Role of molecular studies in the classification of lymphoma

被引:9
作者
Bagg, A [1 ]
机构
[1] Hosp Univ Penn, Dept Pathol & Lab Med, Minimal Residual Dis Resource Lab, Philadelphia, PA 19104 USA
关键词
classification; diagnosis; lymphoid leukemia; lymphoma; microarray; molecular genetics; prognosis; targeted therapy;
D O I
10.1586/14737159.4.1.83
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The classification of lymphomas has historically lacked both precision and accuracy, potentially compromising both optimal diagnosis and therapy. The genetic characterization of key oncogenic events and the advent of expression profiling have afforded the opportunity to understand, diagnose and treat these diseases in a much more rational and targeted manner. As exciting as these new and testable data are, it is also worth noting that molecular genetic analysis of the tumor in isolation will not be the sole arbiter of patient outcome. It is likely that we will remain reliant on traditional and sometimes subjective technologies, albeit probably to a lesser degree, with molecular studies significantly complementing, but certainly not replacing, microscopic, immunophenotypic and cytogenetic approaches. Furthermore, we will perhaps need to extend genotyping to the tumor milieu (the patient) in order to molecularly dissect drug metabolic pathways and the immune response.
引用
收藏
页码:83 / 97
页数:15
相关论文
共 106 条
[1]  
AGUIAR RC, 2002, BLOOD, V96, P4328
[2]  
Akasaka T, 2000, BLOOD, V96, P2907
[3]   BCL6 gene translocation in follicular lymphoma:: a harbinger of eventual transformation to diffuse aggressive lymphoma [J].
Akasaka, T ;
Lossos, IS ;
Levy, R .
BLOOD, 2003, 102 (04) :1443-1448
[4]   Ambivalent role of BCL6 in cell survival and transformation [J].
Albagli-Curiel, O .
ONCOGENE, 2003, 22 (04) :507-516
[5]   High frequency of t(14;18)-translocation breakpoints outside of major breakpoint and minor cluster regions in follicular lymphomas - Improved polymerase chain reaction protocols for their detection [J].
Albinger-Hegyi, A ;
Hochreutener, B ;
Abdou, MT ;
Hegyi, I ;
Dours-Zimmermann, MT ;
Kurrer, MO ;
Heitz, PU ;
Zimmermann, DR .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 160 (03) :823-832
[6]   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
[7]   Isochromosome 7q: the primary cytogenetic abnormality in hepatosplenic gamma delta T cell lymphoma [J].
Alonsozana, ELC ;
Stamberg, J ;
Kumar, D ;
Jaffe, ES ;
Medeiros, LJ ;
Frantz, C ;
Schiffer, CA ;
OConnell, BA ;
Kerman, S ;
Stass, SA ;
Abruzzo, LV .
LEUKEMIA, 1997, 11 (08) :1367-1372
[8]   Detection of BCL2 rearrangements in follicular lymphoma [J].
Aster, JC ;
Longtine, JA .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 160 (03) :759-763
[9]   Immunoglobulin heavy chain gene analysis in lymphomas - A multi-center study demonstrating the heterogeneity of performance of polymerase chain reaction assays [J].
Bagg, A ;
Braziel, RM ;
Arber, DA ;
Bijwaard, KE ;
Chu, AY .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2002, 4 (02) :81-89
[10]   Minimal residual disease: How low do we go? [J].
Bagg, A .
MOLECULAR DIAGNOSIS, 2001, 6 (03) :155-160