lncRNA DHRS4-AS1 海绵状 miR-222-3p 在甲状腺癌诊断中的可行性研究

Endokrynologia Polska Pub Date : 2024-01-01 Epub Date: 2024-10-08 DOI:10.5603/ep.99456
Shuai Xu, Xinyi Zheng, Haibin Wu, Xujun You, Junwei Wu, Hai Zhou, Junhua Wu, Qianqian Liu, Ren-Qun Ye
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引用次数: 0

摘要

导言甲状腺癌是内分泌系统中常见的恶性肿瘤,在我国的发病率持续上升。不断探索甲状腺癌的诊断标志物和分子机制,为治愈患者提供新的可能,是近几十年来研究的重点和方向。本研究以lncRNA DHRS4-AS1为研究靶点,探讨了DHRS4-AS1异常表达对甲状腺癌的调控作用:本文收集了甲状腺癌(116例)和非癌正常组织(82例)样本,采用RT-qPCR技术评估了组织和细胞中DHRS4-AS1和miR-222-3p的表达。CCK-8和流式细胞术用于检测细胞存活状态。通过双荧光素酶报告基因检测分析了DHRS4-AS1海绵化miR-222-3p的机制:结果:在本研究中,DHRS4-AS1在甲状腺组织和细胞样本中均下调,而miR-222-3p的表达则升高。ROC曲线反映了DHRS4-AS1在甲状腺癌中的诊断价值[曲线下面积(AUC)= 0.887,灵敏度=76.7%,特异性=95.1%]。DHRS4-AS1 通过靶向 miR-222-3p 调节甲状腺癌的发展。此外,体外实验表明,过表达 DHRS4-AS1 (pcDNA3.1-DHRS4-AS1)可抑制甲状腺癌细胞的增殖并促进细胞凋亡,同时下调 miR-222-3p 的水平:结论:DHRS4-AS1在甲状腺癌中起着miR-222-3p海绵的作用,过表达DHRS4-AS1可下调细胞增殖并促进细胞凋亡。这些发现证明了DHRS4-AS1作为甲状腺癌诊断因子的潜力。
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Feasibility study of lncRNA DHRS4-AS1 sponge miR-222-3p in the diagnosis of thyroid cancer.

Introduction: Thyroid cancer is a commonly occurring malignant tumour within the endocrine system, the incidence of which has been increasing steadily in our country. It has been the focus and direction of research in recent decades to continuously explore the diagnostic markers and molecular mechanisms of thyroid cancer and provide new possibilities for the healing of patients. In this study, lncRNA DHRS4-AS1 was identified as the research target, and the regulatory function of abnormal expression of DHRS4-AS1 on thyroid cancer was discussed.

Material and methods: Thyroid cancer (116) and non-cancer normal (82) tissue samples were collected in this paper, and the expression of DHRS4-AS1 and miR-222-3p in tissues and cells were evaluated by RT-qPCR. CCK-8 and flow cytometry were used to detect cell survival status. The mechanism of DHRS4-AS1 sponge miR-222-3p was analysed by dual-luciferase reporter gene detection.

Results: In the present study, DHRS4-AS1 was down-regulated in both thyroid tissue and cell samples, while miR-222-3p expression was elevated. The ROC curve reflected the diagnostic value of DHRS4-AS1 in thyroid cancer [area under the curve (AUC) = 0.887, sensitivity = 76.7%, specificity = 95.1%]. DHRS4-AS1 regulates the development of thyroid cancer by targeting miR-222-3p. In addition, in vitro experiments demonstrated that overexpression of DHRS4-AS1 (pcDNA3.1-DHRS4-AS1) inhibited the proliferation of thyroid cancer cells and promoted cell apoptosis, while down-regulating the level of miR-222-3p.

Conclusions: DHRS4-AS1 acts as a miR-222-3p sponge in thyroid cancer, and overexpression of DHRS4 AS1 down-regulates cell proliferation and promotes cell apoptosis. These findings demonstrate the potential of DHRS4-AS1 as a diagnostic factor for thyroid cancer.

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