Low plasma miR-25 expression is a favorite prognosis factor in non-small cell lung cancer

被引:1
作者
Zhang, Y-L [1 ]
Zhang, Z-L [3 ]
Zhu, X-B [2 ]
Xu, L. [1 ]
Lu, P. [1 ]
Xu, M. [1 ]
Liu, W-J [1 ]
Zhang, X-Y [1 ]
Yao, H-M [1 ]
Ye, X-W [1 ]
机构
[1] Guizhou Prov Peoples Hosp, Dept Resp Med, Guiyang, Guizhou, Peoples R China
[2] Zunyi Med Univ, Longgang Cent Hosp Shenzhen, Affiliated Longgang Hosp, Shenzhen, Guangdong, Peoples R China
[3] Zunyi Normal Univ, Coll Life Sci, Zunyi, Guizhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Plasma miR-25; Non-small cell lung cancer; Diagnosis; Prognosis; MICRORNAS; BIOMARKER; PROLIFERATION; DIAGNOSIS; INVASION; METASTASIS; APOPTOSIS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: Circulating microRNAs (miRNAs) are promising biomarkers for the diagnosis and prognosis prediction of cancer. In the study, we aimed to investigate the potential clinical significance of the plasma miR-25 in non-small cell lung carcinoma (NSCLC). PATIENTS AND METHODS: We first compared the miRNAs expression pattern between NSCLC tissues and adjacent normal tissues then. bioinformatic analysis of the downstream targets of miR-25 was performed. The diagnostic and prognostic value of the plasma miR-25 in NSCLC was then evaluated. RESULTS: The expression level of miR-25 was increased in NSCLC tissues compared to the adjacent normal tissues. In addition, bioinformatic analysis of the downstream-targeted genes of miR-25 revealed that many gene ontology functions and pathways were associated with cancer progression. The levels of plasma miR-25 were significantly upregulated in NSCLC patients compared to normal controls. In addition, the plasma miR-25 levels were especially higher in NSCLC patients with positive lymph node metastasis, poorly differentiation or advanced clinical stage. Subsequently, we found that the plasma miR-25 expression levels were dramatically decreased in 45 NSCLC patients after receiving surgical treatment. The receiver operating characteristic (ROC) curve analysis indicated that the plasma miR-25 exhibited high diagnostic sensitivity and specificity to discriminate NSCLC cases from healthy subjects. More interestingly, the combination of the plasma miR-25 and carcinoembryonic antigen (CEA) could effectively enhance the accuracy for distinguishing NSCLC patients from normal controls. Moreover, the plasma miR-25 overexpression was closely correlated with aggressive clinical characteristics and poor survival. Finally, the plasma miR-25 was identified as an independent prognostic marker for the overall survival of NSCLC. CONCLUSIONS: Collectively, our findings demonstrated that the plasma miR-25 might serve as a novel promising biomarker in the diagnosis and prognosis prediction of NSCLC.
引用
收藏
页码:5251 / 5259
页数:9
相关论文
共 33 条
[1]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[2]   MicroRNA signatures in human cancers [J].
Calin, George A. ;
Croce, Carlo M. .
NATURE REVIEWS CANCER, 2006, 6 (11) :857-866
[3]   miR-25 enhances cell migration and invasion in non-small-cell lung cancer cells via ERK signaling pathway by inhibiting KLF4 [J].
Ding, Xiaoli ;
Zhong, Tianyu ;
Jiang, Lixia ;
Huang, Junyun ;
Xia, Yu ;
Hu, Rong .
MOLECULAR MEDICINE REPORTS, 2018, 17 (05) :7005-7016
[4]   Oncomirs - microRNAs with a role in cancer [J].
Esquela-Kerscher, A ;
Slack, FJ .
NATURE REVIEWS CANCER, 2006, 6 (04) :259-269
[5]   Ten Years of Progress in Non Small Cell Lung Cancer [J].
Ettinger, David S. .
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2012, 10 (03) :292-295
[6]   MicroRNA expression and function in cancer [J].
Garzon, Ramiro ;
Fabbri, Muller ;
Cimmino, Amelia ;
Calin, George A. ;
Croce, Carlo M. .
TRENDS IN MOLECULAR MEDICINE, 2006, 12 (12) :580-587
[7]  
He J, 2018, EUR REV MED PHARMACO, V22, P2680, DOI 10.26355/eurrev_201805_14964
[8]  
HE J H, 2017, ONCOL LETT, V14, P6097
[9]   RBM24 suppresses cancer progression by upregulating miR-25 to target MALAT1 in nasopharyngeal carcinoma [J].
Hua, Wen-Feng ;
Zhong, Qian ;
Xia, Tian-Liang ;
Chen, Qi ;
Zhang, Mei-Yin ;
Zhou, Ai-Jun ;
Tu, Zi-Wei ;
Qu, Chen ;
Li, Man-Zhi ;
Xia, Yun-Fei ;
Wang, Hui-Yun ;
Xie, Dan ;
Claret, Francois-Xavier ;
Song, Er-Wei ;
Zeng, Mu-Sheng .
CELL DEATH & DISEASE, 2016, 7 :e2352-e2352
[10]   Upregulated MicroRNA-25 Mediates the Migration of Melanoma Cells by Targeting DKK3 through the WNT/β-Catenin Pathway [J].
Huo, Jia ;
Zhang, Yanfei ;
Li, Ruilian ;
Wang, Yuan ;
Wu, Jiawen ;
Zhang, Dingwei .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (11)