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Has_circ_0008285/miR-211-5p/SIRT-1轴抑制卵巢癌细胞进展。

Has_circ_0008285/miR-211-5p/SIRT-1 Axis Suppress Ovarian Cancer Cells Progression.

作者信息

Elmizadeh Khadijeh, Homaei Ali, Bahadoran Ensiyeh, Abbasi Farzaneh, Moghbelinejad Sahar

机构信息

Department of Obstetrics and Gynecology, School of Medicine, Qazvin University of Medical Science, Qazvin, Iran.

Surgery Department, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, USA.

出版信息

Int J Mol Cell Med. 2023;12(4):401-422. doi: 10.22088/IJMCM.BUMS.12.4.401.

Abstract

The significant functional role of circular RNAs (circRNAs) in the progression of malignant tumors, including ovarian cancer, has been shown in various studies. In this study, we aimed to investigate the abnormal expression of hsa_circ_0008285 and its role in ovarian cancer pathogenesis. Quantitative real time polymerase chain reaction (qRT-PCR) and Western blot methods were used to detect the expression of hsa_circ_0008285 and some target genes in ovarian cancer tissues and related cell lines. To determine the functional roles of hsa_circ_0008285 in ovarian cancer, cell proliferation, apoptosis, and cell invasion assays were performed. Bioinformatics (Target scan, circ intractome) and luciferase reporter analyses were used to predict target genes. Results: In the present study, we first found that hsa_circ_0008285 was up regulated in ovarian cancer tissues and related cell lines. Bioinformatics, experimental data, and luciferase reporter analysis data showed miR-211-5p is a direct target of hsa_circ_0008285, while SIRT-1 is a direct target of miR-211-5p. Overexpression of hsa_circ_0008285 in cancer cells increased the expression of SIRT-1 and progression of cancer cells. Based on these results, inhibition of hsa_circ_0008285 expression could cause upregulation of miR-211-5p and down regulation of SIRT-1 and inhibited the proliferation and invasion of ovarian cancer cells. Conclusion: The results of the present study revealed that hsa_circ_0008285 suppressed ovarian cancer progression by regulating miR-211-5p expression to inhibit SIRT-1 expression.

摘要

多项研究表明,环状RNA(circRNA)在包括卵巢癌在内的恶性肿瘤进展中具有重要的功能作用。在本研究中,我们旨在探究hsa_circ_0008285的异常表达及其在卵巢癌发病机制中的作用。采用定量实时聚合酶链反应(qRT-PCR)和蛋白质免疫印迹法检测卵巢癌组织及相关细胞系中hsa_circ_0008285及一些靶基因的表达。为确定hsa_circ_0008285在卵巢癌中的功能作用,进行了细胞增殖、凋亡及细胞侵袭实验。利用生物信息学方法(Target scan、circ intractome)和荧光素酶报告基因分析预测靶基因。结果:在本研究中,我们首次发现hsa_circ_0008285在卵巢癌组织及相关细胞系中表达上调。生物信息学、实验数据及荧光素酶报告基因分析数据表明,miR-211-5p是hsa_circ_0008285的直接靶标,而SIRT-1是miR-211-5p的直接靶标。癌细胞中hsa_circ_0008285的过表达增加了SIRT-1的表达及癌细胞的进展。基于这些结果,抑制hsa_circ_0008285的表达可导致miR-211-5p上调及SIRT-1下调,并抑制卵巢癌细胞的增殖和侵袭。结论:本研究结果表明,hsa_circ_0008285通过调节miR-211-5p的表达来抑制SIRT-1的表达,从而抑制卵巢癌的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e67/11240052/7c2a11a2da29/ijmcm-12-401-g001.jpg

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