Xie Yan, Hu Xiuhua
Department of Thoracic Surgery, The First Affiliated Hospital of Shandong First Medical University, Jinan, China.
Department of Orthopedic Surgery, The First Affiliated Hospital of Shandong First Medical University, Jinan, China.
J Clin Lab Anal. 2020 Aug;34(8):e23357. doi: 10.1002/jcla.23357. Epub 2020 May 18.
Although long intergenic non-protein coding RNA 691 (LINC00691) has been functionally identified in several tumors, the association between LINC00691 and non-small-cell lung cancer (NSCLC) has not been reported. The objective of our study was to explore the clinical significance of LINC00691 in NSCLC.
RT-PCR was performed to detect LINC00691 levels in 177 pairs of human NSCLC tissues and matched normal lung specimens. A chi-squared test was used to analyze the possible influence of LINC00691 on the clinical progress of NSCLC. Kaplan-Meier methods were used to determine differences in patient survival. The prognostic value of survival variables was evaluated using univariate and multivariate analyses.
We found that LINC00691 levels were increased in tumor specimens compared with matched normal lung tissues (P < .01). Increased LINC00691 levels correlated with lymph node metastasis (P = .025) and advanced TNM stage (P = .002) in NSCLC patients. Moreover, clinical investigations revealed that NSCLC patients with high LINC00691 expression had a shorter overall survival than those with low LINC00691 expression (P = .0042). Finally, Cox regression assays confirmed LINC00691 as an independent prognostic factor for NSCLC patients.
The aberrant expression of LINC00691 may function as a reliable marker for the progression and prognosis of NSCLC in patients.
尽管长链基因间非编码RNA 691(LINC00691)已在多种肿瘤中被鉴定出功能,但LINC00691与非小细胞肺癌(NSCLC)之间的关联尚未见报道。本研究的目的是探讨LINC00691在NSCLC中的临床意义。
采用逆转录聚合酶链反应(RT-PCR)检测177对人NSCLC组织及配对的正常肺组织标本中LINC00691的水平。采用卡方检验分析LINC00691对NSCLC临床进展的可能影响。采用Kaplan-Meier法确定患者生存率的差异。使用单因素和多因素分析评估生存变量的预后价值。
我们发现,与配对的正常肺组织相比,肿瘤标本中LINC00691水平升高(P < 0.01)。NSCLC患者中,LINC00691水平升高与淋巴结转移(P = 0.025)和TNM分期进展(P = 0.002)相关。此外,临床研究显示,LINC00691高表达的NSCLC患者总生存期短于LINC00691低表达的患者(P = 0.0042)。最后,Cox回归分析证实LINC00691是NSCLC患者的独立预后因素。
LINC00691的异常表达可能是NSCLC患者病情进展和预后的可靠标志物。