miR-155 as a Biomarker in B-Cell Malignancies

被引:58
作者
Due, Hanne [1 ,2 ]
Svendsen, Pernille [1 ]
Bodker, Julie Stove [1 ]
Schmitz, Alexander [1 ]
Bogsted, Martin [1 ,3 ,4 ]
Johnsen, Hans Erik [1 ,4 ,5 ]
El-Galaly, Tarec Christoffer [1 ,4 ,5 ]
Roug, Anne Stidsholt [2 ]
Dybkaer, Karen [1 ,4 ]
机构
[1] Aalborg Univ Hosp, Dept Haematol, Hobrovej 18-22, DK-9100 Aalborg, Denmark
[2] Aarhus Univ Hosp, Dept Haematol, Tage Hansens Gade 2, DK-8000 Aarhus C, Denmark
[3] Aalborg Univ, Dept Math Sci, Fredrik Bajers Vej 5, DK-9100 Aalborg, Denmark
[4] Aalborg Univ, Dept Clin Med, Fredrik Bajers Vej 5, DK-9100 Aalborg, Denmark
[5] Aalborg Univ Hosp, Clin Canc Res Ctr, Hobrovej 18-22, DK-9100 Aalborg, Denmark
关键词
CHRONIC LYMPHOCYTIC-LEUKEMIA; GLOBAL MICRORNA EXPRESSION; MARGINAL ZONE LYMPHOMA; GENE-EXPRESSION; MIRNA EXPRESSION; BURKITT-LYMPHOMA; MALT LYMPHOMA; IN-VIVO; RNA; CLL;
D O I
10.1155/2016/9513037
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
MicroRNAs have the potential to be useful biomarkers in the development of individualized treatment since they are easy to detect, are relatively stable during sample handling, and are important determinants of cellular processes controlling pathogenesis, progression, and response to treatment of several types of cancers including B-cell malignancies. miR-155 is an oncomiR with a crucial role in tumor initiation and development of several B-cell malignancies. The present review elucidates the potential of miR-155 as a diagnostic, prognostic, or predictive biomarker in B-cell malignancies using a systematic search strategy to identify relevant literature. miR-155 was upregulated in several malignancies compared to nonmalignant controls and overexpression of miR-155 was further associated with poor prognosis. Elevated expression of miR-155 shows potential as a diagnostic and prognostic biomarker in diffuse large B-cell lymphoma and chronic lymphocytic leukemia. Additionally, in vitro and in vivo studies suggest miR-155 as an efficient therapeutic target, supporting its oncogenic function. The use of inhibiting anti-miR structures indicates promising potential as novel anticancer therapeutics. Reports from 53 studies prove that miR-155 has the potential to be a molecular tool in personalized medicine.
引用
收藏
页数:14
相关论文
共 98 条
[1]   Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling [J].
Alizadeh, AA ;
Eisen, MB ;
Davis, RE ;
Ma, C ;
Lossos, IS ;
Rosenwald, A ;
Boldrick, JG ;
Sabet, H ;
Tran, T ;
Yu, X ;
Powell, JI ;
Yang, LM ;
Marti, GE ;
Moore, T ;
Hudson, J ;
Lu, LS ;
Lewis, DB ;
Tibshirani, R ;
Sherlock, G ;
Chan, WC ;
Greiner, TC ;
Weisenburger, DD ;
Armitage, JO ;
Warnke, R ;
Levy, R ;
Wilson, W ;
Grever, MR ;
Byrd, JC ;
Botstein, D ;
Brown, PO ;
Staudt, LM .
NATURE, 2000, 403 (6769) :503-511
[2]   Splenic marginal zone lymphoma: comprehensive analysis of gene expression and miRNA profiling [J].
Arribas, Alberto J. ;
Gomez-Abad, Cristina ;
Sanchez-Beato, Margarita ;
Martinez, Nerea ;
DiLisio, Lorena ;
Casado, Felipe ;
Cruz, Miguel A. ;
Algara, Patrocinio ;
Piris, Miguel A. ;
Mollejo, Manuela .
MODERN PATHOLOGY, 2013, 26 (07) :889-901
[3]   Biomarkers and surrogate endpoints: Preferred definitions and conceptual framework [J].
Atkinson, AJ ;
Colburn, WA ;
DeGruttola, VG ;
DeMets, DL ;
Downing, GJ ;
Hoth, DF ;
Oates, JA ;
Peck, CC ;
Schooley, RT ;
Spilker, BA ;
Woodcock, J ;
Zeger, SL .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2001, 69 (03) :89-95
[4]   Nanoparticle-based therapy in an in vivo microRNA-155 (miR-155)-dependent mouse model of lymphoma [J].
Babar, Imran A. ;
Cheng, Christopher J. ;
Booth, Carmen J. ;
Liang, Xianping ;
Weidhaas, Joanne B. ;
Saltzman, W. Mark ;
Slack, Frank J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (26) :E1695-E1704
[5]   MicroRNA expression profile in splenic marginal zone lymphoma [J].
Bouteloup, Marie ;
Verney, Aurelie ;
Rachinel, Nicolas ;
Callet-Bauchu, Evelyne ;
Ffrench, Martine ;
Coiffier, Bertrand ;
Magaud, Jean-Pierre ;
Berger, Francoise ;
Salles, Gilles Andre ;
Traverse-Glehen, Alexandra .
BRITISH JOURNAL OF HAEMATOLOGY, 2012, 156 (02) :279-281
[6]   MicroRNA-200 is commonly repressed in conjunctival MALT lymphoma, and targets cyclin E2 [J].
Cai, Jiping ;
Liu, Xiaoyu ;
Cheng, Jinwei ;
Li, You ;
Huang, Xiao ;
Li, Yuzhen ;
Ma, Xiaoye ;
Yu, Hongyu ;
Liu, Huimin ;
Wei, Ruili .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2012, 250 (04) :523-531
[7]   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
[8]   The 2008 WHO classification of lymphoid neoplasms and beyond: evolving concepts and practical applications [J].
Campo, Elias ;
Swerdlow, Steven H. ;
Harris, Nancy L. ;
Pileri, Stefano ;
Stein, Harald ;
Jaffe, Elaine S. .
BLOOD, 2011, 117 (19) :5019-5032
[9]   Role of microRNAs and microRNA machinery in the pathogenesis of diffuse large B-cell lymphoma [J].
Caramuta, S. ;
Lee, L. ;
Ozata, D. M. ;
Akcakaya, P. ;
Georgii-Hemming, P. ;
Xie, H. ;
Amini, R-M ;
Lawrie, C. H. ;
Enblad, G. ;
Larsson, C. ;
Berglund, M. ;
Lui, W-O .
BLOOD CANCER JOURNAL, 2013, 3 :e152-e152
[10]   MicroRNA-155 modulates the interleukin-1 signaling pathway in activated human monocyte-derived dendritic cells [J].
Ceppi, Maurizio ;
Pereira, Patricia M. ;
Dunand-Sauthier, Isabelle ;
Barras, Emmanuele ;
Reith, Walter ;
Santos, Manuel A. ;
Pierre, Philippe .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (08) :2735-2740