC to understand its relationship with chemoresistance and recurrence. In this context, in vitro cultivation-models are important tools for CSC studies. MicroRNAs (miRNAs) play key roles in cancer, CSC regulation and apoptosis. Thus, this study aims to evaluate the tumorsphere model as CSC-enrichment method in EOC studies and investigate apoptosis-related miRNAs in tumorspheres-derived EOC cell lines. TOV-21G and SKOV-3 were cultured in monolayer and tumorspheres. Genetic profiles of cell lines were obtained using COSMIC database. CD24/CD44/CD146/CD177 and ALDH1 markers were evaluated in cell lines and tumorspheres-derived by flow cytometry. Eleven miRNAs were selected by in silico analysis for qPCR analysis. According to COSMIC, TOV-21G and SKOV-3 have eight and nine cancer-related mutations, respectively. TOV-21G showed a CD44+/high/CD24−/low/CD117−/low/CD146−/low/ALDH1low profile in both culture models; thus, no significant difference between cultivation models was identified. SKOV-3 showed a CD44+/high/CD24+/high/ CD117−/low/CD146−/low/ALDH1low profile in both culture models, although the tumorsphere model showed a significant increase in CD24+/high subpopulation (ovarian CSC-like). Among eleven miRNAs, we observed differences in miRNA expression between culture models. MiR-26a was overexpressed in TOV-21G tumorspheres, albeit downregulated in SKOV-3 tumorspheres. MiR-125b-5p, miR-17-5p and miR-221 was downregulated in tumorsphere model in both cell lines. Given that tumorsphere-derived SKOV-3 had a higher ratio of CD24+/high cells, we suggest that miR-26a, miR-125b-5p, miR-17-5p and miR-221 downregulation could be related to poor EOC prognosis.
机译:上皮性卵巢癌(EOC)是最致命的妇科恶性肿瘤,化学抗药性生物标志物的缺乏导致不良的预后。已在EOC中对癌症干细胞(CSC)进行了研究,以了解其与化学耐药性和复发的关系。在这种情况下,体外培养模型是CSC研究的重要工具。微小RNA(miRNA)在癌症,CSC调节和细胞凋亡中起关键作用。因此,本研究旨在评估作为EOC研究中CSC富集方法的肿瘤球模型,并研究源自肿瘤球的EOC细胞系中凋亡相关的miRNA。 TOV-21G和SKOV-3在单层和肿瘤球中培养。使用COSMIC数据库获得细胞系的遗传概况。 CD24 / CD44 / CD146 / CD177和ALDH1标记通过流式细胞术在衍生的细胞系和肿瘤球中评估。通过计算机分析选择了11个miRNA进行qPCR分析。根据COSMIC,TOV-21G和SKOV-3分别具有八个和九个与癌症相关的突变。 TOV-21G显示为CD44 + / high / CD24 -/ low / CD117 -/ low / CD146 -/ low / ALDH1 low 配置文件;因此,没有发现栽培模型之间的显着差异。 SKOV-3显示CD44 + /高 / CD24 + /高 / CD117 -//低 / CD146 -//低 + / high 亚群(卵巢CSC样)显着增加,但两种培养模型中的sup> / ALDH1 low 谱图。在11个miRNA中,我们观察到培养模型之间miRNA表达的差异。 MiR-26a在TOV-21G肿瘤球中过表达,尽管在SKOV-3肿瘤球中被下调。在两种细胞系的肿瘤球模型中,miR-125b-5p,miR-17-5p和miR-221均下调。考虑到肿瘤球来源的SKOV-3具有较高的CD24 + / high 细胞比率,我们建议miR-26a,miR-125b-5p,miR-17-5p和miR-221下调可以与EOC预后不良有关。

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