Prognostic significance of serum miR-17-5p in lung cancer

被引:85
作者
Chen, Qun [1 ]
Si, Qing [1 ]
Xiao, Song [1 ]
Xie, Qiang [1 ]
Lin, Jiangping [1 ]
Wang, Chenhui [1 ]
Chen, Lizhou [1 ]
Chen, Qiaolin [1 ]
Wang, Lin [1 ]
机构
[1] Fujian Med Univ, Dept Oncol, Fuzhou Pulm Hosp, Fuzhou 350008, Peoples R China
关键词
miR-17-5p; Lung cancer; MicroRNA; Prognosis; Serum; Survival; miR-17-92; CELL-PROLIFERATION; MICRORNA; EXPRESSION; CLUSTER; APOPTOSIS; MIR-20A; MARKERS;
D O I
10.1007/s12032-012-0353-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
miR-17-5p is abnormally expressed in various tumor types. The aim of this study was to investigate the expression level of miR-17-5p in serum of patients with lung cancer and to determine whether serum miR-17-5p expression is related to the prognosis of patients with lung cancer. RT-qPCR was used to examine expression of miRNA-17-5p in 20 pairs of lung cancer and adjacent normal tissues, and sera from 221 patients with lung cancer and 54 matched controls. The correlation of serum miR-17-5p with clinicopathological factors or prognosis of patients with lung cancer was analyzed. The expression level of miR-17-5p obviously increased in lung cancer tissues (P = 0.004). Furthermore, serum miR-17-5p expression also significantly increased in patients with lung cancer compared with healthy individuals (P = 0.03). The survival analysis showed that serum miR-17-5p expression was closely related to the survival of patients with lung cancer. Patients with high miR-17-5p expression had shorter survival times [hazard ratio (HR) = 1.767, 95 % CI 1.039-3.005, P = 0.035]. A lower expression level of serum miR-17-5p helps extend the survival of patients with lung cancer. Thus, miR-17-5p may be potential biomarker for prediction the prognosis in patients with lung cancer.
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页数:6
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共 36 条
[1]   Tyrosine phosphatase SHP2 promotes breast cancer progression and maintains tumor-initiating cells via activation of key transcription factors and a positive feedback signaling loop [J].
Aceto, Nicola ;
Sausgruber, Nina ;
Brinkhaus, Heike ;
Gaidatzis, Dimos ;
Martiny-Baron, Georg ;
Mazzarol, Giovanni ;
Confalonieri, Stefano ;
Quarto, Micaela ;
Hu, Guang ;
Balwierz, Piotr J. ;
Pachkov, Mikhail ;
Elledge, Stephen J. ;
van Nimwegen, Erik ;
Stadler, Michael B. ;
Bentires-Alj, Mohamed .
NATURE MEDICINE, 2012, 18 (04) :529-537
[2]   MicroRNA regulation of a cancer network: Consequences of the feedback loops involving miR-17-92, E2F, and Myc [J].
Aguda, Baltazar D. ;
Kim, Yangjin ;
Piper-Hunter, Melissa G. ;
Friedman, Avner ;
Marsh, Clay B. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (50) :19678-19683
[3]  
[Anonymous], COCHRANE DATABASE SY
[4]   Computed tomography screening and lung cancer outcomes [J].
Bach, Peter B. ;
Jett, James R. ;
Pastorino, Ugo ;
Tockman, Melvyn S. ;
Swensen, Stephen J. ;
Begg, Colin B. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2007, 297 (09) :953-961
[5]   Senescence is an endogenous trigger for microRNA-directed transcriptional gene silencing in human cells [J].
Benhamed, Moussa ;
Herbig, Utz ;
Ye, Tao ;
Dejean, Anne ;
Bischof, Oliver .
NATURE CELL BIOLOGY, 2012, 14 (03) :266-+
[6]   miR-17-5p as a Novel Prognostic Marker for Hepatocellular Carcinoma [J].
Chen, Ling ;
Jiang, Meng ;
Yuan, Weijie ;
Tang, Huihuan .
JOURNAL OF INVESTIGATIVE SURGERY, 2012, 25 (03) :156-161
[7]   Nasopharyngeal carcinoma: molecular biomarker discovery and progress [J].
Cho, William Chi-shing .
MOLECULAR CANCER, 2007, 6 (1)
[8]   The miR-17-5p microRNA is a key regulator of the G1/S phase cell cycle transition [J].
Cloonan, Nicole ;
Brown, Mellissa K. ;
Steptoe, Anita L. ;
Wani, Shivangi ;
Chan, Wei Ling ;
Forrest, Alistair Rr ;
Kolle, Gabriel ;
Gabrielli, Brian ;
Grimmond, Sean M. .
GENOME BIOLOGY, 2008, 9 (08)
[9]   MiR-17-92 cluster is associated with 13q gain and c-myc expression during colorectal adenoma to adenocarcinoma progression [J].
Diosdado, B. ;
van de Wiel, Ma ;
Droste, J. S. Terhaar Sive ;
Mongera, S. ;
Postma, C. ;
Meijerink, W. J. H. J. ;
Carvalho, B. ;
Meijer, G. A. .
BRITISH JOURNAL OF CANCER, 2009, 101 (04) :707-714
[10]   A polycistronic microRNA cluster, miR-17-92, is overexpressed in human lung cancers and enhances cell proliferation [J].
Hayashita, Y ;
Osada, H ;
Tatematsu, Y ;
Yamada, H ;
Yanagisawa, K ;
Tomida, S ;
Yatabe, Y ;
Kawahara, K ;
Sekido, Y ;
Takahashi, T .
CANCER RESEARCH, 2005, 65 (21) :9628-9632