The differential expression of galectin-1 and galectin-3 in normal lymphoid tissue and non-Hodgkin's and Hodgkin's lymphomas

被引:46
作者
D'Haene, N
Maris, C
Sandras, F
Dehou, MF
Remmelink, M
Decaestecker, C
Salmon, I
机构
[1] ULB, Pathol Lab, Erasmus Univ Hosp, B-1070 Brussels, Belgium
[2] Ctr Morphol Pathol Prat Anat, Brussels, Belgium
[3] Free Univ Brussels, Inst Pharm, Toxicol Lab, Belgian Res Fund Fundamental Res,FNRS Belgium, B-1050 Brussels, Belgium
关键词
galectin; lymphoma; angiogenesis; diagnosis;
D O I
10.1177/039463200501800304
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The WHO classification of lymphomas was established on the basis of clinical, morphological, immunohistochemical and genetic criteria. However, each entity displays its own spectrum of clinical aggressiveness. Treatment success varies widely and is not predictable. Since galectins are involved in oncogenesis and the physiology of immune cells, we investigated whether galectin-1 and galectin-3 immunohistochemical expression could differ in 25 normal lymphoid tissues, 42 non-Hodgkin's and 14 Hodgkin's lymphomas. Immunohistochemical galectin expression was submitted to semi-quantitative and quantitative (computer-assisted microscopy) evaluations. This study is completed by an analysis (by means of quantitative RT-PCR) of galectin-3 mRNA expression in 3 normal lymph nodes, 3 follicular lymphomas (FLs) and 3 diffuse large B-cell lymphomas (DLBCLs). The data show that in normal lymphoid tissue, lymphocytes do not express galectin-1 and rarely express galectin-3. In contrast, galectin-3 was expressed in 8 of the 16 DLBCL cases and in I of the 8 FL cases. Furthermore, galectin-3 mRNA was expressed 3-times more in the DLBCLs than in the FLs. While the blood vessel walls of the lymphomas expressed galectin-1, the vessel walls of normal lymphoid tissues did not. This expression of galectin-1 in blood vessel walls was correlated with vascular density. The present study thus shows that DLBCL can be distinguished from normal lymphoid tissue and other lymphomas on the basis of galectin-3 expression.
引用
收藏
页码:431 / 443
页数:13
相关论文
共 67 条
[11]   Caspase-3 is dually regulated by apoptogenic factors. mitochondrial release and by SAPK/JNK metabolic pathway in leukemic cells exposed to etoposide-ionizing radiation combined treatment [J].
Di Pietro, R ;
Centurione, L ;
Sabatini, N ;
Bosco, D ;
Sancilio, S ;
Garaci, F ;
Rana, R ;
Cataldi, A .
INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 2004, 17 (02) :181-190
[12]   Cell adhesion receptors in lymphoma dissemination [J].
Drillenburg, P ;
Pals, ST .
BLOOD, 2000, 95 (06) :1900-1910
[13]   Regulation of CD45-induced signaling by galectin-1 in Burkitt lymphoma B cells [J].
Fouillit, M ;
Joubert-Caron, R ;
Poirier, F ;
Bourin, P ;
Monostori, E ;
Levi-Strauss, M ;
Raphael, M ;
Bladier, D ;
Caron, M .
GLYCOBIOLOGY, 2000, 10 (04) :413-419
[14]  
FREEDMAN AS, 1993, SEMIN HEMATOL, V30, P318
[15]   Regulated expression of galectin-1 during T-cell activation involves Lck and Fyn kinases and signaling through MEK1/ERK, p38 MAP kinase and p70S6 kinase [J].
Fuertes, MB ;
Molinero, LL ;
Toscano, MA ;
Ilarregui, JM ;
Rubinstein, N ;
Fainboim, L ;
Zwirner, NW ;
Rabinovich, GA .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2004, 267 (1-2) :177-185
[16]   Detection of TT virus in lymph node biopsies of B-CELL lymphoma and Hodgkin's disease, and its association with EBV infection [J].
Garbuglia, AR ;
Iezzi, T ;
Capobianchi, MR ;
Pignoloni, P ;
Pulsoni, A ;
Sourdis, J ;
Pescarmona, E ;
Vitolo, D ;
Mandelli, F .
INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 2003, 16 (02) :109-118
[17]   Discovery and characterization of an epithelial-specific galectin in the endometrium that forms crystals in the trophectoderm [J].
Gray, CA ;
Adelson, DL ;
Bazer, FW ;
Burghardt, RC ;
Meeusen, ENT ;
Spencer, TE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (21) :7982-7987
[18]  
Holzmann B, 1998, CURR TOP MICROBIOL, V231, P125
[19]   An anti-apoptotic role for galectin-3 in diffuse large B-cell lymphomas [J].
Hoyer, KK ;
Pang, M ;
Gui, D ;
Shintaku, IP ;
Kuwabara, I ;
Liu, FT ;
Said, JW ;
Baum, LG ;
Teitell, MA .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 164 (03) :893-902
[20]  
Iurisci I, 2000, CLIN CANCER RES, V6, P1389