A serum microRNA signature as a prognostic factor for patients with advanced NSCLC and its association with tissue microRNA expression profiles

被引:25
作者
Guo, Jing [1 ,2 ]
Meng, Rui [1 ]
Yin, Zhongyuan [1 ]
Li, Pengcheng [1 ]
Zhou, Rui [1 ]
Zhang, Sheng [1 ]
Dong, Xiaorong [1 ]
Liu, Li [1 ]
Wu, Gang [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Canc Ctr, 1277 JieFang Ave, Wuhan 430022, Hubei, Peoples R China
[2] Qingdao Univ, Affiliated Hosp, Dept Oncol, Qingdao 266003, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
microRNAs; non-small cell lung cancer; biomarker; prognosis; CELL LUNG-CANCER; HEPATOCELLULAR-CARCINOMA; CIRCULATING MICRORNAS; DOWN-REGULATION; SURVIVAL; BIOMARKERS; DIAGNOSIS; PLASMA; ADENOCARCINOMA; PREDICTION;
D O I
10.3892/mmr.2016.5114
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of the present study was to detect microRNA (miRNA) signatures in advanced non-small cell lung cancer (NSCLC), and to study the association between miRNA expression levels in serum and tissue. A cohort of patients who had previously been diagnosed with advanced NSCLC was enrolled in the present study. miRNAs associated with prognosis, which had previously been detected in early stage NSCLC samples, were measured in the serum of the patient groups using a cross-validation method. In addition, serum miRNAs associated with progression-free survival (PFS) were detected in paired fresh tissue samples, in order to analyze the correlation between serum and tissue expression levels. A risk-score analysis was used to develop a four-miRNA signature to predict PFS. miR-1, miR-30d, miR-221 and miR-486 were identified as having a significant correlation with PFS in advanced NSCLC. miR-221 and miR-486 exhibited significant positive correlations between serum and tissue expression. Furthermore, overexpression of miR-221 and reduced expression of miR-486 increased cell proliferation, migration and invasion in vitro. In conclusion, the miRNA signature identified in the present study may be considered an independent prognostic factor of PFS in advanced NSCLC. In addition, the expression levels of miR-221 and miR-486 were significantly correlated between serum and tissue. miR-221 was identified as an oncogenic risk factor, whereas miR-486 exerted protective effects against cancer cell proliferation, migration and invasion.
引用
收藏
页码:4643 / 4653
页数:11
相关论文
共 40 条
[1]   MicroRNA signatures in tissues and plasma predict development and prognosis of computed tomography detected lung cancer [J].
Boeri, Mattia ;
Verri, Carla ;
Conte, Davide ;
Roz, Luca ;
Modena, Piergiorgio ;
Facchinetti, Federica ;
Calabro, Elisa ;
Croce, Carlo M. ;
Pastorino, Ugo ;
Sozzi, Gabriella .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (09) :3713-3718
[2]   MicroRNA-cancer connection: The beginning of a new tale [J].
Calin, George Adrian ;
Croce, Carlo Maria .
CANCER RESEARCH, 2006, 66 (15) :7390-7394
[3]   Characterization of microRNAs in serum: a novel class of biomarkers for diagnosis of cancer and other diseases [J].
Chen, Xi ;
Ba, Yi ;
Ma, Lijia ;
Cai, Xing ;
Yin, Yuan ;
Wang, Kehui ;
Guo, Jigang ;
Zhang, Yujing ;
Chen, Jiangning ;
Guo, Xing ;
Li, Qibin ;
Li, Xiaoying ;
Wang, Wenjing ;
Zhang, Yan ;
Wang, Jin ;
Jiang, Xueyuan ;
Xiang, Yang ;
Xu, Chen ;
Zheng, Pingping ;
Zhang, Juanbin ;
Li, Ruiqiang ;
Zhang, Hongjie ;
Shang, Xiaobin ;
Gong, Ting ;
Ning, Guang ;
Wang, Jun ;
Zen, Ke ;
Zhang, Junfeng ;
Zhang, Chen-Yu .
