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首页> 外文期刊>Journal of clinical laboratory analysis. >CircRNA hsa_circ_0013958 may contribute to the development of ovarian cancer by affecting epithelial‐mesenchymal transition and apoptotic signaling pathways
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CircRNA hsa_circ_0013958 may contribute to the development of ovarian cancer by affecting epithelial‐mesenchymal transition and apoptotic signaling pathways

机译:Circrna hsa_circ_0013958可以通过影响上皮 - 间充质转换和凋亡信号传导途径有助于卵巢癌的发育

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Background CircRNA plays an important role in the development of tumors, but its mechanism of action in ovarian cancer is still unclear. Methods The expression level of hsa_circ_0013958 in 45 pairs of ovarian cancer tissues and cells was quantified by qRT‐PCR, further revealing whether it is related to clinicopathological features and diagnostic value. Next, the effects of hsa_circ_0013958 on the proliferation, migration, invasion, and apoptosis of A2780 and OVCAR‐3 cells were detected by CCK‐8 assay, Transwell assay, and flow cytometry, respectively. Last, the expression levels of epithelial‐mesenchymal transition‐related proteins (E‐cadherin and Vimentin) and apoptosis‐related proteins (Bcl‐2 and Bax) were detected by Western blotting. Results Hsa_circ_0013958 was highly expressed in ovarian cancer tissues and cells, and its expression was closely related to patient FIGO stage and lymph node metastasis. Further, in vitro studies showed that knockdown of hsa_circ_0013958 suppressed proliferation, migration, and invasion of ovarian cancer cells but elevated the cell apoptotic rate. The expression levels of both epithelial‐mesenchymal transition‐related proteins and apoptosis‐related proteins were also changed. Conclusions Hsa_circ_0013958 may contribute to the development of ovarian cancer by affecting epithelial‐mesenchymal transition and apoptotic signaling pathways.
机译:背景Circrna在肿瘤的发展中起着重要作用,但它在卵巢癌中的作用机制仍然不清楚。方法通过QRT-PCR量化45对卵巢癌组织和细胞HSA_CIRC_0013958的表达水平,进一步揭示是否与临床病理特征和诊断价值有关。接下来,通过CCK-8测定,Transwell测定和流式细胞术分别检测HSA_CIRC_0013958对A2780和OVCAR-3细胞的增殖,迁移,侵袭和凋亡的影响。最后,通过蛋白质印迹检测上皮 - 间充质过渡相关蛋白(E-Cadherin和Vimentin)和凋亡相关蛋白(Bcl-2和Bax)的表达水平。结果HSA_CIRC_0013958在卵巢癌组织和细胞中高度表达,其表达与患者FIGO阶段和淋巴结转移密切相关。此外,体外研究表明,HSA_CIRC_0013958的敲低抑制了卵巢癌细胞的增殖,迁移和侵袭,但升高了细胞凋亡率。还改变了上皮 - 间充质过渡相关蛋白和凋亡相关蛋白的表达水平。结论HSA_CIRC_0013958可以通过影响上皮 - 间充质转换和凋亡信号传导途径有助于卵巢癌的发展。

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