Identification of microRNA expression patterns and definition of a microRNA/mRNA regulatory network in distinct molecular groups of multiple myeloma

被引:203
作者
Lionetti, Marta [1 ]
Biasiolo, Marta [2 ]
Agnelli, Luca [1 ]
Todoerti, Katia [1 ]
Mosca, Laura [1 ]
Fabris, Sonia [1 ]
Sales, Gabriele [2 ]
Deliliers, Giorgio Lambertenghi [1 ]
Bicciato, Silvio [3 ]
Lombardi, Luigia [1 ]
Bortoluzzi, Stefania [2 ]
Neri, Antonino [1 ]
机构
[1] Univ Milan, Dept Med Sci, Hematol Ctr Trapianti Midollo Osseo 1, Fdn Ist Ricovero & Cura,Carattere Sci Policlin, I-20122 Milan, Italy
[2] Univ Padua, Dept Biol, Lab Computat Biol, Padua, Italy
[3] Univ Modena & Reggio Emilia, Dept Biomed Sci, Modena, Italy
关键词
TYROSINE-PHOSPHATASE-EPSILON; ALLELIC IMBALANCES; CLASSIFICATION; REVEALS; CANCER; MICROARRAY; GENOMICS; LEUKEMIA; BIOLOGY; CELLS;
D O I
10.1182/blood-2009-08-237495
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To date, little evidence of miRNA expression/deregulation in multiple myeloma has been reported. To characterize miRNA in the context of the major multiple myeloma molecular types, we generated miRNA expression profiles of highly purified malignant plasma cells from 40 primary tumors. Furthermore, transcriptional profiles, available for all patients, were used to investigate the occurrence of miRNA/predicted target mRNA pair anticorrelations, and the miRNA and genome-wide DNA data were integrated in a subset of patients to evaluate the influence of allelic imbalances on miRNA expression. Differential miRNA expression patterns were identified, which were mainly associated with the major IGH translocations; particularly, t(4; 14) patients showed specific overexpression of let-7e, miR-125a-5p, and miR-99b belonging to a cluster at 19q13.33. The occurrence of other lesions (ie, 1q gain, 13q and 17p deletions, and hyperdiploidy) was slightly characterized by specific miRNA signatures. Furthermore, the occurrence of several allelic imbalances or loss of heterozygosity was found significantly associated with the altered expression of miRNAs located in the involved regions, such as let-7b at 22q13.31 or miR-140-3p at 16q22. Finally, the integrative analysis based on computational target prediction and miRNA/mRNA profiling defined a network of putative functional miRNA-target regulatory relations supported by expression data. (Blood. 2009;114:e20-e26)
引用
收藏
页码:E20 / E26
页数:7
相关论文
共 53 条
[1]   Molecular classification of multiple myeloma:: A distinct transcriptional profile characterizes patients expressing CCND1 and negative for 14q32 translocations [J].
Agnelli, L ;
Bicciato, S ;
Mattioli, M ;
Fabris, S ;
Intini, D ;
Verdelli, D ;
Baldini, L ;
Morabito, F ;
Callea, V ;
Lombardi, L ;
Neri, A .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (29) :7296-7306
[2]   Integrative genomic analysis reveals distinct transcriptional and genetic features associated with chromosome 13 deletion in multiple myeloma [J].
Agnelli, Luca ;
Bicciato, Silvio ;
Fabris, Sonia ;
Baldini, Luca ;
Morabito, Fortunato ;
Intini, Daniela ;
Verdelli, Donata ;
Callegaro, Andrea ;
Bertoni, Francesco ;
Lambertenghi-Deliliers, Giorgio ;
Lombardi, Luigia ;
Neri, Antonino .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2007, 92 (01) :56-65
[3]   Upregulation of translational machinery and distinct genetic subgroups characterise hyperdiploidy in multiple myeloma [J].
Agnelli, Luca ;
Fabris, Sonia ;
Bicciato, Silvio ;
Basso, Dario ;
Baldini, Luca ;
Morabito, Fortunato ;
Verdelli, Donata ;
Todoerti, Katia ;
Lambertenghi-Deliliers, Giorgio ;
Lombardi, Luigia ;
Neri, Antonino .
BRITISH JOURNAL OF HAEMATOLOGY, 2007, 136 (04) :565-573
[4]   A SNP Microarray and FISH-Based Procedure to Detect Allelic Imbalances in Multiple Myeloma: An Integrated Genomics Approach Reveals a Wide Gene Dosage Effect [J].
Agnelli, Luca ;
Mosca, Laura ;
Fabris, Sonia ;
Lionetti, Marta ;
Andronache, Adrian ;
Kwee, Ivo ;
Todoerti, Katia ;
Verdelli, Donata ;
Battaglia, Cristina ;
Bertoni, Francesco ;
Deliliers, Giorgio Lambertenghi ;
Neri, Antonino .
GENES CHROMOSOMES & CANCER, 2009, 48 (07) :603-614
[5]   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
[6]   Molecular pathogenesis and a consequent classification of multiple myeloma [J].
Bergsagel, PL ;
Kuehl, WM .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (26) :6333-6338
[7]   MMSET deregulation affects cell cycle progression and adhesion regulons in t(4;14) myeloma plasma cells [J].
Brito, Jose L. R. ;
Walker, Brian ;
Jenner, Matthew ;
Dickens, Nicholas J. ;
Brown, Nicola J. M. ;
Ross, Fiona M. ;
Avramidou, Athanasia ;
Irving, Julie A. E. ;
Gonzalez, David ;
Davies, Faith E. ;
Morgan, Gareth J. .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2009, 94 (01) :78-86
[8]   MicroRNAs and chromosomal abnormalities in cancer cells [J].
Calin, G. A. ;
Croce, C. M. .
ONCOGENE, 2006, 25 (46) :6202-6210
[9]   Chronic lymphocytic leukemia: interplay between noncoding RNAs and protein-coding genes [J].
Calin, George A. ;
Croce, Carlo M. .
BLOOD, 2009, 114 (23) :4761-4770
[10]   MicroRNA-cancer connection: The beginning of a new tale [J].
Calin, George Adrian ;
Croce, Carlo Maria .
CANCER RESEARCH, 2006, 66 (15) :7390-7394