CELL RESEARCH, 2008, 18 (10) :997-1006
[4]   Detection and characterization of placental MicroRNAs in maternal plasma [J].
Chim, Stephen S. C. ;
Shing, Tristan K. F. ;
Hung, Emily C. W. ;
Leung, Tak-yeung ;
Lau, Tze-kin ;
Chiu, Rossa W. K. ;
Lo, Y. M. Dennis .
CLINICAL CHEMISTRY, 2008, 54 (03) :482-490
[5]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247
[6]   Prognostic model of pulmonary adenocarcinoma by expression profiling of eight genes as determined by quantitative real-time reverse transcriptase polymerase chain reaction [J].
Endoh, H ;
Tomida, S ;
Yatabe, Y ;
Konishi, H ;
Osada, H ;
Tajima, K ;
Kuwano, T ;
Takahashi, T ;
Mitsudomi, T .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (05) :811-819
[7]   Non-Small Cell Lung Cancer, Version 2.2013 Featured Updates to the NCCN Guidelines [J].
Ettinger, David S. ;
Akerley, Wallace ;
Borghaei, Hossein ;
Chang, Andrew C. ;
Cheney, Richard T. ;
Chirieac, Lucian R. ;
D'Amico, Thomas A. ;
Demmy, Todd L. ;
Govindan, Ramaswamy ;
Grannis, Frederic W., Jr. ;
Grant, Stefan C. ;
Horn, Leora ;
Jahan, Thierry M. ;
Komaki, Ritsuko ;
Kong, Feng-Ming ;
Kris, Mark G. ;
Krug, Lee M. ;
Lackner, Rudy P. ;
Lennes, Inga T. ;
Loo, Billy W., Jr. ;
Martins, Renato ;
Otterson, Gregory A. ;
Patel, Jyoti D. ;
Pinder-Schenck, Mary C. ;
Pisters, Katherine M. ;
Reckamp, Karen ;
Riely, Gregory J. ;
Rohren, Eric ;
Shapiro, Theresa A. ;
Swanson, Scott J. ;
Tauer, Kurt ;
Wood, Douglas E. ;
Yang, Stephen C. ;
Gregory, Kristina ;
Hughes, Miranda .
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2013, 11 (06) :645-653
[8]   miR-221 and miR-222 expression affects the proliferation potential of human prostate carcinoma cell lines by targeting p27Kip1* [J].
Galardi, Silvia ;
Mercatelli, Neri ;
Giorda, Ezio ;
Massalini, Simone ;
Frajese, Giovanni Vanni ;
Ciafre, Silvia Anna ;
Farace, Maria Giulia .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (32) :23716-23724
[9]   Serum MicroRNAs Are Promising Novel Biomarkers [J].
Gilad, Shlomit ;
Meiri, Eti ;
Yogev, Yariv ;
Benjamin, Sima ;
Lebanony, Danit ;
Yerushalmi, Noga ;
Benjamin, Hila ;
Kushnir, Michal ;
Cholakh, Hila ;
Melamed, Nir ;
Bentwich, Zvi ;
Hod, Moshe ;
Goren, Yaron ;
Chajut, Ayelet .
PLOS ONE, 2008, 3 (09)
[10]   MicroRNA-221 Targets Bmf in Hepatocellular Carcinoma and Correlates with Tumor Multifocality [J].
Gramantieri, Laura ;
Fornari, Francesca ;
Ferracin, Manuela ;
Veronese, Angelo ;
Sabbioni, Silvia ;
Calin, George Adrian ;
Grazi, Gian Luca ;
Croce, Carlo Maria ;
Bolondi, Luigi ;
Negrini, Massimo .
CLINICAL CANCER RESEARCH, 2009, 15 (16) :5073-5081