Clinical significance and detection of microRNA-21 in serum of patients with diffuse large B-cell lymphoma in Chinese population

被引:89
作者
Chen, Weiqun [1 ,2 ,3 ]
Wang, Hui [1 ]
Chen, Heming [4 ]
Liu, Shuiyi [1 ,3 ]
Lu, Hongda [3 ,5 ]
Kong, Deyong [1 ]
Huang, Xiaodong [2 ,3 ]
Kong, Qinzhi [2 ,3 ,5 ]
Lu, Zhongxin [1 ,2 ,3 ]
机构
[1] Cent Hosp Wuhan, Dept Lab Med, Wuhan 430014, Peoples R China
[2] Cent Hosp Wuhan, Dept Cent Lab, Wuhan 430014, Peoples R China
[3] Canc Res Inst Wuhan, Wuhan, Peoples R China
[4] Cent S Univ, Xiangya Hosp 2, Dept Cardiovasc & Thorac Surg, Changsha, Hunan, Peoples R China
[5] Cent Hosp Wuhan, Dept Oncol, Wuhan 430014, Peoples R China
关键词
sera; diffuse large B-cell lymphoma; biomarkers; microRNA-21; EXPRESSION; CANCER; GENE; CARCINOMAS; RESISTANCE; SIGNATURE; PROMOTES; TARGETS;
D O I
10.1111/ejh.12263
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background Expression patterns of microRNAs in serum are involved in potentially non-invasive biomarkers for various diseases. The purpose of this study is to examine the expression of miR-21 in serum of patients with diffuse large B-cell lymphoma (DLBCL) and to validate the significance of miR-21 in early diagnosis, genotyping, treatment options as well as its prognosis estimates of Chinese DLBCL. Methods miR-21 expression was detected by fluorescent quantity polymerase chain reaction (qPCR) in 9 DLBCL cell lines (OCI-Ly1, OCI-Ly3, OCI-Ly4, OCI-Ly7, OCI-Ly8, OCI-Ly10, OCI-Ly18, OCI-Ly19, and HBL), as well as in tumor tissue and serum samples from patients with DLBCL (germinal center B-cell-like (GCB) DLBCL 32; activated B-cell-like (ABC) DLBCL 30) and 50 healthy subjects. Results Expression of miR-21 was increased in DLBCL cell lines. Compared with the miR-21 expression of GCB subgroup (OCI-Ly1, OCI-Ly4, OCI-Ly7, OCI-Ly8, OCI-Ly18, OCI-Ly19), ABC subgroup (OCI-Ly3, OCI-Ly10, and HBL) has higher expression (t=11.18, P<0.01). Circulating miR-21 level in sera from patients with DLBCLwas associated with matched tumor tissue (r(2)=0.931, P<0.0001). Consistent with the in vitro, miR-21 expression levels in serum of patients with DLBCL [21.38(10.26-45.21)] were higher than those in serum of control cases [1.87(1.05-3.97); U=168, P=0.000]. Moreover, miR-21 expression levels in serum of patients with subgroup ABC [28.68(14.92~98.44)] were higher than that of patients with subgroup GCB [18.3(7.32~33.46); U=336, P=0.043]. miR-21 expression in serum of DLBCL with stage I and II were higher than those in stage III and IV (U=62, P=0.013 in GCB type; U=53, P=0.014 in ABC type). Compared with relapse-free survival in patients with DLBCL, high expression of miR-21 was associated with well prognosis (U=259, P=0.035). Conclusion miR-21 expressed in the serum of patients with DLBCL from Chinese was associated with clinical stage, molecular subgroup, and prognosis estimates. miR-21 may be served as a biomarker in early diagnosis, genotyping, treatment options, and prognosis estimating of Chinese DLBCL.
引用
收藏
页码:407 / 412
页数:6
相关论文
共 22 条
[1]
A MicroRNA signature associated with prognosis and progression in chronic lymphocytic leukemia [J].
