Pathobiology and molecular profiling of peripheral T-cell lymphomas.

Details

Serval ID
serval:BIB_4F59E13CD825
Type
Article: article from journal or magazin.
Collection
Publications
Title
Pathobiology and molecular profiling of peripheral T-cell lymphomas.
Journal
Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program
Author(s)
de Leval L., Gaulard P.
ISSN
1520-4383[linking]
ISSN-L
1520-4391[print]
Publication state
Published
Issued date
2008
Pages
272-279
Language
english
Abstract
Peripheral T-cell lymphomas (PTCLs) are a heterogeneous group of rare diseases, usually manifesting clinical aggressiveness. Although important novel insights into the pathobiology of nodal PTCL have been gained recently from molecular profiling studies and clinico-pathological analyses, the pathogenetic molecular lesions remain to be deciphered for most entities. Angioimmunoblastic T-cell lymphoma (AITL) comprises CD4+ CXCL13+ neoplastic cells displaying overlapping immunophenotypical and molecular features with normal follicular helper T cells. This derivation might account for the presence of a prominent non-neoplastic component in AITL tissues and the clinical manifestations of the disease reflective of an immunological dysfunction. ALK+ anaplastic large cell lymphoma (ALCL), defined by ALK gene translocation with various gene partners, is composed of CD30+ ALK+ cells with a cytotoxic phenotype and usually carries a good prognosis. ALK- ALCL, now considered as a distinct disease entity, is morphologically and immunophenotypically similar to ALK+ ALCL, except for ALK expression, but has distinctive molecular features. PTCL, not otherwise specified (PTCL, NOS), the largest PTCL category, which is derived from activated CD4+ (or CD8+) T cells, is markedly heterogeneous, including at the molecular level. Gene expression profiling approaches have identified novel biomarkers of potential therapeutic interest, and suggest the existence of molecularly distinct PTCL, NOS subgroups.
Keywords
B-Lymphocytes/pathology, Gene Expression Profiling, Gene Rearrangement, Genes, T-Cell Receptor, Genetic Variation, Hematologic Neoplasms/classification, Humans, Immunoblastic Lymphadenopathy/classification, Immunoblastic Lymphadenopathy/pathology, Lymphoma, B-Cell/classification, Lymphoma, Large-Cell, Anaplastic/genetics, Lymphoma, Large-Cell, Anaplastic/pathology, Lymphoma, T-Cell, Peripheral/classification, Lymphoma, T-Cell, Peripheral/genetics, Middle Aged, Reed-Sternberg Cells/pathology, T-Lymphocytes, Helper-Inducer/pathology
Pubmed
Open Access
Yes
Create date
27/10/2010 8:41
Last modification date
20/08/2019 14:05
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