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Circular RNA_0015278与甲状腺乳头状癌及临床特征的相关性
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作者 丁华杰 杨绍石 +3 位作者 李莎 史华宁 龚雪 那磊 《河北医药》 CAS 2023年第19期2945-2947,2951,共4页
目的探讨Circular RNA_0015278(circ_0015278)与甲状腺乳头状癌(PTC)及其临床病理特征的相关性。方法回顾分析手术切除的甲状腺乳头状癌患者200例,采用逆转录定量聚合酶链反应(RT-qPCR)检测Circular RNA_0015278在甲状腺乳头状癌(PTC)... 目的探讨Circular RNA_0015278(circ_0015278)与甲状腺乳头状癌(PTC)及其临床病理特征的相关性。方法回顾分析手术切除的甲状腺乳头状癌患者200例,采用逆转录定量聚合酶链反应(RT-qPCR)检测Circular RNA_0015278在甲状腺乳头状癌(PTC)及癌旁组织的表达。结果与癌旁组织比较,甲状腺乳头状癌(PTC)中Circular RNA_0015278表达显著降低(Z=-12.122,P<0.001),ROC分析显示,以相对表达量0.743为截断值,可较好的鉴别PTC肿瘤及癌旁组织(AUC:0.903,95%CI:0.873~0.933)。而PTC肿瘤中Circular RNA_0015278的高表达与患者年龄<45岁(Z=-2.319,P=0.020)、无甲状腺外侵犯(Z=-2.042,P=0.041)、无淋巴结转移(Z=-2.494,P=0.013)及低pTNM分期(Z=-3.719,P=0.001)相关(P<0.05)。而未发现与性别(Z=-1.323,P=0.186)、肿瘤大小(Z=-1.273,P=0.203)具有相关性(P>0.05)。结论PTC肿瘤中Circular RNA_0015278的表达显著降低,而其在PTC肿瘤中高表达与患者年龄<45岁、无甲状腺外侵犯、无淋巴结转移及低pTNM分期具有相关性。 展开更多
关键词 circular RNA_0015278 甲状腺乳头状癌 临床特征
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Increased circulating circular RNA103516 is a novel biomarker for inflammatory bowel disease in adult patients 被引量:9
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作者 Yu-Lan Ye Juan Yin +3 位作者 Tong Hu Li-Ping Zhang Long-Yun Wu Zhi Pang 《World Journal of Gastroenterology》 SCIE CAS 2019年第41期6273-6288,共16页
BACKGROUND Increasing evidence demonstrates that by acting as microRNA sponges modulating gene expression at the transcriptional or post-transcriptional level,circular RNAs(circRNAs)participate in the pathogenesis of ... BACKGROUND Increasing evidence demonstrates that by acting as microRNA sponges modulating gene expression at the transcriptional or post-transcriptional level,circular RNAs(circRNAs)participate in the pathogenesis of a variety of diseases and are considered ideal biomarkers of human disease.AIM To examine the expression of circRNA_103516 in inflammatory bowel disease(IBD)and its associations with clinical phenotypes and inflammatory cytokines.METHODS Peripheral blood mononuclear cells(PBMCs)were obtained from patients with IBD,healthy controls(HCs),and patient controls(PCs).Expression of circRNA_103516 and hsa-miR-19b-1-5p was assessed by quantitative reverse transcription-polymerase chain reaction.Crohn's disease activity index(CDAI),Mayo score,C-reactive protein(CRP)level,and erythrocyte sedimentation rate(ESR)were measured.To assess the inflammatory cytokines tumour necrosis factorα(TNF-α),interferon-γ(IFN-γ),and interleukin-10(IL-10),blood samples were analysed by flow cytometry.RESULTS Ninety Crohn’s disease(CD)and 90 ulcerative colitis(UC)patients,80 HCs,and 35 PCs were included in the study.CircRNA_103516 was upregulated in CD and