Calin, GA ;
Ferracin, M ;
Cimmino, A ;
Di Leva, G ;
Shimizu, M ;
Wojcik, SE ;
Iorio, MV ;
Visone, R ;
Sever, NI ;
Fabbri, M ;
Iuliano, R ;
Palumbo, T ;
Pichiorri, F ;
Roldo, C ;
Garzon, R ;
Sevignani, C ;
Rassenti, L ;
Alder, H ;
Volinia, S ;
Liu, CG ;
Kipps, TJ ;
Negrini, M ;
Croce, CM .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (17) :1793-1801
[2]
Chen CF, 2011, METHODS MOL BIOL, V687, P113, DOI 10.1007/978-1-60761-944-4_8
[3]
Cortez Maria Angelica, 2012, Recent Results Cancer Res, V195, P151, DOI 10.1007/978-3-642-28160-0_13
[4]
Prognostic role of microRNA-21 in various carcinomas: a systematic review andmeta-analysis [J].
Fu, Xiaonan ;
Han, Yijie ;
Wu, Ying ;
Zhu, Xiaoli ;
Lu, Xin ;
Mao, Feng ;
Wang, Xuejing ;
He, Xuelian ;
Zhao, Yuhang ;
Zhao, Yulan .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2011, 41 (11) :1245-1253
[5]
Up-regulation of miR-21 Mediates Resistance to Trastuzumab Therapy for Breast Cancer [J].
Gong, Chang ;
Yao, Yandan ;
Wang, Ying ;
Liu, Bodu ;
Wu, Wei ;
Chen, Jianing ;
Su, Fengxi ;
Yao, Herui ;
Song, Erwei .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (21) :19127-19137
[6]
Confirmation of the molecular classification of diffuse large B-cell lymphoma by immunohistochemistry using a tissue microarray [J].
Hans, CP ;
Weisenburger, DD ;
Greiner, TC ;
Gascoyne, RD ;
Delabie, J ;
Ott, G ;
Müller-Hermelink, HK ;
Campo, E ;
Braziel, RM ;
Jaffe, ES ;
Pan, ZG ;
Farinha, P ;
Smith, LM ;
Falini, B ;
Banham, AH ;
Rosenwald, A ;
Staudt, LM ;
Connors, JM ;
Armitage, JO ;
Chan, WC .
BLOOD, 2004, 103 (01) :275-282
[7]
Downregulation of Spry2 by miR-21 triggers malignancy in human gliomas [J].
Kwak, H-J ;
Kim, Y-J ;
Chun, K-R ;
Woo, Y. M. ;
Park, S-J ;
Jeong, J-A ;
Jo, S. H. ;
Kim, T. H. ;
Min, H. S. ;
Chae, J. S. ;
Choi, E-J ;
Kim, G. ;
Shin, S-H ;
Gwak, H-S ;
Kim, S-K ;
Hong, E-K ;
Lee, G-K ;
Choi, K-H ;
Kim, J. H. ;
Yoo, H. ;
Park, J. B. ;
Lee, S-H .
ONCOGENE, 2011, 30 (21) :2433-2442
[8]
Detection of elevated levels of tumour-associated microRNAs in serum of patients with diffuse large B-cell lymphoma [J].
Lawrie, Charles H. ;
Gal, Shira ;
Dunlop, Heather M. ;
Pushkaran, Beena ;
Liggins, Amanda P. ;
Pulford, Karen ;
Banham, Alison H. ;
Pezzella, Francesco ;
Boultwood, Jacqueline ;
Wainscoat, James S. ;
Hatton, Christian S. R. ;
Harris, Adrian L. .
BRITISH JOURNAL OF HAEMATOLOGY, 2008, 141 (05) :672-675
[9]
MicroRNA expression distinguishes between germinal center B cell-like and activated B cell-like subtypes of diffuse large B cell lymphoma [J].
Lawrie, Charles H. ;
Soneji, Shamit ;
Marafioti, Teresa ;
Cooper, Christopher D. O. ;
Palazzo, Stefano ;
Paterson, Jennifer C. ;
Cattan, Helen ;
Enver, Tariq ;
Mager, Rachel ;
Boultwood, Jacqueline ;
Wainscoat, James S. ;
Hatton, Christian S. R. .
INTERNATIONAL JOURNAL OF CANCER, 2007, 121 (05) :1156-1161
[10]
MicroRNA-21 promotes the cell proliferation, invasion and migration abilities in ovarian epithelial carcinomas through inhibiting the expression of PTEN protein [J].
Lou, Yanhui ;
Yang, Xingsheng ;
Wang, Fuling ;
Cui, Zhumei ;
Huang, Yu .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2010, 26 (06) :819-827