Plasma Long Non-Coding RNA RP11-438N5.3 as a Novel Biomarker for Non-Small Cell Lung Cancer

Qingjuan Chen,1,* Chenjing Zhu,2,* Yingying Jin,3 Xiaomin Si,4 Wan Jiao,4 Wenjing He,4 Wei Mao,4 Ming Li,1 Guomin Luo1 1Department of Oncology, Yongchuan Hospital of Chongqing Medical University, Chongqing 40016, People’s Republic of China; 2Department of Radiation Oncology, Jiangsu Cancer Hospital and Jiangsu Institute of Cancer Research and The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, Jiangsu 210009, People’s Republic of China; 3Department of Oncology, The Second Affiliated Hospital of Xi’an Jiaotong University, Xi’an, Shaanxi Province 710004, People’s Republic of China; 4Department of Oncology, Xianyang Center Hospital, Xi’an, Shaanxi Province 712000, People’s Republic of China*These authors contributed equally to this workCorrespondence: Qingjuan ChenDepartment of Oncology, Yongchuan Hospital of Chongqing Medical University, Chongqing 40016, People’s Republic of ChinaEmail dr.qingjuan.chen@outlook.comBackground: Lung cancer is one of the most common malignancies around the world. The lack of early diagnosis and effective treatment strategies contributes to the poor prognosis of patients with lung cancer. Recent studies have implied the role of long non-coding RNAs (lncRNAs) in oncogenesis. The purpose of our study was to identify specific lncRNAs which were correlated with non-small cell lung cancer (NSCLC) and their potential functions.Materials and Methods: The global plasma lncRNA profiling was performed using LncPathTM Human Cancer Array, and 11 lncRNAs were then selected for quantitative reverse transcription PCR (qRT-PCR) validation in 138 plasma samples from 69 NSCLC patients and 69 healthy controls (HCs). A noteworthy lncRNA, RP11-438N5.3, the function of which was previously unknown, was further explored on the aspect of the correlation of its expression level with clinicopathological factors.Results: The results revealed that plasma level of RP11-438N5.3 was significantly lower in NSCLCs than that in HCs (p < 0.01). Receiver operating characteristic (ROC) analyses showed that the area under the ROC curve (AUC) for plasma RP11-438N5.3 was 0.814 (95% CI, 0.743– 0.885; p< 0.01). High expression of RP11-438N5.3 in plasma correlated with favorable prognosis for NSCLC patients (Hazard ratio = 2.827; 95% CI: 1.036 to 7.718; p = 0.024; Cox regression analysis). Moreover, we found that the plasma level of stromal interaction molecule 1 (STIM1) mRNA was remarkably higher in NSCLC compared with HC (p< 0.01), and the AUC for STIM1 was 0.753 (95% CI, 0.673– 0.833; p< 0.01), RP11-438N5.3 and STIM1 were inversely correlated with each other.Conclusion: Our results indicated that RP11-438N5.3 and STIM1 might provide a new strategy for NSCLC diagnosis. Furthermore, increased circulating RP11-438N5.3 level holds great potential in indicating a beneficial prognosis in NSCLC patients.Keywords: long non-coding RNA, biomarker, non-small cell lung cancer, RP11-438N5.3, stromal interaction molecule 1