UC patients compared with HCs and PCs(P<0.05).The area under the curve of circRNA_103516 for diagnosing CD and UC was 0.790 and 0.687,respectively.In addition,circRNA_103516 levels were increased in active CD and UC compared with remittent groups(P=0.027,P=0.045).Furthermore,in CD,circRNA_103516 correlated positively with CDAI(P<0.001),CRP(P<0.001),ESR(P<0.001),TNFα(P<0.001),and IFN-γ(P<0.001)and negatively correlated with IL-10(P=0.006).In UC patients,circRNA_103516 correlated with Mayo score(P<0.001),CRP(P<0.001),ESR(P<0.001),TNFα(P<0.001),IFN-γ(P=0.011),and IL-10(P=0.002).Additionally,circRNA_103516 correlated positively with stricturing(P=0.018)and penetrating(P=0.031)behaviour.Moreover,hsamiR-19b-1-5p correlated negatively with circRNA_103516 in CD.CONCLUSION CircRNA_103516 levels in PBMCs can be considered an ideal candidate biomarker for diagnosing IBD.Dysregulation of circRNA_103516 may participate in the molecular mechanism of IBD through hsa-miR-19b-1-5p sponging. 展开更多
关键词 circular RNA circular RNA_103516 INFLAMMATORY BOWEL diseases BIOMARKER
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circ_0006174靶向调控miR-876-3p对肺癌细胞恶性生物学行为的影响
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作者 杨祎明 霍前伦 《山东医药》 CAS 2022年第25期43-47,共5页
目的探讨circ_0006174靶向调控miR-876-3p对肺癌细胞恶性生物学行为的影响。方法体外培养A549细胞,随机分为si-circ_0006174组、si-NC组、si-circ_0006174+anti-miR-876-3p组、si-circ_0006174+anti-miRNC组,分别转染si-circ_0006174、s... 目的探讨circ_0006174靶向调控miR-876-3p对肺癌细胞恶性生物学行为的影响。方法体外培养A549细胞,随机分为si-circ_0006174组、si-NC组、si-circ_0006174+anti-miR-876-3p组、si-circ_0006174+anti-miRNC组,分别转染si-circ_0006174、si-NC、si-circ_0006174+anti-miR-876-3p、si-circ_0006174+anti-miR-NC,采用RTqPCR法检测circ_0006174、miR-876-3p表达。收集各组转染后细胞,采用CCK-8法检测细胞增殖情况,采用流式细胞术检测细胞凋亡情况,采用Transwell小室实验检测细胞侵袭和迁移情况,采用Western blotting法检测Bax、Bcl-2、E-cadherin、N-cadherin蛋白表达。通过Circular RNA Interactome在线软件预测circ_0006174与anti-miR-876-3p的靶向结合位点,并通过双荧光素酶报告基因实验验证二者的靶向调控关系。结果si-circ_0006174组circ_0006174相对表达量低于si-NC组,si-circ_0006174+anti-miR-876-3p组miR-876-3p相对表达量低于si-circ_0006174+anti-miRNC组(P均<0.05)。si-circ_0006174组细胞增殖抑制率和细胞凋亡率均高于si-NC组,而si-circ_0006174+anti-miR-876-3p组细胞增殖抑制率和细胞凋亡率均低于si-circ_0006174+anti-miR-NC组(P均<0.05)。si-circ_0006174组细胞侵袭和迁移能力均低于si-NC组,而si-circ_0006174+anti-miR-876-3p组细胞侵袭和迁移能力均高于si-circ_0006174+anti-miR-NC组(P均<0.05)。si-circ_0006174组Bax、E-cadherin蛋白相对表达量均高于si-NC组,Bcl-2、N-cadherin蛋白相对表达量均低于si-NC组(P均<0.05);si-circ_0006174+anti-miR-876-3p组Bax、E-cadherin蛋白相对表达量均低于si-circ_0006174+anti-miR-NC组,Bcl-2、N-cadherin蛋白相对表达量均高于si-circ_0006174+antimiR-NC组(P均<0.05)。经在线软件预测和双荧光素酶报告基因实验验证,circ_0006174能够靶向调控miR-876-3p。结论敲减circ_0006174可能通过靶向调控miR-876-3p抑制肺癌细胞恶性生物学行为。 展开更多
关键词 肺癌 环状RNA_0006174 微小RNA-876-3p 恶性生物学行为
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