Wu Shuangjie, Liu Jun, Wang Xinhai, Li Mengjun, Chen Zongyou, Tang Yifan
Department of General Surgery, Huashan Hospital, Fudan University, 12 Middle Wulumuqi Road, Shanghai 200040, China.
J Cancer. 2017 Oct 23;8(19):4040-4047. doi: 10.7150/jca.21304. eCollection 2017.
Long non-coding RNAs (lncRNAs), which have emerged as important regulatory RNA molecules that have been implicated in carcinogenesis and cancer progression, may also serve as novel potential biomarkers for cancer diagnosis and prognosis. Our previous analysis has identified the lncRNA , the ghrelin antisense strand non-coding RNA gene, as one of the hub genes in the co-expression network of differentially expressed lncRNAs/mRNAs in colorectal cancer (CRC). Here, we further evaluate the expression of in CRC and explore its clinical significance. The expression of in 366 pairs of CRC and adjacent non-cancerous tissues was detected by quantitative RT-PCR assays. The results showed that the expression level of was significantly lower in CRC tissues than in matched non-cancerous tissues ( < 0.001). Decreased expression was observed in 54.4% (199/366) of cases, and was significantly correlated with the occurrence of lymph node metastasis ( = 0.033) and distant metastasis ( = 0.005). A Kaplan-Meier analysis demonstrated that decreased expression contributed to poor disease-free survival (log-rank test, < 0.001) and overall survival (log-rank test, < 0.001). Moreover, a multivariate Cox regression analysis revealed the decreased expression of as an independent prognostic marker of poor outcomes [disease-free survival: hazard ratio (HR) = 2.02, 95% confidence interval (CI) = 1.42-3.88; overall survival: HR = 1.96, 95% CI = 1.34-2.86] in CRC patients. In conclusion, our data suggest that the lncRNA might serve as a candidate biomarker of tumor metastasis and a prognostic indicator in CRC.
长链非编码RNA(lncRNAs)已成为重要的调控RNA分子,与肿瘤发生和癌症进展有关,也可能作为癌症诊断和预后的新型潜在生物标志物。我们之前的分析已确定lncRNA,即胃饥饿素反义链非编码RNA基因,是结直肠癌(CRC)中差异表达的lncRNAs/mRNAs共表达网络中的核心基因之一。在此,我们进一步评估lncRNA在CRC中的表达,并探讨其临床意义。通过定量RT-PCR检测了366对CRC组织和相邻非癌组织中lncRNA的表达。结果显示,CRC组织中lncRNA的表达水平显著低于配对的非癌组织(P<0.001)。54.4%(199/366)的病例中观察到lncRNA表达降低,且与淋巴结转移(P=0.033)和远处转移(P=0.005)的发生显著相关。Kaplan-Meier分析表明,lncRNA表达降低导致无病生存期较差(对数秩检验,P<0.001)和总生存期较差(对数秩检验,P<0.001)。此外,多因素Cox回归分析显示,lncRNA表达降低是CRC患者不良预后的独立预后标志物[无病生存期:风险比(HR)=2.02,95%置信区间(CI)=1.42-3.88;总生存期:HR=1.96,95%CI=1.34-2.86]。总之,我们的数据表明lncRNA可能作为CRC中肿瘤转移的候选生物标志物和预后指标。