학술논문

Expression and Phosphorylation of Eukaryotic Translation Initiation Factor 4E Binding Protein 1 in B-Cell Lymphomas and Reactive Lymphoid Tissues.
Document Type
Article
Source
Archives of Pathology & Laboratory Medicine. Mar2011, Vol. 135 Issue 3, p365-371. 7p. 3 Color Photographs, 1 Diagram, 2 Charts, 1 Graph.
Subject
*PROTEIN metabolism
*RNA metabolism
*B cell lymphoma
*CARRIER proteins
*IMMUNOHISTOCHEMISTRY
*LYMPH nodes
*LYMPHATIC diseases
*LYMPHOID tissue
*TUMOR markers
*WESTERN immunoblotting
*RETROSPECTIVE studies
*GENETICS
Language
ISSN
0003-9985
Abstract
Context.--Cap-mediated messenger RNA translation controlled by the eukaryotic initiation factor 4F (eIF-4F) complex plays a key role in human cancer. eIF-4F activity is controlled by a repressor binding protein (4E-BP1), which promotes translation when phosphorylated. Objective.--To examine the level of expression and phosphorylation of 4E-BP1 in various subtypes of B-cell lymphoma and reactive lymphoid tissues. Design.-Archival formalin-fixed, paraffin-embedded B-cell lymphoma samples and reactive lymphoid tissues were immunostained and examined for expression of 4EBP1 and phosphorylated 4E-BP1. Expression of components of the eIF-4F complex and unphosphorylated and phosphorylated 4E-BP1 was confirmed using Western immunoblotting on lysates of frozen lymphoma samples and reactive tissues. Results.--Immunohistochemical analysis demonstrated weak to undetectable 4E-BP1 staining within benign, reactive germinal centers (N = 10). In contrast, 4E-BP1 was consistently expressed (moderate to strong staining) in 98% of various subtypes of mature B-cell lymphoma (N = 50). 4E-BP1 expression was also demonstrable in all 4 lymph nodes with in situ or partial involvement by follicular lymphoma and in all 12 cases of BCL2-negative lymphoma. The level of phosphorylation of 4E-BP1 in lymphomas, evaluated by immunohistochemistry, was heterogeneous. Conclusions.--The immunohistochemical expression pattern of 4E-BP1 exhibits regional and cellular specificity in reactive lymphoid tissues and may offer a diagnostic tool for distinguishing reactive follicles from neoplastic B-cell proliferations. [ABSTRACT FROM AUTHOR]