• 长链非编码RNA ZNF667-AS1在非小细胞肺癌组织中表达上调
  • 梁海梅.长链非编码RNA ZNF667-AS1在非小细胞肺癌组织中表达上调[J].内科急危重症杂志,2022,28(4):305-307
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    DOI:10.11768/nkjwzzzz20220411
    中文关键词:  非小细胞肺癌  长链非编码RNA  ZNF667-AS1
    英文关键词:
    基金项目:海南省自然科学基金资助(No:818MS136)
    作者单位E-mail
    梁海梅 中南大学湘雅医学院附属海口医院 lianghaimeit88@163.com 
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    中文摘要:
          目的:探讨非小细胞肺癌(NSCLC)组织中长链非编码RNA(lncRNA) 锌指蛋白667反义RNA1(ZNF667-AS1)的表达水平。方法: 97例NSCLC患者被纳入本研究,术中留取新鲜的癌组织及对应癌旁组织,采用实时定量聚合酶链式反应(PCR)法检测lncRNA ZNF667-AS1和血管内皮生长因子(VEGF)的表达,分析lncRNA ZNF667-AS1的表达与NSCLC患者临床病理特征的关系,绘制受试者工作特征(ROC)曲线,评估lncRNA ZNF667-AS1用于诊断NSCLC的价值,分析癌组织中VEGF的表达与lncRNA ZNF667-AS1表达的相关性。结果:PCR检测结果显示,97例NSCLC患者癌组织中lncRNA ZNF667-AS1的平均相对表达量明显高于癌旁组织(P<0.05)。不同性别、年龄、肿瘤直径及病理组织类型的NSCLC患者癌组织中lncRNA ZNF667-AS1相对表达量比较,差异无统计学意义(P均>0.05),但不同组织分化程度、临床分期、浸润程度及有无淋巴结转移的患者癌组织中lncRNA ZNF667-AS1相对表达量比较,差异有统计学意义(P均<0.05)。实时荧光定量PCR检测结果显示,NSCLC癌组织中VEGF的相对表达量明显高于癌旁组织(P<0.01),NSCLC癌组织中lncRNA ZNF667-AS1的相对表达量与VEGF的表达呈正相关(P<0.05)。由ROC曲线可知,lncRNA ZNF667-AS1诊断NSCLC的AUC为0.792(95%CI:0.683-0.911,P﹤0.05),特异性为81.23%,敏感度为86.12%。结论: lncRNA ZNF667-AS1在NSCLC组织中表达上调,其可能作为一种促癌因子参与NSCLC的发生发展过程。
    英文摘要:
          Objective: To investigate the expression level of long non-coding RNA (lncRNA) zinc finger protein 667 antisense RNA1 (ZNF667-AS1) in non-small cell lung cancer tissues. Methods: A total of 97 patients with NSCLC were included in this study. Fresh cancer tissues and corresponding paracancerous tissues were collected during surgery, and real-time quantitative polymerase chain reaction (PCR) was used to detect lncRNA ZNF667-AS1 and vascular endothelial growth factor (VEGF). The relationship between the expression of lncRNA ZNF667-AS1 and the clinicopathological characteristics of NSCLC patients was analyzed. The receiver operating characteristic (ROC) curve was drawn, and the value of lncRNA ZNF667-AS1 in the diagnosis of NSCL was evaluated. Correlation between lncRNA ZNF667-AS1 expression and VEGF expression in lung cancer tissues was analyzed. Results: The PCR results showed that the average relative expression of lncRNA ZNF667-AS1 in cancer tissues of 97 NSCLC patients was significantly higher than that in adjacent tissues (P<0.05). There was no significant difference in the relative expression of lncRNA ZNF667-AS1 in cancer tissues of NSCLC patients with different genders, ages, tumor diameters and pathological tissue types (all P>0.05). The relative expression of lncRNA ZNF667-AS1 in cancer tissues of patients with or without lymph node metastasis showed statistically significant difference (P<0.05). The results of real-time fluorescence quantitative PCR showed that the relative expression of VEGF in NSCLC cancer tissues was significantly higher than that in adjacent tissues (P<0.01), and the relative expression of lncRNA ZNF667-AS1 in NSCLC cancer tissues was positively correlated with the expression of VEGF (P<0.01). The area under the ROC curve (AUC) of lncRNA ZNF667-AS1 in the diagnosis of NSCLC was 0.792 (95% CI: 0.683-0.911, P<0.05), the specificity was 81.23%, and the sensitivity was 86.12%. Conclusion: The expression of lncRNA ZNF667-AS1 is up-regulated in NSCLC tissues, and it may be involved in the occurrence and development of NSCLC as a tumor-promoting factor.