The EML4-ALK transcript but not the fusion protein can be expressed in reactive and neoplastic lymphoid tissues

被引:14
作者
Sozzi, Gabriella [2 ]
Martelli, Maria Paola [1 ]
Conte, Davide [2 ]
Modena, Piergiorgio [2 ]
Pettirossi, Valentina [1 ]
Pileri, Stefano A. [3 ]
Falini, Brunangelo [1 ]
机构
[1] Univ Perugia, Inst Hematol, I-06100 Perugia, Italy
[2] Ist Nazl Tumori, I-20133 Milan, Italy
[3] Univ Bologna, Policlin S Orsola, Unit Hematopathol, Bologna, Italy
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2009年 / 94卷 / 09期
关键词
lung cancer; anaplastic lymphoma kinase (ALK); EML4; fusion transcripts; lymphoma; fusion protein; kinase inhibitors; LARGE-CELL LYMPHOMA; LUNG-CANCER; ANAPLASTIC LYMPHOMA; NPM-ALK; DISEASE; SPECTRUM; GENES;
D O I
10.3324/haematol.2009.008045
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rearrangements involving the ALK gene define two distinct entities in the new 2008 WHO classification of lymphoid neoplasms, i.e. ALK+ anaplastic large cell lymphoma and a rare subset of ALK+ diffuse large B-cell lymphoma. Recently, rearrangements involving ALK and the echinoderm microtubule associated protein-like 4 (EML4) gene were described as a specific genetic alteration in about 6% of non-small cell lung cancer (NSCLC). We investigated the expression of EML4-ALK mRNA and protein in 51 reactive and 58 neoplastic lymphoid tissues. EML4-ALK transcripts were detected in 3/51 (5.9%) of reactive lymphoid tissues and 12/58 (20.7%) of lymphomas of different categories, including follicular lymphoma, diffuse large B-cell lymphoma and Hodgkin's disease. Notably, none of these cases expressed the EML4-ALK fusion protein at Western blotting samples and immunohistochemistry. These results indicate that EML4-ALK rearrangements are not specific of NSCLC and raise yet unsolved questions about their role in promoting human neoplasms.
引用
收藏
页码:1307 / 1311
页数:5
相关论文
共 20 条
[1]   ALK-positive lymphoma:: A single disease with a broad spectrum of morphology [J].
Benharroch, D ;
Meguerian-Bedoyan, Z ;
Lamant, L ;
Amin, C ;
Brugières, L ;
Terrier-Lacombe, MJ ;
Haralambieva, E ;
Pulford, K ;
Pileri, S ;
Morris, SW ;
Mason, DY ;
Delsol, G .
BLOOD, 1998, 91 (06) :2076-2084
[2]   Characterization of t(2;5) reciprocal transcripts and genomic breakpoints in CD30+ cutaneous lymphoproliferations [J].
Beylot-Barry, M ;
Groppi, A ;
Vergier, B ;
Pulford, K ;
Merlio, JP .
BLOOD, 1998, 91 (12) :4668-4676
[3]   ALK is not expressed in Hodgkin disease [J].
Camilleri-Broët, S ;
Audouin, J ;
Fermé, C ;
Brière, J ;
Pulford, K ;
Gaulard, P ;
Diviné, M ;
Macintyre, E ;
Delsol, G ;
Berger, F .
BLOOD, 2001, 97 (06) :1901-1902
[4]  
Delsol G., 2008, WHO Classification of Tumors of Hematopoietic and Lymphoid Tissues, P312
[5]  
Falini B, 1999, BLOOD, V93, P2697
[6]   ALK expression defines a distinct group of T/null lymphomas ("ALK lymphomas") with a wide morphological spectrum [J].
Falini, B ;
Bigerna, B ;
Fizzotti, M ;
Pulford, K ;
Pileri, SA ;
Delsol, G ;
Carbone, A ;
Paulli, M ;
Magrini, U ;
Menestrina, F ;
Giardini, R ;
Pilotti, S ;
Mezzelani, A ;
Ugolini, B ;
Billi, M ;
Pucciarini, A ;
Pacini, R ;
Pelicci, PG ;
Flenghi, L .
AMERICAN JOURNAL OF PATHOLOGY, 1998, 153 (03) :875-886
[7]   Proteins encoded by genes involved in chromosomal alterations in lymphoma and leukemia: clinical value of their detection by immunocytochemistry [J].
Falini, B ;
Mason, DY .
BLOOD, 2002, 99 (02) :409-426
[8]  
Falini B, 1999, BLOOD, V94, P3509
[9]   TPM3-ALK and TPM4-ALK oncogenes in inflammatory myofibroblastic tumors [J].
Lawrence, B ;
Perez-Atayde, A ;
Hibbard, MK ;
Rubin, BP ;
Dal Cin, P ;
Pinkus, JL ;
Pinkus, GS ;
Xiao, S ;
Yi, ES ;
Fletcher, CDM ;
Fletcher, JA .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (02) :377-384
[10]   The NPM-ALK and the ATIC-ALK fusion genes can be detected in non-neoplastic cells [J].
Maes, B ;
Vanhentenrijk, V ;
Wlodarska, I ;
Cools, J ;
Peeters, B ;
Marynen, P ;
De Wolf-Peeters, C .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (06) :2185-2193